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Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum

Introduction: Genome-scale metabolic models (GEMs) are organism-specific knowledge bases which can be used to unravel pathogenicity or improve production of specific metabolites in biotechnology applications. However, the validity of predictions for bacterial proliferation in in vitro settings is ha...

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Autores principales: Bäuerle, Famke, Döbel, Gwendolyn O., Camus, Laura, Heilbronner, Simon, Dräger, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626998/
https://www.ncbi.nlm.nih.gov/pubmed/37936955
http://dx.doi.org/10.3389/fbinf.2023.1214074
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author Bäuerle, Famke
Döbel, Gwendolyn O.
Camus, Laura
Heilbronner, Simon
Dräger, Andreas
author_facet Bäuerle, Famke
Döbel, Gwendolyn O.
Camus, Laura
Heilbronner, Simon
Dräger, Andreas
author_sort Bäuerle, Famke
collection PubMed
description Introduction: Genome-scale metabolic models (GEMs) are organism-specific knowledge bases which can be used to unravel pathogenicity or improve production of specific metabolites in biotechnology applications. However, the validity of predictions for bacterial proliferation in in vitro settings is hardly investigated. Methods: The present work combines in silico and in vitro approaches to create and curate strain-specific genome-scale metabolic models of Corynebacterium striatum. Results: We introduce five newly created strain-specific genome-scale metabolic models (GEMs) of high quality, satisfying all contemporary standards and requirements. All these models have been benchmarked using the community standard test suite Metabolic Model Testing (MEMOTE) and were validated by laboratory experiments. For the curation of those models, the software infrastructure refineGEMs was developed to work on these models in parallel and to comply with the quality standards for GEMs. The model predictions were confirmed by experimental data and a new comparison metric based on the doubling time was developed to quantify bacterial growth. Discussion: Future modeling projects can rely on the proposed software, which is independent of specific environmental conditions. The validation approach based on the growth rate calculation is now accessible and closely aligned with biological questions. The curated models are freely available via BioModels and a GitHub repository and can be used. The open-source software refineGEMs is available from https://github.com/draeger-lab/refinegems.
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spelling pubmed-106269982023-11-07 Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum Bäuerle, Famke Döbel, Gwendolyn O. Camus, Laura Heilbronner, Simon Dräger, Andreas Front Bioinform Bioinformatics Introduction: Genome-scale metabolic models (GEMs) are organism-specific knowledge bases which can be used to unravel pathogenicity or improve production of specific metabolites in biotechnology applications. However, the validity of predictions for bacterial proliferation in in vitro settings is hardly investigated. Methods: The present work combines in silico and in vitro approaches to create and curate strain-specific genome-scale metabolic models of Corynebacterium striatum. Results: We introduce five newly created strain-specific genome-scale metabolic models (GEMs) of high quality, satisfying all contemporary standards and requirements. All these models have been benchmarked using the community standard test suite Metabolic Model Testing (MEMOTE) and were validated by laboratory experiments. For the curation of those models, the software infrastructure refineGEMs was developed to work on these models in parallel and to comply with the quality standards for GEMs. The model predictions were confirmed by experimental data and a new comparison metric based on the doubling time was developed to quantify bacterial growth. Discussion: Future modeling projects can rely on the proposed software, which is independent of specific environmental conditions. The validation approach based on the growth rate calculation is now accessible and closely aligned with biological questions. The curated models are freely available via BioModels and a GitHub repository and can be used. The open-source software refineGEMs is available from https://github.com/draeger-lab/refinegems. Frontiers Media S.A. 2023-10-23 /pmc/articles/PMC10626998/ /pubmed/37936955 http://dx.doi.org/10.3389/fbinf.2023.1214074 Text en Copyright © 2023 Bäuerle, Döbel, Camus, Heilbronner and Dräger. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioinformatics
Bäuerle, Famke
Döbel, Gwendolyn O.
Camus, Laura
Heilbronner, Simon
Dräger, Andreas
Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum
title Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum
title_full Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum
title_fullStr Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum
title_full_unstemmed Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum
title_short Genome-scale metabolic models consistently predict in vitro characteristics of Corynebacterium striatum
title_sort genome-scale metabolic models consistently predict in vitro characteristics of corynebacterium striatum
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626998/
https://www.ncbi.nlm.nih.gov/pubmed/37936955
http://dx.doi.org/10.3389/fbinf.2023.1214074
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