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The pathway for coenzyme M biosynthesis in bacteria

Mercaptoethane sulfonate or coenzyme M (CoM) is the smallest known organic cofactor and is most commonly associated with the methane-forming step in all methanogenic archaea but is also associated with the anaerobic oxidation of methane to CO(2) in anaerobic methanotrophic archaea and the oxidation...

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Autores principales: Wu, Hsin-Hua, Pun, Michael D., Wise, Courtney E., Streit, Bennett R., Mus, Florence, Berim, Anna, Kincannon, William M., Islam, Abdullah, Partovi, Sarah E., Gang, David R., DuBois, Jennifer L., Lubner, Carolyn E., Berkman, Clifford E., Lange, B. Markus, Peters, John W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457059/
https://www.ncbi.nlm.nih.gov/pubmed/36037354
http://dx.doi.org/10.1073/pnas.2207190119
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author Wu, Hsin-Hua
Pun, Michael D.
Wise, Courtney E.
Streit, Bennett R.
Mus, Florence
Berim, Anna
Kincannon, William M.
Islam, Abdullah
Partovi, Sarah E.
Gang, David R.
DuBois, Jennifer L.
Lubner, Carolyn E.
Berkman, Clifford E.
Lange, B. Markus
Peters, John W.
author_facet Wu, Hsin-Hua
Pun, Michael D.
Wise, Courtney E.
Streit, Bennett R.
Mus, Florence
Berim, Anna
Kincannon, William M.
Islam, Abdullah
Partovi, Sarah E.
Gang, David R.
DuBois, Jennifer L.
Lubner, Carolyn E.
Berkman, Clifford E.
Lange, B. Markus
Peters, John W.
author_sort Wu, Hsin-Hua
collection PubMed
description Mercaptoethane sulfonate or coenzyme M (CoM) is the smallest known organic cofactor and is most commonly associated with the methane-forming step in all methanogenic archaea but is also associated with the anaerobic oxidation of methane to CO(2) in anaerobic methanotrophic archaea and the oxidation of short-chain alkanes in Syntrophoarchaeum species. It has also been found in a small number of bacteria capable of the metabolism of small organics. Although many of the steps for CoM biosynthesis in methanogenic archaea have been elucidated, a complete pathway for the biosynthesis of CoM in archaea or bacteria has not been reported. Here, we present the complete CoM biosynthesis pathway in bacteria, revealing distinct chemical steps relative to CoM biosynthesis in methanogenic archaea. The existence of different pathways represents a profound instance of convergent evolution. The five-step pathway involves the addition of sulfite, the elimination of phosphate, decarboxylation, thiolation, and the reduction to affect the sequential conversion of phosphoenolpyruvate to CoM. The salient features of the pathway demonstrate reactivities for members of large aspartase/fumarase and pyridoxal 5′-phosphate–dependent enzyme families.
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spelling pubmed-94570592023-03-01 The pathway for coenzyme M biosynthesis in bacteria Wu, Hsin-Hua Pun, Michael D. Wise, Courtney E. Streit, Bennett R. Mus, Florence Berim, Anna Kincannon, William M. Islam, Abdullah Partovi, Sarah E. Gang, David R. DuBois, Jennifer L. Lubner, Carolyn E. Berkman, Clifford E. Lange, B. Markus Peters, John W. Proc Natl Acad Sci U S A Biological Sciences Mercaptoethane sulfonate or coenzyme M (CoM) is the smallest known organic cofactor and is most commonly associated with the methane-forming step in all methanogenic archaea but is also associated with the anaerobic oxidation of methane to CO(2) in anaerobic methanotrophic archaea and the oxidation of short-chain alkanes in Syntrophoarchaeum species. It has also been found in a small number of bacteria capable of the metabolism of small organics. Although many of the steps for CoM biosynthesis in methanogenic archaea have been elucidated, a complete pathway for the biosynthesis of CoM in archaea or bacteria has not been reported. Here, we present the complete CoM biosynthesis pathway in bacteria, revealing distinct chemical steps relative to CoM biosynthesis in methanogenic archaea. The existence of different pathways represents a profound instance of convergent evolution. The five-step pathway involves the addition of sulfite, the elimination of phosphate, decarboxylation, thiolation, and the reduction to affect the sequential conversion of phosphoenolpyruvate to CoM. The salient features of the pathway demonstrate reactivities for members of large aspartase/fumarase and pyridoxal 5′-phosphate–dependent enzyme families. National Academy of Sciences 2022-08-29 2022-09-06 /pmc/articles/PMC9457059/ /pubmed/36037354 http://dx.doi.org/10.1073/pnas.2207190119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Wu, Hsin-Hua
Pun, Michael D.
Wise, Courtney E.
Streit, Bennett R.
Mus, Florence
Berim, Anna
Kincannon, William M.
Islam, Abdullah
Partovi, Sarah E.
Gang, David R.
DuBois, Jennifer L.
Lubner, Carolyn E.
Berkman, Clifford E.
Lange, B. Markus
Peters, John W.
The pathway for coenzyme M biosynthesis in bacteria
title The pathway for coenzyme M biosynthesis in bacteria
title_full The pathway for coenzyme M biosynthesis in bacteria
title_fullStr The pathway for coenzyme M biosynthesis in bacteria
title_full_unstemmed The pathway for coenzyme M biosynthesis in bacteria
title_short The pathway for coenzyme M biosynthesis in bacteria
title_sort pathway for coenzyme m biosynthesis in bacteria
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457059/
https://www.ncbi.nlm.nih.gov/pubmed/36037354
http://dx.doi.org/10.1073/pnas.2207190119
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