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Elementary Growth Modes provide a molecular description of cellular self-fabrication
In this paper we try to describe all possible molecular states (phenotypes) for a cell that fabricates itself at a constant rate, given its enzyme kinetics and the stoichiometry of all reactions. For this, we must understand the process of cellular growth: steady-state self-fabrication requires a ce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004393/ https://www.ncbi.nlm.nih.gov/pubmed/31986156 http://dx.doi.org/10.1371/journal.pcbi.1007559 |
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author | de Groot, Daan H. Hulshof, Josephus Teusink, Bas Bruggeman, Frank J. Planqué, Robert |
author_facet | de Groot, Daan H. Hulshof, Josephus Teusink, Bas Bruggeman, Frank J. Planqué, Robert |
author_sort | de Groot, Daan H. |
collection | PubMed |
description | In this paper we try to describe all possible molecular states (phenotypes) for a cell that fabricates itself at a constant rate, given its enzyme kinetics and the stoichiometry of all reactions. For this, we must understand the process of cellular growth: steady-state self-fabrication requires a cell to synthesize all of its components, including metabolites, enzymes and ribosomes, in proportions that match its own composition. Simultaneously, the concentrations of these components affect the rates of metabolism and biosynthesis, and hence the growth rate. We here derive a theory that describes all phenotypes that solve this circular problem. All phenotypes can be described as a combination of minimal building blocks, which we call Elementary Growth Modes (EGMs). EGMs can be used as the theoretical basis for all models that explicitly model self-fabrication, such as the currently popular Metabolism and Expression models. We then use our theory to make concrete biological predictions. We find that natural selection for maximal growth rate drives microorganisms to states of minimal phenotypic complexity: only one EGM will be active when growth rate is maximised. The phenotype of a cell is only extended with one more EGM whenever growth becomes limited by an additional biophysical constraint, such as a limited solvent capacity of a cellular compartment. The theory presented here extends recent results on Elementary Flux Modes: the minimal building blocks of cellular growth models that lack the self-fabrication aspect. Our theory starts from basic biochemical and evolutionary considerations, and describes unicellular life, both in growth-promoting and in stress-inducing environments, in terms of EGMs. |
format | Online Article Text |
id | pubmed-7004393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70043932020-02-19 Elementary Growth Modes provide a molecular description of cellular self-fabrication de Groot, Daan H. Hulshof, Josephus Teusink, Bas Bruggeman, Frank J. Planqué, Robert PLoS Comput Biol Research Article In this paper we try to describe all possible molecular states (phenotypes) for a cell that fabricates itself at a constant rate, given its enzyme kinetics and the stoichiometry of all reactions. For this, we must understand the process of cellular growth: steady-state self-fabrication requires a cell to synthesize all of its components, including metabolites, enzymes and ribosomes, in proportions that match its own composition. Simultaneously, the concentrations of these components affect the rates of metabolism and biosynthesis, and hence the growth rate. We here derive a theory that describes all phenotypes that solve this circular problem. All phenotypes can be described as a combination of minimal building blocks, which we call Elementary Growth Modes (EGMs). EGMs can be used as the theoretical basis for all models that explicitly model self-fabrication, such as the currently popular Metabolism and Expression models. We then use our theory to make concrete biological predictions. We find that natural selection for maximal growth rate drives microorganisms to states of minimal phenotypic complexity: only one EGM will be active when growth rate is maximised. The phenotype of a cell is only extended with one more EGM whenever growth becomes limited by an additional biophysical constraint, such as a limited solvent capacity of a cellular compartment. The theory presented here extends recent results on Elementary Flux Modes: the minimal building blocks of cellular growth models that lack the self-fabrication aspect. Our theory starts from basic biochemical and evolutionary considerations, and describes unicellular life, both in growth-promoting and in stress-inducing environments, in terms of EGMs. Public Library of Science 2020-01-27 /pmc/articles/PMC7004393/ /pubmed/31986156 http://dx.doi.org/10.1371/journal.pcbi.1007559 Text en © 2020 de Groot et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article de Groot, Daan H. Hulshof, Josephus Teusink, Bas Bruggeman, Frank J. Planqué, Robert Elementary Growth Modes provide a molecular description of cellular self-fabrication |
title | Elementary Growth Modes provide a molecular description of cellular self-fabrication |
title_full | Elementary Growth Modes provide a molecular description of cellular self-fabrication |
title_fullStr | Elementary Growth Modes provide a molecular description of cellular self-fabrication |
title_full_unstemmed | Elementary Growth Modes provide a molecular description of cellular self-fabrication |
title_short | Elementary Growth Modes provide a molecular description of cellular self-fabrication |
title_sort | elementary growth modes provide a molecular description of cellular self-fabrication |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004393/ https://www.ncbi.nlm.nih.gov/pubmed/31986156 http://dx.doi.org/10.1371/journal.pcbi.1007559 |
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