Describe the role of the enzyme dehydrogenase in photosynthesis
● Catalyses the reduction of NADP in the light-dependent reaction
○ NADP accepts (gains) electrons from photoionisation of chlorophyll / photolysis of water
Describe how rate of dehydrogenase activity in extracts of chloroplasts can be measured
Give examples of variables that could be controlled.
● 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.
● 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.
● End point (colour change) is subjective
● Use a colorimeter
● Measure light absorbance of sample at set time intervals
● Zero colorimeter using the colour standard