Shafaat Hannah S, Rüdiger Olaf, Ogata Hideaki, Lubitz Wolfgang
Max-Planck-Institut für Chemische Energiekonversion, Mülheim an der Ruhr, Germany.
Biochim Biophys Acta. 2013 Aug-Sep;1827(8-9):986-1002. doi: 10.1016/j.bbabio.2013.01.015. Epub 2013 Feb 8.
Hydrogenase proteins catalyze the reversible conversion of molecular hydrogen to protons and electrons. The most abundant hydrogenases contain a [NiFe] active site; these proteins are generally biased towards hydrogen oxidation activity and are reversibly inhibited by oxygen. However, there are [NiFe] hydrogenase that exhibit unique properties, including aerobic hydrogen oxidation and preferential hydrogen production activity; these proteins are highly relevant in the context of biotechnological devices. This review describes four classes of these "nonstandard" [NiFe] hydrogenases and discusses the electrochemical, spectroscopic, and structural studies that have been used to understand the mechanisms behind this exceptional behavior. A revised classification protocol is suggested in the conclusions, particularly with respect to the term "oxygen-tolerance". This article is part of a special issue entitled: metals in bioenergetics and biomimetics systems.
氢化酶蛋白催化分子氢与质子和电子之间的可逆转化。最丰富的氢化酶含有一个[NiFe]活性位点;这些蛋白通常偏向于氢氧化活性,并且会被氧气可逆抑制。然而,存在一些具有独特性质的[NiFe]氢化酶,包括好氧氢氧化和优先产氢活性;这些蛋白在生物技术装置的背景下具有高度相关性。本综述描述了四类这些“非标准”[NiFe]氢化酶,并讨论了用于理解这种特殊行为背后机制的电化学、光谱学和结构研究。在结论中提出了一种修订的分类方案,特别是关于“耐氧性”这一术语。本文是名为:生物能量学和仿生系统中的金属的特刊的一部分。