Nitrogen catabolite repression in Saccharomyces cerevisiae during wine fermentations

FEMS Yeast Res. 2004 Mar;4(6):625-32. doi: 10.1016/j.femsyr.2003.12.004.

Abstract

We carried out fermentations with several nitrogen sources in different concentrations and studied nitrogen regulation by following the transcriptional profile of the general amino-acid permease (GAP1) and the ammonium permeases (MEP1, MEP2, MEP3). In wine fermentations the cells evolve from a nitrogen-repressed situation at the beginning of the process to a nitrogen-derepressed situation as the nitrogen is consumed. These nitrogen-repressed/derepressed conditions determined the different patterns of ammonium and amino-acid consumption. Arginine and alanine were hardly used under the repressed conditions, while the uptake of branched-chain and aromatic amino acids increased.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Transport Systems / metabolism
  • Amino Acids / metabolism
  • Cation Transport Proteins / metabolism
  • Fermentation
  • Gene Expression Regulation, Fungal
  • Nitrogen / metabolism*
  • Quaternary Ammonium Compounds / metabolism
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Wine / microbiology*

Substances

  • Amino Acid Transport Systems
  • Amino Acids
  • Cation Transport Proteins
  • MEP1 protein, S cerevisiae
  • Quaternary Ammonium Compounds
  • Saccharomyces cerevisiae Proteins
  • Nitrogen