• Title of article

    Metabolic engineering of malolactic wine yeast

  • Author/Authors

    Filip Husnik، نويسنده , , John I. and Volschenk، نويسنده , , Heinrich and Bauer، نويسنده , , Jurgen and Colavizza، نويسنده , , Didier and Luo، نويسنده , , Zongli and van Vuuren، نويسنده , , Hennie J.J.، نويسنده ,

  • Issue Information
    دوماهنامه با شماره پیاپی سال 2006
  • Pages
    9
  • From page
    315
  • To page
    323
  • Abstract
    Malolactic fermentation is essential for the deacidification of high acid grape must. We have constructed a genetically stable industrial strain of Saccharomyces cerevisiae by integrating a linear cassette containing the Schizosaccharomyces pombe malate permease gene (mae1) and the Oenococcus oeni malolactic gene (mleA) under control of the S. cerevisiae PGK1 promoter and terminator sequences into the URA3 locus of an industrial wine yeast. The malolactic yeast strain, ML01, fully decarboxylated 5.5 g/l of malate in Chardonnay grape must during the alcoholic fermentation. Analysis of the phenotype, genotype, transcriptome, and proteome revealed that the ML01 yeast is substantially equivalent to the parental industrial wine yeast. The ML01 yeast enjoys ‘Generally Regarded As Safe’ status from the FDA and is the first genetically enhanced yeast that has been commercialized. Its application will prevent the formation of noxious biogenic amines produced by lactic acid bacteria in wine.
  • Keywords
    Oenococcus oeni , Malolactic fermentation , Malate permease , Malolactic enzyme , Saccharomyces cerevisiae
  • Journal title
    Metabolic Engineering
  • Serial Year
    2006
  • Journal title
    Metabolic Engineering
  • Record number

    1428598