A constitutive thiamine metabolism mutation, thi80, causing reduced thiamine pyrophosphokinase activity in Saccharomyces cerevisiae

Author:

Nishimura H1,Kawasaki Y1,Nosaka K1,Kaneko Y1,Iwashima A1

Affiliation:

1. Department of Biochemistry, Kyoto Prefectural University of Medicine, Japan.

Abstract

We identified a strain carrying a recessive constitutive mutation (thi80-1) with an altered thiamine transport system, thiamine-repressible acid phosphatase, and several enzymes of thiamine synthesis from 2-methyl-4-amino-5-hydroxymethylpyrimidine and 4-methyl-5-beta-hydroxyethylthiazole. The mutant shows markedly reduced activity of thiamine pyrophosphokinase (EC 2.7.6.2) and high resistance to oxythiamine, a thiamine antagonist whose potency depends on thiamine pyrophosphokinase activity. The intracellular thiamine pyrophosphate content of the mutant cells grown with exogenous thiamine (2 x 10(-7) M) was found to be about half that of the wild-type strain under the same conditions. These results suggest that the utilization and synthesis of thiamine in Saccharomyces cerevisiae is controlled negatively by the intracellular thiamine pyrophosphate level.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference19 articles.

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2. Isolation of a thiaminbinding protein from Saccharomyces cerevisiae;Iwashima A.;Biochim. Biophys. Acta,1979

3. Soluble and membrane bound thiamine-binding proteins from Saccharomyces cerevisiae;Iwashima A.;Biochim. Biophys. Acta,1979

4. Carrier-mediated transport of thiamin in baker's yeast;Iwashima A.;Biochim. Biophys. Acta,1973

5. Interaction of basic dyes with the thiamine transport system in Saccharomyces cerevisiae;Iwashima A.;Experientia,1981

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