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Light saturation response of inactive photosystem II reaction centers in spinach
Authors:Roger A. Chylla  John Whitmarsh
Affiliation:(1) Institute of Microbiology, Czechoslovak Academy of Sciences, 37981 T"rcaron"ebo"ncaron", Czechoslovakia;(2) Institute of Soil Science and Photosynthesis, USSR Academy of Sciences, 142292 Pushchino, USSR
Abstract:Oxygen evolving photosystem II particles were exposed to 100 and 250 W m–2 white light at 20°C under aerobic, anaerobic and strongly reducing (presence of dithionite) conditions. Three types of photoinactivation processes with different kinetics could be distinguished: (1) The fast process which occurs under strongly reducing (t1/2cong1–3 min) and anaerobic conditions (t1/2cong4–12 min). (2) The slow process (t1/2cong15–40 min) and (3) the very slow process (t1/2>100 min), both of which occur under all three sets of conditions.The fast process results in a parallel decline of variable fluorescence (Fv) and of Hill reaction rate, accompanied by an antiparallel increase of constant fluorescence (Fo). We assume that trapping of QA in a negatively charged stable state, (QA)stab, is responsible for the effects observed.The slow process is characterized by a decline of maximal fluorescence (Fm). In presence of oxygen this decline is due to the well known disappearance of Fv which proceeds in parallel with the inhibition of the Hill reaction; Fo remains essentially constant. Under anaerobic and reducing conditions the decline of Fm represents the disappearance of the increment in Fo generated by the fast process. We assume that the slow process consists in neutralization of the negative charge in the domain of QA in a manner that renders QA non-functional. The charge separation in the RC is still possible, but energy of excitation becomes thermally dissipated.The very slow photoinactivation process is linked to loss of charge separation ability of the PS II RC and will be analyzed in a forthcoming paper.Abbreviations F chlorophyll a fluorescence - Fo, Fv, Fm constant, variable, maximum fluorescence - Fprimeo, Fprimev, Fprimem the same, measured in presence of dithionite (Fprimev suppression method) - PS II photosystem II - RC reaction centre (P680. Pheo) - P680 primary electron donor - Pheo pheophytin, intermediary electron acceptor - QA, QB the primary and secondary electron acceptor - Z, D electron donors to P680 - (QA)stab, (QA H)stab hypothetical modifications of QA resulting from photoinactivation - O-, A- and R-conditions aerobic, anaerobic and strongly reducing (presence of dithionite) conditions - MES 2-(N-morpholine) ethanesulphonic acid - DCPIP 2,6-dichlorphenolindophenol - GGOC mixture of glucose, glucose oxidase and catalase - DT-20 oxygen-evolving PS II particles
Keywords:chlorophyll a fluorescence  oxygen evolving PS II particles  pheophytin  photoinhibition  photosystem II  primary electron acceptor QA
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