Water oxidation mechanism in photosystem II, including oxidations, proton release pathways, O-O bond formation and O2 release

被引:334
作者
Siegbahn, Per E. M. [1 ,2 ]
机构
[1] Stockholm Univ, ALBA NOVA, Dept Phys, SE-10691 Stockholm, Sweden
[2] Stockholm Univ, Arrhenius Lab, Dept Biochem & Biophys, SE-10691 Stockholm, Sweden
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2013年 / 1827卷 / 8-9期
关键词
Density functional theory; Photosystem II; Oxygen evolving complex; O-O bond formation; Energy diagrams; Transition states; OXYGEN-EVOLVING COMPLEX; CHEMICAL CLUSTER APPROACH; MANGANESE COMPLEX; MN CLUSTER; OXIDIZING COMPLEX; STRUCTURAL MODELS; ELECTRON-TRANSFER; CATALYTIC SITE; MN4CA COMPLEX; S-2; STATE;
D O I
10.1016/j.bbabio.2012.10.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present status of DFT studies on water oxidation in photosystem Ills described. It is argued that a full understanding of all steps is close. In each S-transition, the manganese that is oxidized and the proton released are strongly implicated, and structures of all intermediates have been determined. For the S-2-state, recent important experimental findings support key elements of the structure and the mechanism. In this mechanism, the O-O bond is formed between an oxyl radical in the center of the cluster and an Mn-bridging mu-oxo ligand, which was suggested already in 2006. The DFT structure of the oxygen evolving complex, suggested in 2008, is very similar to the recent high-resolution X-ray structure. Some new aspects of the interaction between P-680 and the OEC are suggested. This article is part of a Special Issue entitled: Metals in Bioenergetics and Biomimetics Systems. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1003 / 1019
页数:17
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