A possible role for acid phosphatase with thiamin-binding activity encoded by PHO3 in yeast

FEMS Microbiol Lett. 1989 Jul 1;51(1):55-9. doi: 10.1016/0378-1097(89)90077-3.

Abstract

Periplasmic soluble thiamin-binding protein in Saccharomyces cerevisiae (Iwashima, A. et al. (1979) Biochim. Biophys. Acta 577, 217-220) was demonstrated to be encoded by PHO3 gene that codes for thiamin repressible acid phosphatase (Schweingruber, M.E. et al. (1986) J. Biol. Chem. 261, 15877-15882) by genetic analysis. The pho3 mutant cells of S. cerevisiae in contrast to the parent cells have markedly reduced activity of the uptake of [14C]thiamin phosphates, suggesting that thiamin repressible acid phosphatase plays a role in the hydrolysis of thiamin phosphates in the periplasmic space prior to the uptake of their thiamin moieties by S. cerevisiae.

MeSH terms

  • Acid Phosphatase / genetics
  • Acid Phosphatase / metabolism*
  • Biological Transport, Active
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Chromatography, High Pressure Liquid
  • Genes, Fungal*
  • Mutation
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins*
  • Thiamine / metabolism
  • Thiamine Monophosphate / metabolism
  • Thiamine Pyrophosphate / metabolism

Substances

  • Carrier Proteins
  • Saccharomyces cerevisiae Proteins
  • thiamine-binding protein
  • Thiamine Monophosphate
  • Acid Phosphatase
  • PHO3 protein, S cerevisiae
  • PHO5 protein, S cerevisiae
  • Thiamine Pyrophosphate
  • Thiamine