A Simple Method for Beta-glucosidase Immobilization and Its Application in Soybean Isoflavone Glycosides Hydrolysis
Hu Shenglin, Wang Dongmei, Hong Jiong,
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( Hu Shenglin )
University of Science and Technology of China School of Life Sciences
( Wang Dongmei )
University of Science and Technology of China School of Life Sciences
( Hong Jiong )
University of Science and Technology of China School of Life Sciences
Abstract
In this study, a simple, inexpensive and fast ¥â-glucosidase immobilization system was constructed and evaluated in isoflavone glycosides hydrolysis. A ¥â-glucosidase gene from Thermoascus aurantiacus IFO9748 was recombinantly expressed in Pichia pastoris KM71H and immobilized on regenerated amorphous cellulose (RAC) by fused cellulose binding module 3. Through simple mixing cellulose and crude enzyme for 15 min under room temperature, 96.04% ¥â-glucosidase was immobilized onto RAC. The optimum temperature for ¥â-glucosidase activity was increased by 5¨¬C after immobilization. The half-life (t¨ö) of heat inactivation of immobilized enzyme at 60oC was improved over 8 folds. After 30 rounds recycled at 40oC, 96.9% daidzin and 98.9% genistin could still be hydrolyzed. A continuous hydrolysis system was also constructed, and at the flow rate of 0.2 mL/min after 30 h hydrolysis, 95.6% genistin and 90.2% daidzin can still be hydrolyzed. Combined the simple and high efficient enzyme immobilization procedure and inexpensive cellulose, this scalable and practical system may have broad prospects for industrial utilization.
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immobilized ¥â-Glucosidase; regenerated amorphous cellulose; isoflavone glycosides hydrolysis; cellulose binding module 3
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