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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...

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Autores principales: Burén, Stefan, Jiménez-Vicente, Emilio, Echavarri-Erasun, Carlos, Rubio, Luis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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