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Mechanism of the formation of proton transfer pathways in photosynthetic reaction centers.


ABSTRACT: In photosynthetic reaction centers from purple bacteria (PbRCs) from Rhodobacter sphaeroides, the secondary quinone QB accepts two electrons and two protons via electron-coupled proton transfer (PT). Here, we identify PT pathways that proceed toward the QB binding site, using a quantum mechanical/molecular mechanical approach. As the first electron is transferred to QB, the formation of the Grotthuss-like pre-PT H-bond network is observed along Asp-L213, Ser-L223, and the distal QB carbonyl O site. As the second electron is transferred, the formation of a low-barrier H-bond is observed between His-L190 at Fe and the proximal QB carbonyl O site, which facilitates the second PT. As QBH2 leaves PbRC, a chain of water molecules connects protonated Glu-L212 and deprotonated His-L190 forms, which serves as a pathway for the His-L190 reprotonation. The findings of the second pathway, which does not involve Glu-L212, and the third pathway, which proceeds from Glu-L212 to His-L190, provide a mechanism for PT commonly used among PbRCs.

SUBMITTER: Sugo Y 

PROVIDER: S-EPMC8325351 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Mechanism of the formation of proton transfer pathways in photosynthetic reaction centers.

Sugo Yu Y   Saito Keisuke K   Ishikita Hiroshi H  

Proceedings of the National Academy of Sciences of the United States of America 20210701 30


In photosynthetic reaction centers from purple bacteria (PbRCs) from <i>Rhodobacter sphaeroides</i>, the secondary quinone Q<sub>B</sub> accepts two electrons and two protons via electron-coupled proton transfer (PT). Here, we identify PT pathways that proceed toward the Q<sub>B</sub> binding site, using a quantum mechanical/molecular mechanical approach. As the first electron is transferred to Q<sub>B</sub>, the formation of the Grotthuss-like pre-PT H-bond network is observed along Asp-L213, S  ...[more]

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