Literature DB >> 27956491

Fermentation assays reveal differences in sugar and (off-) flavor metabolism across different Brettanomyces bruxellensis strains.

Sam Crauwels1, Filip Van Opstaele2, Barbara Jaskula-Goiris2, Jan Steensels3, Christel Verreth1, Lien Bosmans1, Caroline Paulussen1, Beatriz Herrera-Malaver3, Ronnie de Jonge4, Jessika De Clippeleer2, Kathleen Marchal5, Gorik De Samblanx1, Kris A Willems1, Kevin J Verstrepen3, Guido Aerts2, Bart Lievens6.   

Abstract

Brettanomyces (Dekkera) bruxellensis is an ascomycetous yeast of major importance in the food, beverage and biofuel industry. It has been isolated from various man-made ecological niches that are typically characterized by harsh environmental conditions such as wine, beer, soft drink, etc. Recent comparative genomics studies revealed an immense intraspecific diversity, but it is still unclear whether this genetic diversity also leads to systematic differences in fermentation performance and (off-)flavor production, and to what extent strains have evolved to match their ecological niche. Here, we present an evaluation of the fermentation properties of eight genetically diverse B. bruxellensis strains originating from beer, wine and soft drinks. We show that sugar consumption and aroma production during fermentation are determined by both the yeast strain and composition of the medium. Furthermore, our results indicate a strong niche adaptation of B. bruxellensis, most clearly for wine strains. For example, only strains originally isolated from wine were able to thrive well and produce the typical Brettanomyces-related phenolic off-flavors 4-ethylguaiacol and 4-ethylphenol when inoculated in red wine. Sulfite tolerance was found as a key factor explaining the observed differences in fermentation performance and off-flavor production. Sequence analysis of genes related to phenolic off-flavor production, however, revealed only marginal differences between the isolates tested, especially at the amino acid level. Altogether, our study provides novel insights in the Brettanomyces metabolism of flavor production, and is highly relevant for both the wine and beer industry. © FEMS 2016. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Keywords:  (Off-)flavors; ecological niche; phenolic acid decarboxylase; vinylphenol reductase; volatile phenols

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Year:  2016        PMID: 27956491     DOI: 10.1093/femsyr/fow105

Source DB:  PubMed          Journal:  FEMS Yeast Res        ISSN: 1567-1356            Impact factor:   2.796


  4 in total

1.  Brettanomyces bruxellensis population survey reveals a diploid-triploid complex structured according to substrate of isolation and geographical distribution.

Authors:  Marta Avramova; Alice Cibrario; Emilien Peltier; Monika Coton; Emmanuel Coton; Joseph Schacherer; Giuseppe Spano; Vittorio Capozzi; Giuseppe Blaiotta; Franck Salin; Marguerite Dols-Lafargue; Paul Grbin; Chris Curtin; Warren Albertin; Isabelle Masneuf-Pomarede
Journal:  Sci Rep       Date:  2018-03-07       Impact factor: 4.379

2.  High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population.

Authors:  Jean-Sébastien Gounot; Cécile Neuvéglise; Kelle C Freel; Hugo Devillers; Jure Piškur; Anne Friedrich; Joseph Schacherer
Journal:  Genome Biol Evol       Date:  2020-06-01       Impact factor: 3.416

3.  Chromosomal genome assembly of the ethanol production strain CBS 11270 indicates a highly dynamic genome structure in the yeast species Brettanomyces bruxellensis.

Authors:  Ievgeniia A Tiukova; Mats E Pettersson; Marc P Hoeppner; Remi-Andre Olsen; Max Käller; Jens Nielsen; Jacques Dainat; Henrik Lantz; Jonas Söderberg; Volkmar Passoth
Journal:  PLoS One       Date:  2019-05-01       Impact factor: 3.240

4.  Assessing the Biofilm Formation Capacity of the Wine Spoilage Yeast Brettanomyces bruxellensis through FTIR Spectroscopy.

Authors:  Maria Dimopoulou; Vasiliki Kefalloniti; Panagiotis Tsakanikas; Seraphim Papanikolaou; George-John E Nychas
Journal:  Microorganisms       Date:  2021-03-12
  4 in total

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