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Direct Binding of Cysteine-367 Thiolate to the Active Site of the [FeFe]-Hydrogenase from Clostridium beijerinckii in the O2-Stable State.

Created on 18 Aug 2026

Authors

Jifu Duan, Federica Arrigoni, Andreas Rutz, Eckhard Hofmann, Claudio Greco, Thomas Happe

Published in

Biochemistry. Volume 65. Issue 16. Pages 2611-2616. Aug 18, 2026.

Abstract

[FeFe]-hydrogenases are very active biocatalysts for H2 conversion. However, their active site is vulnerable to irreversible degradation initiated by O2 binding at the catalytic iron ion (Fed) of the active center. CbA5H, the [FeFe]-hydrogenase from Clostridium beijerinckii, exhibits stability toward oxygen (O2) due to its ability to reversibly enter an inactive state termed Hinact upon contact with O2. We previously proposed that the close distance of approximately 3.1 Å between the thiol of a nearby cysteine (C367) and Fed, based on a 2.9 Å crystal structure of CbA5H in the Hinact state, enables their binding to each other. This binding therefore was suggested to shield Fed from O2 damage. However, there is currently a lack of evidence to support this hypothesis. Furthermore, density functional theory (DFT) calculations based on a homologous model favored hydroxide as the binding ligand of Fed over the thiol of C367. In this study, we present the crystal structure of CbA5H in the Hinact state at an improved resolution of 2.15 Å. The structure reveals a direct binding between the thiol of C367 and Fed with a distance of approximately 2.77 Å, which is well supported by our DFT calculations based on the new crystallographic data. It is noteworthy that the 2.77 Å bond distance is strikingly long when compared with other iron-sulfur bonds. This finding may provide a crucial foundation for understanding the rapid reversibility of the Hinact state.

PMID:
42610741
Bibliographic data and abstract were imported from PubMed on 18 Aug 2026.

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