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[NiFe], [FeFe], and [Fe] hydrogenase models from isomers

The study of hydrogenase enzymes (H(2)ases) is necessary because of their importance to a future hydrogen energy economy. These enzymes come in three distinct classes: [NiFe] H(2)ases, which have a propensity toward H(2) oxidation; [FeFe] H(2)ases, which have a propensity toward H(2) evolution; and...

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Autores principales: Ogo, Seiji, Kishima, Takahiro, Yatabe, Takeshi, Miyazawa, Keishi, Yamasaki, Ryunosuke, Matsumoto, Takahiro, Ando, Tatsuya, Kikkawa, Mitsuhiro, Isegawa, Miho, Yoon, Ki-Seok, Hayami, Shinya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286669/
https://www.ncbi.nlm.nih.gov/pubmed/32577514
http://dx.doi.org/10.1126/sciadv.aaz8181
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author Ogo, Seiji
Kishima, Takahiro
Yatabe, Takeshi
Miyazawa, Keishi
Yamasaki, Ryunosuke
Matsumoto, Takahiro
Ando, Tatsuya
Kikkawa, Mitsuhiro
Isegawa, Miho
Yoon, Ki-Seok
Hayami, Shinya
author_facet Ogo, Seiji
Kishima, Takahiro
Yatabe, Takeshi
Miyazawa, Keishi
Yamasaki, Ryunosuke
Matsumoto, Takahiro
Ando, Tatsuya
Kikkawa, Mitsuhiro
Isegawa, Miho
Yoon, Ki-Seok
Hayami, Shinya
author_sort Ogo, Seiji
collection PubMed
description The study of hydrogenase enzymes (H(2)ases) is necessary because of their importance to a future hydrogen energy economy. These enzymes come in three distinct classes: [NiFe] H(2)ases, which have a propensity toward H(2) oxidation; [FeFe] H(2)ases, which have a propensity toward H(2) evolution; and [Fe] H(2)ases, which catalyze H(−) transfer. Modeling these enzymes has so far treated them as different species, which is understandable given the different cores and ligand sets of the natural molecules. Here, we demonstrate, using x-ray analysis and nuclear magnetic resonance, infrared, Mössbauer spectroscopies, and electrochemical measurement, that the catalytic properties of all three enzymes can be mimicked with only three isomers of the same NiFe complex.
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spelling pubmed-72866692020-06-22 [NiFe], [FeFe], and [Fe] hydrogenase models from isomers Ogo, Seiji Kishima, Takahiro Yatabe, Takeshi Miyazawa, Keishi Yamasaki, Ryunosuke Matsumoto, Takahiro Ando, Tatsuya Kikkawa, Mitsuhiro Isegawa, Miho Yoon, Ki-Seok Hayami, Shinya Sci Adv Research Articles The study of hydrogenase enzymes (H(2)ases) is necessary because of their importance to a future hydrogen energy economy. These enzymes come in three distinct classes: [NiFe] H(2)ases, which have a propensity toward H(2) oxidation; [FeFe] H(2)ases, which have a propensity toward H(2) evolution; and [Fe] H(2)ases, which catalyze H(−) transfer. Modeling these enzymes has so far treated them as different species, which is understandable given the different cores and ligand sets of the natural molecules. Here, we demonstrate, using x-ray analysis and nuclear magnetic resonance, infrared, Mössbauer spectroscopies, and electrochemical measurement, that the catalytic properties of all three enzymes can be mimicked with only three isomers of the same NiFe complex. American Association for the Advancement of Science 2020-06-10 /pmc/articles/PMC7286669/ /pubmed/32577514 http://dx.doi.org/10.1126/sciadv.aaz8181 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Ogo, Seiji
Kishima, Takahiro
Yatabe, Takeshi
Miyazawa, Keishi
Yamasaki, Ryunosuke
Matsumoto, Takahiro
Ando, Tatsuya
Kikkawa, Mitsuhiro
Isegawa, Miho
Yoon, Ki-Seok
Hayami, Shinya
[NiFe], [FeFe], and [Fe] hydrogenase models from isomers
title [NiFe], [FeFe], and [Fe] hydrogenase models from isomers
title_full [NiFe], [FeFe], and [Fe] hydrogenase models from isomers
title_fullStr [NiFe], [FeFe], and [Fe] hydrogenase models from isomers
title_full_unstemmed [NiFe], [FeFe], and [Fe] hydrogenase models from isomers
title_short [NiFe], [FeFe], and [Fe] hydrogenase models from isomers
title_sort [nife], [fefe], and [fe] hydrogenase models from isomers
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286669/
https://www.ncbi.nlm.nih.gov/pubmed/32577514
http://dx.doi.org/10.1126/sciadv.aaz8181
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