| Literature DB >> 31975585 |
Stefan Burén1, Emilio Jiménez-Vicente2, Carlos Echavarri-Erasun1, Luis M Rubio1.
Abstract
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.Entities:
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Year: 2020 PMID: 31975585 PMCID: PMC7318056 DOI: 10.1021/acs.chemrev.9b00489
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622