Photosynthetic water oxidation: binding and activation of substrate waters for O-O bond formation

被引:54
|
作者
Vinyard, David J. [1 ]
Khan, Sahr [1 ]
Brudvig, Gary W. [1 ]
机构
[1] Yale Univ, Dept Chem, New Haven, CT 06520 USA
关键词
OXYGEN-EVOLVING COMPLEX; X-RAY SPECTROSCOPY; PHOTOSYSTEM-II; O-2-EVOLVING COMPLEX; AMMONIA BINDS; DIMANGANESE COMPLEXES; ALTERNATING ELECTRON; CHLORIDE REQUIREMENT; CRYSTAL-STRUCTURE; PROTON-TRANSFER;
D O I
10.1039/c5fd00087d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photosynthetic water oxidation occurs at the oxygen-evolving complex (OEC) of Photosystem II (PSII). The OEC, which contains a Mn4CaO5 inorganic cluster ligated by oxides, waters and amino-acid residues, cycles through five redox intermediates known as Si states (i = 0-4). The electronic and structural properties of the transient S-4 intermediate that forms the O-O bond are not well understood. In order to gain insight into how water is activated for O-O bond formation in the S-4 intermediate, we have performed a detailed analysis of S-state dependent substrate water binding kinetics taking into consideration data from Mn coordination complexes. This analysis supports a model in which the substrate waters are both bound as terminal ligands and react via a water-nucleophile attack mechanism.
引用
收藏
页码:37 / 50
页数:14
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