Cambridge International AS & A Level: BIOLOGY 9700/34

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Cambridge International AS & A Level

* 3 8 6 4 0 7 8 0 2 0 *

BIOLOGY 9700/34
Paper 3 Advanced Practical Skills 2 October/November 2023

2 hours

You must answer on the question paper.

You will need: The materials and apparatus listed in the confidential instructions

INSTRUCTIONS
● Answer all questions.
● Use a black or dark blue pen. You may use an HB pencil for any diagrams or graphs.
● Write your name, centre number and candidate number in the boxes at the top of the page.
● Write your answer to each question in the space provided.
● Do not use an erasable pen or correction fluid.
● Do not write on any bar codes.
● You may use a calculator.
● You should show all your working and use appropriate units.

INFORMATION
● The total mark for this paper is 40.
● The number of marks for each question or part question is shown in brackets [ ].

For Examiner’s Use

Total

This document has 16 pages. Any blank pages are indicated.

DC (PQ/JG) 322734/3
© UCLES 2023 [Turn over
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1 The progress of some enzyme-catalysed reactions can be followed by measuring the time taken
for the substrate to be hydrolysed.

The enzyme amylase catalyses the hydrolysis of starch to maltose.

You will investigate the effect of different concentrations of amylase on the hydrolysis of starch.

You are provided with the materials shown in Table 1.1.

Table 1.1

labelled contents hazard volume / cm3 risk

E 2.0% amylase solution irritant 50


............................

S 1.0% starch solution none 50


............................

W distilled water none 100

iodine iodine solution irritant 25


............................
unknown concentration of
U irritant 10
amylase solution

If any solution comes into contact with your skin, wash off immediately under cold water.

It is recommended that you wear suitable eye protection.

(a) (i) Think about the hazards of using the materials in Table 1.1 and decide whether the risk
of using E, S and iodine is low, medium or high.

Complete Table 1.1, using the words low, medium or high, to state the risk of using E, S
and iodine. You may use each word once, more than once or not at all. [1]

You will need to:

• prepare different concentrations of amylase solution


• record the time taken for the amylase to hydrolyse starch
• use your results to estimate the concentration of an unknown solution of amylase, U.

You will need to use proportional dilution to make different concentrations of amylase solution, E.

You will need to prepare 10 cm3 of each concentration, using E and W.

Table 1.2 shows how to prepare two of the concentrations you will use.

Decide which other concentrations of amylase solution you will use.

© UCLES 2023 9700/34/O/N/23


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(ii) Complete Table 1.2 to show how you will prepare the other concentrations.

Table 1.2

percentage concentration
volume of E / cm3 volume of W / cm3
of amylase solution
2.0 10.0 0.0

0.4 2.0 8.0


[2]

During the investigation you will be sampling at intervals and using iodine solution to test
for the presence of starch. The end-point is reached when the iodine solution is a dark
yellow-brown. There may also be some specks of blue-black present in the iodine solution.
These specks can be ignored.

Carry out step 1 to step 14.

step 1 Prepare the concentrations of amylase solution as shown in Table 1.2, in the
beakers provided. Mix well.

step 2 Label test-tubes with the concentrations of amylase solution prepared in step 1.

step 3 Label the white tile with the numbers shown in Fig. 1.1.

The numbers indicate the sampling times in seconds.

step 4 Put one drop of iodine on the white tile at each sampling time, as shown in Fig. 1.1.

drop of 15 30 45 60
iodine

75 90 105 120

135 150 165 180

Fig. 1.1
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step 5 Put 3 cm3 of S into each of the test-tubes labelled in step 2.

step 6 Put 1 cm3 of the 2.0% amylase solution, E, into the test-tube labelled 2.0%. Use a
glass rod to mix.

step 7 Start timing.

step 8 After 15 seconds, use the glass rod to transfer a drop of the mixture from the
test-tube onto the drop of iodine that is labelled 15, on the white tile.

step 9 Clean the glass rod with a paper towel.

step 10 Repeat step 8 to step 9 at 15-second intervals until the end-point is reached.

step 11 Record in (a)(iii) the time when the end-point is first observed.

If the end-point is not reached at 180 seconds, record as ‘more than 180’.

step 12 Clean the white tile with a damp paper towel and then dry the white tile. Make sure
all the numbers are still visible.

step 13 Put one drop of iodine on the white tile at each sampling time, as shown in Fig. 1.1.

step 14 Repeat step 6 to step 13 using the other concentrations of amylase solution you
prepared in step 1.

(iii) Record your results in an appropriate table.

[5]

(iv) State the independent variable in this investigation.

..................................................................................................................................... [1]

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Carry out step 15 to step 23.

step 15 Put one drop of iodine on the white tile at each sampling time, as shown in Fig. 1.1.

step 16 Label a test-tube with the letter U.

step 17 Put 3 cm3 of S into this test-tube.

step 18 Put 1 cm3 of solution U into the same test-tube. Use a glass rod to mix.

step 19 Start timing.

step 20 After 15 seconds, use the glass rod to transfer a drop of the mixture from the
test-tube onto the drop of iodine that is labelled 15, on the white tile.

step 21 Clean the glass rod with a paper towel.

step 22 Repeat step 20 to step 21 at 15-second intervals until the end-point is reached.

step 23 Record, in (a)(v), the time when the end-point is first observed.

If the end-point is not reached at 180 seconds, record as ‘more than 180’.

(v) State the result for U.

result for U ......................................................... [1]

(vi) Using your results in (a)(iii) and (a)(v), estimate the concentration of amylase in U.

..................................................................................................................................... [1]

(vii) Suggest one source of error in the procedure described in step 10 of this investigation.

..................................................................................................................................... [1]

(viii) Suggest how you could make one improvement to reduce the source of error stated in (a)(vii).

...........................................................................................................................................

...........................................................................................................................................

...........................................................................................................................................

..................................................................................................................................... [1]

(ix) Describe how you would modify the procedure to investigate the effect of pH on the time
taken for amylase to hydrolyse starch.

...........................................................................................................................................

...........................................................................................................................................

...........................................................................................................................................

...........................................................................................................................................

..................................................................................................................................... [2]

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(b) A student investigated the effect of different substrate concentrations on the activity of an
enzyme in the presence of an inhibitor.

The concentration of the inhibitor was standardised.

The results are shown in Table 1.3.

Table 1.3

concentration of substrate rate of reaction


/ mol dm–3 / arbitrary units
0.0 0.000
0.2 0.750
0.4 1.375
0.6 1.800
0.8 2.175
1.0 2.250

(i) Plot a graph of the data in Table 1.3 on the grid in Fig. 1.2.

Use a sharp pencil.

Fig. 1.2
[4]
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(ii) Use your graph in Fig. 1.2 to determine the rate of reaction when the concentration of
substrate is 0.45 mol dm–3.

rate of reaction = .................................. arbitrary units [1]

(iii) The Vmax of this enzyme is 2.250 arbitrary units.

Using this information and the graph in Fig. 1.2, state whether the inhibitor is a competitive
inhibitor or a non-competitive inhibitor.

...........................................................................................................................................

Explain your answer.

...........................................................................................................................................

...........................................................................................................................................

...........................................................................................................................................

..................................................................................................................................... [2]

[Total: 22]

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2 M1 is a slide of a stained transverse section through a plant leaf.

(a) (i) Draw a large plan diagram of the region of the leaf on M1 indicated by the shaded area
in Fig. 2.1.

Use a sharp pencil.

draw this region

Fig. 2.1

Use one ruled label line and label to identify the palisade tissue.

[5]

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(ii) Observe the cells in the upper epidermis on the section of the leaf on M1.
Select a line of four adjacent epidermal cells.

Each cell must touch at least one of the other epidermal cells.

• Make a large drawing of this line of four epidermal cells.


• Use one ruled label line and label to identify the cell wall of one epidermal cell.

[4]

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(b) Fig. 2.2 is a photomicrograph of a stained transverse section of a different leaf from M1.

You are not expected to be familiar with this specimen.

Fig. 2.2

Identify three observable differences, other than colour, between the leaf section in Fig. 2.2
and the leaf section on M1.

Record these three observable differences in Table 2.1.

Table 2.1

feature Fig. 2.2 M1

[4]
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(c) Fig. 2.3 shows a diagram of a stage micrometer scale that is being used to calibrate an
eyepiece graticule.

The length of one division on this stage micrometer is 1.0 mm.

0 10 20 30 40 50 60 70 80 90 100

Fig. 2.3

(i) Use Fig. 2.3 to calculate the actual length of one eyepiece graticule unit.

Show your working and give your answer in micrometres (μm).

actual length = ......................................................... μm


[3]

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Fig. 2.4 is the same photomicrograph as that shown in Fig. 2.2. This was taken using the
same microscope and eyepiece graticule as in Fig. 2.3.

The eyepiece graticule scale has been placed across the midrib of the leaf section.

0
10 20 30 40 50 60 70 80 90 100

Fig. 2.4

(ii) Use the calibration of the eyepiece graticule unit from (c)(i) to calculate the actual
thickness of the midrib of the leaf section in Fig. 2.4.

Show your working and use appropriate units.

actual thickness of the midrib of the leaf section = .......................................................... [1]

(iii) Suggest a possible function of the structure labelled A in Fig. 2.4.

...........................................................................................................................................

...........................................................................................................................................

..................................................................................................................................... [1]

[Total: 18]
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Permission to reproduce items where third-party owned material protected by copyright is included has been sought and cleared where possible. Every
reasonable effort has been made by the publisher (UCLES) to trace copyright holders, but if any items requiring clearance have unwittingly been included, the
publisher will be pleased to make amends at the earliest possible opportunity.

To avoid the issue of disclosure of answer-related information to candidates, all copyright acknowledgements are reproduced online in the Cambridge
Assessment International Education Copyright Acknowledgements Booklet. This is produced for each series of examinations and is freely available to download
at www.cambridgeinternational.org after the live examination series.

Cambridge Assessment International Education is part of Cambridge Assessment. Cambridge Assessment is the brand name of the University of Cambridge
Local Examinations Syndicate (UCLES), which is a department of the University of Cambridge.

© UCLES 2023 9700/34/O/N/23

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