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CO and CN- syntheses by [FeFe]-hydrogenase maturase HydG are catalytically differentiated events.


ABSTRACT: The synthesis and assembly of the active site [FeFe] unit of [FeFe]-hydrogenases require at least three maturases. The radical S-adenosyl-l-methionine HydG, the best characterized of these proteins, is responsible for the synthesis of the hydrogenase CO and CN(-) ligands from tyrosine-derived dehydroglycine (DHG). We speculated that CN(-) and the CO precursor (-):CO2H may be generated through an elimination reaction. We tested this hypothesis with both wild type and HydG variants defective in second iron-sulfur cluster coordination by measuring the in vitro production of CO, CN(-), and (-):CO2H-derived formate. We indeed observed formate production under these conditions. We conclude that HydG is a multifunctional enzyme that produces DHG, CN(-), and CO at three well-differentiated catalytic sites. We also speculate that homocysteine, cysteine, or a related ligand could be involved in Fe(CO)x(CN)y transfer to the HydF carrier/scaffold.

SUBMITTER: Pagnier A 

PROVIDER: S-EPMC4711877 | biostudies-literature | 2016 Jan

REPOSITORIES: biostudies-literature

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CO and CN- syntheses by [FeFe]-hydrogenase maturase HydG are catalytically differentiated events.

Pagnier Adrien A   Martin Lydie L   Zeppieri Laura L   Nicolet Yvain Y   Fontecilla-Camps Juan C JC  

Proceedings of the National Academy of Sciences of the United States of America 20151222 1


The synthesis and assembly of the active site [FeFe] unit of [FeFe]-hydrogenases require at least three maturases. The radical S-adenosyl-l-methionine HydG, the best characterized of these proteins, is responsible for the synthesis of the hydrogenase CO and CN(-) ligands from tyrosine-derived dehydroglycine (DHG). We speculated that CN(-) and the CO precursor (-):CO2H may be generated through an elimination reaction. We tested this hypothesis with both wild type and HydG variants defective in se  ...[more]

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