Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory, Oxford OX1 3QR, UK.
Curr Opin Chem Biol. 2012 Apr;16(1-2):26-34. doi: 10.1016/j.cbpa.2012.01.012. Epub 2012 Feb 25.
The bacterial [NiFe]-hydrogenases have been classified as either 'standard' or 'O2-tolerant' based on their ability to function in the presence of O2. Typically, these enzymes contain four redox-active metal centers: a Ni-Fe-CO-2CN- active site and three electron-transferring Fe-S clusters. Recent research suggests that, rather than differences at the catalytic active site, it is a novel Fe-S cluster electron transfer (ET) relay that controls how [NiFe]-hydrogenases recover from O2 attack. In light of recent structural data and mutagenic studies this article reviews the molecular mechanism of O2-tolerance in [NiFe]-hydrogenases and discusses the biosynthesis of the unique Fe-S relay.
根据在氧气存在下的功能,细菌[NiFe]-氢化酶被分为“标准”或“耐氧”型。通常,这些酶包含四个氧化还原活性金属中心:一个 Ni-Fe-CO-2CN-活性位点和三个电子转移 Fe-S 簇。最近的研究表明,控制[NiFe]-氢化酶如何从 O2 攻击中恢复的不是催化活性位点的差异,而是新型 Fe-S 簇电子转移(ET)中继,该中继控制[NiFe]-氢化酶对 O2 的耐受性。鉴于最近的结构数据和诱变研究,本文综述了[NiFe]-氢化酶耐 O2 性的分子机制,并讨论了独特的 Fe-S 中继的生物合成。