Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322, United States.
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
Chem Rev. 2020 Jun 24;120(12):5082-5106. doi: 10.1021/acs.chemrev.9b00556. Epub 2020 Mar 16.
Nitrogenase is the enzyme that catalyzes biological N reduction to NH. This enzyme achieves an impressive rate enhancement over the uncatalyzed reaction. Given the high demand for N 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 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, is also discussed, and remaining challenges in understanding nitrogenase substrate reduction are considered.
固氮酶是一种能够催化生物固氮将 N 还原为 NH 的酶。该酶在未催化的反应中实现了令人印象深刻的速率增强。考虑到对 N 固定的高需求以支持食品和化学品生产,以及工业 Haber-Bosch 氮固定反应对化石燃料的严重依赖,因此强烈需要阐明固氮酶如何在良性条件下实现这一困难的反应,以此作为设计下一代合成催化剂的依据。这篇综述总结了近年来在解决固氮酶如何催化一系列底物还原方面的进展。首先考虑了新的关于 N 和质子还原机制的见解。接下来,总结了近年来在理解还原多种其他氮化合物方面的进展,这些化合物不被认为是生理底物。还讨论了对广泛的 C 基底物(包括 CO 和 CO)还原的理解进展,以及理解固氮酶底物还原的剩余挑战。