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The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture

We have developed a wine fermentation procedure that takes advantage of the metabolic features of a previously characterized Metschnikowia pulcherrima strain in order to reduce ethanol production. It involves the use of M. pulcherrima/Saccharomyces cerevisiae mixed cultures, controlled oxygenation c...

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Detalles Bibliográficos
Autores principales: Morales, Pilar, Rojas, Virginia, Quirós, Manuel, Gonzalez, Ramon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428804/
https://www.ncbi.nlm.nih.gov/pubmed/25582558
http://dx.doi.org/10.1007/s00253-014-6321-3
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author Morales, Pilar
Rojas, Virginia
Quirós, Manuel
Gonzalez, Ramon
author_facet Morales, Pilar
Rojas, Virginia
Quirós, Manuel
Gonzalez, Ramon
author_sort Morales, Pilar
collection PubMed
description We have developed a wine fermentation procedure that takes advantage of the metabolic features of a previously characterized Metschnikowia pulcherrima strain in order to reduce ethanol production. It involves the use of M. pulcherrima/Saccharomyces cerevisiae mixed cultures, controlled oxygenation conditions during the first 48 h of fermentation, and anaerobic conditions thereafter. The influence of different oxygenation regimes and initial inoculum composition on yeast physiology and final ethanol content was studied. The impact of oxygenation on yeast physiology goes beyond the first aerated step and influences yields and survival rates during the anaerobic stage. The activity of M. pulcherrima in mixed oxygenated cultures resulted in a clear reduction in ethanol yield, as compared to S. cerevisiae. Despite relatively low initial cell numbers, S. cerevisiae always predominated in mixed cultures by the end of the fermentation process. Strain replacement was faster under low oxygenation levels. M. pulcherrima confers an additional advantage in terms of dissolved oxygen, which drops to zero after a few hours of culture, even under highly aerated conditions, and this holds true for mixed cultures. Alcohol reduction values about 3.7 % (v/v) were obtained for mixed cultures under high aeration, but they were associated to unacceptable volatile acidity levels. In contrast, under optimized conditions, only 0.35 g/L acetic acid was produced, for an alcohol reduction of 2.2 % (v/v), and almost null dissolved oxygen during the process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-014-6321-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-44288042015-05-18 The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture Morales, Pilar Rojas, Virginia Quirós, Manuel Gonzalez, Ramon Appl Microbiol Biotechnol Applied Microbial and Cell Physiology We have developed a wine fermentation procedure that takes advantage of the metabolic features of a previously characterized Metschnikowia pulcherrima strain in order to reduce ethanol production. It involves the use of M. pulcherrima/Saccharomyces cerevisiae mixed cultures, controlled oxygenation conditions during the first 48 h of fermentation, and anaerobic conditions thereafter. The influence of different oxygenation regimes and initial inoculum composition on yeast physiology and final ethanol content was studied. The impact of oxygenation on yeast physiology goes beyond the first aerated step and influences yields and survival rates during the anaerobic stage. The activity of M. pulcherrima in mixed oxygenated cultures resulted in a clear reduction in ethanol yield, as compared to S. cerevisiae. Despite relatively low initial cell numbers, S. cerevisiae always predominated in mixed cultures by the end of the fermentation process. Strain replacement was faster under low oxygenation levels. M. pulcherrima confers an additional advantage in terms of dissolved oxygen, which drops to zero after a few hours of culture, even under highly aerated conditions, and this holds true for mixed cultures. Alcohol reduction values about 3.7 % (v/v) were obtained for mixed cultures under high aeration, but they were associated to unacceptable volatile acidity levels. In contrast, under optimized conditions, only 0.35 g/L acetic acid was produced, for an alcohol reduction of 2.2 % (v/v), and almost null dissolved oxygen during the process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-014-6321-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-01-13 2015 /pmc/articles/PMC4428804/ /pubmed/25582558 http://dx.doi.org/10.1007/s00253-014-6321-3 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Applied Microbial and Cell Physiology
Morales, Pilar
Rojas, Virginia
Quirós, Manuel
Gonzalez, Ramon
The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
title The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
title_full The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
title_fullStr The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
title_full_unstemmed The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
title_short The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
title_sort impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture
topic Applied Microbial and Cell Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428804/
https://www.ncbi.nlm.nih.gov/pubmed/25582558
http://dx.doi.org/10.1007/s00253-014-6321-3
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