Authors
Oliver Lenz, Lars Lauterbach, Stefan Frielingsdorf, Bärbel Friedrich
Publication date
2015/3
Book
Biohydrogen
Pages
61-88
Publisher
De Gruyter
Description
Hydrogenases are nature’s catalysts designed to extract protons from molecular hydrogen (H2) thereby forming a reactive hydride species (H−). Those enzymes capable of catalyzing the complete reaction, H2↔ 2 e−+ 2 H+, come in two different flavors, namely [NiFe]-and [FeFe]-hydrogenases [1, 2, 3]. They are assigned according to the metal content in their active sites.[FeFe]-hydrogenases, which are described in detail in Chapters 3 and 7, are usually highly active in the direction of proton reduction and display turnover rates of up to 20,000 hydrogen molecules per second [4]. However,[FeFe]-hydrogenases are exclusively synthesized under strictly anoxic conditions in their host organisms, and are immediately, and in most cases irreversibly, inactivated by traces of O2. The proposed mechanism of O2-mediated inactivation is described in Chapters 3 and 5. This property makes it extremely difficult to use these …
Total citations
201520162017201820192020202120222023202444344374114
Scholar articles
O Lenz, L Lauterbach, S Frielingsdorf, B Friedrich - Biohydrogen, 2015
O Lenz, L Lauterbach, S Frielingsdorf, B Friedrich - 2015
A Applegate, U Ermler, B Friedrich, S Frielingsdorf… - 2015