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

被引:464
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
相关论文
共 237 条
[121]   ROLE OF CHLORIDE-ION IN PHOTOSYSTEM-II .1. EFFECTS OF CHLORIDE-ION ON PHOTOSYSTEM-II ELECTRON-TRANSPORT AND ON HYDROXYLAMINE INHIBITION [J].
KELLEY, PM ;
IZAWA, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 502 (02) :198-210
[122]   Kinetic isotope effects for nonadiabatic proton transfer reactions in a polar environment. 2. Comparison with an electronically diabatic description [J].
Kiefer, PM ;
Hynes, JT .
JOURNAL OF PHYSICAL CHEMISTRY A, 2004, 108 (52) :11809-11818
[123]   Structural changes of D1 C-terminal α-carboxylate during S-state cycling in photosynthetic oxygen evolution [J].
Kimura, Y ;
Mizusawa, N ;
Yamanari, T ;
Ishii, A ;
Ono, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (03) :2078-2083
[124]   Chelator-induced disappearance of carboxylate stretching vibrational modes in S2/S1 FTIR spectrum in oxygen-evolving complex of photosystem II [J].
Kimura, Y ;
Ono, TA .
BIOCHEMISTRY, 2001, 40 (46) :14061-14068
[125]   PERSPECTIVES ON THE STRUCTURE OF THE PHOTOSYNTHETIC OXYGEN-EVOLVING MANGANESE COMPLEX AND ITS RELATION TO THE KOK CYCLE [J].
KLEIN, MP ;
SAUER, K ;
YACHANDRA, VK .
PHOTOSYNTHESIS RESEARCH, 1993, 38 (03) :265-277
[126]   PROBES OF MECHANISM AND TRANSITION-STATE STRUCTURE IN THE ALCOHOL-DEHYDROGENASE REACTION [J].
KLINMAN, JP .
CRC CRITICAL REVIEWS IN BIOCHEMISTRY, 1981, 10 (01) :39-78
[127]   Site-directed mutagenesis of basic arginine residues 305 and 342 in the CP 43 protein of photosystem II affects oxygen-evolving activity in Synechocystis 6803 [J].
Knoepfle, N ;
Bricker, TM ;
Putnam-Evans, C .
BIOCHEMISTRY, 1999, 38 (05) :1582-1588
[128]   TEMPERATURE-DEPENDENCE OF S-STATE TRANSITION IN A THERMOPHILIC CYANOBACTERIUM, SYNECHOCOCCUS-VULCANUS COPELAND MEASURED BY ABSORPTION CHANGES IN THE ULTRAVIOLET REGION [J].
KOIKE, H ;
HANSSUM, B ;
INOUE, Y ;
RENGER, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 893 (03) :524-533
[129]   COOPERATION OF CHARGES IN PHOTOSYNTHETIC O2 EVOLUTION .1. A LINEAR 4STEP MECHANISM [J].
KOK, B ;
FORBUSH, B ;
MCGLOIN, M .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1970, 11 (06) :457-&
[130]   Near-IR irradiation of the S2 state of the water oxidizing complex of photosystem II at liquid helium temperatures produces the metalloradical intermediate attributed to S1YZ• [J].
Koulougliotis, D ;
Shen, JR ;
Ioannidis, N ;
Petrouleas, V .
BIOCHEMISTRY, 2003, 42 (10) :3045-3053