Abstract
The HypC and HypD maturases are required for the biosynthesis of the Fe(CN)(2)CO cofactor in the large subunit of [NiFe]-hydrogenases. Using infrared spectroscopy we demonstrate that an anaerobically purified, Strep-tagged HypCD complex from Escherichia coli exhibits absorption bands characteristic of diatomic CO and CN(-) ligands as well as CO(2). Metal and sulphide analyses revealed that along with the [4Fe-4S](2+) cluster in HypD, the complex has two additional oxygen-labile Fe ions. We prove that HypD cysteine 41 is required for the coordination of all three ligands. These findings suggest that the HypCD complex carries minimally the Fe(CN)(2)CO cofactor.
Copyright © 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acids / chemistry
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Amino Acids / metabolism
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Binding Sites
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Carbon Monoxide / chemistry
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Carbon Monoxide / metabolism*
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Cations, Divalent
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Coenzymes / chemistry
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Coenzymes / metabolism
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Cyanides / chemistry
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Cyanides / metabolism*
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Escherichia coli / enzymology
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Escherichia coli / genetics*
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Escherichia coli Proteins / chemistry
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Escherichia coli Proteins / genetics
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Escherichia coli Proteins / metabolism*
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Hydrogenase / chemistry
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Hydrogenase / genetics
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Hydrogenase / metabolism*
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Iron / chemistry
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Iron / metabolism
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Ligands
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Plasmids
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Protein Binding
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Proteins / chemistry
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Proteins / genetics
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Proteins / metabolism*
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Recombinant Proteins / chemistry
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Recombinant Proteins / genetics
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Recombinant Proteins / metabolism
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Spectrophotometry, Infrared
Substances
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Amino Acids
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Cations, Divalent
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Coenzymes
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Cyanides
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Escherichia coli Proteins
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HypC protein, E coli
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HypD protein, Bacteria
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Ligands
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Proteins
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Recombinant Proteins
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Carbon Monoxide
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Iron
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nickel-iron hydrogenase
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Hydrogenase