电子转移
电子传输链
化学
电子受体
光化学
光系统
氧化还原
光系统I
接受者
动力学
电子供体
马库斯理论
光合作用
氧气
光系统II
反应速率常数
催化作用
有机化学
生物化学
物理
凝聚态物理
量子力学
作者
Dmitry A. Cherepanov,Georgy E. Milanovsky,Anastasia A. Petrova,А. Н. Тихонов,Alexey Yu. Semenov
出处
期刊:Biokhimiya
[Pleiades Publishing]
日期:2017-11-01
卷期号:82 (11): 1249-1268
被引量:30
标识
DOI:10.1134/s0006297917110037
摘要
This review considers the state-of-the-art on mechanisms and alternative pathways of electron transfer in photosynthetic electron transport chains of chloroplasts and cyanobacteria. The mechanisms of electron transport control between photosystems (PS) I and II and the Calvin–Benson cycle are considered. The redistribution of electron fluxes between the noncyclic, cyclic, and pseudocyclic pathways plays an important role in the regulation of photosynthesis. Mathematical modeling of light-induced electron transport processes is considered. Particular attention is given to the electron transfer reactions on the acceptor side of PS I and to interactions of PS I with exogenous acceptors, including molecular oxygen. A kinetic model of PS I and its interaction with exogenous electron acceptors has been developed. This model is based on experimental kinetics of charge recombination in isolated PS I. Kinetic and thermodynamic parameters of the electron transfer reactions in PS I are scrutinized. The free energies of electron transfer between quinone acceptors A 1A /A 1B in the symmetric redox cofactor branches of PS I and iron–sulfur clusters F X , F A , and F B have been estimated. The second-order rate constants of electron transfer from PS I to external acceptors have been determined. The data suggest that byproduct formation of superoxide radical in PS I due to the reduction of molecular oxygen in the A1 site (Mehler reaction) can exceed 0.3% of the total electron flux in PS I.
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