Back to Search
Start Over
Biosynthesis of Nitrogenase Cofactors.
- Source :
-
Chemical reviews [Chem Rev] 2020 Jun 24; Vol. 120 (12), pp. 4921-4968. Date of Electronic Publication: 2020 Jan 24. - Publication Year :
- 2020
-
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.
Details
- Language :
- English
- ISSN :
- 1520-6890
- Volume :
- 120
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Chemical reviews
- Publication Type :
- Academic Journal
- Accession number :
- 31975585
- Full Text :
- https://doi.org/10.1021/acs.chemrev.9b00489