Kinetic analysis of yeast galactokinase: Implications for transcriptional activation of the GAL genes

David J. Timson, Richard J. Reece

    Research output: Contribution to journalArticlepeer-review


    Galactokinase (EC catalyses the first step in the catabolism of galactose. Yeast galactokinase, Gal1p, and the closely related but catalytically inactive Gal3p, also function as ligand sensors in the GAL genetic switch. In the presence of galactose and ATP (the substrates of the reaction catalysed by Gal1p) Gal1p or Gal3p can bind to Gal80p, a transcriptional repressor. This relieves the inhibition of a transcriptional activator, Gal4p, and permits expression of the GAL genes. In order to learn more about the mechanism of ligand sensing by Gal3p and Gal1p, we studied the kinetics of the reaction catalysed by Gal1p. Galactose-1-phosphate, a product of the reaction, is a mixed inhibitor both with respect to galactose and to ATP suggesting that the reaction proceeds via a compulsory, ordered, ternary complex mechanism. There is little variation in either the turnover number or the specificity constants in the pH range 6.0-9.5, implying that no catalytic base is required in the reaction. These data are discussed both in the context of galactokinase enzymology and their implications for the mechanism of transcriptional induction. © 2002 Société française de biochimie et biologie moléculaire/Éditions scientifiques et médicales Elsevier SAS. All rights reserved.
    Original languageEnglish
    Pages (from-to)265-272
    Number of pages7
    Issue number4
    Publication statusPublished - 2002


    • Enzyme mechanism
    • Gal3p
    • Gal80p
    • Galactosemia
    • Gene expression


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