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An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control
Growth and environmental responses are essential for living organisms to survive and adapt to constantly changing environments. In order to simulate new conditions and capture dynamic responses to environmental shifts in a developing whole-cell model of E. coli, we incorporated additional regulation...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391491/ https://www.ncbi.nlm.nih.gov/pubmed/35986058 http://dx.doi.org/10.1038/s41540-022-00242-9 |
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author | Ahn-Horst, Travis A. Mille, Luis Santiago Sun, Gwanggyu Morrison, Jerry H. Covert, Markus W. |
author_facet | Ahn-Horst, Travis A. Mille, Luis Santiago Sun, Gwanggyu Morrison, Jerry H. Covert, Markus W. |
author_sort | Ahn-Horst, Travis A. |
collection | PubMed |
description | Growth and environmental responses are essential for living organisms to survive and adapt to constantly changing environments. In order to simulate new conditions and capture dynamic responses to environmental shifts in a developing whole-cell model of E. coli, we incorporated additional regulation, including dynamics of the global regulator guanosine tetraphosphate (ppGpp), along with dynamics of amino acid biosynthesis and translation. With the model, we show that under perturbed ppGpp conditions, small molecule feedback inhibition pathways, in addition to regulation of expression, play a role in ppGpp regulation of growth. We also found that simulations with dysregulated amino acid synthesis pathways provide average amino acid concentration predictions that are comparable to experimental results but on the single-cell level, concentrations unexpectedly show regular fluctuations. Additionally, during both an upshift and downshift in nutrient availability, the simulated cell responds similarly with a transient increase in the mRNA:rRNA ratio. This additional simulation functionality should support a variety of new applications and expansions of the E. coli Whole-Cell Modeling Project. |
format | Online Article Text |
id | pubmed-9391491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93914912022-08-21 An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control Ahn-Horst, Travis A. Mille, Luis Santiago Sun, Gwanggyu Morrison, Jerry H. Covert, Markus W. NPJ Syst Biol Appl Article Growth and environmental responses are essential for living organisms to survive and adapt to constantly changing environments. In order to simulate new conditions and capture dynamic responses to environmental shifts in a developing whole-cell model of E. coli, we incorporated additional regulation, including dynamics of the global regulator guanosine tetraphosphate (ppGpp), along with dynamics of amino acid biosynthesis and translation. With the model, we show that under perturbed ppGpp conditions, small molecule feedback inhibition pathways, in addition to regulation of expression, play a role in ppGpp regulation of growth. We also found that simulations with dysregulated amino acid synthesis pathways provide average amino acid concentration predictions that are comparable to experimental results but on the single-cell level, concentrations unexpectedly show regular fluctuations. Additionally, during both an upshift and downshift in nutrient availability, the simulated cell responds similarly with a transient increase in the mRNA:rRNA ratio. This additional simulation functionality should support a variety of new applications and expansions of the E. coli Whole-Cell Modeling Project. Nature Publishing Group UK 2022-08-19 /pmc/articles/PMC9391491/ /pubmed/35986058 http://dx.doi.org/10.1038/s41540-022-00242-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ahn-Horst, Travis A. Mille, Luis Santiago Sun, Gwanggyu Morrison, Jerry H. Covert, Markus W. An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control |
title | An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control |
title_full | An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control |
title_fullStr | An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control |
title_full_unstemmed | An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control |
title_short | An expanded whole-cell model of E. coli links cellular physiology with mechanisms of growth rate control |
title_sort | expanded whole-cell model of e. coli links cellular physiology with mechanisms of growth rate control |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391491/ https://www.ncbi.nlm.nih.gov/pubmed/35986058 http://dx.doi.org/10.1038/s41540-022-00242-9 |
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