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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...

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Detalles Bibliográficos
Autores principales: Decamps, Laure, Rice, Derek B., DeBeer, Serena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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