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Expanding a dynamic flux balance model of yeast fermentation to genome-scale

BACKGROUND: Yeast is considered to be a workhorse of the biotechnology industry for the production of many value-added chemicals, alcoholic beverages and biofuels. Optimization of the fermentation is a challenging task that greatly benefits from dynamic models able to accurately describe and predict...

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Autores principales: Vargas, Felipe A, Pizarro, Francisco, Pérez-Correa, J Ricardo, Agosin, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118138/
https://www.ncbi.nlm.nih.gov/pubmed/21595919
http://dx.doi.org/10.1186/1752-0509-5-75
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author Vargas, Felipe A
Pizarro, Francisco
Pérez-Correa, J Ricardo
Agosin, Eduardo
author_facet Vargas, Felipe A
Pizarro, Francisco
Pérez-Correa, J Ricardo
Agosin, Eduardo
author_sort Vargas, Felipe A
collection PubMed
description BACKGROUND: Yeast is considered to be a workhorse of the biotechnology industry for the production of many value-added chemicals, alcoholic beverages and biofuels. Optimization of the fermentation is a challenging task that greatly benefits from dynamic models able to accurately describe and predict the fermentation profile and resulting products under different genetic and environmental conditions. In this article, we developed and validated a genome-scale dynamic flux balance model, using experimentally determined kinetic constraints. RESULTS: Appropriate equations for maintenance, biomass composition, anaerobic metabolism and nutrient uptake are key to improve model performance, especially for predicting glycerol and ethanol synthesis. Prediction profiles of synthesis and consumption of the main metabolites involved in alcoholic fermentation closely agreed with experimental data obtained from numerous lab and industrial fermentations under different environmental conditions. Finally, fermentation simulations of genetically engineered yeasts closely reproduced previously reported experimental results regarding final concentrations of the main fermentation products such as ethanol and glycerol. CONCLUSION: A useful tool to describe, understand and predict metabolite production in batch yeast cultures was developed. The resulting model, if used wisely, could help to search for new metabolic engineering strategies to manage ethanol content in batch fermentations.
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spelling pubmed-31181382011-06-19 Expanding a dynamic flux balance model of yeast fermentation to genome-scale Vargas, Felipe A Pizarro, Francisco Pérez-Correa, J Ricardo Agosin, Eduardo BMC Syst Biol Research Article BACKGROUND: Yeast is considered to be a workhorse of the biotechnology industry for the production of many value-added chemicals, alcoholic beverages and biofuels. Optimization of the fermentation is a challenging task that greatly benefits from dynamic models able to accurately describe and predict the fermentation profile and resulting products under different genetic and environmental conditions. In this article, we developed and validated a genome-scale dynamic flux balance model, using experimentally determined kinetic constraints. RESULTS: Appropriate equations for maintenance, biomass composition, anaerobic metabolism and nutrient uptake are key to improve model performance, especially for predicting glycerol and ethanol synthesis. Prediction profiles of synthesis and consumption of the main metabolites involved in alcoholic fermentation closely agreed with experimental data obtained from numerous lab and industrial fermentations under different environmental conditions. Finally, fermentation simulations of genetically engineered yeasts closely reproduced previously reported experimental results regarding final concentrations of the main fermentation products such as ethanol and glycerol. CONCLUSION: A useful tool to describe, understand and predict metabolite production in batch yeast cultures was developed. The resulting model, if used wisely, could help to search for new metabolic engineering strategies to manage ethanol content in batch fermentations. BioMed Central 2011-05-19 /pmc/articles/PMC3118138/ /pubmed/21595919 http://dx.doi.org/10.1186/1752-0509-5-75 Text en Copyright ©2011 Vargas et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vargas, Felipe A
Pizarro, Francisco
Pérez-Correa, J Ricardo
Agosin, Eduardo
Expanding a dynamic flux balance model of yeast fermentation to genome-scale
title Expanding a dynamic flux balance model of yeast fermentation to genome-scale
title_full Expanding a dynamic flux balance model of yeast fermentation to genome-scale
title_fullStr Expanding a dynamic flux balance model of yeast fermentation to genome-scale
title_full_unstemmed Expanding a dynamic flux balance model of yeast fermentation to genome-scale
title_short Expanding a dynamic flux balance model of yeast fermentation to genome-scale
title_sort expanding a dynamic flux balance model of yeast fermentation to genome-scale
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118138/
https://www.ncbi.nlm.nih.gov/pubmed/21595919
http://dx.doi.org/10.1186/1752-0509-5-75
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