Structural and Spectroscopic Insights into Catalytic Intermediates of a [NiFe]-hydrogenase from Group 3.

IF 2.8 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChemBioChem Pub Date : 2025-10-13 DOI:10.1002/cbic.202500692
Marion Jespersen, Christian Lorent, Olivier N Lemaire, Ingo Zebger, Tristan Wagner
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引用次数: 0

Abstract

Hydrogenases catalyze reversible H2 production and are potential models for renewable energy catalysts. Here, the full redox landscape of a group 3 [NiFe]-hydrogenase from methanothermococcus thermolithotrophicus is elucidated, resembling group 1 enzymes. Structural and spectroscopic analyses reveal a catalytic-ready state with nickel seesaw coordination, enabling intermediate trapping and advancing mechanistic understanding of oxygen-sensitive [NiFe] enzymes.

[NiFe]-氢化酶催化中间体的结构和光谱研究
氢化酶催化可逆制氢,是可再生能源催化剂的潜在模型。本文阐明了产自热嗜养甲烷球菌的第3组[NiFe]-氢化酶的完整氧化还原过程,类似于第1组酶。结构和光谱分析揭示了镍跷跷板配位的催化就绪状态,实现了中间捕获和推进对氧敏感酶的机制理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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