Accumulating the hydride state in the catalytic cycle of [FeFe]-hydrogenases

H(2) turnover at the [FeFe]-hydrogenase cofactor (H-cluster) is assumed to follow a reversible heterolytic mechanism, first yielding a proton and a hydrido-species which again is double-oxidized to release another proton. Three of the four presumed catalytic intermediates (H(ox), H(red)/H(red) and H...

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Detalles Bibliográficos
Autores principales: Winkler, Martin, Senger, Moritz, Duan, Jifu, Esselborn, Julian, Wittkamp, Florian, Hofmann, Eckhard, Apfel, Ulf-Peter, Stripp, Sven Timo, Happe, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524980/
https://www.ncbi.nlm.nih.gov/pubmed/28722011
http://dx.doi.org/10.1038/ncomms16115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524980/
https://www.ncbi.nlm.nih.gov/pubmed/28722011
http://dx.doi.org/10.1038/ncomms16115

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