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Electronic structural changes of Mn in the oxygen-evolving complex of photosystem II during the catalytic cycle.


ABSTRACT: The oxygen-evolving complex (OEC) in photosystem II (PS II) was studied in the S0 through S3 states using 1s2p resonant inelastic X-ray scattering spectroscopy. The spectral changes of the OEC during the S-state transitions are subtle, indicating that the electrons are strongly delocalized throughout the cluster. The result suggests that, in addition to the Mn ions, ligands are also playing an important role in the redox reactions. A series of Mn(IV) coordination complexes were compared, particularly with the PS II S3 state spectrum to understand its oxidation state. We find strong variations of the electronic structure within the series of Mn(IV) model systems. The spectrum of the S3 state best resembles those of the Mn(IV) complexes Mn3(IV)Ca2 and saplnMn2(IV)(OH)2. The current result emphasizes that the assignment of formal oxidation states alone is not sufficient for understanding the detailed electronic structural changes that govern the catalytic reaction in the OEC.

SUBMITTER: Glatzel P 

PROVIDER: S-EPMC3683399 | biostudies-literature | 2013 May

REPOSITORIES: biostudies-literature

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Electronic structural changes of Mn in the oxygen-evolving complex of photosystem II during the catalytic cycle.

Glatzel Pieter P   Schroeder Henning H   Pushkar Yulia Y   Boron Thaddeus T   Mukherjee Shreya S   Christou George G   Pecoraro Vincent L VL   Messinger Johannes J   Yachandra Vittal K VK   Bergmann Uwe U   Yano Junko J  

Inorganic chemistry 20130506 10


The oxygen-evolving complex (OEC) in photosystem II (PS II) was studied in the S0 through S3 states using 1s2p resonant inelastic X-ray scattering spectroscopy. The spectral changes of the OEC during the S-state transitions are subtle, indicating that the electrons are strongly delocalized throughout the cluster. The result suggests that, in addition to the Mn ions, ligands are also playing an important role in the redox reactions. A series of Mn(IV) coordination complexes were compared, particu  ...[more]

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