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An Fe(6)C Core in All Nitrogenase Cofactors
The biological process of dinitrogen reduction to ammonium occurs at the cofactors of nitrogenases, the only enzymes that catalyze this challenging chemical reaction. Three types of nitrogenases have been described, named according to the heterometal in their cofactor: molybdenum, vanadium or iron n...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826452/ https://www.ncbi.nlm.nih.gov/pubmed/35975943 http://dx.doi.org/10.1002/anie.202209190 |
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author | Decamps, Laure Rice, Derek B. DeBeer, Serena |
author_facet | Decamps, Laure Rice, Derek B. DeBeer, Serena |
author_sort | Decamps, Laure |
collection | PubMed |
description | The biological process of dinitrogen reduction to ammonium occurs at the cofactors of nitrogenases, the only enzymes that catalyze this challenging chemical reaction. Three types of nitrogenases have been described, named according to the heterometal in their cofactor: molybdenum, vanadium or iron nitrogenases. Spectroscopic and structural characterization allowed the unambiguous identification of the cofactors of molybdenum and vanadium nitrogenases and revealed a central μ(6)‐carbide in both of them. Although genetic studies suggested that the cofactor of the iron nitrogenase contains a similar Fe(6)C core, this has not been experimentally demonstrated. Here we report Valence‐to‐Core X‐ray Emission Spectroscopy providing experimental evidence that this cofactor contains a carbide, thereby making the Fe(6)C core a feature of all nitrogenase cofactors. |
format | Online Article Text |
id | pubmed-9826452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98264522023-01-09 An Fe(6)C Core in All Nitrogenase Cofactors Decamps, Laure Rice, Derek B. DeBeer, Serena Angew Chem Int Ed Engl Communications The biological process of dinitrogen reduction to ammonium occurs at the cofactors of nitrogenases, the only enzymes that catalyze this challenging chemical reaction. Three types of nitrogenases have been described, named according to the heterometal in their cofactor: molybdenum, vanadium or iron nitrogenases. Spectroscopic and structural characterization allowed the unambiguous identification of the cofactors of molybdenum and vanadium nitrogenases and revealed a central μ(6)‐carbide in both of them. Although genetic studies suggested that the cofactor of the iron nitrogenase contains a similar Fe(6)C core, this has not been experimentally demonstrated. Here we report Valence‐to‐Core X‐ray Emission Spectroscopy providing experimental evidence that this cofactor contains a carbide, thereby making the Fe(6)C core a feature of all nitrogenase cofactors. John Wiley and Sons Inc. 2022-09-07 2022-10-10 /pmc/articles/PMC9826452/ /pubmed/35975943 http://dx.doi.org/10.1002/anie.202209190 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Decamps, Laure Rice, Derek B. DeBeer, Serena An Fe(6)C Core in All Nitrogenase Cofactors |
title | An Fe(6)C Core in All Nitrogenase Cofactors |
title_full | An Fe(6)C Core in All Nitrogenase Cofactors |
title_fullStr | An Fe(6)C Core in All Nitrogenase Cofactors |
title_full_unstemmed | An Fe(6)C Core in All Nitrogenase Cofactors |
title_short | An Fe(6)C Core in All Nitrogenase Cofactors |
title_sort | fe(6)c core in all nitrogenase cofactors |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826452/ https://www.ncbi.nlm.nih.gov/pubmed/35975943 http://dx.doi.org/10.1002/anie.202209190 |
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