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Biosynthesis of Nitrogenase Cofactors
[Image: see text] Nitrogenase harbors three distinct metal prosthetic groups that are required for its activity. The simplest one is a [4Fe-4S] cluster located at the Fe protein nitrogenase component. The MoFe protein component carries an [8Fe-7S] group called P-cluster and a [7Fe-9S-C-Mo-R-homocitr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318056/ https://www.ncbi.nlm.nih.gov/pubmed/31975585 http://dx.doi.org/10.1021/acs.chemrev.9b00489 |
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author | Burén, Stefan Jiménez-Vicente, Emilio Echavarri-Erasun, Carlos Rubio, Luis M. |
author_facet | Burén, Stefan Jiménez-Vicente, Emilio Echavarri-Erasun, Carlos Rubio, Luis M. |
author_sort | Burén, Stefan |
collection | PubMed |
description | [Image: see text] Nitrogenase harbors three distinct metal prosthetic groups that are required for its activity. The simplest one is a [4Fe-4S] cluster located at the Fe protein nitrogenase component. The MoFe protein component carries an [8Fe-7S] group called P-cluster and a [7Fe-9S-C-Mo-R-homocitrate] group called FeMo-co. Formation of nitrogenase metalloclusters requires the participation of the structural nitrogenase components and many accessory proteins, and occurs both in situ, for the P-cluster, and in external assembly sites for FeMo-co. The biosynthesis of FeMo-co is performed stepwise and involves molecular scaffolds, metallochaperones, radical chemistry, and novel and unique biosynthetic intermediates. This review provides a critical overview of discoveries on nitrogenase cofactor structure, function, and activity over the last four decades. |
format | Online Article Text |
id | pubmed-7318056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73180562020-06-26 Biosynthesis of Nitrogenase Cofactors Burén, Stefan Jiménez-Vicente, Emilio Echavarri-Erasun, Carlos Rubio, Luis M. Chem Rev [Image: see text] Nitrogenase harbors three distinct metal prosthetic groups that are required for its activity. The simplest one is a [4Fe-4S] cluster located at the Fe protein nitrogenase component. The MoFe protein component carries an [8Fe-7S] group called P-cluster and a [7Fe-9S-C-Mo-R-homocitrate] group called FeMo-co. Formation of nitrogenase metalloclusters requires the participation of the structural nitrogenase components and many accessory proteins, and occurs both in situ, for the P-cluster, and in external assembly sites for FeMo-co. The biosynthesis of FeMo-co is performed stepwise and involves molecular scaffolds, metallochaperones, radical chemistry, and novel and unique biosynthetic intermediates. This review provides a critical overview of discoveries on nitrogenase cofactor structure, function, and activity over the last four decades. American Chemical Society 2020-01-24 2020-06-24 /pmc/articles/PMC7318056/ /pubmed/31975585 http://dx.doi.org/10.1021/acs.chemrev.9b00489 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Burén, Stefan Jiménez-Vicente, Emilio Echavarri-Erasun, Carlos Rubio, Luis M. Biosynthesis of Nitrogenase Cofactors |
title | Biosynthesis of Nitrogenase Cofactors |
title_full | Biosynthesis of Nitrogenase Cofactors |
title_fullStr | Biosynthesis of Nitrogenase Cofactors |
title_full_unstemmed | Biosynthesis of Nitrogenase Cofactors |
title_short | Biosynthesis of Nitrogenase Cofactors |
title_sort | biosynthesis of nitrogenase cofactors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318056/ https://www.ncbi.nlm.nih.gov/pubmed/31975585 http://dx.doi.org/10.1021/acs.chemrev.9b00489 |
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