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A B
enzyme enzyme
activity activity
0 50 100 0 50 100
temperature / °C temperature / °C
C D
enzyme enzyme
activity activity
0 50 100 0 50 100
temperature / °C temperature / °C
2. The diagram represents enzyme action.
+ +
W X Y
A W X Y
B X W Y
C X Y W
D Y W X
The substrate fits into the enzyme at the active site and is split into the
products, which are released.
This is known as the lock and key hypothesis.
3. The diagram represents a chemical reaction.
reactants product
A B C
D
Enzymes are proteins and have a specific shape, held in place by bonds.
This is extremely important around the active site area as the specific shape
is what ensures the substrates will fit into the active site and enable the
reaction to proceed.
The substrates fit into the active site of the enzyme like a key fits into a
lock.
D is the only enzyme shape which has a complementary shape to the
reactants and subsequent product:
4. A food stain on a table cloth is where meat cooked in oil has been spilt.
Which combination of enzymes should be in the washing powder to remove the stain?
A B
product
active site
substrate product
enzyme enzyme
C D
enzyme substrate
product
The substrate fits into the enzyme at the active site and the product is
released once the reaction has taken place.
6. The table shows the conditions in four test-tubes containing equal amounts of starch and salivary
amylase.
temperature
pH
/ °C
A 2 27
B 2 37
C 7 27
D 7 37
active site
With which substrate would this enzyme most easily form an enzyme-substrate complex?
A B C D
✓ Enzymes are proteins and have a specific shape, held in place by bonds.
✓ This is extremely important around the active site area as the specific shape
is what ensures the substrate will fit into the active site and enable the
reaction to proceed.
✓ The substrate is a complementary shape to the active site and fits into it as
a key fits into a lock.
A
B
C
D
enzyme at pH 1.5
and temperature 37 °C
✓ Enzymes are proteins and have a specific shape, held in place by bonds.
This is extremely important around the active site area as the specific shape
is what ensures the substrate will fit into the active site and enable the
reaction to proceed.
✓ Enzymes work at specific pHs and changing the pH will denature the
enzyme, causing the bonds to break and the shape of the active site to
change.
✓ This means that the substrate will no longer fit into the active site and
therefore the rate of reaction will be much lower.
A is incorrect as removing the products will not have any effect on the
rate of reaction.
A carbohydrates
B enzymes
C fatty acids
D hormones
A B C D
water-bath
at 37 °C
Remember protease enzymes from the stomach work best at an acidic pH.
The numbers of bubbles of oxygen released per minute were counted at each temperature.
temperature / °C 15 25 35 45 55
number of bubbles / bubbles per minute 96 98 82 36 1
The results suggest the optimum temperature for the enzyme is between which two values?
A 15 °C and 35 °C
B 35 °C and 45 °C
C 35 °C and 55 °C
D 45 °C and 55 °C
Beyond 35⁰C the number of bubble produced per minute drops significantly
to 36, showing that the rate of reaction has slowed down.
This is an indication that the increase in temperature has had an effect on
the working of the enzymes.
14. Which graph shows the effect of temperature between 20 °C and 35 °C on the activity of a human
digestive enzyme?
A B
rate of rate of
reaction reaction
20 35 20 35
temperature / °C temperature / °C
C D
rate of rate of
reaction reaction
20 35 20 35
temperature / °C temperature / °C
15. Lactase is a human enzyme that catalyses the breakdown of lactose in milk.
A 0 °C B 18 °C C 37 °C D 100 °C
rate of
reaction
1 2 3 4 5 6 7 8 9 10 11 12 13
pH
A at pH 1 and pH 13
B at pH 3 and pH 11
C at pH 5 and pH 9
D at pH 7
Enzymes are proteins and have a specific shape, held in place by bonds. This
is extremely important around the active site area as the specific shape is
what ensures the substrate will fit into the active site and enable the
reaction to proceed.
Heating to high temperatures(beyond the optimum) will break the bonds
that hold the enzyme together and it will lose its shape. This is known as
denaturation. Substrates cannot fit into denatured enzymes as the shape of
their active site has been lost.
Optimum temperature for the majority of enzymes is around 40⁰C.
B is incorrect as white blood cells destroy foreign cells, not body enzymes. This is
not temperature dependent.
C is incorrect as enzymes enable digestion to take place, they are not generally
digested themselves. Again, this is not temperature dependent.
y-axis
x-axis
What are the labels for the x-axis and the y-axis?
x-axis y-axis
A pH rate of reaction
B pH
H time
C rate of reaction pH
D time
im pH
The independent variable is always placed on the x axis. This is the factor
that is changed when investigating. In this case, the experiment would be
carried out at different pHs and so this is what is changed.
The dependent variable is always palced on the y axis. This is the factor that
is measured to obtain the results. In this case, the rate of reaction of the
enzyme would be measured at different pHs.
19. The enzyme catalase, found in potato, speeds up the breakdown of hydrogen peroxide. The
reaction releases a froth of oxygen bubbles.
The diagram shows an experiment to find the effect of changes in pH on the rate of this reaction.
piece of potato
dilute hydrogen peroxide solution
The table shows the time taken for the froth of bubbles to reach the top of the test-tube at
different pH values.
A pH 4 B pH 5 C pH 6 D pH 7
The quicker the froth reaches the top of the test tube, the faster the
enzyme is working.
20. What is a characteristic of all catalysts?
1 2
enzyme substrate
A 1 2
B 1 3
C 3 1
D 3 2
1 = substrate
2 = products
3 = enzyme
22. The table shows the temperature and pH at which four different enzymes are most active.
optimum temperature
optimum pH
/ °C
A 25 10
B 37 7
C 40 2
D 50 5
enzyme 1
amino acids proteins
enzyme 2
proteins amino acids
Amino acids are small molecules and are the basic units of proteins.
Whether the rate increases or not depends on how high the temperature
now is.
If the increase in 10°C has taken it beyond the optimum temperature then
the rate will slow down.
If the increase in 10°C takes it closer towards the optimum temperature
then the rate will speed up.
Six different test-tubes are set up, each containing a mixture of amylase and starch solution.
Which condition should not be kept the same in each of the six test-tubes?
A concentration of amylase
B pH
C temperature
D volume of starch solution
enzyme 2
enzyme 1 enzyme 3
rate of
reaction
1 2 3 4 5 6 7 8 9 10 11 12 13 14
pH
For enzyme 1, the rate of reaction is quickest at pH 1.5, making this its
optimum pH.
For enzyme 2, the rate of reaction is quickest at pH 7, making this its
optimum pH.
For enzyme 3, the rate of reaction is quickest at pH 14, making this its
optimum pH.
A acids
B alkalis
C enzymes
D hormones
Enzymes are biological catalysts which means they speed up the rate of a
reaction without being changed themselves.
Digestion is an example of a reaction that requires the action of enzymes to
speed up the breakdown of large food molecules.
A, B and D are all incorrect as none of these will speed up the rate of reaction to
breakdown large substrate molecules into smaller products.
29. The graph shows the effect of pH on the activity of two enzymes.
enzyme
activity
1 2 3
pH
A 1 B 3 C 5 D 8
30. Four identical mixtures of starch and amylase were kept at different temperatures. The graph
shows the time taken for the starch to be completely digested at each temperature.
time for
starch to
be digested
A B C D
temperature
The rate of reaction is the quickest when the starch takes the least time to
be digested.
31. Equal quantities of a protein-digesting enzyme were added to 5 cm3 of protein solutions of
different pH. Each tube was kept at 37 °C.
The amount of amino acid in each tube was measured after 3 minutes. The results are shown in
the table.
1 10
2 9
3 7
4 2
5 1
6 1
7 1
8 0
A 1 B 7 C 8 D 10
The more amino acid present, the quicker the enzyme is working to digest
the protein.
32. Four test-tubes were set up as shown in the diagram.
B is incorrect as the amylase has been boiled which means that it will
have denatured and not work at all.
D is incorrect as the amylase has been boiled which means that it will
have denatured and not work at all.
33. A human digestive enzyme breaks down its substrate at a fast rate at 35 °C.
What would occur if the enzyme and substrate were kept at 75 °C?
Enzymes are proteins and have a specific shape, held in place by bonds. This
is extremely important around the active site area as the specific shape is
what ensures the substrate will fit into the active site and enable the
reaction to proceed.
Enzymes work fastest at their ‘optimum temperature’ – in this question, the
optimum temperature is likely 37⁰C (this is human body temperature
meaning this enzyme is probably a human enzyme).
Heating to high temperatures(beyond the optimum) will break the bonds
that hold the enzyme together and it will lose its shape. This is known as
denaturation. Substrates cannot fit into denatured enzymes as the shape of
their active site has been lost.
Denaturation is irreversible - once enzymes are denatured they cannot
regain their proper shape and activity will stop.
34. The diagram shows the action of amylase.
amylase part of a
starch molecule
A carbohydrates
B DNA
C fats
D proteins
A 0 °C B 27 °C C 40 °C D 65 °C
A 15 °C B 35 °C C 45 °C D 65 °C
9 The better the enzyme works, the quicker the reaction will be finished.
38. The graph shows how the rate of an enzyme-controlled reaction changes with temperature.
rate of
reaction
temperature X
Heating to high temperatures (beyond the optimum) will break the bonds
that hold the enzyme together and it will lose its shape. This is known as
denaturation. Substrates cannot fit into denatured enzymes as the shape of
their active site has been lost.
Denaturation is irreversible - once enzymes are denatured they cannot
regain their proper shape and activity will stop.
A B
rate of rate of
reaction reaction
20 70 20 70
temperature / °C temperature / °C
C D
rate of rate of
reaction reaction
20 70 20 70
temperature / °C temperature / °C
Low temperatures do not denature enzymes; they simply make them move
more slowly and so the rate of reaction is slower; up to the optimum
temperature, heating enzymes makes them work more quickly.
Heating to high temperatures(beyond the optimum) will break the bonds
that hold the enzyme together and it will lose its shape. This is known as
denaturation. Substrates cannot fit into denatured enzymes as the shape of
their active site has been lost.
Denaturation is irreversible - once enzymes are denatured they cannot
regain their proper shape and activity will stop.
40. Which substance is an enzyme?
A bile
B fibrinogen
C lipase
D maltose
Remember that enzymes often end in ‘ase’ unless they are protease
enzymes.