Papers

International journal
Oct, 2020

Formation of the High-Spin S-2 State Related to the Extrinsic Proteins in the Oxygen Evolving Complex of Photosystem II

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
  • Shota Taguchi
  • ,
  • Liangliang Shen
  • ,
  • Guangye Han
  • ,
  • Yasufumi Umena
  • ,
  • Jian-Ren Shen
  • ,
  • Takumi Noguchi
  • ,
  • Hiroyuki Mino

Volume
11
Number
20
First page
8908
Last page
8913
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1021/acs.jpclett.0c02411
Publisher
AMER CHEMICAL SOC

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.

Link information
DOI
https://doi.org/10.1021/acs.jpclett.0c02411
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32990440
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000582569600062&DestApp=WOS_CPL
ID information
  • DOI : 10.1021/acs.jpclett.0c02411
  • ISSN : 1948-7185
  • Pubmed ID : 32990440
  • Web of Science ID : WOS:000582569600062

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