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DOI10.1073/pnas.2000895117
Acquirement of water-splitting ability and alteration of the charge-separation mechanism in photosynthetic reaction centers
Tamura H.; Saito K.; Ishikita H.
发表日期2020
ISSN0027-8424
起始页码16373
结束页码16382
卷号117期号:28
英文摘要In photosynthetic reaction centers from purple bacteria (PbRC) and the water-oxidizing enzyme, photosystem II (PSII), charge separation occurs along one of the two symmetrical electron-transfer branches. Here we report the microscopic origin of the unidirectional charge separation, fully considering electron–hole interaction, electronic coupling of the pigments, and electrostatic interaction with the polarizable entire protein environments. The electronic coupling between the pair of bacteriochlorophylls is large in PbRC, forming a delocalized excited state with the lowest excitation energy (i.e., the special pair). The charge-separated state in the active branch is stabilized by uncharged polar residues in the transmembrane region and charged residues on the cytochrome c2 binding surface. In contrast, the accessory chlorophyll in the D1 protein (ChlD1) has the lowest excitation energy in PSII. The charge-separated state involves ChlD1•+ and is stabilized predominantly by charged residues near the Mn4CaO5 cluster and the proceeding proton-transfer pathway. It seems likely that the acquirement of water-splitting ability makes ChlD1 the initial electron donor in PSII. © 2020 National Academy of Sciences. All rights reserved.
英文关键词Artificial photosynthesis; Excitation energy transfer; Oxygen evolution; P680; Unidirectional electron transfer
语种英语
scopus关键词bacteriochlorophyll; chlorophyll; cytochrome c2; water; amino acid; bacteriochlorophyll; oxygen; Article; bioenergy; electron transport; excitation; molecular stability; nonhuman; photosynthesis; photosystem II; polarization; priority journal; protein binding; Proteobacteria; proton transport; separation technique; static electricity; chemistry; electron; electron transport; metabolism; photosynthesis; protein subunit; Amino Acids; Bacteriochlorophylls; Electron Transport; Electrons; Oxygen; Photosynthetic Reaction Center Complex Proteins; Photosystem II Protein Complex; Protein Subunits; Proteobacteria; Water
来源期刊Proceedings of the National Academy of Sciences of the United States of America
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/160263
作者单位Tamura, H., Department of Applied Chemistry, University of Tokyo, Tokyo, 113-8654, Japan, Research Center for Advanced Science and Technology, University of Tokyo, Tokyo, 153-8904, Japan; Saito, K., Department of Applied Chemistry, University of Tokyo, Tokyo, 113-8654, Japan, Research Center for Advanced Science and Technology, University of Tokyo, Tokyo, 153-8904, Japan; Ishikita, H., Department of Applied Chemistry, University of Tokyo, Tokyo, 113-8654, Japan, Research Center for Advanced Science and Technology, University of Tokyo, Tokyo, 153-8904, Japan
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Tamura H.,Saito K.,Ishikita H.. Acquirement of water-splitting ability and alteration of the charge-separation mechanism in photosynthetic reaction centers[J],2020,117(28).
APA Tamura H.,Saito K.,&Ishikita H..(2020).Acquirement of water-splitting ability and alteration of the charge-separation mechanism in photosynthetic reaction centers.Proceedings of the National Academy of Sciences of the United States of America,117(28).
MLA Tamura H.,et al."Acquirement of water-splitting ability and alteration of the charge-separation mechanism in photosynthetic reaction centers".Proceedings of the National Academy of Sciences of the United States of America 117.28(2020).
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