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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...
Autores principales: | Winkler, Martin, Senger, Moritz, Duan, Jifu, Esselborn, Julian, Wittkamp, Florian, Hofmann, Eckhard, Apfel, Ulf-Peter, Stripp, Sven Timo, Happe, Thomas |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
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 |
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