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Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway
Escherichia coli excretes acetate upon growth on fermentable sugars, but the regulation of this production remains elusive. Acetate excretion on excess glucose is thought to be an irreversible process. However, dynamic (13)C-metabolic flux analysis revealed a strong bidirectional exchange of acetate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301487/ https://www.ncbi.nlm.nih.gov/pubmed/28186174 http://dx.doi.org/10.1038/srep42135 |
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author | Enjalbert, Brice Millard, Pierre Dinclaux, Mickael Portais, Jean-Charles Létisse, Fabien |
author_facet | Enjalbert, Brice Millard, Pierre Dinclaux, Mickael Portais, Jean-Charles Létisse, Fabien |
author_sort | Enjalbert, Brice |
collection | PubMed |
description | Escherichia coli excretes acetate upon growth on fermentable sugars, but the regulation of this production remains elusive. Acetate excretion on excess glucose is thought to be an irreversible process. However, dynamic (13)C-metabolic flux analysis revealed a strong bidirectional exchange of acetate between E. coli and its environment. The Pta-AckA pathway was found to be central for both flux directions, while alternative routes (Acs or PoxB) play virtually no role in glucose consumption. Kinetic modelling of the Pta-AckA pathway predicted that its flux is thermodynamically controlled by the extracellular acetate concentration in vivo. Experimental validations confirmed that acetate production can be reduced and even reversed depending solely on its extracellular concentration. Consistently, the Pta-AckA pathway can rapidly switch from acetate production to consumption. Contrary to current knowledge, E. coli is thus able to co-consume glucose and acetate under glucose excess. These metabolic capabilities were confirmed on other glycolytic substrates which support the growth of E. coli in the gut. These findings highlight the dual role of the Pta-AckA pathway in acetate production and consumption during growth on glycolytic substrates, uncover a novel regulatory mechanism that controls its flux in vivo, and significantly expand the metabolic capabilities of E. coli. |
format | Online Article Text |
id | pubmed-5301487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53014872017-02-15 Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway Enjalbert, Brice Millard, Pierre Dinclaux, Mickael Portais, Jean-Charles Létisse, Fabien Sci Rep Article Escherichia coli excretes acetate upon growth on fermentable sugars, but the regulation of this production remains elusive. Acetate excretion on excess glucose is thought to be an irreversible process. However, dynamic (13)C-metabolic flux analysis revealed a strong bidirectional exchange of acetate between E. coli and its environment. The Pta-AckA pathway was found to be central for both flux directions, while alternative routes (Acs or PoxB) play virtually no role in glucose consumption. Kinetic modelling of the Pta-AckA pathway predicted that its flux is thermodynamically controlled by the extracellular acetate concentration in vivo. Experimental validations confirmed that acetate production can be reduced and even reversed depending solely on its extracellular concentration. Consistently, the Pta-AckA pathway can rapidly switch from acetate production to consumption. Contrary to current knowledge, E. coli is thus able to co-consume glucose and acetate under glucose excess. These metabolic capabilities were confirmed on other glycolytic substrates which support the growth of E. coli in the gut. These findings highlight the dual role of the Pta-AckA pathway in acetate production and consumption during growth on glycolytic substrates, uncover a novel regulatory mechanism that controls its flux in vivo, and significantly expand the metabolic capabilities of E. coli. Nature Publishing Group 2017-02-10 /pmc/articles/PMC5301487/ /pubmed/28186174 http://dx.doi.org/10.1038/srep42135 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Enjalbert, Brice Millard, Pierre Dinclaux, Mickael Portais, Jean-Charles Létisse, Fabien Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway |
title | Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway |
title_full | Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway |
title_fullStr | Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway |
title_full_unstemmed | Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway |
title_short | Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway |
title_sort | acetate fluxes in escherichia coli are determined by the thermodynamic control of the pta-acka pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301487/ https://www.ncbi.nlm.nih.gov/pubmed/28186174 http://dx.doi.org/10.1038/srep42135 |
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