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Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments
BACKGROUND: S. cerevisiae has attracted considerable interest in recent years as a model for ecology and evolutionary biology, revealing a substantial genetic and phenotypic diversity. However, there is a lack of knowledge on the diversity of metabolic networks within this species. RESULTS: To ident...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820951/ https://www.ncbi.nlm.nih.gov/pubmed/27044358 http://dx.doi.org/10.1186/s12934-016-0456-0 |
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author | Nidelet, Thibault Brial, Pascale Camarasa, Carole Dequin, Sylvie |
author_facet | Nidelet, Thibault Brial, Pascale Camarasa, Carole Dequin, Sylvie |
author_sort | Nidelet, Thibault |
collection | PubMed |
description | BACKGROUND: S. cerevisiae has attracted considerable interest in recent years as a model for ecology and evolutionary biology, revealing a substantial genetic and phenotypic diversity. However, there is a lack of knowledge on the diversity of metabolic networks within this species. RESULTS: To identify the metabolic and evolutionary constraints that shape metabolic fluxes in S. cerevisiae, we used a dedicated constraint-based model to predict the central carbon metabolism flux distribution of 43 strains from different ecological origins, grown in wine fermentation conditions. In analyzing these distributions, we observed a highly contrasted situation in flux variability, with quasi-constancy of the glycolysis and ethanol synthesis yield yet high flexibility of other fluxes, such as the pentose phosphate pathway and acetaldehyde production. Furthermore, these fluxes with large variability showed multimodal distributions that could be linked to strain origin, indicating a convergence between genetic origin and flux phenotype. CONCLUSIONS: Flux variability is pathway-dependent and, for some flux, a strain origin effect can be found. These data highlight the constraints shaping the yeast operative central carbon network and provide clues for the design of strategies for strain improvement. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0456-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4820951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48209512016-04-06 Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments Nidelet, Thibault Brial, Pascale Camarasa, Carole Dequin, Sylvie Microb Cell Fact Research BACKGROUND: S. cerevisiae has attracted considerable interest in recent years as a model for ecology and evolutionary biology, revealing a substantial genetic and phenotypic diversity. However, there is a lack of knowledge on the diversity of metabolic networks within this species. RESULTS: To identify the metabolic and evolutionary constraints that shape metabolic fluxes in S. cerevisiae, we used a dedicated constraint-based model to predict the central carbon metabolism flux distribution of 43 strains from different ecological origins, grown in wine fermentation conditions. In analyzing these distributions, we observed a highly contrasted situation in flux variability, with quasi-constancy of the glycolysis and ethanol synthesis yield yet high flexibility of other fluxes, such as the pentose phosphate pathway and acetaldehyde production. Furthermore, these fluxes with large variability showed multimodal distributions that could be linked to strain origin, indicating a convergence between genetic origin and flux phenotype. CONCLUSIONS: Flux variability is pathway-dependent and, for some flux, a strain origin effect can be found. These data highlight the constraints shaping the yeast operative central carbon network and provide clues for the design of strategies for strain improvement. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0456-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-05 /pmc/articles/PMC4820951/ /pubmed/27044358 http://dx.doi.org/10.1186/s12934-016-0456-0 Text en © Nidelet et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Nidelet, Thibault Brial, Pascale Camarasa, Carole Dequin, Sylvie Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments |
title | Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments |
title_full | Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments |
title_fullStr | Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments |
title_full_unstemmed | Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments |
title_short | Diversity of flux distribution in central carbon metabolism of S. cerevisiae strains from diverse environments |
title_sort | diversity of flux distribution in central carbon metabolism of s. cerevisiae strains from diverse environments |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820951/ https://www.ncbi.nlm.nih.gov/pubmed/27044358 http://dx.doi.org/10.1186/s12934-016-0456-0 |
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