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Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism
Saccharomyces non‐cerevisiae yeasts are gaining momentum in wine fermentation due to their potential to reduce ethanol content and achieve attractive aroma profiles. However, the design of the fermentation process for new species requires intensive experimentation. The use of mechanistic models coul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034642/ https://www.ncbi.nlm.nih.gov/pubmed/36722662 http://dx.doi.org/10.1111/1751-7915.14211 |
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author | Moimenta, Artai R. Henriques, David Minebois, Romain Querol, Amparo Balsa‐Canto, Eva |
author_facet | Moimenta, Artai R. Henriques, David Minebois, Romain Querol, Amparo Balsa‐Canto, Eva |
author_sort | Moimenta, Artai R. |
collection | PubMed |
description | Saccharomyces non‐cerevisiae yeasts are gaining momentum in wine fermentation due to their potential to reduce ethanol content and achieve attractive aroma profiles. However, the design of the fermentation process for new species requires intensive experimentation. The use of mechanistic models could automate process design, yet to date, most fermentation models have focused on primary metabolism. Therefore, these models do not provide insight into the production of secondary metabolites essential for wine quality, such as aromas. In this work, we formulate a continuous model that accounts for the physiological status of yeast, that is, exponential growth, growth under nitrogen starvation and transition to stationary or decay phases. To do so, we assumed that nitrogen starvation is associated with carbohydrate accumulation and the induction of a set of transcriptional changes associated with the stationary phase. The model accurately described the dynamics of time series data for biomass and primary and secondary metabolites obtained for various yeast species in single culture fermentations. We also used the proposed model to explore different process designs, showing how the addition of nitrogen could affect the aromatic profile of wine. This study underlines the potential of incorporating yeast physiology into batch fermentation modelling and provides a new means of automating process design. |
format | Online Article Text |
id | pubmed-10034642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100346422023-03-24 Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism Moimenta, Artai R. Henriques, David Minebois, Romain Querol, Amparo Balsa‐Canto, Eva Microb Biotechnol Research Articles Saccharomyces non‐cerevisiae yeasts are gaining momentum in wine fermentation due to their potential to reduce ethanol content and achieve attractive aroma profiles. However, the design of the fermentation process for new species requires intensive experimentation. The use of mechanistic models could automate process design, yet to date, most fermentation models have focused on primary metabolism. Therefore, these models do not provide insight into the production of secondary metabolites essential for wine quality, such as aromas. In this work, we formulate a continuous model that accounts for the physiological status of yeast, that is, exponential growth, growth under nitrogen starvation and transition to stationary or decay phases. To do so, we assumed that nitrogen starvation is associated with carbohydrate accumulation and the induction of a set of transcriptional changes associated with the stationary phase. The model accurately described the dynamics of time series data for biomass and primary and secondary metabolites obtained for various yeast species in single culture fermentations. We also used the proposed model to explore different process designs, showing how the addition of nitrogen could affect the aromatic profile of wine. This study underlines the potential of incorporating yeast physiology into batch fermentation modelling and provides a new means of automating process design. John Wiley and Sons Inc. 2023-02-01 /pmc/articles/PMC10034642/ /pubmed/36722662 http://dx.doi.org/10.1111/1751-7915.14211 Text en © 2023 The Authors. Microbial Biotechnology published by Applied Microbiology International and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Moimenta, Artai R. Henriques, David Minebois, Romain Querol, Amparo Balsa‐Canto, Eva Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
title | Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
title_full | Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
title_fullStr | Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
title_full_unstemmed | Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
title_short | Modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
title_sort | modelling the physiological status of yeast during wine fermentation enables the prediction of secondary metabolism |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034642/ https://www.ncbi.nlm.nih.gov/pubmed/36722662 http://dx.doi.org/10.1111/1751-7915.14211 |
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