The possible role of proton-coupled electron transfer (PCET) in water oxidation by photosystem II

被引:462
|
作者
Meyer, Thomas J. [1 ]
Huynh, My Hang V.
Thorp, H. Holden
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] High Explos Sci & Technol Grp, Los Alamos Natl Lab, Dynam Mat Properties & Energet Mat Sci Div, Los Alamos, NM 87545 USA
关键词
coupled electron-proton transfer; electron transfer; photosynthesis; photosystem II; proton transport;
D O I
10.1002/anie.200600917
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
All higher life forms use oxygen and respiration as their primary energy source. The oxygen comes from water by solar-energy conversion in photosynthetic membranes. In green plants, light absorption in photosystem II (PSII) drives electron-transfer activation of the oxygen-evolving complex (OEC). The mechanism of water oxidation by the OEC has long been a subject of great interest to biologists and chemists. With the availability of new molecular-level protein structures from X-ray crystallography and EXAFS, as well as the accumulated results from numerous experiments and theoretical studies, it is possible to suggest how water may be oxidized at the OEC. An integrated sequence of light-driven reactions that exploit coupled electron-proton transfer (EPT) could be the key to water oxidation. When these reactions are combined with long-range proton transfer (by sequential local proton transfers), it may be possible to view the OEC as an intricate structure that is "wired for protons". © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:5284 / 5304
页数:21
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