ISOLATION AND PARTIAL CHARACTERIZATION OF BETA-GALACTOSIDASE ACTIVITYPRODUCED BY A THERMOTOLERANT STRAIN OF KLUYVEROMYCES-MARXIANUS DURINGGROWTH ON LACTOSE-CONTAINING MEDIA

Citation
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
Citations number
14
Categorie Soggetti
Biothechnology & Applied Migrobiology
ISSN journal
01410229
Volume
17
Issue
8
Year of publication
1995
Pages
696 - 699
Database
ISI
SICI code
0141-0229(1995)17:8<696:IAPCOB>2.0.ZU;2-M
Abstract
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.