Cargando…
[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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783544914894651392 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7286669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ogoseiji nifefefeandfehydrogenasemodelsfromisomers AT kishimatakahiro nifefefeandfehydrogenasemodelsfromisomers AT yatabetakeshi nifefefeandfehydrogenasemodelsfromisomers AT miyazawakeishi nifefefeandfehydrogenasemodelsfromisomers AT yamasakiryunosuke nifefefeandfehydrogenasemodelsfromisomers AT matsumototakahiro nifefefeandfehydrogenasemodelsfromisomers AT andotatsuya nifefefeandfehydrogenasemodelsfromisomers AT kikkawamitsuhiro nifefefeandfehydrogenasemodelsfromisomers AT isegawamiho nifefefeandfehydrogenasemodelsfromisomers AT yoonkiseok nifefefeandfehydrogenasemodelsfromisomers AT hayamishinya nifefefeandfehydrogenasemodelsfromisomers |