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A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T)
Coenzyme A (CoA) thioesters are formed during anabolic and catabolic reactions in every organism. Degradation pathways of growth‐supporting substrates in bacteria can be predicted by differential proteogenomic studies. Direct detection of proposed metabolites such as CoA thioesters by high‐performan...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107677/ https://www.ncbi.nlm.nih.gov/pubmed/36331165 http://dx.doi.org/10.1002/cbic.202200584 |
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author | Bruns, Stefan Cakić, Nevenka Mitschke, Nico Kopke, Bernd Johann Rabus, Ralf Wilkes, Heinz |
author_facet | Bruns, Stefan Cakić, Nevenka Mitschke, Nico Kopke, Bernd Johann Rabus, Ralf Wilkes, Heinz |
author_sort | Bruns, Stefan |
collection | PubMed |
description | Coenzyme A (CoA) thioesters are formed during anabolic and catabolic reactions in every organism. Degradation pathways of growth‐supporting substrates in bacteria can be predicted by differential proteogenomic studies. Direct detection of proposed metabolites such as CoA thioesters by high‐performance liquid chromatography coupled with high‐resolution mass spectrometry can confirm the reaction sequence and demonstrate the activity of these degradation pathways. In the metabolomes of the anaerobic sulfate‐reducing bacterium Desulfobacula toluolica Tol2(T) grown with different substrates various CoA thioesters, derived from amino acid, fatty acid or alcohol metabolism, have been detected. Additionally, the cell extracts of this bacterium revealed a number of CoA analogues with molecular masses increased by 1 dalton. By comparing the chromatographic and mass spectrometric properties of synthetic reference standards with those of compounds detected in cell extracts of D. toluolica Tol2(T) and by performing co‐injection experiments, these analogues were identified as inosino‐CoAs. These CoA thioesters contain inosine instead of adenosine as the nucleoside. To the best of our knowledge, this finding represents the first detection of naturally occurring inosino‐CoA analogues. |
format | Online Article Text |
id | pubmed-10107677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101076772023-04-18 A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T) Bruns, Stefan Cakić, Nevenka Mitschke, Nico Kopke, Bernd Johann Rabus, Ralf Wilkes, Heinz Chembiochem Research Articles Coenzyme A (CoA) thioesters are formed during anabolic and catabolic reactions in every organism. Degradation pathways of growth‐supporting substrates in bacteria can be predicted by differential proteogenomic studies. Direct detection of proposed metabolites such as CoA thioesters by high‐performance liquid chromatography coupled with high‐resolution mass spectrometry can confirm the reaction sequence and demonstrate the activity of these degradation pathways. In the metabolomes of the anaerobic sulfate‐reducing bacterium Desulfobacula toluolica Tol2(T) grown with different substrates various CoA thioesters, derived from amino acid, fatty acid or alcohol metabolism, have been detected. Additionally, the cell extracts of this bacterium revealed a number of CoA analogues with molecular masses increased by 1 dalton. By comparing the chromatographic and mass spectrometric properties of synthetic reference standards with those of compounds detected in cell extracts of D. toluolica Tol2(T) and by performing co‐injection experiments, these analogues were identified as inosino‐CoAs. These CoA thioesters contain inosine instead of adenosine as the nucleoside. To the best of our knowledge, this finding represents the first detection of naturally occurring inosino‐CoA analogues. John Wiley and Sons Inc. 2022-12-08 2023-01-17 /pmc/articles/PMC10107677/ /pubmed/36331165 http://dx.doi.org/10.1002/cbic.202200584 Text en © 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Bruns, Stefan Cakić, Nevenka Mitschke, Nico Kopke, Bernd Johann Rabus, Ralf Wilkes, Heinz A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T) |
title | A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T)
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title_full | A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T)
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title_fullStr | A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T)
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title_full_unstemmed | A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T)
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title_short | A Novel Coenzyme A Analogue in the Anaerobic, Sulfate‐Reducing, Marine Bacterium Desulfobacula toluolica Tol2(T)
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title_sort | novel coenzyme a analogue in the anaerobic, sulfate‐reducing, marine bacterium desulfobacula toluolica tol2(t) |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107677/ https://www.ncbi.nlm.nih.gov/pubmed/36331165 http://dx.doi.org/10.1002/cbic.202200584 |
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