ISOLATION AND PARTIAL CHARACTERIZATION OF BETA-GALACTOSIDASE ACTIVITYPRODUCED BY A THERMOTOLERANT STRAIN OF KLUYVEROMYCES-MARXIANUS DURINGGROWTH ON LACTOSE-CONTAINING MEDIA
D. Brady et al., ISOLATION AND PARTIAL CHARACTERIZATION OF BETA-GALACTOSIDASE ACTIVITYPRODUCED BY A THERMOTOLERANT STRAIN OF KLUYVEROMYCES-MARXIANUS DURINGGROWTH ON LACTOSE-CONTAINING MEDIA, Enzyme and microbial technology, 17(8), 1995, pp. 696-699
A thermotolerant yeast strain, Kluyveromyces marxianus IMB3, has previ
ously been shown to be capable of ethanol production following growth
on lactose-containing media at 45 degrees C. Here, we demonstrate that
the organism is capable of producing inducible beta-galactosidase act
ivity in the presence of lactose. The majority of the activity appears
to be cell associated. Enzyme, isolated following disruption of the c
ells, has been partially characterized and shown to have a K-m of 5 mM
for the substrate o-nitrophenyl-beta-D-galactoside, whereas that for
lactose was found to be 40 mM. The activity was shown to have an optim
al operating temperature of 50 degrees C, although the half-life of th
e enzyme was shown to be <5 min at that temperature. The half-life of
the isolated enzyme at 45 degrees C, the optimal fermenting temperatur
e of the yeast, was shown to be 15 min. The enzyme was stable at 30 de
grees C for at least 8 h. The optimum pH was 7.5. When we analyzed the
result using nondenaturing polyacrylamide gradient gel electrophoresi
s together with zymogram staining with methylumbelliferyl-beta-D-galac
toside as substrate, two distinct forms of activity were observed foll
owing prolonged incubation with substrate. The results suggest that al
though this yeast is capable of ethanol production at 45 degrees C, th
ermotolerance is not reflected in the enzyme activity associated with
assimilation of lactose.