4.5 Article

Requirement of Chloride for the Downhill Electron Transfer Pathway from the Water-Splitting Center in Natural Photosynthesis

期刊

JOURNAL OF PHYSICAL CHEMISTRY B
卷 126, 期 1, 页码 123-131

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.1c09176

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资金

  1. JSPS KAKENHI [JP18H05155, JP18H01937, JP20H03217, JP20H05090, JP18H01186, JP16H06560]
  2. JST CREST [JPMJCR1656]
  3. Interdisciplinary Computational Science Program in CCS, University of Tsukuba
  4. Department of Biotechnology, Government of India [BT/RLF/Re-entry/41/2020]

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Depletion of Cl- in PSII affects the proton transfer pathway and significantly increases the redox potential of S-2/S-3 transition. The binding between D2-Lys317 and D1-Asp61 influences the subsequent proton transfer process.
In photosystem II (PSII), Cl- is a prerequisite for the second flash-induced oxidation of the Mn4CaO5 cluster (the S-2 to S-3 transition). We report proton transfer from the substrate water molecule via D1-Asp61 and electron transfer via redox-active D1-Tyr161 (TyrZ) to the chlorophyll pair in Cl--depleted PSII using a quantum mechanical/molecular mechanical approach. The low-barrier H-bond formation between the substrate water molecule and D1-Asp61 remained unaffected upon the depletion of Cl-. However, the binding site, D2-Lys317, formed a salt bridge with D1-Asp61, leading to the inhibition of the subsequent proton transfer. Remarkably, the redox potential (E-m) of S-2/S-3 increased significantly, making electron transfer from S-2 to TyrZ energetically uphill, as observed in Ca2+-depleted PSII. The uphill electron transfer pathway was induced by the significant increase in E-m(S-2/S-3) caused by the loss of charge compensation for D2-Lys317 upon the depletion of Cl-, whereas it was induced by the significant decrease in E-m(TyrZ) caused by the rearrangement of the water molecules at the Ca2+ binding moiety upon the depletion of Ca2+.

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