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The potential of several alternative genetic engineering based strategies in order to accelerate Saccharomyces cerevisiae autolysis for wine production has been studied. Both constitutively autophagic and defective in autophagy strains have been studied. Although both alternatives lead to impaired survival under starvation conditions, only constitutively autophagic strains, carrying a multicopy plasmid with the csc1-1 allele under the control of the TDH3 promoter, undergo accelerated autolysis in the experimental conditions tested. Fermentation performance is impaired in the autolytic strains, but industrial strains carrying the above-mentioned construction are still able to complete second fermentation of a model base wine. We suggest the construction of industrial yeasts showing a constitutive autophagic phenotype as a way to obtain second fermentation yeast strains undergoing accelerated autolysis.
Saccharomyces cerevisiae Proteins, Ethanol, Genes, Fungal, Colony Count, Microbial, Gene Expression, Wine, Saccharomyces cerevisiae, Culture Media, Industrial Microbiology, Glucose, Sparkling wine, Genetic engineering, Fermentation, Autophagy, Food Microbiology, Amino Acids, Autolysis, Promoter Regions, Genetic, Alleles, Plasmids
Saccharomyces cerevisiae Proteins, Ethanol, Genes, Fungal, Colony Count, Microbial, Gene Expression, Wine, Saccharomyces cerevisiae, Culture Media, Industrial Microbiology, Glucose, Sparkling wine, Genetic engineering, Fermentation, Autophagy, Food Microbiology, Amino Acids, Autolysis, Promoter Regions, Genetic, Alleles, Plasmids
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