An easily regenerable enzyme reactor prepared from polymerized high internal phase emulsions

被引:9
|
作者
Ruan, Guihua [1 ,2 ]
Wu, Zhenwei [1 ]
Huang, Yipeng [1 ]
Wei, Meiping [1 ]
Su, Rihui [1 ]
Du, Fuyou [1 ,2 ]
机构
[1] Guilin Univ Technol, Coll Chem & Bioengn, Guangxi Key Lab Electrochem & Magnetochem Funct M, Guangxi 541004, Peoples R China
[2] Guilin Univ Technol, Guangxi Collaborat Innovat Ctr Water Pollut Contr, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Immobilized enzymatic reactor; Protein digestion; High internal phase emulsion; PolyHIPE monoliths; TRYPSIN IMMOBILIZATION; PROTEIN DIGESTION; HIGH-EFFICIENCY; SILICA; PROTEOLYSIS; MONOLITHS; SUPPORT; MATRIX; NANOPARTICLES; MICROSPHERES;
D O I
10.1016/j.bbrc.2016.03.049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A large-scale high-efficient enzyme reactor based on polymerized high internal phase emulsion monolith (polyHIPE) was prepared. First, a porous cross -linked polyHIPE monolith was prepared by in-situ thermal polymerization of a high internal phase emulsion containing styrene, divinylbenzene and polyglutaraldehyde. The enzyme of TPCK-Trypsin was then immobilized on the monolithic polyHIPE. The performance of the resultant enzyme reactor was assessed according to the conversion ability of Nebenzoyl-L-arginine ethyl ester to 1%-benzoyl-r-arginine, and the protein digestibility of bovine serum albumin (BSA) and cytochrome (Cyt-C). The results showed that the prepared enzyme reactor exhibited high enzyme immobilization efficiency and fast and easy -control protein digestibility. BSA and Cyt-C could be digested in 10 min with sequence coverage of 59% and 78%, respectively. The peptides and residual protein could be easily rinsed out from reactor and the reactor could be regenerated easily with 4 M HCl without any structure destruction. Properties of multiple interconnected chambers with good permeability, fast digestion facility and easily reproducibility indicated that the polyHIPE enzyme reactor was a good selector potentially applied in proteomics and catalysis areas. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:54 / 60
页数:7
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