Formation of the High-Spin S2 State Related to the Extrinsic Proteins in the Oxygen Evolving Complex of Photosystem II

被引:12
作者
Taguchi, Shota [1 ]
Shen, Liangliang [2 ]
Han, Guangye [2 ]
Umena, Yasufumi [3 ,4 ]
Shen, Jian-Ren [2 ,3 ,4 ]
Noguchi, Takumi [1 ]
Mino, Hiroyuki [1 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Div Mat Sci, Nagoya, Aichi 4648602, Japan
[2] Chinese Acad Sci, Photosynth Res Ctr, Inst Bot, Key Lab Photobiol, Beijing 100093, Peoples R China
[3] Okayama Univ, Res Inst Interdisciplinary Sci, Okayama 7008530, Japan
[4] Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
CRYSTAL-STRUCTURE; MANGANESE; CLUSTER; MECHANISM; S-2-STATE; BINDING; LIGHT; FIELD; SITE;
D O I
10.1021/acs.jpclett.0c02411
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
The high-spin S-2 state was investigated with photosystem II (PSII) from spinach, Thermosynechococcus vulcanus, and Cyanidioschyzon merolae. In extrinsic protein-depleted PSII, high-spin electron paramagnetic resonance (EPR) signals were not detected in either species, whereas all species showed g similar to 5 signals in the presence of a high concentration of Ca2+ instead of the multiline signal. In the intact and PsbP/Qdepleted PSII from spinach, the g = 4.1 EPR signal was detected. These results show that formation of the high-spin S-2 state of the manganese cluster is regulated by the extrinsic proteins through a charge located near the Mn4 atom in the Mn4CaO5 cluster but is independent of the intrinsic proteins. The shift to the g similar to 5 state is caused by tilting of the z-axis in the Mn4 coordinates through hydrogen bonds or external divalent cations. The structural modification may allow insertion of an oxygen atom during the S-2-to-S-3 transition.
引用
收藏
页码:8908 / 8913
页数:6
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