Chapter 3 Biological Macromolecules
Chapter 3 Biological Macromolecules
Chapter 3 Biological Macromolecules
Chapter 3
Learning Objec-ves (1 of 2)
1. Summarize the properties of carbon that have made it important for
the evolution of a wide diversity of organisms.
2. Describe how functional groups are important for the functions of
biological molecules.
3. Define isomer and state the relevance of isomers to biochemical
reactions.
4. Define a dehydration synthesis reaction and hydrolysis.
5. Differentiate between monosaccharides, disaccharides, and
polysaccharides, the different forms of carbohydrate molecules.
Learning Objec-ves (2 of 2)
6. Describe the structure and properties of lipids.
7. List major protein functions in living organisms.
8. Discuss the structure of amino acids, the formation of
polypeptides, and the four levels of protein structure.
9. Describe the structure of nucleotides and how they link together
to form DNA and RNA.
10. The structure of DNA and how it differs from RNA.
Regulatory Protein and DNA
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Organic Molecules
• Four major classes of organic molecules are found in living organisms:
carbohydrates, lipids, proteins, and nucleic acids
• In organic molecules, carbon atoms bond covalently to each other
and to other atoms in molecules that range in size from a few atoms
to thousands or millions of atoms
• Molecules consisting of carbon linked only to hydrogen atoms are
called hydrocarbons
• Hydrocarbons consist of carbon and hydrogen.
• Covalent bonds store considerable energy.
• Hydrocarbons are nonpolar. And when functional groups ARE ADDED,
THEY CONFER chemical properties to the molecule
A. Two-carbon hydrocarbons with single, double,
and triple bonding
10
Stereoisomers
COOH COOH
H C R R C H
L isomer D isomer
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A. Glucose B. Fructose
(an aldehyde) (a ketone)
H H H
H C OH C O C O
C O Structural H C OH Stereo- H C OH
isomer isomer
HO C H HO C H HO C H
H C OH H C OH HO C H
H C OH H C OH H C OH
H C OH H C OH H C OH
H H H
Fructose Glucose Galactose
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Biological Molecules – Proteins, Carbohydrates,
Lipids, and Nucleic Acids
• Polymer – built by linking monomers
• Monomer – small, similar chemical subunits
Dehydration synthesis
–Formation of large molecules by the removal of water
–Monomers are joined to form polymers
Hydrolysis
–Breakdown of large molecules by the addition of water
–Polymers are broken down to monomers
14
Dehydration Synthesis
Hydrolysis
Carbohydrates
• Molecules with a 1:2:1 raIo of carbon, hydrogen, oxygen
• Empirical formula (CH2O)n
• C—H covalent bonds hold much energy
• Monosaccharides contain three to seven carbon atoms
• Two monosaccharides polymerize to form a disaccharide
• Carbohydrate polymers with more than 10 linked
monosaccharide monomers are polysaccharides
• Energy storage molecules – glycogen and starch are
polysaccharides
• Structural carbohydrates example – Cellulose is a
polysaccharide
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Monosaccharides
• Simplest carbohydrate
• 6 carbon sugars play important roles
• Glucose C6H12O6
• All monosaccahrides occur in linear form
• Example of common hexoses are Glucose, Fructose, and
Galactose
• Enzymes that act on different sugars can distinguish structural
and stereoisomers of this basic six-carbon skeleton
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Glyceraldehyde Ribose Mannose
(3 carbons; (5 carbons; (6 carbons;
a triose) a pentose) a hexose)
α-Glucose
or
D. Space-filling model
β-Glucose
DISACCHARIDES
• Disaccharides are assembled from
two monosaccharides covalently
joined by a dehydration synthesis
reaction
• Example: Maltose is formed by a
glycosidic bond linking two α-
glucose molecules with oxygen as a
bridge between the 1 carbon of the
first glucose and the 4 carbon of the
second glucose unit – an α (1→4)
linkage
• Other common disaccharides
include sucrose (glucose + fructose)
and lactose (glucose + galactose)
Polysaccharides
• Long chains of monosaccharides
– Linked through dehydration synthesis
– Polysaccharides may be linear, unbranched molecules, or they
may contain one or more branches in which side chains of
sugar units are attached to a main chain
• Energy storage
– Plants use starch
– Animals use glycogen
• Structural support
– Plants use cellulose
– Arthropods and fungi use chitin (modified glucose containing
nitrogen-containing groups)
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AMYLOSE AND GLYCOGEN
A. Amylose, a plant
starch
Amylose, formed from
Ed Reschke/Getty Images
α-glucose units joined
end to end in alpha (1->4)
linkages. The coiled
structures are induced
by the bond angles in
the α -linkages.
B. Glycogen, found in
animal tissues
Glycogen, formed
from glucose units joined
in chains by α( 1-> 4 )
linkages; side branches
DeAgostini/Getty Images
are linked to the chains
by α(1 ->6) linkages
(boxed in blue).