The mechanism for proton-coupled electron transfer from tyrosine in a model complex and comparisons with Yz oxidation in photosystem II

被引:45
作者
Sjödin, M
Styring, S
Åkermark, B
Sun, LC
机构
[1] Univ Uppsala, Dept Phys Chem, S-75121 Uppsala, Sweden
[2] Lund Univ, Dept Biochem, S-22100 Lund, Sweden
[3] Stockholm Univ, Dept Organ Chem, S-10691 Stockholm, Sweden
关键词
photosystem II; proton-coupled electron transfer; tyrosine; ruthenium; photochemistry;
D O I
10.1098/rstb.2002.1142
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the water-oxidizing reactions of photosystem II (PSII), a tyrosine residue plays a key part as an intermediate electron-transfer reactant between the primary donor chlorophylls (the pigment P-680) and the water-oxidizing Mn cluster. The tyrosine is deprotonated upon oxidation, and the coupling between the proton reaction and electron transfer is of great mechanistic importance for the understanding of the water-oxidation mechanism. Within a programme on artificial photosynthesis, we have made and studied the proton-coupled tyrosine oxidation in a model system and been able to draw mechanistic conclusions that we use to interpret the analogous reactions in PSII.
引用
收藏
页码:1471 / 1478
页数:8
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