
doi: 10.1007/bf00130844
β-D-Glucosidase, alone and after copolymerizing with a resorcinol polymer, was immobilized on a PM 10 ultrafiltration membrane, κ-carrageenan and DEAE (DE52) cellulose. The best support for both enzyme preparations, in terms of high Vmax values, was the ultrafiltration membrane. Compared with free β-D-glucosidase, both preparations immobilized on ultrafiltration membranes exhibited: different pH optima, enhanced thermostability, and were more suitable for continuous hydrolysis of substrate.
FoR 09 (Engineering), FoR 10 (Technology), FoR 06 (Biological Sciences), biotechnology
FoR 09 (Engineering), FoR 10 (Technology), FoR 06 (Biological Sciences), biotechnology
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