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Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor
The Mo-nitrogenase catalyses the ambient reduction of N(2) to NH(3) at the M-cluster, a complex cofactor that comprises two metal-sulphur partial cubanes ligated by an interstitial carbide and three belt-sulphurs. A recent crystallographic study suggests binding of N(2) via displacement of the belt-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540607/ https://www.ncbi.nlm.nih.gov/pubmed/36213009 http://dx.doi.org/10.1038/s41929-022-00782-7 |
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author | Lee, Chi Chung Kang, Wonchull Jasniewski, Andrew J. Stiebritz, Martin T. Tanifuji, Kazuki Ribbe, Markus W. Hu, Yilin |
author_facet | Lee, Chi Chung Kang, Wonchull Jasniewski, Andrew J. Stiebritz, Martin T. Tanifuji, Kazuki Ribbe, Markus W. Hu, Yilin |
author_sort | Lee, Chi Chung |
collection | PubMed |
description | The Mo-nitrogenase catalyses the ambient reduction of N(2) to NH(3) at the M-cluster, a complex cofactor that comprises two metal-sulphur partial cubanes ligated by an interstitial carbide and three belt-sulphurs. A recent crystallographic study suggests binding of N(2) via displacement of the belt-sulphur(s) of the M-cluster upon turnover. However, the direct proof of N(2) binding and belt-sulphur mobilization during catalysis remains elusive. Here we show that N(2) is captured on the M-cluster via electron- and sulphur-depletion, and that the N(2)-captured state is catalytically competent in generating NH(3). Moreover, we demonstrate that product release only occurs when sulphite is supplied along with a reductant, that sulphite is inserted as sulphide into the belt-sulphur displaced positions, and that there is a dynamic in-and-out of the belt-sulphurs during catalysis. Together, these results establish the mobilization of the cofactor belt-sulphurs as a crucial, yet overlooked, mechanistic element of the nitrogenase reaction. |
format | Online Article Text |
id | pubmed-9540607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-95406072022-11-16 Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor Lee, Chi Chung Kang, Wonchull Jasniewski, Andrew J. Stiebritz, Martin T. Tanifuji, Kazuki Ribbe, Markus W. Hu, Yilin Nat Catal Article The Mo-nitrogenase catalyses the ambient reduction of N(2) to NH(3) at the M-cluster, a complex cofactor that comprises two metal-sulphur partial cubanes ligated by an interstitial carbide and three belt-sulphurs. A recent crystallographic study suggests binding of N(2) via displacement of the belt-sulphur(s) of the M-cluster upon turnover. However, the direct proof of N(2) binding and belt-sulphur mobilization during catalysis remains elusive. Here we show that N(2) is captured on the M-cluster via electron- and sulphur-depletion, and that the N(2)-captured state is catalytically competent in generating NH(3). Moreover, we demonstrate that product release only occurs when sulphite is supplied along with a reductant, that sulphite is inserted as sulphide into the belt-sulphur displaced positions, and that there is a dynamic in-and-out of the belt-sulphurs during catalysis. Together, these results establish the mobilization of the cofactor belt-sulphurs as a crucial, yet overlooked, mechanistic element of the nitrogenase reaction. 2022-05 2022-05-16 /pmc/articles/PMC9540607/ /pubmed/36213009 http://dx.doi.org/10.1038/s41929-022-00782-7 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms |
spellingShingle | Article Lee, Chi Chung Kang, Wonchull Jasniewski, Andrew J. Stiebritz, Martin T. Tanifuji, Kazuki Ribbe, Markus W. Hu, Yilin Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
title | Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
title_full | Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
title_fullStr | Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
title_full_unstemmed | Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
title_short | Evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
title_sort | evidence of substrate binding and product release via belt-sulfur mobilization of the nitrogenase cofactor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540607/ https://www.ncbi.nlm.nih.gov/pubmed/36213009 http://dx.doi.org/10.1038/s41929-022-00782-7 |
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