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Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions

BACKGROUND: Viability in a non dividing state is referred to as chronological life span (CLS). Most grape juice fermentation happens when Saccharomyces cerevisiae yeast cells have stopped dividing; therefore, CLS is an important factor toward winemaking success. RESULTS: We have studied both the phy...

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Autores principales: Orozco, Helena, Matallana, Emilia, Aranda, Agustín
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503821/
https://www.ncbi.nlm.nih.gov/pubmed/22873488
http://dx.doi.org/10.1186/1475-2859-11-104
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author Orozco, Helena
Matallana, Emilia
Aranda, Agustín
author_facet Orozco, Helena
Matallana, Emilia
Aranda, Agustín
author_sort Orozco, Helena
collection PubMed
description BACKGROUND: Viability in a non dividing state is referred to as chronological life span (CLS). Most grape juice fermentation happens when Saccharomyces cerevisiae yeast cells have stopped dividing; therefore, CLS is an important factor toward winemaking success. RESULTS: We have studied both the physical and chemical determinants influencing yeast CLS. Low pH and heat shorten the maximum wine yeast life span, while hyperosmotic shock extends it. Ethanol plays an important negative role in aging under winemaking conditions, but additional metabolites produced by fermentative metabolism, such as acetaldehyde and acetate, have also a strong impact on longevity. Grape polyphenols quercetin and resveratrol have negative impacts on CLS under winemaking conditions, an unexpected behavior for these potential anti-oxidants. We observed that quercetin inhibits alcohol and aldehyde dehydrogenase activities, and that resveratrol performs a pro-oxidant role during grape juice fermentation. Vitamins nicotinic acid and nicotinamide are precursors of NAD(+), and their addition reduces mean longevity during fermentation, suggesting a metabolic unbalance negative for CLS. Moreover, vitamin mix supplementation at the end of fermentation shortens CLS and enhances cell lysis, while amino acids increase life span. CONCLUSIONS: Wine S. cerevisiae strains are able to sense changes in the environmental conditions and adapt their longevity to them. Yeast death is influenced by the conditions present at the end of wine fermentation, particularly by the concentration of two-carbon metabolites produced by the fermentative metabolism, such as ethanol, acetic acid and acetaldehyde, and also by the grape juice composition, particularly its vitamin content.
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spelling pubmed-35038212012-11-22 Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions Orozco, Helena Matallana, Emilia Aranda, Agustín Microb Cell Fact Research BACKGROUND: Viability in a non dividing state is referred to as chronological life span (CLS). Most grape juice fermentation happens when Saccharomyces cerevisiae yeast cells have stopped dividing; therefore, CLS is an important factor toward winemaking success. RESULTS: We have studied both the physical and chemical determinants influencing yeast CLS. Low pH and heat shorten the maximum wine yeast life span, while hyperosmotic shock extends it. Ethanol plays an important negative role in aging under winemaking conditions, but additional metabolites produced by fermentative metabolism, such as acetaldehyde and acetate, have also a strong impact on longevity. Grape polyphenols quercetin and resveratrol have negative impacts on CLS under winemaking conditions, an unexpected behavior for these potential anti-oxidants. We observed that quercetin inhibits alcohol and aldehyde dehydrogenase activities, and that resveratrol performs a pro-oxidant role during grape juice fermentation. Vitamins nicotinic acid and nicotinamide are precursors of NAD(+), and their addition reduces mean longevity during fermentation, suggesting a metabolic unbalance negative for CLS. Moreover, vitamin mix supplementation at the end of fermentation shortens CLS and enhances cell lysis, while amino acids increase life span. CONCLUSIONS: Wine S. cerevisiae strains are able to sense changes in the environmental conditions and adapt their longevity to them. Yeast death is influenced by the conditions present at the end of wine fermentation, particularly by the concentration of two-carbon metabolites produced by the fermentative metabolism, such as ethanol, acetic acid and acetaldehyde, and also by the grape juice composition, particularly its vitamin content. BioMed Central 2012-08-08 /pmc/articles/PMC3503821/ /pubmed/22873488 http://dx.doi.org/10.1186/1475-2859-11-104 Text en Copyright ©2012 Orozco 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
Orozco, Helena
Matallana, Emilia
Aranda, Agustín
Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
title Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
title_full Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
title_fullStr Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
title_full_unstemmed Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
title_short Two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
title_sort two-carbon metabolites, polyphenols and vitamins influence yeast chronological life span in winemaking conditions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503821/
https://www.ncbi.nlm.nih.gov/pubmed/22873488
http://dx.doi.org/10.1186/1475-2859-11-104
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