Biosynthesis of Nitrogenase Cofactors
Author(s) -
Stefan Burén,
Emilio JiménezVicente,
Carlos EchávarriErasun,
Luis M. Rubio
Publication year - 2020
Publication title -
chemical reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 20.528
H-Index - 700
eISSN - 1520-6890
pISSN - 0009-2665
DOI - 10.1021/acs.chemrev.9b00489
Subject(s) - nitrogenase , chemistry , cofactor , biosynthesis , cluster (spacecraft) , stereochemistry , enzyme , crystallography , biochemistry , nitrogen fixation , organic chemistry , computer science , nitrogen , programming language
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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