逐步 O-诱导的 CO 脱氢酶[NiFe(OH)(μ-S)]活性位点簇的重排和拆解。
Stepwise O -Induced Rearrangement and Disassembly of the [NiFe (OH)(μ -S) ] Active Site Cluster of CO Dehydrogenase.
机构信息
Institut für Biologie, Humboldt-Universität zu Berlin, Unter den Linden 6, 10099, Berlin, Germany.
出版信息
Angew Chem Int Ed Engl. 2023 Aug 7;62(32):e202305341. doi: 10.1002/anie.202305341. Epub 2023 Jun 30.
Ni,Fe-containing carbon monoxide dehydrogenases (CODHs) catalyze the reversible reduction of carbon dioxide to carbon monoxide. CODHs are found in anaerobic microorganisms and can rapidly lose their activity when exposed to air. What causes the loss of activity is unclear. In this study, we analyzed the time-dependent structural changes induced by the presence of air on the metal centers of CODH-II. We show that inactivation is a multistep process. In a reversible step, the open coordination site on the Ni ion is blocked by a Ni,Fe-bridging μ-sulfido or chlorido ligand. Blocking this open coordination site with a cyanide ligand stabilizes the cluster against O -induced decomposition, indicating that O attacks at the Ni ion. In the subsequent irreversible phase, nickel is lost, the Fe ions rearrange and the sulfido ligands disappear. Our data are consistent with a reversible reductive reactivation mechanism to protect CODHs from transient over-oxidation.
含镍铁的一氧化碳脱氢酶(CODHs)能够催化二氧化碳可逆还原为一氧化碳。CODHs 存在于厌氧微生物中,当暴露于空气中时,其活性会迅速丧失。导致活性丧失的原因尚不清楚。在这项研究中,我们分析了空气中存在时 CODH-II 金属中心引起的时变结构变化。我们表明,失活是一个多步骤的过程。在一个可逆步骤中,Ni 离子上的开放配位位点被 Ni,Fe 桥连的 μ-硫代或氯代配体所阻塞。用氰化物配体阻塞这个开放配位位点可以稳定配合物免受 O 引起的分解,表明 O 攻击的是 Ni 离子。在随后的不可逆阶段,镍丢失,Fe 离子重排,硫代配体消失。我们的数据与一个可逆的还原再激活机制一致,该机制可以保护 CODHs 免受瞬时过度氧化。