一氧化碳脱氢酶
化学
一氧化碳
星团(航天器)
配体(生物化学)
氧化态
晶体结构
金属
离子
无机化学
结晶学
催化作用
有机化学
受体
程序设计语言
生物化学
计算机科学
作者
Jae‐Hun Jeoung,Holger Dobbek
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2007-11-30
卷期号:318 (5855): 1461-1464
被引量:478
标识
DOI:10.1126/science.1148481
摘要
Anaerobic CO dehydrogenases catalyze the reversible oxidation of CO to CO 2 at a complex Ni-, Fe-, and S-containing metal center called cluster C. We report crystal structures of CO dehydrogenase II from Carboxydothermus hydrogenoformans in three different states. In a reduced state, exogenous CO 2 supplied in solution is bound and reductively activated by cluster C. In the intermediate structure, CO 2 acts as a bridging ligand between Ni and the asymmetrically coordinated Fe, where it completes the square-planar coordination of the Ni ion. It replaces a water/hydroxo ligand bound to the Fe ion in the other two states. The structures define the mechanism of CO oxidation and CO 2 reduction at the Ni-Fe site of cluster C.
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