Affiliation:
1. Instituto de Fermentaciones Industriales (CSIC), Madrid, Spain
2. Instituto de Ciencias de la Vid y el Vino (CSIC, Universidad de La Rioja, and Gobierno de La Rioja), Logroño, Spain
Abstract
ABSTRACT
Stabilization against protein haze was one of the first positive properties attributed to yeast mannoproteins in winemaking. In previous work we demonstrated that deletion of
KNR4
leads to increased mannoprotein release in laboratory
Saccharomyces cerevisiae
strains. We have now constructed strains with
KNR4
deleted in two different industrial wine yeast backgrounds. This required replacement of two and three alleles of
KNR4
for the EC1118 and T73-4 backgrounds, respectively, and the use of three different selection markers for yeast genetic transformation. The actual effect of the genetic modification was dependent on both the genetic background and the culture conditions. The fermentation performance of T73-4 derivatives was clearly impaired, and these derivatives did not contribute to the protein stability of the wine, even though they showed increased mannoprotein release in vitro. In contrast, the EC1118 derivative with both alleles of
KNR4
deleted released increased amounts of mannoproteins both in vitro and during wine fermentation assays, and the resulting wines were consistently less susceptible to protein haze. The fermentation performance of this strain was slightly impaired, but only with must with a very high sugar content. These results pave the way for the development of new commercial strains with the potential to improve several mannoprotein-related quality and technological parameters of wine.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
77 articles.
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