| Literature DB >> 32237739 |
Casey Van Stappen1, Laure Decamps1, George E Cutsail1, Ragnar Bjornsson1, Justin T Henthorn1, James A Birrell1, Serena DeBeer1.
Abstract
<span class="Chemical">Nitrogenn>ases <span class="Chemical">are responsible for biological nitrogen fixation, a crucial step in the biogeochemical nitrogen cycle. These enzymes utilize a two-component protein system and a series of iron-sulfur clusters to perform this reaction, culminating at the FeMco active site (M = Mo, V, Fe), which is capable of binding and reducing N2 to 2NH3. In this review, we summarize how different spectroscopic approaches have shed light on various aspects of these enzymes, including their structure, mechanism, alternative reactivity, and maturation. Synthetic model chemistry and theory have also played significant roles in developing our present understanding of these systems and are discussed in the context of their contributions to interpreting the nature of nitrogenases. Despite years of significant progress, there is still much to be learned from these enzymes through spectroscopic means, and we highlight where further spectroscopic investigations are needed.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32237739 PMCID: PMC7318057 DOI: 10.1021/acs.chemrev.9b00650
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622