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Electrogenic reduction of the primary electron donor P700 + in photosystem I by redox dyes

The kinetics of reduction of the photo-oxidized primary electron donor P700 + by redox dyes N,N,N′, N′-tetramethyl- p-phenylendiamine, 2,6-dichlorophenol-indophenol and phenazine methosulfate was studied in proteoliposomes containing Photosystem I complexes from cyanobacteria Synechocystis sp. PCC 6...

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Published in:FEBS letters 1997-09, Vol.414 (2), p.193-196
Main Authors: Gourovskaya, Kira N., Mamedov, Mahir D., Vassiliev, Ilya R., Golbeck, John H., Semenov, Alexey Yu
Format: Article
Language:English
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Summary:The kinetics of reduction of the photo-oxidized primary electron donor P700 + by redox dyes N,N,N′, N′-tetramethyl- p-phenylendiamine, 2,6-dichlorophenol-indophenol and phenazine methosulfate was studied in proteoliposomes containing Photosystem I complexes from cyanobacteria Synechocystis sp. PCC 6803 using direct electrometrical technique. In the presence of high concentrations of redox dyes, the fast generation of a membrane potential related to electron transfer between P700 and the terminal iron-sulfur clusters F A/F B was followed by a new electrogenic phase in the millisecond time domain, which contributes approximately 20% to the overall photoelectric response. This phase is ascribed to the vectorial transfer of an electron from the redox dye to the protein-embedded chlorophyll of P700 +. Since the contribution of this electrogenic phase in the presence of artificial redox dyes is approximately equal to that of the phase observed earlier in the presence of cytochrome c 6, it is likely that electrogenic reduction of P700 + in vivo occurs due to vectorial electron transfer within RC molecule rather than within the cytochrome c 6-P700 complex.
ISSN:0014-5793
1873-3468
DOI:10.1016/S0014-5793(97)00994-0