Cargando…

Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction

Growth is a fundamental process of life. Growth requirements are well-characterized experimentally for many microbes; however, we lack a unified model for cellular growth. Such a model must be predictive of events at the molecular scale and capable of explaining the high-level behavior of the cell a...

Descripción completa

Detalles Bibliográficos
Autores principales: O’Brien, Edward J, Lerman, Joshua A, Chang, Roger L, Hyduke, Daniel R, Palsson, Bernhard Ø
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817402/
https://www.ncbi.nlm.nih.gov/pubmed/24084808
http://dx.doi.org/10.1038/msb.2013.52
_version_ 1782478069653569536
author O’Brien, Edward J
Lerman, Joshua A
Chang, Roger L
Hyduke, Daniel R
Palsson, Bernhard Ø
author_facet O’Brien, Edward J
Lerman, Joshua A
Chang, Roger L
Hyduke, Daniel R
Palsson, Bernhard Ø
author_sort O’Brien, Edward J
collection PubMed
description Growth is a fundamental process of life. Growth requirements are well-characterized experimentally for many microbes; however, we lack a unified model for cellular growth. Such a model must be predictive of events at the molecular scale and capable of explaining the high-level behavior of the cell as a whole. Here, we construct an ME-Model for Escherichia coli—a genome-scale model that seamlessly integrates metabolic and gene product expression pathways. The model computes ∼80% of the functional proteome (by mass), which is used by the cell to support growth under a given condition. Metabolism and gene expression are interdependent processes that affect and constrain each other. We formalize these constraints and apply the principle of growth optimization to enable the accurate prediction of multi-scale phenotypes, ranging from coarse-grained (growth rate, nutrient uptake, by-product secretion) to fine-grained (metabolic fluxes, gene expression levels). Our results unify many existing principles developed to describe bacterial growth.
format Online
Article
Text
id pubmed-3817402
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher European Molecular Biology Organization
record_format MEDLINE/PubMed
spelling pubmed-38174022013-11-06 Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction O’Brien, Edward J Lerman, Joshua A Chang, Roger L Hyduke, Daniel R Palsson, Bernhard Ø Mol Syst Biol Article Growth is a fundamental process of life. Growth requirements are well-characterized experimentally for many microbes; however, we lack a unified model for cellular growth. Such a model must be predictive of events at the molecular scale and capable of explaining the high-level behavior of the cell as a whole. Here, we construct an ME-Model for Escherichia coli—a genome-scale model that seamlessly integrates metabolic and gene product expression pathways. The model computes ∼80% of the functional proteome (by mass), which is used by the cell to support growth under a given condition. Metabolism and gene expression are interdependent processes that affect and constrain each other. We formalize these constraints and apply the principle of growth optimization to enable the accurate prediction of multi-scale phenotypes, ranging from coarse-grained (growth rate, nutrient uptake, by-product secretion) to fine-grained (metabolic fluxes, gene expression levels). Our results unify many existing principles developed to describe bacterial growth. European Molecular Biology Organization 2013-10-01 /pmc/articles/PMC3817402/ /pubmed/24084808 http://dx.doi.org/10.1038/msb.2013.52 Text en Copyright © 2013, 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 Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Article
O’Brien, Edward J
Lerman, Joshua A
Chang, Roger L
Hyduke, Daniel R
Palsson, Bernhard Ø
Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
title Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
title_full Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
title_fullStr Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
title_full_unstemmed Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
title_short Genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
title_sort genome-scale models of metabolism and gene expression extend and refine growth phenotype prediction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817402/
https://www.ncbi.nlm.nih.gov/pubmed/24084808
http://dx.doi.org/10.1038/msb.2013.52
work_keys_str_mv AT obrienedwardj genomescalemodelsofmetabolismandgeneexpressionextendandrefinegrowthphenotypeprediction
AT lermanjoshuaa genomescalemodelsofmetabolismandgeneexpressionextendandrefinegrowthphenotypeprediction
AT changrogerl genomescalemodelsofmetabolismandgeneexpressionextendandrefinegrowthphenotypeprediction
AT hydukedanielr genomescalemodelsofmetabolismandgeneexpressionextendandrefinegrowthphenotypeprediction
AT palssonbernhardø genomescalemodelsofmetabolismandgeneexpressionextendandrefinegrowthphenotypeprediction