IB Biology Study Notes

IB Biology Study Notes
Unit 1 – Cells
1.1
 Living Organisms are composed of cells, they are the smallest unit of life, they
come from pre existing cells.
 A virus is a non-cellular structure consisting of DNA or RNA surrounded by a

protein coat.
Advantages of Light Microscopes Advantages of Electron Microscopes

 Enables user to see larger structures  Magnifies over 500,000x
within eukaryotes and distinguish individual  Resolving power for biological specimen
prokaryotes. around 1nm
 They are user-friendly: small, portable,  3-D view instead of one.
easily-prepared slides, relatively cheap to  Interior view
buy and maintain.  See organelles than cannot be observed
 Both living and dead material may be w/ light microscope
viewed.
 Material is rarely distorted by
preparation.
 Thicker materials may be viewed
 Allows experimenter to view image
directly.
 Allows for specimen to be observed in
natural state.
 Slides are simple to prepare
 Faster
 Color
 Can observe movement.
 An organelle is a discrete structure within a cell, and has a specific function
Membrane Thickness – 1 nm
Viruses – 100 nm
Bacteria – 1um
Organelles – up to 10 um
Most cells – up to 100 um
 Surface area to volume ratio – as the size increases the ratio decreases, thus
decreases the rate of exchange.
 Unicellular organisms carry out all of the functions of life, including metabolism,
response, homeostasis, growth, reproduction and nutrition.
1.2
 Prokaryote – a cell that lacks any membrane bound organelles. Prokaryotes

belong to their own kingdom, bacteria.
Cell Wall – Gives cell it’s shape, protects the cell and prevents the cell from absorbing
too much water
Ribosomes – small granules found in all cells. Made of RNA and protein, they are
important in protein synthesis. Produce protein for use inside cells
Slime/Capsule – surrounds the cell wall of bacteria, it helps to keep the cell from being
digested or drying out.
Flagellum – An organelle that propels a cell
Plasma Membrane – Controls the movement of things in and out of the cell. Protects
organelles inside from the outside environment. Made of phospholipids
 Prokaryotic cells divide by binary fission
1.3
 N:Nucleus
 PM: plasma membrane
 M: mitochondria
 rER: Rough endoplasmic
reticulum
 GA: Golgi apparatus
 L: Lysosome
 MV: Microvilli
see 2.3.2 form functions of the cell

components.
2.3.2 Annotate the diagram from 2.3.1 with the functions of each named structure.
Nucleus: This is the largest of the organelles. The nucleus contains the chromosomes which
during interphase are to be found the nucleolus.
 The nucleus has a double membrane with pores(NP).

 The nucleus controls the cells functions through the
expression of genes.
 Some cells are multi nucleated such as the muscle fibre
Plasma membrane: controls which substances can enter and exit a cell. It is a fluid
structure that can radically change shape. see 2.4
 The membrane is a double layer of water
repellant molecules.
 Receptors in the outer surface detect signals
to the cell and relay these to the interior.
 The membrane has pores that run through
the water repellant layer called channel
proteins.
Mitochondria: location of aerobic respiration and a majot synthesis of ATP region..
 Double membrane organelle.

 Inner membrane has folds called
cristae. This is the site of oxidative
phosphorylation.
 Centre of the structure is called the
matrix and is the location of the
Krebs cycle.
 Oxygen is consumed in the synthesis
of ATP on the inner membrane
 The more active a cell the greater the
number of mitochondria.
Rough endoplasmic reticulum (rER): protein synthesis and packaging into vesicles.
rER form a network of tubules with a maze

like structure.
 In general these run away from the nucleus

 The 'rough' on the reticulum is caused by the
presence of ribosomes.
 Proteins made here are secreted out of the
cell
Ribosomes: the free ribosome produces proteins for internal use within the cell.
Golgi apparatus: modification of proteins prior to secretion.
 proteins for secretion are modified

 possible addition of carbohydrate or
lipid components to protein
 packaged into vesicles for secretion
Lysozyme:
 Vesicles in the above diagram that have formed on the golgi apparatus.
 Containing hydrolytic enzymes.
 Functions include the digestion of old organelles, engulfed bacteria and viruses.
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2.3.3 Identify structures from 2.3.1 in electron micrographs of liver cells.(2)
Identify: To find an answer from a given number of possibilities.
To identify structures within an electron micrograph it is necessary to know the scale at

which the image has been taken. Look around the image to find the nucleus and then the
mitochondria. In a plant cell there will also be the cell wall, chloroplasts and the vacuole to
identify.
Nucleus:
In an electron micrograph the nucleus will be the largest of the

organelles.
In this image there is a dark stained region called the nucleolus

which is the location of the DNA.
The membrane has pores which allow the entry of cell signal
molecules, nucleotides and the exit of mRNA.
Generally the nucleus appears spherical however there are cells in which the nucleus has
more unusual shape such as the multi-lobbed white blood cells.
Plasma membrane:
This image shows the junction between two liver

cells. The image has been manipulated for clarity to
see the two adjoining plasma membranes.
Notice the mitochondria to the left and the rER to the

right of the membranes.
Mitochondria:
This micrograph of a mitochondria shows:
 Double outer membrane

 Folded inner membrane called the
cristae.
 Matrix of the mitochondria
These features are common to all mitochondria. Notice the rER above the mitochondria for
scale and the dark granules of glycogen below the organelle.
Endoplasmic reticulum (rER).
The rER runs vertical in the image. Note the

dark spots which are the ribosomes.
 A cell with a great deal of rER is producing

proteins for secretion outside of the cell.
 The network of endoplasmic tubules allows
proteins to be moved around within the
cytoplasm before final packaging and secretion.
Golgi apparatus:
The golgi apparatus in the diagram

forms a stack of membrane envelopes
on top of each other.
 Vesicles containing proteins fuse with

the structure.
 The proteins are modified inside the
apparatus usually with the addition of
non-protein substances.
Lysozyme:
 simple membrane bound vesicle containing hydrolytic enzymes

 produced in the golgi apparatus.
 used to digest engulfed bacteria or viruses or old organelles
 used to digest macromolecules
 hydrolytic enzymes are retained within the vesicle membrane to prevent
autodigestion of the cell.
2.3.4 Comparison of prokaryotic and eukaryotic cells (3).
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Diffusion: passive movement of particles from a region of high concentration to a region
of low concentration.
Osmosis is the passive movement of water molecules from regions of lower solute
concentration to a region of higher solute concentration
2.5.1 Outline the stages in the cell cycle, including interphase (G1, S, G 2), mitosis
and cytokinesis (2).
outline means to give a brief summary
The cell cycle describes the major phases of activity in the division of a cell. The length of
the cell cycle depends on the particular function of the cell. For example bacterial cells can
divide every 30 minutes under suitable conditions, skin cells divide about every 12 hours on
average, liver cells every 2 years, and muscle cells never divide at all after maturing.
The total length

of a cell cycle
varies depending
on the specialised
function of a cell.
 Interphase (grey)
is the longest
phase which itself
occurs in three
stages.
 G1 The cell
performs its
normal
differentiated
function. Protein
synthesis/ mitochondria replication/ chloroplast replication.
 S DNA replication. At this point the mass of DNA in the cell has doubled.
 G2 Preparation for cell division
 Phases of mitosis (see 2.5.4)
 Cytokinesis: division of the cytoplasm to form two daughter cells.
An appreciation of mitosis only comes when you have studied the structure of nucleic acids,
DNA replication and some gene expression. At that point you will understand better the
significance of the S phase= DNA replication.
2.5.2 State that tumours (cancers) are the result of uncontrolled cell division and
that these can occur in any organ or
tissue(1)
calculation. State means to give a specific name, value or other brief answer without
explanation or
'Tumours are not foreign invaders. They arise from the same material used by the body to
construct its own tissues. Tumours use the same components -human cells- to form the
jumbled masses that disrupt biological order and function and, if left unchecked, to bring
the whole complex, life sustaining edifice that is the human body crashing down'.
R. Weinberg, R. (1998) One Renegade Cell. London:Phoenix, Science Masters Series.
'Cancer is, in essence a genetic disease'
Volgestein and Kinzler
 Tumours (cancers) are a cell mass formed as a result

of uncontrolled cell division.
 They can occur in any tissue.
 Stomach cancer
Not on the syllabus and just for interest
Cells are normally in state of repressed mitosis. The default condition is for the cell to
progress into mitosis and cytokinesis. In a tumour something happens (mutation to the
proto-oncogene) to release the repression of cell division. There appear to be atleast two
groups of genes which are important in the formation of tumours:
a) Oncogenes, which if accidentally or inappropriately activated increase the risk of tumour

formation.
b) Tumour Suppressor genes (TSG) which as the name suggests normally are actively
suppressing tumours. If these are switched off by a mutation then the suppression is lost.
Evolution of Cancer:
1. Multi step carcinogenisis: Cancers do not arise as invasive malignant metastatic
(spreading) tumours. Rather they follow a series of steps that begins with a contained
benign growth. A cell will eventually arise within the benign mass which is more aggressive
in its growth rate and with a tendency to invade surrounding tissue. These cells have a
selective advantage and will become the dominant cell type within the tumour. The cancer
has now progresses to an aggressive invasive form. In the next stage a further mutation to
a cell makes this cell not only aggressive and invasive but with a tendency to break up and
spread to other tissues (metastasis). This latter tumour stage is the malignant tumour
2. Oncogene activation: There are within a cell many proteins that are either cell signals
or control proteins within the cell cycle. The proteins are coded for by genes that are
referred to as proto-oncogenes. When transformed by mutagenic agents( chemicals,
radiation) they are transformed (mutated) into oncogenes. It is these oncogenes that when
expressed will cause a loss of control of division within that cell. There is then the
production of a protein that signals the cell internally to increase the rate of cell division.
Since this gives these cells a selective advantage they become more common at the
expense of non-mutated cells. These types of genes that create transform cell function were
discovered as early as 1910.
3. Tumour Suppressor deactivation. An alternative or additional feature is the idea of

tumour suppression which holds cell division in check. The tumour suppressor could simply
be a protein that inhibits the cell cycle. Alternatively there are proteins that repair DNA
which also suppress tumour suppression by maintaining the integrity of DNA. Therefore the
suppression is removed and the cell progresses into uncontrolled cell division.
This might suggestion from this description therefore is that the development of a cancer
will require atleast two mutations; one of the proto-oncogene; two of the tumour
suppressor.
Cancer exerts its deleterious effect on the body by: destroying the surrounding adjacent
tissues: e.g. compressing nerves, eroding blood vessels, or causing perforation of organs:
replacing normal functioning cells in distant sites: e.g. replacing blood forming cells in the
bone marrow, replacing bones leading to increased calcium levels in the blood, or in the
heart muscles so that the heartfails.
2.5.3 State that interphase is an active period in the life of a cell when many
metabolic reactions occur, including protein synthesis, DNA replication
and an increase in the number of mitochondria and/or chloroplasts (1).
State means to give a specific name, value or other brief answer without explanation or
calculation.
 The cell specialises to a particular function in a process called differentiation.

 Through gene expression and protein synthesis there is a specialisation of cell
structure and function.
 During this interphase the cell carries out this specialist function.
 The length of the interphase varies from one type of cell to another.
 G1 follows cytokinesis. The cell is involved in the synthesis of various proteins which
allow the cell to specialise.
 S-phase involves the replication of DNA molecules which takes place prior to the
phases of mitosis.
 G2 preparation for the phases of mitosis which involves the replication of
mitochondria and in the case of plants, the chloroplast.
2.5.4 Describe the events that occur in the four phases of mitosis (prophase,
metaphase, anaphase and telophase (2).
Describe means to give a detailed account.
Super coiling: Eukaryotic DNA is combined with histone proteins and non-histone proteins
to form chromatin. The method of folding of chromatin is specific to each chromosome
leaving genes in predictable positions and a distinctive overall chromosome shape. The
human cell has a DNA length of about 1.8 m this has to be packed into a nucleus which has
only a 5 um diameter. This packaging process requires up to a X 15,000 reduction. This
super coiling makes the structure so dense that it can be see with a light microscope during
the phases of mitosis.
In this sequence only one chromosome is illustrated so that we can more clearly follow the
process. In a human a complete diagram would have 46 chromosomes each replicating and
condensing and separating.
a)The cell membrane is intact

during this the interphase. The
chromosomes cannot be seen
during G1,S and G2.
b) G1,Within the nucleus, genes

on the chromosome are being
expressed to carry out normal
cell function (interphase).
Remember you cannot see
chromosomes at this stage. The
diagram has a 'see's through'
the nuclear membrane so you
can see inside. In reality it
would look just like cell a).
c) S-phase in which DNA

replication occurs and the
chromosomes are copied. The copies called sister chromatids are held together by a
protein to form the centromere. It is still not possible to see this happen with an intact cell.
d) Early Prophase in which the sister chromatids have condensed by super coiling. Note
the formation of the spindle microtubules and their attachment to centrioles. The nuclear
membrane will now break down to reveal sister chromatids. The internal arrangements of
chromosomes can now be seen with a light microscope.
e) Metaphase the chromosomes arranged on the equator of the cell each attached to a
spindle microtubule at the centromere
f) Anaphase: The spindle microtubules contract and pull apart the sister chromatids one to
each pole of the cell. The centromere splits allowing the sister chromatids to be separate.
g) Telophase: at each pole there are separate groups of the replicated chromosomes the
spindles is degenerating
h) Cytokinesis: the cell membrane begins to separate, dividing the cell into two new cells.
The nuclear membrane is reforming around each cell.
i) Two daughter cells are formed. They are genetically identical to each other and in effect
the basis of a clone. (see 2.5.6)
Notice that cell a) begins with one chromosome and that by step h) there are two cells each
with a copy of that chromosome.
As suggested by cell theory, all cells have come from other cells.
2.5.5 Explain how mitosis produces two genetically identical nuclei (3).
Explain means to give a detailed account of causes, reasons or mechanisms.
 The process of cell division produces genetically identical daughter cells.
 Conservation of chromosome number. The chromosome number in each of the

daughter cells is the same as that of the original parental cell
 During the S-phase, each chromosome is copied exactly. The two copies of each
chromosome are held together by a protein structure called a centromere.
 Therefore just prior to the beginning of the phases of mitosis there is actually double
the number of chromosomes present in a cell.
 Each chromosome in this state is represented by a pair of sister chromatids. These
give the now classic cross image of the DNA
(see image below)
This pair of sister chromatids image was taken

during one of the phases of mitosis.
The two sister chromatids are held together at the

centromere
The arms of the chromatids are visible because of a

condensation of the molecule called super coiling.
This condenses the molecule some x 15,000 times of its original length The pairs of sister
chromatids is a non-random organisation. The position of genes is predicable within the
structure seen here. Also there is a unique shape to each of the chromosomes.
Mitosis makes sure that each cell obtains a copy of each of the chromosomes in the parental
cell.
However, it is the process of DNA replication during the S-phase that actually copies each
DNA molecules to make mitosis possible.
State that growth, embryonic development, tissue repair and asexual

reproduction involve mitosis(1).
calculation.
 Growth: multicellular organisms increase their size through growth. This growth
involves increasing the number of cells through mitosis. These cells will differentiate
and specialise their function.
 Embryonic development is when the fertilised egg cell (zygote) divides to form the
multicellular organism. Each cell in the organisms is identical (genetically) to all the
other cells. However, each cell will express only a few of its genes to determine its
overall specialisms, a process called differentiation. In this way a stem cell may
becomes a muscle, or it may become a nerve cell or any one of the many different
kinds of cells found in a complex multicellular organism. The best book about this
process for the interested reader is
 Tissue Repair: As tissues are damaged they can recover through replacing damaged
or dead cells. This is easily observed in a skin wound. More complex organ
regeneration can occur in some species of amphibian.
 Asexual Reproduction: This the production of offspring from a single parent using
mitosis. The offspring are therefore genetically identical to each other and to their
“parent”- in other words they are clones. Asexual reproduction is very common in
nature, and in addition we humans have developed some new, artificial methods.
Bacteria DO NOT asexually reproduce by mitosis but rather by a process called
Binary Fission.
3.2.2 Identify amino acids, glucose, ribose and fatty acids from diagrams showing
their structure(2).
Identify means to find an answer from a given number of possibilities.
The following are examples of the most common organic molecules in living things:
Monosaccharide sugars. These are the monomers from which larger polymer molecules
are constructed. Molecules like glucose and fructose
are metabolically active molecules usually stored in
an inactive, insoluble polysaccharide form.
 Glucose: C6H12O6 this is a hexose sugar (six

carbons) most commonly found in this ring
structure.
 Glucose will be known to most students as a
product of photosynthesis or the substrate
molecule for respiration.
 Glucose is also found in a polymer as starch,
glycogen or cellulose.
 All bonds are covalent.
 Glucose is a reducing sugar and will give
positive (Brick red) precipitate in a Benedicts
test.
 Glucose is metabolically active compound
Glucose is soluble and has osmotic effects when

in solution
This is an alternative diagram of glucose where the carbons are

assumed to be at each of the corners or ends of the lines
(bonds). In this image the carbons are numbered so you can
compare to the diagram above. Normally such numbers would
be omitted form a diagram. These shorthand diagrams allow
organic molecules to be drawn faster. There are examples further down the page of this
type of diagram.
 Ribose: Pentose (5 carbon sugar).

 Ribose is part of one the important organic
molecules in photosynthesis, ribulose
bisphosphate. (RUBP)
 A modified version of ribose, deoxyribose is
perhaps best known for its role in Deoxyribonucleic
acid or DNA where it forms part of the sugar
phosphate backbone. The chemical properties of
deoxyribose are very different from the properties of ribulose
 Both Ribose and Glucose will attract water molecules (hydrogen bonding ) to form
solutions.
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Amino Acids: There are 20 common amino acids found in the protein structures of living
things. Amino acids are monomers which combine to form the larger polypeptides. In turn
polypeptides combine to form proteins. Proteins molecules are the basis of enzymes and
many cellular and extra cellular components.
This model shows the structure of the

general amino acid. If you build one in a
molecular kit you will appreciate better the
3D structure.
 Each of the common amino acids has the

same structure as the one shown except that
the R group is different.
 Amino acids are soluble

This is an alternative way to draw the general

amino acid structure.
 This diagram illustrates the 'amino' group which

is -NH2
 There is also the acidic group -COOH which ionizes in solution to form an -COO-and
H+groups
 This acid group is known as a carboxylic acid group .
This is an illustration of the smallest of the

amino acids, Glycine.
 Notice that Glycine has an amino group,

carboxylic acid group and a R group = H
 A common source of glycine is sugar cane.
This image shows a common amino acids,

Alanine
 Note the similarity in structure with glycine

but this time the R group is -CH3
 Students are not required to know the
structure of all 20 common amino acids
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Fatty Acids: These molecules are the basis of triglycerides and many other types of lipid.
These molecules are also the basis of the phospholipid molecules that form the bilayer of
the cell membrane.
The image shows a basic

saturated (no double bonds)
fatty acid.
 There is a methyl group (-CH3)

at one end of the chain.
 Chain is the formed from a series
of covalently bonded carbons
saturated with hydrogens.
 The chain is non-polar and
hydrophobic
 The carbonyl group is polar
making this ends of the molecule hydrophilic.
The complex diagram of the fatty acid can be abbreviated to this simpler diagram.
This image show the unsaturated

double bond which is characteristic of
animal fats.
 If there are many double bonds the fatty acid is known as polyunsaturated.
Micelle
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 In water fatty acid molecules arrange

themselves into spheres called
micelles.
 The polar carbonyl groups on the
outside in contact with water
molecules.
 The non-polar tail sections are in the
centre away from water.
 This is an important aspect of fat
digestion and membrane structure.
3.2.3 List three examples each of monosaccharides, disaccharides and

polysaccharides(1)
List means to Give a sequence of names or other brief answers with no explanation.
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3.2.4 State one function of glucose, lactose and glycogen in animals, and of
fructose, sucrose and cellulose in plants(1)
calculation.
3.2.6 State three functions of lipids(1).
calculation.
3.2.7 Compare the use of carbohydrates and lipids in energy storage(3).
Compare means to give an account of similarities and differences between two (or more)
items, referring to both (all) of them throughout.
3.3.1 Outline DNA nucleotide structure in terms of sugar (deoxyribose), base and
phosphate(2)
Outline means to give a brief account or summary. .


Sugar is deoxyribose which differs

from ribose in having one less oxygen
on carbon 2.
 Phosphate is the PO4-3 group.

 Bases are nitrogen based ring structures of which there are 4 different kinds.
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3.3.2 State the names of the four bases in DNA (1).
calculation.
Nucleosides are the

combination of sugar and
base only and are not
required for the syllabus.
You will however see the
terms used in the literature.
 These are the four bases which are universally found in living things.
 In 1950 Edwin Chargaff determined that within an organism there was same approx
the same amount of A as T and the same amount of G=C.
 Chargaff surveyed a wide variety of organsims and found in the ratio of A:T, G:C
consistently across the range of his specimens
 These ratios became known as Chargaff's ratio's and would later prove to be a
significant clue to the structure of DNA.
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3.3.3 Outline how DNA nucleotides are linked together by covalent bonds into a
single strand (2).
Outline means to give a brief summary.

 DNA
is
composed of two polynucleotides chains.

 Nucleotides are covalently bonded between the phosphate of one nucleotide to the
C3 of the second nucleotide.
 The phosphate group creates a bridge connecting C5 on one pentose with the C3 on
the next pentose.
 The bond is a phosphodiester bond which indicates that there are two covalent bonds
formed between the -OH and the acidic phosphate group.
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Polynucleotide
The image is of one polynucleotide chain.
Note:
 The sugar phosphate backbone which

provides the stable backbone of one of
the helices.
 Covalent bonds that link the
nucleotides along the backbone of the
molecule.
 The bases projecting into the centre.
 At one end there is pentose with 5' (said "five prime" ) carbon which is free from
bonding.
 At the other end there is a 3' carbon free from bonding to other nucleotides.
 Additional nucleotides are joined to the 3' end of the existing polynucleotide chain.
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3.3.4 Explain how a DNA double helix is formed using complementary base
pairing and hydrogen bonds (3).
History:
complementary means matching, is different from complimentary, which means being nice.
You may recall that in 1950 Edwin Chargaff working in Columbia University USA had
determined that the mass of the bases(in a DNA speciment) formed ratios of A:T and G:C.
This held true when taking samples from individuals within a population or when comparing
species across large classification divides. In the cell of any organism the mass of Adenine
seems to be about the same as the mass of Thymine. The mass of Cytosine seems to be
about the same as the mass of Guanine.
Three years later the significance of Chargaff's Rule was realize by Watson and Crick at the
Cavendish Laboratory in Cambridge, England. Watson an American geneticist and Crick an
English physicist began model building DNA based on a collection of results from other
researchers, including Chargaff. The model building technique uses the principles of
chemistry such as molecular structure and bond angles as then developed by Linus Pauling.
Together with the data from X-ray crystallography studies (the combined work of Wilkins
and Franklin ) they began to build DNA and part of that process involved the pairing of the
bases in the centre of the helix.
The molecular distance from Adenine combined with Thymine is the same as the molecular
distance between Guanine combined with cytosine. This gave a uniform distance that could
fill the centre of the helix.
The complementary bases are formed (A-T, G-C) when hydrogen bonded occur between the
two bases in a pair.
Refer to the diagram and notes in the next section..
3.3.5 Draw and label a simple diagram of the molecular structure of DNA(1) .
Draw means to be able to represent by means of pencil

lines.
This image of DNA shows the arrangement of the two

polynucleotide chains but not the helical shape which can
be seen in the space filled model below.
This is image shows:
 Two polynucleotide chains.

 Two anti-parallel chains. (definition).
a)The number followed by the prime (') determined the

carbon in deoxyribose free from bonding to another
nucleotide.
b) Note that the two chains are in opposite directions 3'

to 5' is parallel to 5' to 3' chain.
 The anti-parallel chains have a uniform distance

(2nm) between the outside of the two sugar
phosphate backbones
 Complementary base pairs: Inside the double
helix bases form one strand hydrogen bond to
bases on the opposite strand but always in the
following way:
a) Adenine hydrogen binds to Thymine
b) Cytosine hydrogen bonds to Guanine

The three-dimensional structure of DNA was discovered
in 1953 by Watson and Crick in Cambridge, using the
experimental data of Wilkins and Franklin in London, for
which work they won a Nobel prize. Ms Franklin
however died before the award and the Nobel Prize is
never awarded posthumously.
The main features of the structure are:
 DNA is double-stranded, so there are two

polynucleotide stands alongside each other.
 The strands are antiparallel, i.e. they run in

opposite directions thus 5' to 3' is parallel to 3'
to 5'.
 The two strands are wound round each other to
form a double helix (not a spiral, despite what
some textbooks say).
 The two strands are joined together

by hydrogen bonds between the bases.
 The bases therefore form base pairs, which are

like rungs of a ladder.
 The base pairs are specific. A only binds to T

(and T with A), and C only binds to G (and G with C).
 These are called complementary base pairs (or sometimes Watson-Crick base pairs).
(A-T and G-C)
 This means that whatever the sequence of bases along one strand, the sequence of
bases on the other stand must be complementary to it.
3.4.1 Explain DNA replication in terms of unwinding the double helix and
separation of the strands by helicase,
followed by formation of the new complementary strands by DNA
polymerase.(3)

1. The original double
helix molecule.
2. Helicase enzyme
breaks the hydrogen
bonds between
complementary base
pairs. This unzips the
double helix at a
position called the
replication fork.
3. There is an
abundant supply of
nucleotides in the
nucleus for the
formation of the new
polynucleotides.
4. Nucleotides base
pair to the bases in the
original strands.
5. DNA polymerase
joins together the nucleotides together with strong covalent phosphodiester bonds To form
a new complementary polynucleotide strand.
6. The double strand reforms a double helix under the influence of an enzyme.
7 Two copies of the DNA molecule form behind the replication fork. These are the new
daughter chromosomes.
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Speed of replication:
 DNA replication can take a few hours and this limits the speed of cell division.
 Bacteria can replicate quickly because of the relatively small amount of DNA.
 Eukaryotic organism's accelerate DNA replication by having thousands of replication
forks along the length of the DNA molecule.
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3.4.2 Explain the significance of complementary base pairing in the conservation

of the base sequence of DNA.(3)
 The significance of the mechanism outlined above is that the DNA molecule is copied
precisely from one cell generation to the next.
 In a unicellular organism this means that the total genome is successfully copied into
each new generation.
 In the multi-cellular organism all cells contain an exact copy of the total genome
(even though not fully expressed).
 Genes (base sequences) are faithfully passed from one generation to the next.
 The genes (base sequences) which the reader possess have been passed from
generation to generation until they arrived in you now. With minor and rare
modification the base sequences copied by DNA replication and successfully passed
on through sexual reproduction. Your base sequences have been copied for
thousands of years.
3.5.1Compare the structure of RNA and DNA.(3).
Compare means to give an account of similarities and differences between two (or more)
items, referring to both (all) of them throughout.
3.5.2 Outline DNA transcription in terms of the formation of an RNA strand

complementary to the DNA strand by RNA polymerase.(2).
Outline means to give a brief account or summary.

This model illustrate the process of transcription that takes place in the nucleus. The DNA
base sequence of the gene is copied into messenger RNA (mRNA)
The DNA helix is

opened at the
position of the
gene.
 The helix is
unwound by RNA
polymerase
 RNA nucleotides are found in the nucleus space.
 One of the polynucleotide chains act as a template for mRNA
 Free nucleotides base pair with DNA nucleotides
 The phosphodiester bonds on the mRNA chain are formed by RNA polymerase
 mRNA is a single polynucleotide chain but the base thymine is replaced by Uracil.
 After the mRNA is complete the molecule detach's from the DNA and leaves the
nucleus for the cytoplasm ribosomes.
 The DNA helix reforms.
3.5.3 Describe the genetic code in terms of codons composed of triplets of bases.
(2)
'You can treat the genetic code like a dictionary in which sixty-four words in one language
(the sixty-four possible triplets of a four-letter alphabet) are mapped onto twenty-one
words in another language (twenty amino acids plus a punctuation mark). The odds of
arriving at the same 64:21 mapping are less than one in a million million million million
million. Yet the genetic code is in fact literally identical in all animals, plants and bacteria
that have ever been looked at. All living things are certainly descended from a single
ancestor'
R.Dawkins, (1995),River out of Eden.
Well actually the code is nearly Universal. Interestingly the DNA in the mitochondria and
chloroplast is slightly different in both prokaryotic and eukaryotic organisms. There are also
some Protists in which UAA and UAG code for glutamine rather than acting as stop codons.
The significance of these differences is as yet unclear
The genetic code:
 A polynucleotide is a sequence of bases

 Bases are either A T G or C
 There are 4 bases which operate in sets of 3 (a triplet).= 43possible triplets of DNA
=64 triplets
 There are 20 common amino acids
 Therefore 64 triplets are mapped to 20 amino acids
 However there is a 'punctuation' triplets.
 Therefore the mapping of the code is 64: 21
3.5.4 Explain the process of translation, leading to polypeptide formation.(3)
 mRNA is translated into an amino acid sequence (mapping above)
The location of translation is the ribosomes

in the cytoplasm.
 Ribosomes are also composed of RNA

(rRNA) which acts as a catalyst for the
translation of the mRNA.
 Free ribosomes form polypeptides (proteins
) for internal cell use.
 Ribosomes on the endoplasmic reticulum synthesis proteins for secretion.
mRNA from the nucleus locates onto

the ribosome.
The start codon (initiation codon) AUG


occupies one of two rib some site.
 In this image the second site is
occupied by CUG codon.
 The ribosome moves along the mRNA
 One mRNA can have many ribosomes (polysome) which accelerates protein
synthesis.

Activation is a process in which Transfer RNA (tRNA) molecules attach to specific
amino acids.
 The tRNA molecule an anti-codon, three bases that are complementary to the codons
on mRNA.
 In heterotrophs the amino acids for activation come form consumed protein in the
diet.
The first codon (AUG) bonds to the

tRNA anti-codon UAC.
 This tRNA carried the amino acid

Methionine.
 The second tRNA (GAC) binds to the
second site with mRNA codon CUG
 The second tRNA carried the amino
acid Leucine.
 Note that codon-anticodon binding is
antiparallel
The link between the tRNA and the

amino acid Methionine is broken.
 The bond energy is transferred to form

a peptide bond between methionine
and Leucine.
 The first tRNA is released form the
ribosome first site.
 This tRNA molecule moves away to
pick up more methionine.

The ribosome move one mRNA codon

to the right (in this image).
 mRNA now occupied site one on the

ribosome
 The mRNA codon is UGC which has the
complementary tRNA of ACG and is
charged with Serine.
 This occupied site site on the
ribosome.
The bond between tRNA and Leucine is

broken.
 The bond energy is transferred to form

a peptide bond between Leucine and
Serine.
 The tRNA for leucine is released form
site one.
 Then ribosome shift to the right and
the process repeats itself until the stop
codon is encountered.
 As the amino acid chain is built the polypeptide self assembles into the correct
shape. It essentially folds up due to intra-molecular forces such as hydrogen bonds.
3.5.5 Discuss the relationship between one gene and one polypeptide.(3)
Discuss means to Give an account including, where possible, a range of arguments for and
against the relative importance of various factors, or comparisons of alternative hypotheses.
Theory: One gene is transcribed and translated to produce one polypeptide.
Some proteins are composed of a number of polypeptides and in this theory each
polypeptide has its own gene.
e.g. haemoglobin is composed of 4 polypeptides (2 of each type) and there is a gene for
each type of polypeptide.
This theory, like so many in biology has exceptions. e.g.
1) Some genes code for types of RNA which do not produce polypeptides.
2) Some genes control the expression of other genes.
3.6.1 Define enzyme and active site.(1)
Define means to give the precise meaning of a word, phrase or physical quantity.
globular proteins
 catalysts which speed up

biological reactions
 unchanged by the reaction
 specific to their substrate

 active site is the
position on the enzyme
occupied by the
substrate
 affected by temperature and pH
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3.6.2 Explain enzyme–substrate specificity. (3)

a) Large
globular
protein enzyme
b) Active
Site where the
substrate
combines to
the enzyme
c)Substrate
which fits the
active site
d) Activated complex. The substrate is weakened to allow the reaction.
e)Unchanged enzyme/ re-used at low concentrations
f) Product of the reaction
other keypoints from the hypothesis:
 The active site is often composed of open loops of polar amino acids on the exterior
of the enzyme molecule.
 Enzyme specificity is due to the complementary shape of the active site and the
substrate.
 Enzymes work at low concentrations because they are unaffected by the reaction and
can return for more substrate.
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3.6.3 Explain the effects of temperature, pH and substrate concentration on
enzyme activity.(3)
Effect of temperature on the rate of an enzyme catalysed reaction:
(a) As the temperature increases enzyme

stability decreases. The kinetic energy of
the enzyme atoms increases causing
vibrations in the enzyme molecule that
lead to the hydrogen bonds to breaking,
shape changes in the active site.
(b) As the temperature increases the

kinetic energy of the substrate and enzyme
molecules also increases. Therefore more
collisions of the substrate with the active
site and the formation of activated
complex's and product. The rate of
reaction is increasing.
(c) The optimal temperature (X) is the

highest rate of reaction. Compromise
between decreasing enzyme stability and
kinetic energy of the reactants.
(d) Higher temperature increases the kinetic energy of the enzyme atoms so much that
they break bonds, change shape of the active site.
The main diagram is often simplified to this diagram which still shows
the three key stages in the reaction.
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The effect of pH on the rate of an enzyme catalysed reaction:
pH also affects the rate

of reaction of an
enzyme catalysed
reaction.
 At the optimal pH (a) or

(b) the maximum rate
of reaction is achieved.
 Above or below the
optimal pH the rate
decreases.
 The change in rate is
because bonds are
made and broken which change the shape of the active site and therefore decrease
the rate of reaction.
 The two enzyme shown in the image illustrate the fact that different enzymes can
have very different optimal pH.
 e.g. Blue curve = pepsin (a)= pH3, Red curve =salivary amylase (b)= pH 7.2
Effect of substrate
concentration on the rate of an
enzyme catalysed reaction:
(a) As the substate concentration is

increased the rate of reaction
increases.
There are more collisions between the substrate and the enzyme such that more activated
complex's are formed and therefore product per unit time.
(b) Further increases in substrate also increase the rate but proportionately less than
previously.
The number of occupied active site is increasing and there is competition for the active site.
(c) The rate is constant.
The enzyme active site is fully saturated with substrate such that adding more substrate
does not increase the rate of reaction. The enzymes molecules are fully occupied converting
substrate to product and any substrate must await a free active site before conversion to
product.
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3.6.4 Define denaturation.(1)
Denaturation is a structural change in a protein that results in the loss (usually

permanent) of its biological properties.
Temperature:(see section 3.6.3)
 Temperature rises cause the average kinetic energy of the enzyme atoms to
increase.
 This vibration breaks the weakest bonds first, which in the enzyme are the hydrogen
bonds.
 The breaking of bonds, changes the shape of the enzyme.
 Change the shape of the enzyme changes the shape of the active site.
 Change the shape of the active site prevents substrate from entering.
 The rate of reaction reduces or stops.
pH: (see section 3.6.3)
 At pH lower than the optimal pH the concentration of H+ in the solution will be higher
than normal.
 The hydrogens will tend to be attracted to electronegative regions of the enzyme
protein.
 Bonds are formed or changed as a consequence of the additional H+ which changes
the shape of the enzyme molecule.
 Changes in shape, change the active site shape.
 Changes in active site shape reduces the ability of the substrate to bind with the
active site.
 This reduces the rate of reaction that changes substrate to product.
 The rate of reaction reduces.
 For pH values above the optimum breaks bonds in the same way and have the same
reductions in the rate of reaction
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3.6.5 Explain the use of lactase in the production of lactose-free milk.(3)
 Lactose is a disaccharide (glucose + Galactose) milk sugar

 Around 90% of all humans show some kind of lactose intolerance.
 People who are lactose intolerant can drink milk if it is lactose free.
 Lactase is an enzyme extracted from yeast that can digest the milk sugar to glucose
and galactose.
4.1.1 State that eukaryote chromosomes are made of DNA and proteins.(1)
calculation.
 The chromosome is composed of

two main molecules.
a) DNA
b) Proteins called histones.
 This image was taken shortly after

DNA a replication but before the
prophase. It is composed of two
daughter chromatids joined at the
centromere.
 The chromosome is super coiled by a factor around x16,000. The DNA molecule is
about 1.8m long but is located in the nucleus which is only 10um in diameter!
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4.1.2 Define gene, allele and genome. (1)
 Gene:a heritable factor that controls

a specific characteristic.
 Allele: one specific form of a gene,
differing form other alleles by one or
a few bases only and occupying the
same gene locus as other alleles of
that gene.
 Genome: the whole genetic
information of the organism.
4.1.3 Define gene mutation. (1)
 Gene mutation is a change in the base sequence of an allele.

 The changed base sequence may produce a different amino acid sequence in the
protein translated.
 The changed base sequence may not change the protein because of the degenerate
nature of the genetic code.
 The expression of the mutated gene may or may not be beneficial to the organism.
 Substances that cause mutation are called mutagens and include chemicals and
radiation.
Mutation was coined by Hugo de Vries a dutch researcher who at the time was testing the
work of mendel. His research at the begriming of the 20th Century even suggested that
sudden changes in gene might explain an evolutionary 'jumping' mechanisms rather than
the gradual mechanisms suggested by Darwinism. Subsequently it has been shown that the
plant that de Vries was working on has unusual genetic behaviour.
Mutations are not rare, even as you read these pages you are accumulating thousands of
mutations and if you are male the mutation rate is even higher. Most mutations will not
improve condition but just occasionally against all the odds this is the case. Mutation of
course creates the raw material for the process of evolution. Cellular machinery acts against
mutation with the presence of all sort of enzymes that correct the frequent errors.
Nevertheless look around you and take in the diversity of life, at any level you care to
consider the cause of this variation is mutation.
The production of mutation is in its self a series of random mistakes. Mutagens are the
cause of mutations, radiation is a well know examples but there is also chemical-
mutagenesis as discovered by Charlotte Albach. As mentioned the mutation is random and
not directional, an animal exposed to a cold environment is just as likely to produce
mutations which have advantages in warm climates as it is to a cold climate but it is even
more likely to produce a mutation that has nothing to do with climate.
That said the rate of mutation is balance between the environmental mutagen attaching the
genome and the corrective mechanisms such as the polymerase enzymes or corrective DNA
enzymes. But why does mutation occur at all? Or for that matter why is the rate not very
very high? The answer is not clear but perhaps the rate of mutation is a consequence of
evolution itself. No mutation would result in an inflexible genome incapable of responding
(as a gene pool) to the environmental changes of time. Too much mutation would render
the organsims largely non functional and compromise its survival. The 'allowed' rate
provides sufficient variation to respond to environmental change whilst not compromising
the integrity of the organisms physiology. An interesting discover which in directly support
this view is the discovery that some bacteria
 A mutation story
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4.1.4 Explain the consequence of a base substitution mutation in relation to the

processes of transcription and translation, using the example of sickle-cell
anemia.(3)
Sickle cell anaemia is a genetic disease.
Frequency ia about 1 in 655 African Americans
The disease is inherited not contracted by infectious routes.
Sickle cell anaemia at the tissue level:
(a) Normal haemoglobin has two of four

proteins changed in the mutation.
(b) The normal biconcave disc shape of the

red blood cell is changed to a 'sickle' shape.
(c) In addition to not carrying oxygen

correctly (anaemia) the cells also causes
local clots (infarctions) such as is shown in
the kidney tubules. This leads to necrosis
(death) of the tubules, kidney damage, kidney failure and possible to death.
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Genetics of
Sickle Cell.
The gene
locus for
the normal
beta chain
of
haemoglobin is on chromosome 11.
 The normal allele carried the triplet GAG at the sixth amino acid position for the beta
chain (146 amino acids).
 This transcribed and translates into the negatively charged Glutamic acid.
 The mutation changes a single base (T replaces A) and this transcribes and
translates into the amino acid Valine.
 Valine has a neutral charge and the result is a change in the shape of the beta chain
with long needle like structures forming.
 This gene is noted for many mutations and it is estimated that some 5% of humans
carry one or other variants.
.2.1 State that meiosis is a reduction

division of a diploid nucleus to
form haploid nuclei.(1)
State means to give a specific name, value or

other brief answer without explanation or
calculation.
Meiosis is a reduction division of a diploid

nucleus(2n) to form a haploid nucleus (n).
For clarity the nuclear membrane has been

omitted from the diagram.
 (a) The cell is in G1 of the interphase and has a total of 2 chromosomes, 2n=2.
 (b) The S phase of the interphase is DNA replication.
 (c) In G2 of the interphase the cell has two daughter chromatids per chromosome,
the cell mass of DNA has doubled.
 (d) Meiosis occurs in a series of phases similar to mitosis ut with significant
differences.
 (e) The diploid cell has divided to form haploid gamete cells (n=1).
 (f) The homologous pair of chromosomes has been separated (red from blue).
One diploid cell which undergoes meiosis produces four haploid gametic cells.
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4.2.2 Define homologous chromosomes. (1)
Define means to give the precise meaning

of a word, phrase or physical quantity.
 Homologous chromosomes form

pairs within the nucleus and during
cell division.
 The name suggest that both
members of the pair share certain
structural characteristics.
 They are the same length of
chromosomes.
 They have the same shape of
chromosomes.
 They carry the same genes in the
same gene loci.
 The forms of the gene found on the homologous pairs are the alleles of the gene that
an individual may posses. Note that for every gene there are normally two alleles in
the individual.
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4.2.3 Outline the process of meiosis, including pairing of homologous
chromosomes and crossing over, followed by two divisions, which results
in four haploid cells. (2)
Outline means to give a brief account or summary.
Meiosis is a form of cell division that produces gametes. It takes place in the reproductive
organs and shows variation in how long the process occurs. Although meiosis can produce
millions of gametes in a short period of time in comparison to mitosis in the body it is
relatively rare.
The stages of meiosis are shown below but begins with some diagrams about Interphase as
a reminder. In the diagrams homologous pairs are shown in different colours ((red with
blue), (purple with green)). The organism shown is an animal cell with a diploid number
(2n)= 4. Therefore we expect to see four gametes each with a haploid number (n) =2.
Meiosis I: This is the first of two sets of divisions. In meiosis one the prophase, metaphase,
anaphase and telophase will divide the cell into two and separate the homologous pairs.
This is perhaps the most significant step in terms of genetics.
Interphase:
(a) The nuclear membrane is intact and the chromosomes inside

cannot be seen. At this stage the chromosomes are not greatly
coiled or condensed which allows genes to be expressed. Each
DNA molecule is about 1.8m long but still wound sufficiently
such that it can be contained inside a 10um nucleus.
(b) In the G1 stage of the Interphase each chromosome is a

single DNA molecule (+histones). Here we can see (although in-
reality you cannot since the nucleus is intact) that there are four
chromosomes and the diploid number of the cell is 2n=4. Red
and blue are a homologous pair as are green and purple.
(c) In S1 of the interphase the DNA molecules replicate. Each copy (sister chromatids) are
held together at the centromere (black dot). The cell is now preparing for the meiotic
division in which:
Chromosome number will be halved and the Homologous chromosomes will be separated
(d):Early prophase, the nuclear membrane is breaking down.
The spindle of microtubules is forming from opposite ends of the

cell.
Centrioles organise the spindle construction at the poles of the

cell.
(e) The pairs of sister chromatids attach to the spindle

microtubules at the centromere.
The DNA is condensing by super coiling, this will reach it peak in

the metaphase.
(f) The pairs of chromatids will move up and down the between the poles but gradually
move towards the equatorial plate (centre) of the cell.
The nucleus has now disappeared and the chromosomes are dense enough to be seen with
a light microscope. Note that the red and blue homologous pair are 'crossing over' , see
metaphase for details.
Prophase is the longest of the meiotic phases of cell division. In humans the process of
meiosis in the testes can take up to a month form the diploid cell to the mature sperms cell.
In human females the process begins as a foetus whilst still in the uterus but does not
complete until the instance of fertilisation many years later.
(g) The metaphase is marked by all pairs of sister chromatids
aligned on the equator.
The chromosomes are at their most condensed and therefore

most visible at the metaphase.
(h) Cross-over. Notice that the chromosome of one

homologous chromosome is exchanging with the chromosome of
the parallel non-sister chromosome.
Cross-over is the exchange of genetic material between non-

sister chromatids during Prophase I but is most readily seen
during the metaphase.
The point at which the chromosomes exchange genetic information is called

the chiasma. This may occur many times along a chromosome and not just once as shown
in the diagram.
(i) Early anaphase with the homologous pairs are aligned

together on the equatorial plate of the cell
The spindle microtubules contract and pull the homologous pairs

(alleles) apart.
The homologous pairs separate one to either pole. This is the

case with all homologous pairs.
(j) Late anaphase the pairs of chromatids are moving to the

poles.
Notice that there has been an exchange of genetic material on

the 'arm' of the red and blue homologous pair.
New combinations of genes are not found on the same chromosome.
(K) Illustrates how to identify anaphase by the 'arrow' shape make by the pair of sister
chromatids points towards the poles.
(l) chromosomes are now in two sets at opposite ends of the cell.
Each set contains one from each of the homologous pairs.
In some species a nuclear membrane may form, in others there is

a progression straight into Prophase II.
The cell membrane 'pinches' towards the centre in a 'cleavage

furrow' the membrane will fuse at a central point and the cell will
have divided in half.
This marks the end of meiosis one (reduction division) in which the homologous pairs have
been separated.
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Meiosis II: involves the separation of the sister chromatids

and looks very like mitosis.
(m) The nuclear membrane breaks down if present.
Spindles reform ( shown here in the vertical plane only to

distinguish from the diagrams above).
Centrioles begin the organisation of the spindle microtubules.

Pairs of sister chromatids will attach one to each spindle microtubule set.
(n) All Pairs of sister chromatids aligned on the equatorial

plate of the cell.
(o) The spindle fibres contract and the pairs of sister

chromatids separate.
Each pole receives one of the chromosomes ( one chromatid).
(p) Nuclear membranes form around each of the tetrad of

haploid game cells.
Notice that each cell contains two chromosomes n=2

(haploid).
Notice that the homologous pairs are separated (no red

with blue, no purple with green)
There are some unusual chromosomes with exchanged genetic material due to cross-over.
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Non-syllabus information:
Fertilisation = n + n = 2n
Two cells (from meiosis) one the female (egg) the other the male sperm (n) will join
together their sets of chromosomes to form a new complete diploid set, this is called
fertilisation.
The diploid offspring are genetically unique and show differences to other individuals both
their parents, siblings and others in the population. The members of a population show
differences (variation) for a given characteristic. This is the basis of one of the remarkable
contributions of Charles Darwin to biology, population thinking , which is to say that a
population shows variation. Of course Darwin new little of the details of meiosis.
4.2.4 Explain that non-disjunction can lead to changes in chromosome number,

illustrated by reference to Down
syndrome (trisomy 21). Objective level (3)
Non-disjunction is an error in meiosis produce cells with unusual combinations of

chromosomes.
(a) This is the diploid parental cell (2n=2)
(b) S-phase involves DNA replication during the

interphase.
(c) Pairs of sister chromatids are formed during

the interphase
(d) meiosis should separate; i) Homologous

pairs ii) sister chromatids, so that each cell
contains one chromosome (in this example).
(e) Has an extra red chromosome so that sister

chromatids have failed to separate during
meiosis II. This games has one extra
chromosomes
(f) This gamete has one less chromosome that it should have (none in this case).
(g) These gametes are normal
Non-disjunction can also occur during meiosis I in which case all the tetrad are affected.
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Example: Downs Syndrome
Trisomy 21: An individual with Down's

syndrome has three copies of
chromosome 21.
During meiosis the sister chromatids have

not been separated (non-disjunction) so
that the gamete has had 24
chromosomes (23 + i extra chromosome
number 21).
At fertilisation when the chromosomes

form new homologous pairs the 21stpair
actually is a triplet.
The image to the left shows a set of

human chromosomes in their homologous
pairs.
Chromosome 21 shows trisomy.
Down's is called a syndrome because it shows wide variation in the symptoms and signs of
the condition. Individuals can experience learning and social problems along with additional
physiological abnormalities. That said, I have personally met an individual with Down's
syndrome so mild that they had passed many public examinations. As always we must be
ever so careful to jump top conclusions about assigning labels to individuals.
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4.2.5 State that, in karyotyping, chromosomes are arranged in pairs according to

their size and structure.(1).
State measn to give a specific name, value or other brief answer without explanation or
calculation.
 Pictures can be taken of the human chromosomes during the metaphase.

 They can then be arranged into pairs on the basis of size and structure.
 The chromosomes appear as pairs of sister chromatids.

 There are 23 pairs (46 chromosomes) therefore this is human
 In this case the 23rdpair in this case are one long pair of chromatids (X-chromosome)
and one very short (Y chromosome).
 This is a male human.
 There is no visible chromosomal abnormality.
4.3.1 Define genotype, phenotype, dominant allele, recessive allele, codominant

alleles, locus, homozygous, heterozygous, carrier and test cross.(1)
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4.3.2 Determine the genotypes and phenotypes of the offspring of a monohybrid

cross using a Punnett grid.(3)
Determine means to find the only possible answer.
It is possible using genetic crosses to determine the genotype and phenotype of the
offspring. The method used is called the Punnett square which is a simple grid which allows
the genotypes and phenotypes to be determined methodically.
When you begin genetic crosses it is worth writing out in full the calculation and only later
start to abbreviate your calculations. This may seem very time consuming but it will prepare
you properly for the questions asked in the examination.
In the following example a very long hand form is used that includes images of
chromosomes and alleles to help us track what it taking place. I strongly advise that
students always think about what is taking place in the stages of meiosis and fertilisation.
Monohybrid genetic crosses: genetics involving one gene.
 Example: Pea plants and the texture of their seed coats.

 The characteristic of seed coat texture is controlled by by one gene with two alleles.
 The seed coat can be either smooth or rough.
 Smooth coat is dominant to rough coat.
 One parent is homozygous dominant and the other is homozygous recessive.
Step 1: Write an allele key

using the upper case letter for
the dominant allele and the
lower case latter for the
recessive. (here S and s). It is
actually better to use easily
distinguished letter such as L
and l, Q and q and so on.
Step 2: Write out the parental

phenotype cross.
Step 3: Write down the

genotypes of the
parents(diploid).
In this case they are both

homozygous
Step 4: Write down the

genotype of the gametes
(haploid).
In this case since both alleles

are the same in appearance
they can only produce on
genotype of gamete for this
gene.
Step 5 : In the Punnett square write down the possible fertilisations.
Remember these are just probabilities (chance fertilisations).
Step 6: Write out the genotypes and ratio of the offspring.
Step 7. Write out the phenotypic ratio.
The drawings help to visualize where the alleles are going. However the aim is just to use
the allele code letters.
F= filial (first generation of the homozygous parent cross.) Note that they are all
heterozygous.
F1 Cross = F1 (heterozygote) x F1 (heterozygote)
Phenotype = Smooth coat seed x Smooth coated seed:
Step 1: use the same allele key as

above.
Step 2: Smooth Coat X Smooth coat
Step 3: Ss X Ss
Meiosis will separate the homologous

pairs (Ss).
Step 4: Gamete genotypes are S and

s for both parents.
Step 5: Enter possible fertilisations

into the Punnett grid. Note this time
each parent will produce two types of
gamete. The chance of producing on
or other type of gamete is p= 0.5
( 50%) or 1 in 2.
Step 6. Write out the gamete

genotype and ratio.
1 SS : 2Ss: 1ss
Step 7: Write out the phenotypic ratio:
3 Smooth coats: 1 Rough Coat

Remember that homozygous dominant cannot be distinguished from the heterozygote so
they all appear the same.
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Points to remember:
 All parental alleles must segregate in meiosis to form gametes.

 There is an equal probability of each allele carried occurring in the gamete.
 Fertilisation is a random process with each gamete(allele) from one parent having an
equal chance of fertilizing any of other gamete ( alleles) of the other parent.
 The genotypes of any particular offspring genotype or phenotype are only
probabilities.
 One fertilisation of two gametes does not affect he probability of the other possible
fertilisations.
In the previous example F1 x F1 the ratio produced is 3:1
 The probability of the offspring developing to produce smooth coated seeds is 3 in 4

or 75%
 The larger the population of offspring the closer the phenotypic ratio will be to 3:1
 The smaller the population the more likely a larger deviation from the 3:1 ratio.
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4.3.3 State that some genes have more than two alleles (multiple alleles).(1)
calculation.
 Some genes have more than two alleles.

 An individual can only possess two alleles.
 The population may contain many alleles for a given gene.
 Multiple alleles increases the number of different phenotypes.
 Multiple alleles can be dominant, recessive or co-dominant to each other.
 Example: Rabbit coat colour(C) has four alleles which have the dominance hierarchy:
C > cch > ch> c
This produces 5 phenotypes, Dark(C_) , Chinchilla( cchcch), light grey (cchch ,cchc), Point
restricted (ch ch, chc) and albino (cc)
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4.3.4 Describe ABO blood groups as an example of codominance and multiple

alleles. (2)
Describe means to a detailed account
The ABO blood group system

is an example of both a
multiple allele and
codominance condition.
There are three alleles the

base letter = I stands for
immunoglobulin
IA and IB are codominant to each other. Both these alleles are dominant to i
The Allele hierarchy is IA = IB > i
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4.3.5 Explain how the sex chromosomes control gender by referring to the
inheritance of X and Y chromosomes in humans.(3)
Gender in humans is controlled by the

23rd pair of chromosomes.
XX is female and XY is male.
The female possess two X chromosomes

one inherited from the father the other
from the mother. They are both the
longer chromosomes
The male possess one X chromosome inherited from the mother and the much shorter Y
chromosome inherited form the father.
The image to the left represents the difference in the XX and XY combination. The y
chromosome length is greatly exaggerated in this image.
This image represent a theoretical

cross between a human male and
female
 The female can provide only one

type of chromosome (X)
 The male however provides sperm
cells either with and X or with a Y.
 Theoretically this means that in any
fertilisation there is a P=0.5
( 50% , 1 in 2) chance of having
either a boy or a girl.
 This is the basis of many genetic
crosses and the one adopted here.

 However studies of families shows that some families tend to have more boys than
girl and some families have more girls than boys. The inheritance of this tendency is
explored in the excellent book about the Y-chromosome:
Sykes, B. (2003). Adams Curse. New York: Norton Paperback
 The genetic basis of gender is associated with the SRY gene (Sex determining region
of the Y chromosome) that was identified as the previously hypothesised trf gene.
This gene is normally found at the very tip of the y-chromosome but has also been
found on the X-chromosome due to translocation errors. In such a case it is possible
to be male and yet have XX chromosomes.
 New Scientist 1
 New Scientist 2
 Sexual differentiation (wiki)
 SRY Gene (wiki)
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4.3.6 State that some genes are present on the X chromosome and absent from
the shorter Y chromosome in humans.(1)
calculation.
Male:
 Some genes are

present on the X-
chromosome but
missing on the
shorter Y-
chromosome.
 The image of the
male 23rdpair of
homologous
chromosomes
represent the size
difference in the
two chromosomes.
 In the non-
homologous
region of the X-
chromosome a
male will only
have one allele for
any gene in this
region.
 Genes in the
homologous region have two alleles per gene and function just as other genes
already described.
Female:
 The complete length of the X-chromosome has a homologous pair on the other X-
chromosome.
 Genes on the x-chromosome of female therefore have two alleles just like another
gene on the other chromosomes.
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4.3.7 Define sex linkage.(1)
Define means to give a precise meaning of a word, phrase or physical quantity.
Genes on the non-homologous region of the X - chromosome are said to be sex linked.
Females have two such chromosomes (therefore two alleles) and males only one.
Phenotypes associated with recessive alleles are more common in males than in females.
Assuming that this plant species is dioecious
 The recessive allele (a) is found on

the non-homologous region of the X-
chromosome.
 Males only get one allele for this
gene.
 Males have a 50% chance of being
recessive.
 Female have a lower risk (33.3 %)
since they always receive 2 alleles.
 'Recessive' males can pass on this
condition( X-chromosome) to the
'daughter'.
 Cannot pass these conditions to the
'sons' as they pass the y-
chromosome with no alleles.
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4.3.8 Describe the inheritance of colour blindness and hemophilia as examples of
sex linkage.(2)
Describe means to give a deatiled account
 Red Green colourblindness is

a sex linked condition.
 The gene loci is on the non-
homologous region of the X-
chromosomes.
 Red Green colour blindness is
more common in males than
in females.
 Males always inherit the
colourblind allele form their
mothers.
 Males cannot pass on
colourblindness to their sons
since the Y-allele does not
have any of the
colourblindness alleles.
Inheritance of colourblindness:
Calculation: Calculate the phenotypic ratio of a cross between a female carrier for red green
colour blindness and a normal vision male.
Answer.
Haemophilia
Haemophilia is a recessive, sex-

linked genetic disorder.
 Persons suffering from

haemophilia are unable to
produce clotting factor.
 The haemophiliac allele (Xh)is
recessive to the normal allele
(XH).
 The gene is located on the non-
homologous region of the x-
chromosome.
 Haemophilia is more common in
men than women.
 Males inherit the allele from their mother and develop the disease.
 Since (until recently) the prognosis for survival was poor and haemophiliac males did
not survive to pass on the allele to their daughters (its on the X-chromosome).
Therefore female haemophilia where rare.
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Haemophilia can occur in

the children where the
mother is a carrier and a
normal male.
 The mother is
heterozygous for the
allele (XH Xh) .
 The father carries the
normal allele on the x-
chromosome and none
on the Y chromosomes
(XH Y).
 We can see that from such a cross the probability of being a haemophiliac male is
P=0.25 ( 25% or 1 in 4).
 Today with treatment haemophiliac males can survive until sexual maturity but they
cannot have daughters who are normal for this condition, why?
 Historically the haemophiliac allele has played a significant role in history and not
least amongst the royal families of europe.
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4.3.9 State that a human female can be homozygous or heterozygous with respect
to sex-linked genes.(1)
calculation.
 Females can be
homozygous or
heterozygous for the
sex-linked alleles
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4.3.10 Explain that female carriers are heterozygous for X-linked recessive alleles.
(3)
 Carrier are individuals that are heterozygous for the allele.

 The have both the dominant and the recessive (disease) allele.
 Females have two long x chromosomes (two alleles) but males have only one such
chromosome (one allele).
 Heterozygous famales can carry the disease causing allele but are normal as they
also have the dominant allele.
 To carry a disease causing allele in the heterozygote and be normal is called a '
Carrier'.
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4.3.11 Predict the genotypic and phenotypic ratios of offspring of monohybrid

crosses involving any of the above patterns of inheritance.(3)
Predict means to give an expected result.
1.The ability to taste the chemical PTC is determined by a single gene in humans with the
ability to taste given by the dominant allele T and inability to taste by the recessive allele
t. Suppose two heterozygous tasters (Tt) have a large family.
a. Predict the proportion of their children who will be tasters and non-tasters.
b. Use a Punnett square to illustrate how you make these predictions.is the likelihood that
their first child will be a taster?
c. What is the likelihood that their fourth child will be a taster?
d. what is the likelihood that the first three children of this couple will be non tasters.
answer
2.In certain trees, smooth bark is dominant over wrinkled.
a. Cross two trees that are heterozygous for smooth bark.

b. If there are 100 offspring produced, how many will have wrinkled bark.
answer
3. A rooster with grey feathers is mated with a hen of the same phenotype. Among their
offspring 15 chicks are grey, 6 are black and 8 are white.
a. What is the simplest explanation for the inheritance of these colours in chickens?
b. What offspring would you expect from the mating of a grey rooster and a black hen?
answer
4.In Mountain Boomers, the genes for length of tail exhibit co-dominance.
a. Use a Punnett Square to predict the result of a cross between a homozygous Long-tailed
and a homozygous Short-tailed Mountain Boomer.
b. Suggest what the the offspring might look like?
answer
5. In roses, red petal is dominant over white petal. Use the allele key R for the red allele
and r for the white allele.
a. Cross two heterozygous red roses,

b. Describe the phenotype of the offspring.
answer
6. In dogs, wire hair is due to a dominant gene (W) and smooth hair is due to its recessive
allele (w).
a. If a homozygous wire-haired dog is mated with a smooth-haired dog, what type of

offspring could be produced?
b. What type of offspring could be produced in the F2?
c. Two wire-haired dogs are mated. Among the offspring of their first litter is a smooth-
haired pup. If these two wire-haired dogs mate again, what are the chances that they will
produce another smooth-haired pup? What are the chances that the pup will be wire-
haired?
d. A wire-haired male is mated with a smooth-haired female. The mother of the wire-haired
male was smooth-haired. What are the phenotypes and genotypes of the pups they could
produce?
answer
7.In snapdragons, red flower colour is incompletely dominant over white flower colour; the
heterozygous plants have pink flowers.
a.If a red-flowered plant is crossed with a white-flowered plant, what are the genotypes and
phenotypes of the plants of the F1 generation?
b. What genotypes and phenotypes can be produced in the F2 generation?
c. What kinds of offspring can be produced if a red-flowered plant is crossed with a pink-
flowered plant?
d.What kinds of offspring can be produced if a pink-flowered plant is crossed with a white-
flowered plant?
answer
8. In cattle, roan coat colour (mixed red and white hairs) occurs in the heterozygous (Rr)
offspring of red (RR) and white (rr) homozygotes. When two roan cattle are crossed, the
phenotypes of the progeny are found to be in the ratio of 1 red : 2 roan : 1 white. Which of
the following crosses could produce he highest percentage of roan cattle?
(a) red x white; (b) roan x roan; (c) white x roan; (d) red x roan; (e) all of the above
crosses would give the same percentage of roan.
answer
9.Roan colour in cattle is the result of the absence of dominance between red and white
colour genes. How would one produce a herd of pure-breeding roan-coloured cattle?
answer
10.In some cats, black colour is due to a sex-linked (X-linked) recessive gene (b); the
dominant allele (B) produces orange colour The heterozygote (Bb) is calico.
a. What kinds of offspring would be expected from the cross of an orange male and a black
female?
answer
11. Haemophilia is a sex-linked trait where XH gives normal blood clotting and is dominant
to the haemophilia allele Xh.
a. Give the genotypes of 1) a woman with normal blood clotting whose father had
haemophilia and 2) a normal man whose father had haemophilia.
b. What is the probability that a mating between these two individuals will produce a child,
regardless of sex, that has haemophilia?
c. If this couple has a daughter, what is the probability that the daughter will be a carrier of
the haemophilia trait? What is the probability a daughter would have haemophilia?
d. If this couple has a son, what is the probability he will have haemophilia?
answer
12. If a woman who is red-green colour blind mates with a man with normal vision, what
phenotypes would one expect their children to have?
answer
13. Cystic fibrosis is found on the autosomal chromosomes. It is a recessive disorder in

which the allele key is dominant CFand Cf for the recessive allele.
a. A child is diagnosed with cystic fibrosis show with a diagram the likely genotype of their
parents?
b. What is the probability of the next child from this couple being not having the disease?
answer
More monohybrid questions.
Even more monohybrid questions
More sex linkage questions.
Sex linkage (Arizona) set 1
Sex linkage (Arizona) set 2
TOKBIT 4.3.11
Quote:
'Statisticians are convinced that Mendel's results are too close to exact ratios to be genuine'.
'....whether it is right to discard results that do not fit a theory as Louis Pasteur is known to
have done,....'
 To what extent are statements like these made with the benefit of hind site or with
the benefit of historical perspective?
 Is it correct to judge the work of another person by the value system and
methodologies of a historically later date?
External Links
Mendel Web homepage

Comment:
It is most important when considering the above statements that we do not lapse into an all
too easily adopted cynical evaluation of the work of people like Mendel, Pasteur, Darwin and
more recently Watson and Crick. Historical revision of events of course is valuable but only
if it has us reflects on our own conduct. I would suggest it is more important to realize that
scientific work today which seems entirely valid (by today's standards) may well fail the the
quality assurance standards of future generations. The work of the scientist mentioned and
so many more besides stands as pivotal moments in scientific history. Students of the IB
diploma might like to reflect on how their own work will be evaluated when they participate
in the group 4 projects!
4.3.12 Deduce the genotypes and phenotypes of individuals in pedigree charts.(3)
Deduce means to give reach a conclusion from the information given.
Often geneticists will carry out planned experiments in which breeding pairs are selected
and the offspring phenotypes counted. However this is not acceptable or possible when
working with humans. Instead geneticists have to collect information form about individuals
and relatives within a family and construct diagrams of inheritance(family trees) called
pedigrees.
The chart show the typical symbol found in a

pedigree chart.
 Circles are female(1),(3),(5), (6).

 Squares are male (2), (4), (7).
 Black means that the individual is affected by
the condition,(3).
 White indicates that the individual is
unaffected by the condition.
 Mating: Female 1 and male 2 (Horizontal
line)
 Children: Female (3) and male (4) are the
children of (1) and (2).
 Individuals (6) and (7) are the paternal
grandchildren of (1) and (2).

Phenylketonuria (PKU) is a metabolic

disorder and a recessive genetic
condition.
 The pedigree shows the inheritance

through a particular family.
 Which individuals can we be sure about
their genotype?
 Since it was not possible to identify the
condition of 12 and 13 suggest their
genotype and phenotype and how the
diagram may need modifying?
4.4.1 Outline the use of polymerase chain reaction (PCR) to copy and amplify
minute quantities of DNA. (2)
Outline means to give a brief account or summary
PCR is the cloning of DNA

(amplification).
 Copies are made and the

amount of DNA can be rapidly
increased. Useful if the source
of DNA is small.
 Temperature is used instead

of enzymes like helicases
(95oC ).
 DNA polymerase is thermostable to protect it against the reaction temperatures.

 This is an automated process and can produce sufficient DNA in 20 cycles.
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4.4.2 State that, in gel electrophoresis, fragments of DNA move in an electric field
and are separated according to their size.(1)
calculation.
Sample of
fragmented DNA is
placed in one of the
wells on the gel.
 An electrical current
is passed across the
gel.
 Fragment separation
is based on charge and size.
 Large fragments move slowly.
 Negative fragments are moved to the right.
Gel after staining:

This diagram shows the separation of 6 separate mixtures of DNA.
 The dark bands to the left are those with a large molecular mass or a positive charge
 (a) contains 5 fragments of DNA. Each bands corresponds to a group of DNA
molecules of the same size and charge.
 (b) and (c) have the same bands. They are identical
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4.4.3 State that gel electrophoresis of DNA is used in DNA profiling.(1)
calculation.
 Gel electrophoresis is used in DNA profiling.

 Satellite (Tandem repeating) DNA are highly repetitive sequences of DNA from
the non coding region of DNA.
 Different individuals have a unique length to their satellite regions.
 These can be used to differentiate between one individual and another.
 There are different types of 'DNA fingerprinting' for different circumstance
(a) The mothers chromosome provides a DNA

STR cutting the chromosome with particular
restriction enzymes.
(b)The fathers chromosome provides the same

fragment using the same restriction enzymes.
(c) The mother DNA fragment placed in the well

of the gel.
(d) The mother DNA fragment placed in the well

of the gel.
(e) Mothers fragment produces 5 STR and moves

a short distance along the electrophoresis gel.
(f) fathers fragment produces 2 STR and moves a

longer distance along the electrophoresis gel.
(g) The child is heterozygous for the fragment having on homologous chromosome form the
father and one form the mother.
Both 5 STR and 2 STR are shown in the electrophoresis.
The technique can be used in:
 Forensic crime investigations

 Parentage Issues
 Animal breeding pedigrees
 Disease detection
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4.4.4 Describe the application of DNA profiling to determine paternity and also in
forensic investigations.(2).
Paternity Investigation:
Trying to determine who are the biological parents of a child.
 The DNA fragments in the child comes from the mother and
father.
 A band present in the child must come either from the mother
or from the father
 Comparing male 1 with the child then male 2 with the child.
Interpretation:
 The bands on the child's fragments are either found on the mother or the male1.
 Male 1 therefore is this father of this child.
 None of the Male 2 bands appear in the child
Forensic Investigation:
A specimen of DNA is taken from the victim or the crime

scene.
 DNA samples are taken from the 3 suspects.

 The bands are compared to associate the suspects but to
eliminate the victims DNA from the specimens
Interpretation:
 Note that the bands on the specimen are matched by the

bands on the Suspect 1.
 This means that Suspect 1 was present at the crime scene.
 The law will still require to prove a crime was committed and then that Suspect 1
committed the crime
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4.4.5 Analyse DNA profiles to draw conclusions about paternity or forensic

investigations.(3)
Analyse means to interpret data to reach conclusions.
In the above example the description has been extended to an interpretation.

4.4.6 Outline three outcomes of the sequencing of the complete human genome.
(2)
Outline means to give a brief account or summmary.
Begun formally in 1990 the international projects aims where:
 identify all the approximate 30,000 genes in human DNA.
 determine the sequences of the 3 billion chemical base pairs that make up human
DNA.
 store this information in database.
 improve tools for data analysis.
 transfer related technologies to the private sector.
 address the ethical, legal, and social issues (ELSI) that may arise from the project.
 To help achieve these goals, researchers also are studying the genetic makeup of
several nonhuman organisms. These include the common human gut bacterium
Escherichia coli, the fruit fly, and the laboratory mouse.
External Links:
 Sanger Institute
 US GOV
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4.4.7 State that, when genes are transferred between species, the amino acid
sequence of polypeptides translated from them is unchanged because the
genetic code is universal.(1)
calculation.
 The genetic code is universal

 All known organisms use the same genetic code.
 Therefore in principle if we transfer a gene from one species to another it should still
be transcribed and translated into the same protein.
As with all of biology its the 'exceptions that prove the rule' and so it is with the 'Universal
genetic code. There are in fact some prokaryotes which have one or two different code
specifications. However they do not adopt a radically different system. Once more this
demonstrates the emergent properties of complex biological systems.
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4.4.8 Outline a basic technique used for gene transfer involving plasmids, a host
cell (bacterium, yeast or other cell), restriction enzymes (endonucleases)
and DNA ligase. (2)
Outline means to give a brief account of summary.
Stage 1: obtaining the gene for transfer:
Restriction enzymes
are used to cut out the
useful gene that is to
be transferred.
 Note the 'sticky ends' of unattached hydrogen bonds.
Stage 2. Preparing a vector for the transferred gene:
Plasmids are small circular DNA molecules found in

bacteria.
 These can be cut with the same restriction enzyme

as above.
 This leaves the same complementary 'sticky ends'

in the plasmid
 The plasmid can be cut at particular sites. These

are called restriction sites and some are named in
the diagram.
Stage3.
Recombinant
DNA
(a) plas
mid
that will
be the
vector
 (b) plas
mid cut at restriction site Pstl
 (c) Source DNA cut with same restriction enzyme as plasmid to (d)
 (e) Recombinant DNA
 (f) unaffected plasmid
Expression vectors: usually if a eukaryotic gene is inserted into the genome of a prokaryote
it make very little of the desired gene product. Therefore additional factors are included in
the vector plasmid 'package' which includes types of RNA. The final plasmid as outlined
above containing these additional factors is called an' Expression vector'.
Stage4. Isolation of transformed cells
Recombinant DNA is
introduced into the host cells
 Many cells remain

untransformed
 Some cells are transformed to contain the recombinant DNA.
 These transformed cells must be separated from untransformed
Stage 5. Product manufacture.
The transformed
bacterial cells are
isolated.
 They are introduced into

a Fermenter to be
cloned.
 The bacterial population

grows by asexual
reproduction.
 The Recombinant DNA is

copied along with the
rest of the bacterial
genome.
 In a fermenter the conditions for growth and reproduction are controlled.
 Once the bacteria express the transformed gene the product is produced.
 The next (long ) step is to isolate and purify the product. This is called downstream
processing.
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4.4.9 State two examples of the current uses of genetically modified crops or
animals.(1)
calculation.
• Genetically modified organism (GMO) is an organism containing a

transplanted gene.
• The organism will express the gene and synthesis the protein.
Factor IX : A human clotting factor is produces by genetically modified sheep. The

protein (factor IX) is expressed in milk from which it must be isolated before use by
haemophiliacs.
A ewe is treated with fertility drugs to create super-

ovulation.
Eggs are inseminated.
Each fertilised egg has the transgene injected.
A surrogate ewe has the egg implanted for gestation.
Lambs are born which are transgenic, GMO for this factor IX
gene.
Each Lamb when mature can produce milk.

The factor IX protein is in the milk and so must be isolated and purified before use in
human.
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Tomato salt tolerance:
Plants find it hard to grow in salty conditions since this hypertonic soil water results in
desiccation, wilting and death of the plant.
Tomato plants have now been genetically modified to carry the gene for salt tolerance.
The origin of the gene was a weed called Arabidopsis thaliana.
The transgenic tomato plant can tolerate plants.
This now provides the opportunity for a crop to be grown in an otherwise sterile soil.
Links:
Rice with retinol:
Retinol deficiency:
Retinol (Vitamin A1) is essential for the development of an effective immune system,
normal vision and growth. Where a child lacks Retinol they have stunted growth and in
extreme cases blindness. A serious complication arises from the combined of malnutrition,
disease and retinol deficiency. The coincidence of these three conditions together is seen in
some third word nations. In Zambia more than 54% of the population of children have
retinol deficient diets. Even if children have sufficient food (calories) the problem is that is
not a balanced diet. These children experience retarded growth for their age group and
vision problems are common. Vision problems usually begin with a loss of night vision and
then ultimately complete blindness. As might be expected these communities find it very
difficult to support children with these multiple problems. To make matters worse diseases
such as malaria and measles (known killer diseases) disable or kill large numbers of children
as they have ineffective immune systems, another consequence of retinol deficiency.
 Rice does not contain retinol or beta-carotene (used by the body to make retinol).
 Rice does contain a molecule that is normally used to make beta-carotene.
 The gene and enzymes to manufacture are missing from rice.
 Genetically modified rice contains the gene for the manufacture of beta-carotene.
 Source of the gene is either Erwinia bacterium or the common daffodil.
 The transgenic rice is usually yellow in colour because of the accumulation of beta-
carotene.
 This transgenic rice is then crossed with local strains of rice.
Herbicides: Roundup
 Weeds growing amongst a crop use up soil nutrients that would otherwise be used
by the crop plant.
 This competition of resources reduces the productivity of the crop plant and
therefore the efficiency of farming.
 Herbicides can be used prior to crop planting to kills weeds.
 The herbicide cannot be used after crops have been sown as they will also kill the
crop.
 The major herbicide in use is called 'Glyphosate', anyone who has gardened will
know this as 'Roundup' which is the market name for the product.
 However, Cotton, Corn and Soybeans have been genetically modified to contain an
enzyme that breaks down glyphosate.
 This makes these crops resistant to the herbicide.
 Herbicide can then be use after the crop has grown to prevent the reoccurrence of
weed competition.
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4.4.10 Discuss the potential benefits and possible harmful effects of one example
of genetic modification.(3)
Discuss means to give an account including, where possible, a range of arguments for and
The advantages and disadvantages of GMO is a controversial topic with wide political,
environmental, health and social effects. The following issues can be applied specifically to
the above examples of GMO.
The benefits of GMO include:
 Increased yields particularly in regions of food shortage.

 Yields of crops with specific dietary requirement such as vitamins and minerals.
 Crops that do not spoil so easily during storage.
 GM animals produce similar effect including higher meat yields.
The disadvantages or concerns about GMO usually can be found:
 The foods (animal and plant) are considered un-natural and unsafe for human
consumption.
 There is a risk of the escape of 'genes' into the environment where they may be
passed to other organisms with unknown effects.
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4.4.11 Define clone.(1)
define means to give the precise meaning of a word, phrase or physical quantity.
Syllabus statement: ' Clone: a group of genetically identical organisms or a group of cells
derived from a single parent'.
4.4.12 Outline a technique for cloning using differentiated animal cells.(2)
Outline means to give a brief account or

sumarry.
 Somatic cells are differentiated

that is specialised to a particular
function. In the case of Dolly
(1996) the cell was taken from the
udder of the original sheep (1) that
was to be cloned.
 Sheep (2) provides the egg cell

after being stimulated to
superovulated by the use of the
hormone FSH.
 The nucleus is removed from the

egg cell. This removes the genetic
information of sheep (2).
 The cells are fused combining the

nucleus of sheep (1) with the egg
cell from sheep(2). The egg cell
retains its ability to replicate
chromosomes and divide by
mitosis.
 The cell is grown 'in-vitro' until it reaches the16 cell stage this will then be implanted
into a surrogate mother sheep.
 Sheep (3) is the surrogate mother sheep and is not related to any of the other
sheep. There is a normal gestation period before the 'Clone lamb' is born.
 Lamb (4) is dolly the clone of sheep (1). They are genetically identical. However
they will experience a different set of environmental conditions.It should be noted
that this technique was tried many times before it was successful.
4.4.13 Discuss the ethical issues of therapeutic cloning in humans.(3)
Discuss means to give an account including, where possible, a range of arguments for and
The discussion is about the creation of an embryo to supply stem cells for medical use.
 Research what is meant by therapeutic cloning.

 Decide what the ethical issues are in therapeutic cloning.
 What is an embryo?
 Where would they be obtained from? Alternatives?
 Try to make yourself aware of the stance of interest groups on the issues.
6.1.1 Explain why digestion of large food molecules is essential.(3)
 Most food molecules are large polymers and insoluble

 They must first be digested to smaller soluble molecules before they can be absorbed
into the blood
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6.1.2 Explain the need for enzymes in digestion.(3)
 Enzymes are biological catalysts that increase the rate of reaction
 Digestive enzymes are secreted into the lumen of the gut
 Digestive enzyme increase the rate of reaction of the hydrolysis of insoluble food
molecules to soluble end products
 Digestive enzymes increase the rate of reaction at body temperature
 This image illustrates the

reduction in activation energy
that is achieved by the use of
an enzyme
 Notice that the normal

reaction requires a higher
activation energy which would
correspond to a high body
temperature. This is usually
not possible in living
organisms.
 The enzyme-catalysed reaction

has a lower activation energy. This lower activation energy would correspond to body
temperature but is only possible in the presence of an enzyme
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6.1.3 State the source, substrate, products and optimum pH conditions for one
amylase, one protease and one lipase.(1)
Example 1 Pancreatic amylase:

Conditions:
 Source the Pancreas

 Optimal pH 7.5-7.8
 Substrate is starch
(amylose)
 End product is the
disaccharide maltose
 Action: hydrolysis of 1-4
glycosidic bonds
Example 2: Pepsin is a protease produced in the stomach
Conditions:
 Source is the stomach

 Optimal pH is 2
 Substrate is a polypeptide chains
of amino acids
 End product is small polypeptides
 Action is the hydrolysis of
peptide bonds within the
polypeptide chain
(endopeptidase).
Example 3: Pancreatic lipases:
Source is the pancreas
 The optimal pH is 7.2

 The substrate is a
triglyceride lipid
 The product is glycerol
and fatty acid chains
 The action of pancreatic amylases also requires the presence of bile salts that
emulsify the lipid. This emulsification has two effects:
1. Increases the surface area of the lipid for the digestion of fat
2. Exposes the glycerol 'head' structure to the enzyme
 Action: hydrolysis of ester bonds between the glycerol molecules and the fatty acid
chains.
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6.1.4 Draw and label a diagram of the digestive system.(1)
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6.1.5 Outline the function of the stomach, small intestine and large intestine.(2)
1. Stomach:
The stomach stores the food from a meal and begins protein digestion.
(a) Lumen of the stomach which stores the food

from a meal
(b) Gastric pits from which mucus , enzymes and

acid are secreted
(c) Mucus secreting cells. Mucus protects the

surface of the stomach from auto-digestion
(d) Parietal cells that produce HCL which kills

microorganism that enter the digestive system
(food & tracheal mucus). This also converts inactive pepsinogen to active pepsin
(e) Chief cells: produces pepsinogen a protease enzyme
2. small Intestine
In the small intestine digestion is completed.
The products of digestion are absorbed into the blood stream.
(a) Villus which increase the surface area for

absorption of the products of digestion
(b) Microvilli border of the epithelial cell increases the surface are for absorption.
(c) Lacteals are connect to the lymphatic system for the transport of lipids.
(d) In the wall of the small intestine are the blood vessels to transport absorbed products to
the general circulation, There are also the muscle to maintain peristalsis
3. Large Intestine or colon:
The colon is responsible for the reabsorption of water from the gut.
(a) The lumen of the colon
(b) The mucus producing goblet cells
(b) Muscular walls to maintain peristalsis
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6.1.6 Distinguish between

absorption and
assimilation.(2)
Insoluble food molecules are

digested to soluble products in the
lumen of the gut.
Absorption:
1. The soluble products are first taken up by various mechanisms into the epithelial
cells that line the gut.
2. These epithelial cells then load the various absorbed molecules into the blood
stream.
Assimilation:
1. The soluble products of digestion are then transported to the various tissues by the
circulatory system.
2. The cells of the tissues then absorb the molecules for use within this tissues
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6.1.7Explain how the structure of the villus is related to its role in absorption and
transport of the products of digestion.(3)
The structure of the villus increases the surface are for the absorption of digested food
molecules.
(a) folds
increase
SA:VOL
ration by
X3
(b) Villi
project
into the
lumen of
the gut increasing the surface area by X 10
(c) Microvilli are outward folds of the plasma membrane increasing the surface area another
X10
This sequence of light microscope and electron micrograph images show the same sequence
as the diagram above.
Histological adaptations within the villus.
 Blood supply in the villus

which absorb the end
products of digestion from the
epithelial cells
 The lacteals (green) that

receive the lipoproteins
before transporting them to
the circulatory system.
 Muscular walls that maintain

the movement of chyme by peristalsis.
6.2.1 Draw and label a diagram

of the heart showing the
four chambers,
associated blood
vessels, valves and the
route of blood through
the heart.(1)
 Each atrium fills with blood from the veins.
 Ventricles are filled with blood from their respective atria.
 Blood exits the ventricles (and heart) in arteries.
 The red arrows suggest oxygenated blood
 Blue arrows represent deoxygenated blood.
 Blood enters the heart under lower pressure in veins, it exists the heart in arteries
under high pressure.
Heart Valves
 Vales maintain a one way flow of

blood.
 Atrio-ventricular vales open to let
blood flow from atria to the
ventricles.
 The atrio-ventricular valves close
to prevent a back flow of blood
into the atria.
 Semi-lunar valves open to allow
high pressure blood to pulse into
the arteries.
 Semi-lunar valves close to
prevent black flow of blood into
the ventricles form arteries.
 The left atrio-ventricular valve is
also know as the bicuspid valve.
 The right atrio-ventricular valve is
also known as the tricuspid valve.
Pressure of blood to the left is
greater than pressure to the right
Valve flaps (cusps) pushed open.
Blood flows to the right.
The pressure on the right is greater

than the pressure on the left.
Cusps pushed closed.
Back flow stops
6.2.2 State that the coronary arteries supply heart muscle with oxygen and
nutrients.(1)
 The heart has its own blood
vessels.
 Blood passing through the
chambers of the heart does not
provide nutrient or oxygen to
the heart muscle cells.
 Coronary arteries are branches
of the aorta which provide the
heart muscle with a supply of
oxygen and nutrient.
 The coronary arteries branch
and spread through the heart
muscle supplying the individual
muscles cells.
6.2.3 Explain the action of the heart in

terms of collecting blood, pumping
blood, and opening and closing of
valves.(3)
Diastole
 The heart muscle is relaxed this is called diastole.
 There is no pressure in the heart chambers.
 Blood tries to flow back into the heart but closes the semi-lunar valves.
Diastole
 Both atria fill with blood returning to the

heart in the veins.
 The right atria fills with blood returning in
the vena cava from the body tissues
(deoxygenated).
 The atrio-ventricular valves are still closed
and the atria fill up.
 When the pressure in the atria is greater
than the pressure in the ventricles the
atrio-ventricular valves will open.
Late Diastole
 In this diagram the heart is still relaxed

(diastole).
 The pressure of blood returning to the
heart and filling the atria is now high
enough to open the atrio-ventricular
valves.
 The pressure in the atria is greater than
the pressure in the ventricles.
 Atrio-ventricular valves open
 Ventricles begin to fill with blood.
Atrial systole
 Both atria contract together (see control of

heart rate)
 The muscles of the atria contract.
 volume of the atria reduces.
 Pressure of blood increases
 Blood flow into the ventricle, filling this
chamber and causing the ventricle wall to
stretch.
Ventricular Systole
 The ventricle contracts (systole)

 The pressure increases in the ventricle
 The atrio-ventricular valve closes
 The pressure rises further
 Pressure in the ventricle is greater than the
artery, semi-lunar valve opens
 Blood pulses into the arteries
6.2.4 Outline the control of the heartbeat in terms of myogenic muscle

contraction, the role of the
pacemaker, nerves, the medulla
of the brain and epinephrine
(adrenaline).(2)
 Myogenic muscle contraction describes

the way the heart generates its own
impulse to contract. It does not
require external nerve input.
 In the wall of the right atrium there are a group of specialised cells(SAN).
 Cells of the Sino-Atrial Node generate an impulse that can spread across the muscle
cell of both atria (red pathway).
 The impulse causes a contraction of both atria together.
 The impulse cannot spread to the muscle cells of the ventricles.
 The impulse is picked up by a sensory ending called the atrio-ventricular node (AVN).
The atria have already contracted sending

blood down into the ventricles.
The ventricles are stretched and full of blood.
(A) The impulse to contract (generated in the

SAN) is picked up by the AVN .
(B) The impulse to 'contract' travels down the

septum of the heart, insulated from ventricle
muscle fibres
(C) The impulse emerges first at the apex of

the heart. This causes this region to contract
first.
(D) The impulse now emerges higher up

causing this region to contract.
(E). This region contract last.
The effect is to spread the contraction from the apex upwards, pushing blood towards the
semi-lunar valves.
Modification of myogenic contraction
The basic myogenic contraction can be

accelerated or slowed by nerve input form the
brain stem or medulla.
There are two nerves:
 Decelerator nerve (parasympathetic)

which decreases the rate of
depolarisation at the SAN. Note that the
synapse releases acetyl choline.
 Accelerator nerve (sympathetic) which
accelerates the rate of depolarisation at
the SAN. Synapse releases nor-
adrenaline.
Epinephrine (adrenaline) and heart rate
 The hormone epinephrine is produced in the

adrenal glands (an endocrine gland).
 The hormone travels through the blood to its target tissue, the sino-atrial
node(SAN).
 Epinephrine increases the rate of depolarisation of the SAN.
 This accelerates heart rate.
 This reaction is associated with the 'fight or flight response'.
6.2.5 Explain the relationship between the structure and function of arteries,
capillaries and veins.(3).
a) Arteries have muscular

walls and outer layer of
collagen for support.
The collagen resists the

expansion due to the high
pressure of blood.
The muscle layer

contracts on the pulse of
blood maintaining
pressure all the way to
the tissues.
b) Veins have carry blood under low pressure the lumen is wide to reduce the resistance to
blood flow.
c) Capillaries have only a single layer of endothelium through which exchange can occur in
the tissues.
General functions of arteries and veins.
Arteries carry blood away form the heart under

high pressure.
Veins return blood to the heart under lower

pressure.
Capillaries are the site of exchange of blood with

tissue fluid and cells.
6.2.6 State that blood is

composed of
plasma,
erythrocytes,
leucocytes
(phagocytes and
lymphocytes) and
platelets.(1)
Plasma is largely water and makes up about 55% of the total blood volume.
This is the main transporting part of blood and takes advantage of the solvent properties of
water.
The items listed to the left are shown for discussion only.
Erythrocytes are the

red blood cells.
Leucocytes are the

white blood cells
Relative numbers are

shown for illustration
purposes only.
6.2.7 State that the following are transported by the blood: nutrients, oxygen,
carbon dioxide, hormones, antibodies, urea and heat.(1)
The items listed above take advantage of the properties of water (as a solvent):
 Nutrients
 Carbon dioxide
 Hormones
 Antibodies
 Urea
or its thermal properties:
 heat
Oxygen and carbon dioxide rely in the RBC for their transport:
6.3.1Define pathogen. (1)
 A pathogen is an organism that can cause disease.

 Pathogens include bacteria, viruses, protista, fungi and other parasitic multicellular
organisms.
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6.3.2 Explain why antibiotics are effective against bacteria but not against
viruses.(3)
Antibiotics block specific metabolic pathways found in bacteria, but not in

eukaryotic cells.
These graphs show how the two kinds of drug (see below) affect bacterial growth curves.
 Bactericidal or fungicidal antibiotics kill microbes.

 Others are antibiotics are static (bacteriostatic, fungistatic, etc.), which means
they stop further growth, but don't kill existing cells.
 Both are useful medically, because if the growth of an infective pathogen is stopped,
the body's immune system will be able to kill it.
 Antibiotics can be selectively toxic by targeting such features as the bacterial cell
wall, 70S ribosomes, and enzymes that are specific to bacteria. In this way the
human eukaryotic cells are unaffected.
Viruses reproduce using the host cell metabolic pathways that are not affected by
antibiotics.
 Viruses do not have metabolic pathways like bacteria and therefore antibiotics do not
work on viruses.
 Viruses can only be treated by their specific anti-microbial agent and antibiotics
should never be prescribed for viral infections (such as flu).
6.3.3 Outline the role of skin and mucous membranes in defence against
pathogens.(2)
Skin :
 The skin is a tough outer layer called the epidermis, which is 20-30 cells thick whose
cells are toughened by the protein keratin. Beneath this is the layer called the dermis
(20-40 times thicker) making up the main skin layer and contains sensory receptor
cells, blood capillaries and hairs. Deeper down the skin divides to produce new cells
which replace those lost from the surface.
 The lining of the lung is another way that pathogen can enter the body. The trachea,
bronchi and bronchioles are protected from infection by mucus to which various
particles when inhaled. Other cells have cilia, hair like extensions of the cell
membrane move the mucus upward to the epiglottis. Here the mixture of mucus and
micro-organisms are swallowed down into the acid of the stomach.
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6.3.4 Outline how phagocytic leucocytes ingest pathogens in the blood and in
body tissues.(2)
The second line of defence is the non-specific immune system, a host of quick, non-specific
methods of killing microbes that have passed the first line of defence and entered the body.
Phagocytes are large,

irregularly-shaped leukocytes
that destroy bacteria, viruses,
and dust particles.
 The phagocytes show amoeboid

movement, constantly changing
shape, as they engulf microbes.
The engulf vesicles join
together to form phagozomes.
 The phagosome then fuses with

lysosomes which contain containing lysozymes. These enzymes killing and digesting
the microbes.
 The process is called phagosytosis
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6.3.5 Distinguish between antigens and antibodies.(2)
Antigen is often used to describe something that has infected the body. However it is more
accurate to describe them as follows:
 An antigen is a large molecule (protein, glycoprotein, lipoprotein or polysaccharide)

on the outer surface of a cell.
 All living cells have these antigens as part of their cell membrane or cell wall.
 The capsid proteins of viruses and even individual protein molecules can also be
classed as antigens.
 Their purpose is for cell communication, and cells from different individuals have
different antigens, while all the cells of the same individual have the same antigens.
 Antigens are genetically controlled, so close relative have more similar antigens than
unrelated individuals.
 Blood groups are an example of antigens on red blood cells, but all cells have them.
The link with infection is that when a pathogen or toxin enters the body it this that the
immune system reacts against.
Antibodies are proteins secreted from lymphocytes that destroy pathogen and antigen
infections
 B-cells make antibodies.
 An antibody (also called an immunoglobulin) is a protein molecule that can bind

specifically to an antigen.
 Antibodies all have a similar structure composed of 4 polypeptide chains (2 heavy

chains and 2 light chains) joined together by strong disulphide bonds to form a Y-
shaped structure.
 The stem of the Y is called the constant region because in all immunoglobulin's it has
the same amino acid sequence, and therefore same structure.
 The ends of the arms of the Y are called the variable regions of the molecule because
different immunoglobulin molecules have different amino acid structure and
therefore different structures.
 These variable regions are where the antigens bind to form a highly specific antigen-
antibody complex, much like an enzyme-substrate complex.
 Each B-cell has around 10 5 membrane-bound antibody molecules on its surface and
can also secrete soluble antibodies into its surroundings.
 Every human has around 108 different types of B cell, each making antibodies with
slightly different variable regions.
 Between them, these antibodies can therefore bind specifically to 108 different
antigens, so there will be an antibody to match almost every conceivable antigen
that might enter the body.
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6.3.6 Explain
antibody
production.
(3)
(a) There are many

different lymphocytes.
(b) The antigen infects and is presented to the lymphocytes
(c) The lymphocyte with a surface epitope complementary to the antigen is selected.
(d) The Lymphocyte clones to produce many plasma cells. This occurs in the lymph nodes.
(e) The clone of plasma cells
(f) The gene for the antibody is expressed and secreted into the plasma and tissue fluid.
(g) The antibody circulated in body fluids destroying the infectious antigen
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6.3.7 Outline the

effects of HIV
on the
immune
system.(2)
HIV is a virus that

selectively infects
Lymphocytes
(a) Different
lymphocytes
(b) HIV virus
(c) Infection as the

virus attaches then
enters the host
lymphocyte.
(d) The infected

lymphocyte is
'disabled' by the virus
(e) When an antigen infection is presented the lymphocyte cannot produce antibodies.
(f) The antigen is not challenged by the immune system and is able to freely proliferate
The consequence is that the infected individual will have no immune and develop that
disease.
Therefore an individual who is HIV +ve (infected ) will eventually develop a disease which
will go unchecked. The consequence is that that disease will severely damage the infected
person and will eventually bring about their death.
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6.3.8 Discuss the cause, transmission and social implications of AIDS.(3)
AIDS: Acquired Immuno deficiency syndrome.
 Acquired relates the infectious nature of AIDS through the transmission of the HIV
virus.
 Immuno deficient relates to the way diseases cannot be resisted.
 Syndrome relates to the variation in the way the disease manifest itself. People who
develop AIDS can be a affected by quite different set of diseases.
Cause: is the HIV retro-virus that selectively infects cells of the immune system effectively
disabling primary and secondary response to infection.
Transmission: Through contact with the body fluids of an infected person. In particular the
fluids are blood and semen, vaginal mucus. There is a very low risk ( almost zero)
associated with salivary mucus.
6.4.1 Distinguish between ventilation, gas exchange and cell respiration.(2)
1. Ventilation:
 The flow of air in and out of the alveoli is called ventilation and has two stages:
inspiration (or inhalation) and expiration (or exhalation).
 Lungs are not muscular and cannot ventilate themselves, but instead the whole
thorax moves and changes size, due to the action of two sets of muscles: the
intercostal muscles and the diaphragm.
2. Gas Exchange:
This is the diffusion of gases (oxygen and
carbon dioxide)
There are two sites for gas exchange
 (a)Alveoli: Oxygen diffuses into the

blood from the alveoli and carbon
dioxide diffuses from the blood into
the alveoli
 (b)Tissues: Oxygen diffuses from blood into the cells and carbon dioxide diffuses
from cells to the blood
3. Cell Respiration
 Aerobic respiration uses oxygen in the mitochondria and produces carbon dioxide
 Anaerobic respiration does not use oxygen but still produces carbon dioxide
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6.4.2 Explain the need for a ventilation system.(3)
 A ventilation system is needed to maintain concentration gradients in the alveoli
 The steep concentration gradient across the respiratory surface is maintained in two
ways: by blood flow on one side and by air flow on the other side. The ventilation
system replaces diffuses oxygen (keeping the concentration high) and removes
carbon dioxide (keeping the concentration low).
 This means oxygen can always diffuse down its concentration gradient from the air
to the blood, while at the same time carbon dioxide can diffuse down its
concentration gradient from the blood to the air.
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6.4.3 Describe the features of alveoli that adapt them to gas exchange.(2)
Large surface area due to the

combined spherical shape
(600 million alveoli = 80 m2)
 Flattened epithelial cells of

alveoli and close association
with capillaries
 Short diffusion distance from alveoli to blood (0.5-1.0 um)
 Dense capillary network
 Moist surface for the solution of gases

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6.4.4 Draw and label a diagram of the ventilation system, including trachea, lungs,
bronchi, bronchioles and alveoli.(1).
(a) Trachea
(b) Cartilage ring support
(c) Bronchi (plural) Bronchus

(single)
(d) Lung
(e) Heart
(f) Sternum
(g) Rib cage
(h) Bronchioles (j) Alveoli (k) Diaphragm
6.4.5 Explain the mechanism of ventilation of the lungs in terms of volume and
pressure
changes
caused by
the internal
and external
intercostal
muscles, the
diaphragm
and
abdominal
muscles.(3)
The diaphragm
contracts and
flattens
downwards.
 The external intercostal muscles contract, pulling the ribs up and out
 this increases the volume of the thorax this increases the lung and alveoli volume
 this decreases the pressure of air in the alveoli below atmospheric (Boyle's law)air
flows in to equalise the pressure
The diaphragm
relaxes and
curves upwards
 the external
intercostal
muscles relax, allowing the ribs to fall
 this decreases the volume of the thorax
 this decreases the lung and alveoli volume
 this increases the pressure of air in the alveoli above atmospheric (Boyle's law)air
flows out to equalise the pressure.
 The abdominal muscles contract, pushing the diaphragm upwards

 The internal intercostal muscles contract, pulling the ribs downward
 This gives a larger and faster expiration, used in exercise
6.5.1 State that the nervous system consists of the central nervous system (CNS)
and peripheral nerves, and is composed of cells called neurons that can
carry rapid electrical impulses.(1)
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6.5.2 Draw and label a diagram of the structure of a motor neuron.(1)
Electron micrograph cross section

 A neuron has a cell body with extensions leading off it.
 Numerous dendrons and dendrites provide a large surface area for connecting with
other neurons, and carry nerve impulses towards the cell body.
 A single long axon carries the nerve impulse away from the cell body.
 The axon is only 10µm in diameter but can be up to 4m in length in a large animal (a
piece of spaghetti the same shape would be 400m long)!
 Most neurons have many companion cells called Schwann cells, which wrap their cell
membrane around the axon many times in a spiral to form a thick insulating lipid
layer called the myelin sheath.
 Nerve impulse can be passed from the axon of one neuron to the dendron of another
at a synapse. A nerve is a discrete bundle of several thousand neuron axons.
Humans have three types of neuron:
 Sensory neurons have long axons and transmit nerve impulses from sensory
receptors all over the body to the central nervous system.
 Motor neurons also have long axons and transmit nerve impulses from the central
nervous system to effectors (muscles and glands) all over the body.
 Interneurones (also called connector neurons or relay neurons) are usually much
smaller cells, with many interconnections.
6.5.3 State that nerve impulses are conducted from receptors to the CNS by
sensory neurons, within the CNS by relay neurons, and from the CNS to
effectors by motor neurons.(1)
 There are various

receptor around
the body such as
skin and the eye.
 Stimuli (think of
them as energy
forms) are
detected by the
receptors and turned into an nerve impulse (chemical energy).
 Nerve impulses from sensory nerves are conducted to the central nervous system
along sensory neurons.
 The impulse is sent to the relay neurons that move it around inside the central
nervous system (brain and spine).
• Motor neurons take the relayed nerve impulse to the effectors (often muscles)
which then produce the response.
This is a cross
section through
the vertebrate
spinal column.
 The receptor is
deep in the biceps
muscle.
 Sensory neuron
conducts nerve
impulses from the
receptor to the
central nervous system.
 The relay nerve conduct the impulse through the spinal cord and in a reflex back to
the motor neuron.
 The motor neuron connects to the effector which in this case is the biceps muscle.
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6.5.4 Define resting potential and action potential (depolarization and

repolarization).(1).
To record the electrical activity of a nerve

it is placed in an isotonic fluid bath.
 A reference electrode is placed in the

surrounding fluid.
 A recording electrode is inserted into the
cytoplasm of the axon.
 The electrical disturbances are measured and displayed on the oscilloscope.
Membrane potentials:
 Resting potential is the negative charge registered when the nerve is at rest and
not conducting a nerve impulse.
 Action potential is the positive electrochemical charge generated at the nerve
impulse. Normally this is seen as the 'marker' of the nerve impulse position.
 Depolarisation is a change from the negative resting potential to the positive action
potential.
 Re-polarisation is the change in the electrical potential from the positive action
potential back to the negative resting potential.
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6.5.5 Explain how a nerve impulse passes along a non-myelinated neuron.(3).
To understand the Resting Potential and Action Potential first consider an ion pump found in
the plasma membrane
Sodium-Potassium ATPase
 This uses the energy from ATP splitting to simultaneously pump 3 sodium ions out of
the cell and 2 potassium ions in.
 If this was to continue unchecked there would be no sodium or potassium ions left to
pump, but there are also sodium and potassium ion channels in the membrane.
 These channels are normally closed, but even when closed, they “leak”, allowing
sodium ions to leak in and potassium ions to leak out, down their respective
concentration gradients.
 The combination of the Na +K +ATPase pump and the leak channels cause a stable
imbalance of Na + and K + ions across the membrane.
 This imbalance causes a potential difference across all animal cell membranes, called
the membrane potential.
 The membrane potential is always negative inside the cell, and varies in size from –
20 to –200 mV in different cells and species.
 The Na +K+ ATPase is thought to have evolved as an osmoregulator to keep the
internal water potential high and so stop water entering animal cells and bursting
them. Plant cells don’t need this as they have strong cells walls to prevent bursting.
Resting Potential & Action Potential
 In nerve and muscle cells the membranes are electrically excitable, which means
that they can change their membrane potential, and this is the basis of the nerve
impulse.
 The sodium and potassium channels in these cells are voltage-gated, which means
that they can open and close depending on the voltage across the membrane.
 Early experiments on nerves focused on the non-myelinated Squid Giant Axon .
 An electrodes is placed inside the cell and one outside the cell (reference).
 The electrodes are attached to an oscilloscope
 The nerve cell is stimulated to generate a nerve impulse and the voltage change
recorded on the oscilloscope.
 The normal membrane potential of these nerve cells is –70mV (inside the axon), and
since this potential can change in nerve cells it is called the resting potential.
 When a stimulating pulse was applied a brief reversal of the membrane potential,
lasting about a millisecond, was recorded. This brief reversal is called the action
potential:
RP: Resting Potential
DP: Depolarisation
AP: Action Potential
ReP: Re-polarisation
RFP: Refractory Period
TH: Threshold
The Action Potential has two stages depolarisation (DP) and Re-polarisation(ReP)
Depolarisation .(DP)
 The stimulating electrodes cause the membrane

potential to change a little.
 The voltage-gated ion channels can detect this
change, and when the potential reaches –
30mV(TH) the sodium channels open for 0.5ms
 The causes sodium ions to rush in, making the
inside of the cell more positive.
 This phase is referred to as a depolarisation
since the normal voltage polarity (negative inside) is reversed (becomes positive
inside).
Re-polarisation (ReP).
 The membrane potential reaches 0V.

 The potassium channels open for 0.5ms,
causing potassium ions to rush out.
 This makes the inside more negative again.
 Since this restores the original polarity, it is
called re-polarisation
How the nerve impulse travels along the axon:
 Once an action potential has started it is moved (propagated) along an axon

automatically.
 The local reversal of the membrane potential is detected by the surrounding voltage-
gated ion channels, which open when the potential
Section a) Refractory potential:
The axon is in a refractory (ReP)period which means that diffusion backwards of Na+ from
the action potential is not able to depolarise the membrane channels. This means the
impulse travels in one direction
Section b) Action Potential:
The voltage gates have been opened and there is a high concentration of Na+ in the axon.
This diffuses to the next set of voltage gates depolarising from resting potential.
Section c: Resting potential:
The Na+will diffuse to this position. If the voltage reaches threshold (TH) then the channel
will open Na+will flood in and a new action potential site will be established.
Threshold (TH):
 The ion channels are either open or closed; there is no half-way position. This means
that the action potential always reaches +40mV as it moves along an axon, and it is
never attenuated (reduced) by long axons. In other word the action potential is all-
or-nothing.
Re factory Period (ReP):
 After an ion channel has opened, it needs a “rest period” before it can open again.
 This is called the refractory period, and lasts about 2 ms.
 This means that, although the action potential affects all other ion channels nearby,
the upstream ion channels cannot open again since they are in their refractory
period, so only the downstream channels open, causing the action potential to move
one-way along the axon.
 The delay caused by refractory period also prevents the summation of Action
potentials (one impulse cannot catch up another impulse)
Human Nerve propagation:
It should be noted that the description given above of nerve conduction is for a squid giant
axon. This is a typical arrangement in the invertebrates. To increase the rate of nerve
conduction the axon diameter is increased. However, vertebrates have a different method of
accelerating their nerve conduction but this is not part of the IB syllabus for this particular
unit. You can however read about this method of nerve conduction called saltatory
conduction.
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6.5.6 Explain the principles of synaptic transmission.(3)
 The junction between two neurons is called a synapse.

 An action potential cannot cross the synaptic cleft between neurons, and instead the
nerve impulse is carried by chemicals called neurotransmitters.
 These chemicals are made by the cell that is sending the impulse (the pre-synaptic
neuron) and stored in synaptic vesicles at the end of the axon.
 The cell that is receiving the nerve impulse (the post-synaptic neuron) has chemical-
gated ion channels in its membrane, called neuroreceptors.
 These have specific binding sites for the neurotransmitters
1. At the end of the

pre-synaptic neuron
there are voltage-gated
calcium channels. When
an action potential
reaches the synapse
these channels open,
causing calcium ions to
flow into the cell.
2. These calcium ions

cause the synaptic
vesicles to fuse with the
cell membrane,
releasing their contents
(the neurotransmitter
chemicals) by
exocytosis.
3. The neurotransmitters diffuse across the synaptic cleft.
4. The neurotransmitter binds to the neuroreceptors in the post-synaptic membrane,

causing the channels to open. In the example shown these are sodium channels, so sodium
ions flow in.
5. This causes a depolarisation of the post-synaptic cell membrane, which may initiate an
action potential.
6. The neurotransmitter is broken down by a specific enzyme in the synaptic cleft; for
example the enzyme acetylcholinesterase breaks down the neurotransmitter acetylcholine.
The breakdown products are absorbed by the pre-synaptic neuron by endocytosis and used
to re-synthesis more neurotransmitter, using energy from the mitochondria. This stops the
synapse being permanently on.
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6.5.7 State that the endocrine system consists of glands that release hormones
that are transported in the blood.(1)
The gland secretes these

hormones into the blood
stream
 The hormone travels in blood

to the target tissue (effector)
that brings about a response.
 The response modifies the internal environment and this becomes feedback stimuli
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6.5.8 State that homeostasis involves maintaining the internal environment

between limits, including blood pH, carbon dioxide concentration, blood
glucose concentration, body temperature and water balance.(1)
Homeostasis involves maintaining the internal environment (tissue fluid, blood) between
limits.
Examples:
 Blood pH
 Blood carbon dioxide levels
 blood glucose concentration
 body temperature
 water balance
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6.5.9 Explain that homeostasis involves monitoring levels of variables and
correcting changes in levels by negative feedback mechanisms.(3)
 This model represents the main features of a negative feedback model .

 Specialised receptors detect changes within the internal conditions
 This information is relayed to a central coordinator that determines the level of
response
 The coordinator in turn relays such a decision to the effector that is specialised to
produce the response behaviour
 Notice that this response will modify the internal environment and that these new
conditions will in turn become the new stimuli.
 The cycle will continue until conditions are reduced back to within narrow acceptable
limits (fixed regulation point).
 Notice that system works responding to conditions which are lower than and higher
than the fixed regulation point.
 Very efficient systems allow very little in the way of undershoot and overshoot.
This model is an
alternative
representation of the
negative feedback
cycle but this time
emphasising the
deviation from a
fixed regulation
point.
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6.5.10 Explain the control of body temperature, including the transfer of heat in
blood, and the roles of the hypothalamus, sweat glands, skin arterioles and
shivering.(3).
The control of body temperature includes the transfer of heat in blood, the role of sweat
glands and skin arterioles, and shivering.
Model of
temperature control:
 The sensors
are found in
the
hypothalamus.
 Effectors are found in the skin and in muscles.
 The fixed point for regulation is around 37.8 degrees centigrade.
Note the particular features of skin

which are involved in temperature
regulation:
Hairs with the erector Pilli

muscle
 Sweat glands
 Blood arterioles
 The skin is an effector in the
control of body temperature.
 It is particularly important to prevent cooling or overheating of the core (essential
organs and brain)
The hypothalamus as the co-ordinator of temperature regulation:
Vasoconstriction: is a cold adaptation narrowing of arterioles that reduces blood flow to

the surface of the skin is coupled with a dilation of the horizontal shunt vessels. This
prevents heat loss from blood near the skin surface and retains heat in the body core for
essential organs.
Vasodilation: is an adaptation to warm conditions in which arterioles dilate sending more

blood closer to the skin surface from where heat can be radiated to the surrounding
environment. The horizontal shunt vessels are constricted sending most blood closer to the
skin surface. Additionally sweat (mainly water) is released onto the surface of the skin
where it enters the vapour phase when warmed by the heat carried by blood. Therefore the
vapour of sweat carried
away heat energy from
blood.
Cold: when cold the

following events occur to
reduce heat loss and raise
temperature.
Lower than regulation

temperature blood reaches
the hypothalamus.
The hypothalamus signals

the vasoconstriction
(narrowing) of arterioles
Muscle effectors are

produces the rapid
contraction relaxation of
muscles known as shivering
which produces more body
heat.
Hot:
 Sweat is secreted onto the surface of skin when body temperature is high
 Sweat is largely composed of water which has a high specific heat capacity (absorbs
a heat easily)
 Body heat is transferred from skin and blood to the sweat
 The sweat evaporates transferring heat away and in doing so cools the body
Hair and temperature control:
 In warm weather the erector-pilli muscle are relaxed and the hairs lie flat.
 This prevents a build up of a 'boundary layer' of warm air.
 Air movement will further accelerate the loss of heat.
 In cold weather the erector-pilli muscle contracts and the hair moves vertical. This
traps a 'boundary layer' of warm air that reduces the temperature gradient and in
turn reduces heat loss.
 Other longer term adaptations take place when exposed to continuously high or low
temperatures. These effects are often linked to the metabolic rate of the organism
and are atleast in part influenced by the endocrine system.
 Whilst a significant mechanism for the control of heat loss in many mammals the
relatively hairless body of humans derives very little benefit from this mechanism.
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6.5.11 Explain the control of blood glucose concentration, including the roles of
glucagon, insulin and α and β cells in
the pancreatic islets.(3)
Blood sugar concentration is regulated for a number of reason amongst which:
Osmosis. content of a tissue is determined by the concentration of the surrounding tissues.
Respiration: Some tissues are entirely dependent on blood sugar as a respiratory substrate
being unable to either store glucose of metabolise fat.
Model:
a) Low glucose
concentration is
detected by the
pancreas.
b) Alpha cells in the

pancreatic islets secret
glucagon.
c)Glucagon flows through the blood to receptors on liver cells.
d)Liver responds by adding glucose to blood stream.
h) High blood glucose levels stimulate the beta pancreatic cells
a) Beta pancreatic cells secrete insulin.
f)Insulin flows through the blood to the receptors on liver cells.
g)Insulin stimulates the liver to remove blood glucose and store this as glycogen (insoluble)
Blood sugar regulation alternative diagram (labels correspond to both diagrams)
Note from the

second diagram that
the glucose levels
remain within a set
of narrow limits. The
regulation point for
blood glucose is
around 5 mmol dm-3.
The response and

change in blood
glucose levels becomes the new stimuli for receptors
This is a typical feedback control.
Additional features of blood sugar regulation:
• Insulin stimulates the 'glucose-transporter molecules' in the cell membrane of

liver cells to take up glucose.
• Insulin is responsible for the conversion of glucose to glycogen but also to fat.
• Insulin stimulates the incorporation of 'glucose-transporter molecules into the
cell membrane of the muscle cells. Then the glucose is taken up and stored as
glycogen as in the liver. Muscles will store around 900g of glycogen in
comparison to the average 100 g in the liver.
• Adipose (fat cells) are also stimulated to take up the glucose and begin its
conversion to fat.
• Almost all cells are influenced in this way by insulin, except that is for the
cells of the nervous system which require a constant blood glucose level.
• After the absorption of glucose most cells will switch their metabolism to the
beta oxidation of fat and preserve their glycogen stores. This cannot be done
by the cells of the nervous system which of course is another reason to
maintain blood sugar levels.
Ask around your class for people who whilst not diabetics experience mild hyperglycaemia
or have experienced this as on the odd occasion. They will describe that if they do not eat
regularly that they experience muscle weakness, lethargy, mild visual disturbance. The
interesting features are those that affect their nervous system and have some remarkable
resemblance to mild migraine symptoms.
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6.5.12 Distinguish between type I and type II diabetes. (2)
Type I diabetes (early or juvenile onset):
 Auto-immune disease in which the beta-cells pancreatic are destroyed.

 Unable to produce insulin.
 Responds well to regular injection of insulin probably manufactured as the genetically
engineered humulin.
Type II diabetes (Adult onset):
 Reduced sensitivity of the liver cells to insulin.

 Reduced number of receptors on the liver cell membrane.
In both types of diabetes there is:
 a build of glucose in the blood stream and it will then subsequently appear in urine.
(test with a Clinistic )
 High concentrations of blood glucose (hyperglycaemia) results in the movement of
water from cells by osmosis.
 This extra fluid in the blood results in larger quantities of urine production.
 A lack of glucose in cells means that fats then proteins have to be metabolised in
respiration.
 Particularly the breakdown of protein for energy creates organ damage.
6.6.1 Draw and label diagrams of the adult male and female reproductive
systems.(1)
Male reproductive system:
Female reproductive system:
top
6.6.2 Outline the role of hormones in the menstrual cycle, including FSH (follicle
stimulating hormone), LH (luteinizing hormone), estrogen and
progesterone.(2).
 Sexual maturity in women is marked by the beginning of the menstrual cycles. These
cycles coordinate the development and release of an egg with the conditions required
in the uterus to support a pregnancy.
 The cycle is controlled by hormones from both the brain (FSH and LH) and the
ovary(oestrogen and progesterone).
 The natural cycle repeats until there is either a pregnancy or the woman reaches
menopause and the end of the reproductive phase of her life.
 FSH and LH are two hormone that are active at significant phases of human
development including primary and secondary sexual characteristics. They are both
significant hormones in the primary sex determination. Following puberty human
become fertile and in females this is manifest as the menstrual cycle.
Anterior Pituitary Hormones:
Follicle Stimulating hormone (FSH)
 Stimulates the development of a primary follicles (oocytes).

 Increases the number of follicular cells which in turn produce oestrogens.
 Produces follicular fluids.
 Develops the oocyte in the follicle.
Luteinising Hormone (LH):
 surges in mid cycle (12 days) to bring about ovulation.

 high LH is associated with a resumption of meiosis in the oocyte. Meiosis has been
arrested in Prophase I since the embryonic stage. Only at the point of fertilisation
does meiosis complete.
 stimulates the development of the corpus luteum.
Ovarian Hormones
Oestrogen:
 Stimulates the development of the endometrium (lining of the uterus) and it

associated blood supply.
 During the first half of the cycle there is positive feedback through increased
sensitivity of the follicle cells to FSH (Up-regulation of receptors on the follicular cell
plasma membrane).
 During the second half of the cycle (high oestrogen) there is negative feedback on
FSH and LH.
Progesterone:
 maintains the lining of the endometrium

 negative feedback on FSH and LH
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6.6.3 Annotate a graph showing hormone levels in the menstrual cycle,

illustrating the relationship between changes in hormone levels and
ovulation, menstruation and thickening of the endometrium.(2 )
a)
Follicle
Stimulating Hormone (FSH) is secreted by the pituitary gland of the brain and stimulates
the development of a primary follicle.
(b) Primary follicle cells secrete oestrogen which in turn increase the secretion of FSH in a
positive feedback.
(c) The oestrogen thickens the lining of the uterus in preparation for a fertilised egg.
(d) The peak of oestrogen secretion at day 12 causes the pituitary to release a surge of LH.
This loosens the now mature egg which is released in ovulation
 LH reduces the secretion of Oestrogen

 LH stimulates the empty follicle to develop into the corpus luteum
e) Progesterone and oestrogen together stop any more LH and FSH being secreted from the
pituitary. (negative feedback)
 This prevents further follicle development or ovulation.
(f) Progesterone maintains the lining of the thickened endometrium in preparation for the
implantation of a fertilised egg.
(g) If implantation does not take place then the Corpus luteum degenerates and fails.
The progesterone production stops.
 The endometrium breaks down and the 'menstrual period' begins

 The inhibition of FSH and LH by ovarian hormones has been removed and so they
begin their secretions again of FSH.
 A new cycle has begun.
top
6.6.4 List three roles of testosterone in males.(1)
1. Week 7 of embryonic development, testosterone initiates the development of male

genitalia.
2. Around mid teens, testosterone initiates the development of secondary sexual

characteristics
 increase in muscle mass

 increase in the length of the long bones (height)
 increase in the length of the vocal cords (voice deepens)
 spermatogenesis
 growth of the penis and testis
3. Post puberty testosterone maintains the production of sperm cells and the male sex
drive.
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6.6.5 Outline the process of in vitro fertilization (IVF).(2)
One of the common reasons that a couple cannot produce a pregnancy is the low sperm
count of the male. This can be rectified by concentrating the male sperm before being
placed into the uterus of the female using a catheter.
Other reasons for infertility include stenosis (blockage) of the cervix which again can be
overcome by simple procedures and the mechanical introduction of sperm through this
passage (as above).
In more complex cases of infertility it is necessary to fertilize the egg cell outside of the
body before introducing the embryos into the uterus for implantation.
One of the assisted reproductive technologies is called 'In Vitro fertilisation' or IVF. First
performed by Sir Robert Winston in 1978 Oldham England. Louise Brown was the first of
millions of 'test tube babies'.
The first stage of the technique maybe preceded by the taking of inhibitors of FSH and LH
but this stage maybe missed through monitoring using ultrasound.
top
6.6.6 Discuss the ethical issues associated with IVF.(3)
Advantages of IVF: there are as many reasons for this treatment as there are people
seeking this treatment. As examples
 over comes infertility

 allow families for people who must be sterilised e.g.. radiography/chemo therapy
cancer patients
Disadvantages of IVF:
 what happens to unwanted embryo's

 what happens to orphaned embryo's
 should infertility be by-passed

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 A virus is a non-cellular structure consisting of DNA or RNA surrounded by a

Advantages of Light Microscopes Advantages of Electron Microscopes

Most cells – up to 100 um

 Prokaryote – a cell that lacks any membrane bound organelles. Prokaryotes

Flagellum – An organelle that propels a cell

 Prokaryotic cells divide by binary fission

see 2.3.2 form functions of the cell

 The nucleus has a double membrane with pores(NP).

Mitochondria: location of aerobic respiration and a majot synthesis of ATP region..

 Double membrane organelle.

rER form a network of tubules with a maze

 In general these run away from the nucleus

Golgi apparatus: modification of proteins prior to secretion.

 proteins for secretion are modified

2.3.3 Identify structures from 2.3.1 in electron micrographs of liver cells.(2)

Identify: To find an answer from a given number of possibilities.

To identify structures within an electron micrograph it is necessary to know the scale at

In an electron micrograph the nucleus will be the largest of the

In this image there is a dark stained region called the nucleolus

This image shows the junction between two liver

Notice the mitochondria to the left and the rER to the

This micrograph of a mitochondria shows:

 Double outer membrane

Endoplasmic reticulum (rER).

The rER runs vertical in the image. Note the

 A cell with a great deal of rER is producing

The golgi apparatus in the diagram

 Vesicles containing proteins fuse with

 simple membrane bound vesicle containing hydrolytic enzymes

2.3.4 Comparison of prokaryotic and eukaryotic cells (3).

outline means to give a brief summary

The total length

R. Weinberg, R. (1998) One Renegade Cell. London:Phoenix, Science Masters Series.

'Cancer is, in essence a genetic disease'

Volgestein and Kinzler

 Tumours (cancers) are a cell mass formed as a result

Not on the syllabus and just for interest

a) Oncogenes, which if accidentally or inappropriately activated increase the risk of tumour

3. Tumour Suppressor deactivation. An alternative or additional feature is the idea of

 The cell specialises to a particular function in a process called differentiation.

Describe means to give a detailed account.

a)The cell membrane is intact

b) G1,Within the nucleus, genes

c) S-phase in which DNA

Explain means to give a detailed account of causes, reasons or mechanisms.

 The process of cell division produces genetically identical daughter cells.

 Conservation of chromosome number. The chromosome number in each of the

This pair of sister chromatids image was taken

The two sister chromatids are held together at the

The arms of the chromatids are visible because of a

State that growth, embryonic development, tissue repair and asexual

Identify means to find an answer from a given number of possibilities.

 Glucose: C6H12O6 this is a hexose sugar (six

Glucose is soluble and has osmotic effects when

This is an alternative diagram of glucose where the carbons are

 Ribose: Pentose (5 carbon sugar).

This model shows the structure of the

 Each of the common amino acids has the

This is an alternative way to draw the general