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Energetics of the S2 State Spin Isomers of the Oxygen-Evolving Complex of Photosystem II
Author(s) -
David J. Vinyard,
Sahr Khan,
Mikhail Askerka,
Víctor S. Batista,
Gary W. Brudvig
Publication year - 2017
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/acs.jpcb.7b00110
Subject(s) - energetics , photosystem ii , oxygen , oxygen evolving complex , spin (aerodynamics) , chemical physics , chemistry , photochemistry , photosynthesis , physics , thermodynamics , biochemistry , organic chemistry
The S 2 redox intermediate of the oxygen-evolving complex in photosystem II is present as two spin isomers. The S = 1/2 isomer gives rise to a multiline electron paramagnetic resonance (EPR) signal at g = 2.0, whereas the S = 5/2 isomer exhibits a broad EPR signal at g = 4.1. The electronic structures of these isomers are known, but their role in the catalytic cycle of water oxidation remains unclear. We show that formation of the S = 1/2 state from the S = 5/2 state is exergonic at temperatures above 160 K. However, the S = 1/2 isomer decays to S 1 more slowly than the S = 5/2 isomer. These differences support the hypotheses that the S 3 state is formed via the S 2 state S = 5/2 isomer and that the stabilized S 2 state S = 1/2 isomer plays a role in minimizing S 2 Q A - decay under light-limiting conditions.

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