4.8 Article

Regulated Electron Tunneling of Photoinduced Primary Charge Separated State in the Photosystem II Reaction Center

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 8, Issue 6, Pages 1179-1184

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.7b00044

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan [25288004, 26620065, 16H04097]
  2. JSPS [26011113]
  3. MEXT/JSPS [26620003]
  4. Grants-in-Aid for Scientific Research [26620065, 26620003, 14J11113, 25288004, 16H04097] Funding Source: KAKEN

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In initial events of the photosynthesis by higher plants, the photosystem II (PSII) generates photoinduced primary charge-separated (CS) state composed of reduced pheophytin (Pheo(D1)(-center dot)) and oxidized special pair (P+center dot) in chlorophyll a (Chla) P-D1/P-D2 in the D-1/D-2 heterodimer, ultimately leading to the water oxidation at the oxygen-evolving Mn4CaO5 cluster by P+center dot. To understand the mechanism of the efficient generation of initially localized CS state (P-D1(+center dot) Pheo(D1)(-center dot)), we have characterized cofactor geometries and electronic coupling of the photoinduced primary CS state in quinone prereduced membrane of PSII from spinach using the time-resolved electron paramagnetic resonance method. It has been revealed that the electronic coupling between the charges is significantly weak in the CS state separated by 1.5 nm, showing the importance of regulated cofactor-cofactor electronic interaction between a vinyl substituent in Pheo(D1) and an accessory chlorophyll to inhibit the energy-wasting charge recombination after the primary electron-transfer processes.

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