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Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli
Understanding the genetic basis of adaptation is a central problem in biology. However, revealing the underlying molecular mechanisms has been challenging as changes in fitness may result from perturbations to many pathways, any of which may contribute relatively little. We have developed a combined...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913397/ https://www.ncbi.nlm.nih.gov/pubmed/20531407 http://dx.doi.org/10.1038/msb.2010.33 |
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author | Goodarzi, Hani Bennett, Bryson D Amini, Sasan Reaves, Marshall L Hottes, Alison K Rabinowitz, Joshua D Tavazoie, Saeed |
author_facet | Goodarzi, Hani Bennett, Bryson D Amini, Sasan Reaves, Marshall L Hottes, Alison K Rabinowitz, Joshua D Tavazoie, Saeed |
author_sort | Goodarzi, Hani |
collection | PubMed |
description | Understanding the genetic basis of adaptation is a central problem in biology. However, revealing the underlying molecular mechanisms has been challenging as changes in fitness may result from perturbations to many pathways, any of which may contribute relatively little. We have developed a combined experimental/computational framework to address this problem and used it to understand the genetic basis of ethanol tolerance in Escherichia coli. We used fitness profiling to measure the consequences of single-locus perturbations in the context of ethanol exposure. A module-level computational analysis was then used to reveal the organization of the contributing loci into cellular processes and regulatory pathways (e.g. osmoregulation and cell-wall biogenesis) whose modifications significantly affect ethanol tolerance. Strikingly, we discovered that a dominant component of adaptation involves metabolic rewiring that boosts intracellular ethanol degradation and assimilation. Through phenotypic and metabolomic analysis of laboratory-evolved ethanol-tolerant strains, we investigated naturally accessible pathways of ethanol tolerance. Remarkably, these laboratory-evolved strains, by and large, follow the same adaptive paths as inferred from our coarse-grained search of the fitness landscape. |
format | Text |
id | pubmed-2913397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-29133972010-08-02 Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli Goodarzi, Hani Bennett, Bryson D Amini, Sasan Reaves, Marshall L Hottes, Alison K Rabinowitz, Joshua D Tavazoie, Saeed Mol Syst Biol Article Understanding the genetic basis of adaptation is a central problem in biology. However, revealing the underlying molecular mechanisms has been challenging as changes in fitness may result from perturbations to many pathways, any of which may contribute relatively little. We have developed a combined experimental/computational framework to address this problem and used it to understand the genetic basis of ethanol tolerance in Escherichia coli. We used fitness profiling to measure the consequences of single-locus perturbations in the context of ethanol exposure. A module-level computational analysis was then used to reveal the organization of the contributing loci into cellular processes and regulatory pathways (e.g. osmoregulation and cell-wall biogenesis) whose modifications significantly affect ethanol tolerance. Strikingly, we discovered that a dominant component of adaptation involves metabolic rewiring that boosts intracellular ethanol degradation and assimilation. Through phenotypic and metabolomic analysis of laboratory-evolved ethanol-tolerant strains, we investigated naturally accessible pathways of ethanol tolerance. Remarkably, these laboratory-evolved strains, by and large, follow the same adaptive paths as inferred from our coarse-grained search of the fitness landscape. European Molecular Biology Organization 2010-06-08 /pmc/articles/PMC2913397/ /pubmed/20531407 http://dx.doi.org/10.1038/msb.2010.33 Text en Copyright © 2010, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits distribution and reproduction in any medium, provided the original author and source are credited. Creation of derivative works is permitted but the resulting work may be distributed only under the same or similar licence to this one. This licence does not permit commercial exploitation without specific permission. |
spellingShingle | Article Goodarzi, Hani Bennett, Bryson D Amini, Sasan Reaves, Marshall L Hottes, Alison K Rabinowitz, Joshua D Tavazoie, Saeed Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli |
title | Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli |
title_full | Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli |
title_fullStr | Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli |
title_full_unstemmed | Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli |
title_short | Regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in E. coli |
title_sort | regulatory and metabolic rewiring during laboratory evolution of ethanol tolerance in e. coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913397/ https://www.ncbi.nlm.nih.gov/pubmed/20531407 http://dx.doi.org/10.1038/msb.2010.33 |
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