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Reduction of Substrates by Nitrogenases.

Authors :
Seefeldt LC
Yang ZY
Lukoyanov DA
Harris DF
Dean DR
Raugei S
Hoffman BM
Source :
Chemical reviews [Chem Rev] 2020 Jun 24; Vol. 120 (12), pp. 5082-5106. Date of Electronic Publication: 2020 Mar 16.
Publication Year :
2020

Abstract

Nitrogenase is the enzyme that catalyzes biological N <subscript>2</subscript> reduction to NH <subscript>3</subscript> . This enzyme achieves an impressive rate enhancement over the uncatalyzed reaction. Given the high demand for N <subscript>2</subscript> fixation to support food and chemical production and the heavy reliance of the industrial Haber-Bosch nitrogen fixation reaction on fossil fuels, there is a strong need to elucidate how nitrogenase achieves this difficult reaction under benign conditions as a means of informing the design of next generation synthetic catalysts. This Review summarizes recent progress in addressing how nitrogenase catalyzes the reduction of an array of substrates. New insights into the mechanism of N <subscript>2</subscript> and proton reduction are first considered. This is followed by a summary of recent gains in understanding the reduction of a number of other nitrogenous compounds not considered to be physiological substrates. Progress in understanding the reduction of a wide range of C-based substrates, including CO and CO <subscript>2</subscript> , is also discussed, and remaining challenges in understanding nitrogenase substrate reduction are considered.

Details

Language :
English
ISSN :
1520-6890
Volume :
120
Issue :
12
Database :
MEDLINE
Journal :
Chemical reviews
Publication Type :
Academic Journal
Accession number :
32176472
Full Text :
https://doi.org/10.1021/acs.chemrev.9b00556