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Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must

Winemaking is a stressful procedure for yeast cells. The presence of high levels of carbohydrates at the beginning of the fermentation and the subsequent increase of ethanol levels alongside with other environmental factors force the cell to undergo a continuous adaptation process. Ideally, yeast st...

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Autores principales: Kassoumi, Konstantina, Kousoulou, Penny, Sevastos, Dimitrios, Vamvakas, Sotirios-Spyridon, Papadimitriou, Konstantinos, Kapolos, John, Koliadima, Athanasia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834448/
https://www.ncbi.nlm.nih.gov/pubmed/35159565
http://dx.doi.org/10.3390/foods11030413
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author Kassoumi, Konstantina
Kousoulou, Penny
Sevastos, Dimitrios
Vamvakas, Sotirios-Spyridon
Papadimitriou, Konstantinos
Kapolos, John
Koliadima, Athanasia
author_facet Kassoumi, Konstantina
Kousoulou, Penny
Sevastos, Dimitrios
Vamvakas, Sotirios-Spyridon
Papadimitriou, Konstantinos
Kapolos, John
Koliadima, Athanasia
author_sort Kassoumi, Konstantina
collection PubMed
description Winemaking is a stressful procedure for yeast cells. The presence of high levels of carbohydrates at the beginning of the fermentation and the subsequent increase of ethanol levels alongside with other environmental factors force the cell to undergo a continuous adaptation process. Ideally, yeast strains should be able to adapt to this changing environment fast and they must be able to ferment at low temperatures with the highest possible fermentation rates. Additionally, the balanced utilization of glucose and fructose—the two major hexoses in grapes—is also important as any residual fructose may confers unwanted sweetness. As proteins, Msn2/4 are known to play pivotal roles in cell stress response, the question that arise regards the differentially cell response driven by specific point mutations in these two proteins, and the subsequent effects on alcoholic fermentation. Four different mutants in which serine residues have been replaced by alanine are studied in this paper. Our results indicate that substitution at position 533 of Msn4 protein (W_M4_533) significantly increases the fermentation rate even at low temperatures (12 °C), by lowering the fermentation’s activation energy. Similar results but to a lesser extent were obtained by the S582A substitution in Msn2 protein. In addition, W_M4_533 seems to have a more balanced utilization of must hexoses. From the present work it is concluded that genetic modification Msn2/4 represents a promising procedure for shortening the fermentation time, even at low temperatures, which in many cases constitutes an important technological requirement.
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spelling pubmed-88344482022-02-12 Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must Kassoumi, Konstantina Kousoulou, Penny Sevastos, Dimitrios Vamvakas, Sotirios-Spyridon Papadimitriou, Konstantinos Kapolos, John Koliadima, Athanasia Foods Article Winemaking is a stressful procedure for yeast cells. The presence of high levels of carbohydrates at the beginning of the fermentation and the subsequent increase of ethanol levels alongside with other environmental factors force the cell to undergo a continuous adaptation process. Ideally, yeast strains should be able to adapt to this changing environment fast and they must be able to ferment at low temperatures with the highest possible fermentation rates. Additionally, the balanced utilization of glucose and fructose—the two major hexoses in grapes—is also important as any residual fructose may confers unwanted sweetness. As proteins, Msn2/4 are known to play pivotal roles in cell stress response, the question that arise regards the differentially cell response driven by specific point mutations in these two proteins, and the subsequent effects on alcoholic fermentation. Four different mutants in which serine residues have been replaced by alanine are studied in this paper. Our results indicate that substitution at position 533 of Msn4 protein (W_M4_533) significantly increases the fermentation rate even at low temperatures (12 °C), by lowering the fermentation’s activation energy. Similar results but to a lesser extent were obtained by the S582A substitution in Msn2 protein. In addition, W_M4_533 seems to have a more balanced utilization of must hexoses. From the present work it is concluded that genetic modification Msn2/4 represents a promising procedure for shortening the fermentation time, even at low temperatures, which in many cases constitutes an important technological requirement. MDPI 2022-01-31 /pmc/articles/PMC8834448/ /pubmed/35159565 http://dx.doi.org/10.3390/foods11030413 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kassoumi, Konstantina
Kousoulou, Penny
Sevastos, Dimitrios
Vamvakas, Sotirios-Spyridon
Papadimitriou, Konstantinos
Kapolos, John
Koliadima, Athanasia
Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must
title Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must
title_full Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must
title_fullStr Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must
title_full_unstemmed Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must
title_short Fermentation Efficiency of Genetically Modified Yeasts in Grapes Must
title_sort fermentation efficiency of genetically modified yeasts in grapes must
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834448/
https://www.ncbi.nlm.nih.gov/pubmed/35159565
http://dx.doi.org/10.3390/foods11030413
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