| Literature DB >> 23399489 |
Hannah S Shafaat1, Olaf Rüdiger, Hideaki Ogata, Wolfgang Lubitz.
Abstract
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.Entities:
Keywords: Electrochemistry; Hydrogen; Oxygen-tolerant; Renewable energy; Spectroscopy
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Year: 2013 PMID: 23399489 DOI: 10.1016/j.bbabio.2013.01.015
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002