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Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster
The active site of [FeFe] hydrogenase, the H-cluster, consists of a canonical [4Fe–4S](H) subcluster linked to a unique binuclear [2Fe](H) subcluster containing three CO, two CN(−) and a bridging azadithiolate (adt, NH(CH(2)S(−))(2)) ligand. While it is known that all five diatomic ligands are deriv...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148037/ https://www.ncbi.nlm.nih.gov/pubmed/34123248 http://dx.doi.org/10.1039/c9sc05900h |
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author | Rao, Guodong Tao, Lizhi Britt, R. David |
author_facet | Rao, Guodong Tao, Lizhi Britt, R. David |
author_sort | Rao, Guodong |
collection | PubMed |
description | The active site of [FeFe] hydrogenase, the H-cluster, consists of a canonical [4Fe–4S](H) subcluster linked to a unique binuclear [2Fe](H) subcluster containing three CO, two CN(−) and a bridging azadithiolate (adt, NH(CH(2)S(−))(2)) ligand. While it is known that all five diatomic ligands are derived from tyrosine, there has been little knowledge as to the formation and installation of the adt ligand. Here, by using a combination of a cell-free in vitro maturation approach with pulse electronic paramagnetic resonance spectroscopy, we discover that serine donates the nitrogen atom and the CH(2) group to the assembly of the adt ligand. More specifically, both CH(2) groups in adt are sourced from the C3 methylene of serine. |
format | Online Article Text |
id | pubmed-8148037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81480372021-06-11 Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster Rao, Guodong Tao, Lizhi Britt, R. David Chem Sci Chemistry The active site of [FeFe] hydrogenase, the H-cluster, consists of a canonical [4Fe–4S](H) subcluster linked to a unique binuclear [2Fe](H) subcluster containing three CO, two CN(−) and a bridging azadithiolate (adt, NH(CH(2)S(−))(2)) ligand. While it is known that all five diatomic ligands are derived from tyrosine, there has been little knowledge as to the formation and installation of the adt ligand. Here, by using a combination of a cell-free in vitro maturation approach with pulse electronic paramagnetic resonance spectroscopy, we discover that serine donates the nitrogen atom and the CH(2) group to the assembly of the adt ligand. More specifically, both CH(2) groups in adt are sourced from the C3 methylene of serine. The Royal Society of Chemistry 2019-12-18 /pmc/articles/PMC8148037/ /pubmed/34123248 http://dx.doi.org/10.1039/c9sc05900h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Rao, Guodong Tao, Lizhi Britt, R. David Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster |
title | Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster |
title_full | Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster |
title_fullStr | Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster |
title_full_unstemmed | Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster |
title_short | Serine is the molecular source of the NH(CH(2))(2) bridgehead moiety of the in vitro assembled [FeFe] hydrogenase H-cluster |
title_sort | serine is the molecular source of the nh(ch(2))(2) bridgehead moiety of the in vitro assembled [fefe] hydrogenase h-cluster |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148037/ https://www.ncbi.nlm.nih.gov/pubmed/34123248 http://dx.doi.org/10.1039/c9sc05900h |
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