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Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling

Anaerobic microbial metabolism drives critical functions within global ecosystems, host–microbiota interactions, and industrial applications, yet remains ill-defined. Here we advance a versatile approach to elaborate cellular metabolism in obligate anaerobes using the pathogen Clostridioides diffici...

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Autores principales: Pavao, Aidan, Girinathan, Brintha, Peltier, Johann, Altamirano Silva, Pamela, Dupuy, Bruno, Muti, Isabella H., Malloy, Craig, Cheng, Leo L., Bry, Lynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154198/
https://www.ncbi.nlm.nih.gov/pubmed/36894723
http://dx.doi.org/10.1038/s41589-023-01275-9
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author Pavao, Aidan
Girinathan, Brintha
Peltier, Johann
Altamirano Silva, Pamela
Dupuy, Bruno
Muti, Isabella H.
Malloy, Craig
Cheng, Leo L.
Bry, Lynn
author_facet Pavao, Aidan
Girinathan, Brintha
Peltier, Johann
Altamirano Silva, Pamela
Dupuy, Bruno
Muti, Isabella H.
Malloy, Craig
Cheng, Leo L.
Bry, Lynn
author_sort Pavao, Aidan
collection PubMed
description Anaerobic microbial metabolism drives critical functions within global ecosystems, host–microbiota interactions, and industrial applications, yet remains ill-defined. Here we advance a versatile approach to elaborate cellular metabolism in obligate anaerobes using the pathogen Clostridioides difficile, an amino acid and carbohydrate-fermenting Clostridia. High-resolution magic angle spinning nuclear magnetic resonance (NMR) spectroscopy of C. difficile, grown with fermentable (13)C substrates, informed dynamic flux balance analysis (dFBA) of the pathogen’s genome-scale metabolism. Analyses identified dynamic recruitment of oxidative and supporting reductive pathways, with integration of high-flux amino acid and glycolytic metabolism at alanine’s biosynthesis to support efficient energy generation, nitrogen handling and biomass generation. Model predictions informed an approach leveraging the sensitivity of (13)C NMR spectroscopy to simultaneously track cellular carbon and nitrogen flow from [U-(13)C]glucose and [(15)N]leucine, confirming the formation of [(13)C,(15)N]alanine. Findings identify metabolic strategies used by C. difficile to support its rapid colonization and expansion in gut ecosystems. [Image: see text]
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spelling pubmed-101541982023-05-04 Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling Pavao, Aidan Girinathan, Brintha Peltier, Johann Altamirano Silva, Pamela Dupuy, Bruno Muti, Isabella H. Malloy, Craig Cheng, Leo L. Bry, Lynn Nat Chem Biol Article Anaerobic microbial metabolism drives critical functions within global ecosystems, host–microbiota interactions, and industrial applications, yet remains ill-defined. Here we advance a versatile approach to elaborate cellular metabolism in obligate anaerobes using the pathogen Clostridioides difficile, an amino acid and carbohydrate-fermenting Clostridia. High-resolution magic angle spinning nuclear magnetic resonance (NMR) spectroscopy of C. difficile, grown with fermentable (13)C substrates, informed dynamic flux balance analysis (dFBA) of the pathogen’s genome-scale metabolism. Analyses identified dynamic recruitment of oxidative and supporting reductive pathways, with integration of high-flux amino acid and glycolytic metabolism at alanine’s biosynthesis to support efficient energy generation, nitrogen handling and biomass generation. Model predictions informed an approach leveraging the sensitivity of (13)C NMR spectroscopy to simultaneously track cellular carbon and nitrogen flow from [U-(13)C]glucose and [(15)N]leucine, confirming the formation of [(13)C,(15)N]alanine. Findings identify metabolic strategies used by C. difficile to support its rapid colonization and expansion in gut ecosystems. [Image: see text] Nature Publishing Group US 2023-03-09 2023 /pmc/articles/PMC10154198/ /pubmed/36894723 http://dx.doi.org/10.1038/s41589-023-01275-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pavao, Aidan
Girinathan, Brintha
Peltier, Johann
Altamirano Silva, Pamela
Dupuy, Bruno
Muti, Isabella H.
Malloy, Craig
Cheng, Leo L.
Bry, Lynn
Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling
title Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling
title_full Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling
title_fullStr Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling
title_full_unstemmed Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling
title_short Elucidating dynamic anaerobe metabolism with HRMAS (13)C NMR and genome-scale modeling
title_sort elucidating dynamic anaerobe metabolism with hrmas (13)c nmr and genome-scale modeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154198/
https://www.ncbi.nlm.nih.gov/pubmed/36894723
http://dx.doi.org/10.1038/s41589-023-01275-9
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