JBC, Vol. 252, Issue 4, 1162-1166, Feb, 1977
Purification and properties of galactokinase from Saccharomyces cerevisiae
M. A. Schell and D. B. Wilson
Galactokinase (EC 2.7.1.6; ATP:D-galactose-1-phosphotransferase) was
purified to homogeneity with a 50% yield from cells of Saccharomyces
cerevisiae which were fully induced for the production of the galactose
metabolizing enzymes. The purification was accomplished by:(a) ammonium
sulfate fractionation, (b) streptomycin sulfate precipitation. (c)
DEAE-cellulose chromatography, (d) hydroxylapatite chromatography, and
finally (e) Bio-Gel A-0.5 m gel filtration. The resulting preparation of
galactokinase was judged to be at least 95% pure by the following criteria:
(a) sodium dodecyl sulfate-polyacrylamide gel electrophoresis, (b)
ultracentrifuge analysis, (c) nondissociating polyacrylamide gel
electrophoresis, and (d) Bio-Gel A-0.5 m gel filtration. The purified
enzyme preparation was used to determine the Km values for the two
substrates, galactose and ATP, which were found to be 0.60 and 0.15 mM,
respectively. Vmax was also determined and found to be 3.35 mmol/h/mg. This
corresponds to a turnover rate of 3350 molecules of galactose
phosphorylated/min/enzyme molecule. The effect of pH on the
galactokinase-catalyzed phosphorylation of galactose was determined; the
results showed the pH optimum of the reaction to be in the range of pH 8.0
to 9.0. The enzyme is highly specific for galactose since galactokinase did
not appear to phosphorylate any of the other sugars tested at a rate
greater than 0.5% of the rate of galactose phosphorylation. Amino acid
analysis was performed on the enzyme preparation and the results were used
to calculate the partial specific volume (v) of 0.736. The NH2-terminal
sequence was determined for the first 3 residues. The molecular weight and
subunit composition were determined by ultracentrifugation and
polyacrylamide gel electrophoresis under dissociating and nondissociating
conditions. The data obtained indicated that galactokinase is a monomeric
protein of molecular weight 58,000.