Required Practiced 8 Flashcards
investigation into the effect of a named factor on the rate of dehydrogenase activity in extracts of chloroplasts
Describe the role of the enzyme dehydrogenase in photosythesis
- catalyses the reduction of NADP in the light-dependent reaction
- NADP gains electrons from photoionisation of chlorophyll/photolysis of water
Describe how rate of dehydrogenase activity in extracts of chloroplasts can
be measured
- Extract chloroplasts from a leaf sample using the method in ‘2.1.3 Methods of studying cells’
- Set up test tubes as follows:
A. Control 1 - set volume of DCPIP (redox indicator dye, electron acceptor), water and
chloroplasts in isolation medium, covered in foil to block light
B. Control 2 - set volume of DCPIP, water and isolation medium without chloroplasts
C. Standard - set volume of water and chloroplasts in isolation medium, without DCPIP
D. Experiment - set volume of DCPIP, water and chloroplasts in isolation medium - Shine light on test tubes and time how long to it takes for DCPIP to turn from blue (oxidised) to
colourless (reduced) in tube D (tube A and B should show no change)
○ Compare to a colour standard (tube C) to identify end point - Rate of dehydrogenase activity (s
-1
) = 1 / time taken
To investigate the effect of a named factor (eg. effect of wavelength of light), you do what ?
repeat and change that factor
Give examples of variables that
could be controlled. (3)
● Source of chloroplasts
● Volume of chloroplast suspension
● Volume / concentration of DCPIP
Explain the purpose of control 1
(tube A). (2)
● Shows light is required for DCPIP to decolourise
● Shows that chloroplasts alone do not cause DCPIP to decolourise
Explain why DCPIP in control 1
stays blue. (2)
● No light so no photoionisation of chlorophyll
● So no electrons released to reduce DCPIP
Explain the purpose of control 2
(tube B). (2)
● Shows chloroplasts are required for DCPIP to decolourise
● Shows that light alone does not cause DCPIP to decolourise
Explain why DCPIP changes from
blue to colourless. (2)
● DCPIP is a redox indicator / DCPIP gets reduced by electrons
● From photoionisation of chlorophyll
Suggest a limitation with the
method and how the experiment
could be modified to overcome
this. (4)
● End point (colour change) is subjective
● Use a colorimeter
● Measure light absorbance of sample at set time intervals
● Zero colorimeter using the colour standard