| Literature DB >> 30509463 |
Oliver Lenz1, Lars Lauterbach2, Stefan Frielingsdorf2.
Abstract
Dioxygen-tolerant [NiFe]-hydrogenases are defined by their ability to catalyze the reaction, H2⇌2H++2e- even in the presence of O2. Catalytic and probably also noncatalytic mechanisms protect their active sites from being inactivated by reactive oxygen species, which makes them attractive subjects of investigation from both fundamental and applied perspectives. Prominent representatives of the O2-tolerant [NiFe]-hydrogenases have been isolated from the chemolithoautotrophic model organism Ralstonia eutropha H16, which can thrive in a simple mineral medium supplemented with the gases H2, O2, and CO2. In this chapter, we describe methods for cultivation and genetic manipulation of R. eutropha, both of which are prerequisites for the reproducible manufacturing of high-quality hydrogenase preparations. The purification procedures for two different O2-tolerant [NiFe]-hydrogenases from R. eutropha are described in detail, as well as the corresponding biochemical procedures used for the determination of the catalytic properties of these sophisticated enzymes.Entities:
Keywords: Affinity chromatography; Alcaligenes eutrophus; Biofuel cell; Catalytic hydrogen–deuterium exchange; Chemolithotrophy; Clark electrode; Cofactor recycling; Cupriavidus necator; Enzyme purification; Genetic manipulation; Hydrogen oxidation; Hydrogen production; Hydrogenase; Hydrogenomonas; Iron; Iron–sulfur clusters; Knallgas; Metalloenzyme; Nickel; Oxygen tolerance; Photometric assay; Plasmid; Protein engineering; Ralstonia eutropha; Wautersia eutropha; [NiFe]-hydrogenase
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Year: 2018 PMID: 30509463 DOI: 10.1016/bs.mie.2018.10.008
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600