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A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics
Eukaryotic organisms play an important role in industrial biotechnology, from the production of fuels and commodity chemicals to therapeutic proteins. To optimize these industrial systems, a mathematical approach can be used to integrate the description of multiple biological networks into a single...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352978/ https://www.ncbi.nlm.nih.gov/pubmed/34373465 http://dx.doi.org/10.1038/s41467-021-25158-6 |
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author | Oftadeh, Omid Salvy, Pierre Masid, Maria Curvat, Maxime Miskovic, Ljubisa Hatzimanikatis, Vassily |
author_facet | Oftadeh, Omid Salvy, Pierre Masid, Maria Curvat, Maxime Miskovic, Ljubisa Hatzimanikatis, Vassily |
author_sort | Oftadeh, Omid |
collection | PubMed |
description | Eukaryotic organisms play an important role in industrial biotechnology, from the production of fuels and commodity chemicals to therapeutic proteins. To optimize these industrial systems, a mathematical approach can be used to integrate the description of multiple biological networks into a single model for cell analysis and engineering. One of the most accurate models of biological systems include Expression and Thermodynamics FLux (ETFL), which efficiently integrates RNA and protein synthesis with traditional genome-scale metabolic models. However, ETFL is so far only applicable for E. coli. To adapt this model for Saccharomyces cerevisiae, we developed yETFL, in which we augmented the original formulation with additional considerations for biomass composition, the compartmentalized cellular expression system, and the energetic costs of biological processes. We demonstrated the ability of yETFL to predict maximum growth rate, essential genes, and the phenotype of overflow metabolism. We envision that the presented formulation can be extended to a wide range of eukaryotic organisms to the benefit of academic and industrial research. |
format | Online Article Text |
id | pubmed-8352978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83529782021-08-19 A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics Oftadeh, Omid Salvy, Pierre Masid, Maria Curvat, Maxime Miskovic, Ljubisa Hatzimanikatis, Vassily Nat Commun Article Eukaryotic organisms play an important role in industrial biotechnology, from the production of fuels and commodity chemicals to therapeutic proteins. To optimize these industrial systems, a mathematical approach can be used to integrate the description of multiple biological networks into a single model for cell analysis and engineering. One of the most accurate models of biological systems include Expression and Thermodynamics FLux (ETFL), which efficiently integrates RNA and protein synthesis with traditional genome-scale metabolic models. However, ETFL is so far only applicable for E. coli. To adapt this model for Saccharomyces cerevisiae, we developed yETFL, in which we augmented the original formulation with additional considerations for biomass composition, the compartmentalized cellular expression system, and the energetic costs of biological processes. We demonstrated the ability of yETFL to predict maximum growth rate, essential genes, and the phenotype of overflow metabolism. We envision that the presented formulation can be extended to a wide range of eukaryotic organisms to the benefit of academic and industrial research. Nature Publishing Group UK 2021-08-09 /pmc/articles/PMC8352978/ /pubmed/34373465 http://dx.doi.org/10.1038/s41467-021-25158-6 Text en © The Author(s) 2021 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 Oftadeh, Omid Salvy, Pierre Masid, Maria Curvat, Maxime Miskovic, Ljubisa Hatzimanikatis, Vassily A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
title | A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
title_full | A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
title_fullStr | A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
title_full_unstemmed | A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
title_short | A genome-scale metabolic model of Saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
title_sort | genome-scale metabolic model of saccharomyces cerevisiae that integrates expression constraints and reaction thermodynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352978/ https://www.ncbi.nlm.nih.gov/pubmed/34373465 http://dx.doi.org/10.1038/s41467-021-25158-6 |
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