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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...
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| Pubblicato in: | Nat Commun |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5524980/ https://ncbi.nlm.nih.gov/pubmed/28722011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms16115 |
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