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优化里氏木霉纤维素酶通过修饰的 ReliZyme HA403 和 Sepabeads EC-EP 载体的共价固定化,用于纤维素水解,在缓冲液和离子液体/缓冲液介质中。

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.

机构信息

a Department of Chemistry , Faculty of Sciences and Letters, University of Cukurova , Adana , Turkey.

b Advanced Technology Education, Research and Application Center, Mersin University , Mersin , Turkey.

出版信息

Artif Cells Nanomed Biotechnol. 2016 Aug;44(5):1276-84. doi: 10.3109/21691401.2015.1024842. Epub 2015 Mar 26.

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.

摘要

将里氏木霉纤维素酶共价固定到改性 ReliZyme HA403 和 Sepabeads EC-EP 载体上。使用响应面法确定最佳固定化条件。研究了在离子液体(IL)中使用共溶剂的游离和固定化纤维素酶制剂对纤维素的水解作用。在含有 25%(v/v)1-丁基-3-甲基咪唑六氟磷酸盐的缓冲介质中的水解活性比在缓冲介质中的活性高 2.6 倍、1.6 倍和 5.5 倍。固定在 Sepabeads EC-EP 载体和改性 ReliZyme HA403 载体上的纤维素酶制剂在重复使用 5 次后,保留的初始活性分别为 32%和 57%。

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