PLANT PHYSIOLOGY · 1969 · 192 citations · 12 references
Life SciencesBiochemistryPlant BiologyPhotosynthesisPlant BiochemistryRedox BiochemistryChloroplast BiochemistryOxygen EvolutionPhotocatalysisPhotochemical KineticsPhotochemistryPhotosystem IiAssayAssay SensitivityOxygen Evolution InhibitionOxygen Evolution MechanismOxygen Evolution ReactionPhotochemical Reaction MechanismsPhotosensitizing CompoundsPrimary Photochemistry
The use of diphenylcarbazide as an electron donor coupled to the photoreduction of 2,6-dichlorophenolindophenol by tris-washed chloroplasts or subchloroplast fragments provides a simple and sensitive assay for photosystem 2 of chloroplasts. By varying the concentration of tris buffer at pH 8.0 during an incubation period it is shown that the destruction of oxygen evolution activity is accompanied by a corresponding emergence of an ability to photooxidize diphenylcarbazide, as evidenced by absorbance changes due to diphenylcarbazide at 300 nm. The temperature-sensitive oxidation of diphenylcarbazide is inhibited by DCMU and by high ionic strengths. This activity appears to measure the primary photochemical reaction of photosystem 2.
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