首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Optimization of covalent immobilization of Trichoderma reesei cellulase onto modified ReliZyme HA403 and Sepabeads EC-EP supports for cellulose hydrolysis, in buffer and ionic liquids/buffer media
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Optimization of covalent immobilization of Trichoderma reesei cellulase onto modified ReliZyme HA403 and Sepabeads EC-EP supports for cellulose hydrolysis, in buffer and ionic liquids/buffer media

机译:优化里氏木霉纤维素酶在修饰的ReliZyme HA403和Sepabeads EC-EP上共价固定在缓冲液和离子液体/缓冲液中的纤维素水解能力

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Abstract The covalent immobilization of Trichoderma reesei cellulase onto modified ReliZyme HA403 and Sepabeads EC-EP supports were carried out. The optimal immobilization conditions were determined using response surface methodology. The hydrolysis of cellulose using the free and immobilized cellulase preparations in ionic liquids (IL) using cosolvents was investigated. The hydrolytic activities in buffer medium containing 25% (v/v) of 1-butyl-3-methylimidazolium hexafluorophosphate were around 2.6-, 1.6-, and 5.5-fold higher than the activities in buffer medium. The retained initial activities were 32% and 57%, respectively for cellulase preparations immobilized onto Sepabeads EC-EP support and onto modified ReliZyme HA403 support after 5 reuses.
机译:摘要将里氏木霉纤维素酶共价固定在改良的ReliZyme HA403和Sepabeads EC-EP载体上。使用响应表面方法确定最佳固定条件。使用游离溶剂和固定化纤维素酶制剂在离子液体(IL)中使用助溶剂对纤维素进行了水解研究。含有25%(v / v)1-丁基-3-甲基咪唑鎓六氟磷酸盐的缓冲液中的水解活性比缓冲液中的水解活性高约2.6、1.6和5.5倍。 5次重复使用后,固定在Sepabeads EC-EP支撑物和修饰的ReliZyme HA403支撑物上的纤维素酶制剂保留的初始活性分别为32%和57%。

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