Metabolic engineering of malolactic wine yeast

Metab Eng. 2006 Jul;8(4):315-23. doi: 10.1016/j.ymben.2006.02.003. Epub 2006 Apr 18.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Genetic Enhancement / methods*
  • Malate Dehydrogenase / genetics
  • Malate Dehydrogenase / metabolism*
  • Organic Anion Transporters / genetics
  • Organic Anion Transporters / metabolism*
  • Protein Engineering / methods
  • Recombinant Proteins / metabolism
  • Saccharomyces cerevisiae / physiology*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Schizosaccharomyces / enzymology
  • Schizosaccharomyces / genetics*
  • Vitis / metabolism*
  • Wine / microbiology*

Substances

  • Bacterial Proteins
  • Organic Anion Transporters
  • Recombinant Proteins
  • Saccharomyces cerevisiae Proteins
  • malate permease protein, Bacteria
  • malolactic enzyme
  • Malate Dehydrogenase