SSU1 mediates sulphite efflux in Saccharomyces cerevisiae

Yeast. 2000 Jul;16(10):881-8. doi: 10.1002/1097-0061(200007)16:10<881::AID-YEA576>3.0.CO;2-3.

Abstract

Ssu1p, a plasma membrane protein involved in sulphite metabolism in Saccharomyces cerevisiae, was found to be required for efficient sulphite efflux. An SSU1 null mutant accumulated significantly more sulphite than wild-type, whereas cells expressing multicopy SSU1 accumulated significantly less. Cells expressing FZF1-4, a dominant allele of a transcriptional activator of SSU1 that confers sulphite resistance, also accumulated less sulphite. beta-galactosidase activity in the FZF1-4 strain carrying an SSU1::lacZ fusion was found to be 8.5-fold higher than in a strain carrying wild-type FZF1, confirming that the heightened resistance was correlated with hyperactivation of SSU1. Multicopy SSU1 was also found to increase the sulphite resistance of a number of unrelated sulphite-sensitive strains by a factor of 3- to 8-fold. Rates of efflux of free sulphite from cells expressing multicopy SSU1 or FZF1-4 were significantly greater than that from wild-type or from a SSU1 null mutant. Rates of efflux of bound sulphite from wild-type, a SSU1 null mutant, a FZF1-4 mutant, or cells expressing multicopy SSU1 were not significantly different, suggesting that Ssu1p specifically mediates efflux of the free form of sulphite.

MeSH terms

  • Anion Transport Proteins*
  • Biological Transport
  • Drug Resistance, Microbial
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism*
  • Gene Expression Regulation, Fungal
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mutation
  • Oxidoreductases Acting on Sulfur Group Donors / metabolism
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins*
  • Sulfites / metabolism*
  • Sulfites / pharmacology
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors*
  • beta-Galactosidase / metabolism

Substances

  • Anion Transport Proteins
  • FZF1 protein, S cerevisiae
  • Fungal Proteins
  • Membrane Proteins
  • Saccharomyces cerevisiae Proteins
  • Ssu1 protein, S cerevisiae
  • Sulfites
  • Trans-Activators
  • Transcription Factors
  • Oxidoreductases Acting on Sulfur Group Donors
  • beta-Galactosidase