Synthesis and characterization of surface-functionalized paramagnetic nanoparticles and their application to immobilization of α-acetolactate decarboxylase

被引:11
|
作者
Qian, Siriguleng [1 ]
Wang, Chun [1 ]
Wang, Hongying [1 ]
Yu, Fang [1 ]
Zhang, Chunzhi [1 ]
Yu, Hongshan [1 ]
机构
[1] Dalian Polytech Univ, Sch Biol Engn, Dalian 116034, Peoples R China
关键词
Paramagnetic surface-functionalized nanoparticles; K-m; Immobilized enzyme; alpha-Acetolactate decarboxylase; ENZYME IMMOBILIZATION; SHELL; LIPASE; CORE; MICROSPHERES;
D O I
10.1016/j.procbio.2015.05.012
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
In this paper, a facile paramagnetic Fe3O4@SiO2-NH2 nanoparticles (PMN Fe3O4@SiO2-NH2 NPs) have been successfully synthesized and characterized, which were applied to alpha-acetolactate decarboxylase (alpha-ALDC) immobilization using 1, 1'-carbonyldiimidazole (CDI) as the covalent reagent. The synthesized nanoparticles exhibited satisfactory paramagnetic under magnetic field, high single-crystalline and abundant amino groups on the surface. The alpha-ALDC loading capacity onto nanoparticles was 48.70 +/- 1.25 mu g/mg carrier and the activity of retained alpha-ALDC remained 69.39 +/- 1.16% in comparison with free alpha-ALDC. Enzyme kinetics analysis showed that immobilized alpha-ALDC had lower affinity to its substrate than that of free alpha-ALDC based on higher Km and little lower limax of immobilized alpha-ALDC. After storage at 4 degrees C in disodium hydrogen phosphate and citric acid (DHPCA) buffer (20 mM, pH 6) for 14 days, immobilized alpha-ALDC retained 65.35% of its initial activity, while the activity of free alpha-ALDC only kept 39.22% in the same conditions. After 5 times re-use, immobilized alpha-ALDC still retained 31.03% of its initial activity for preventing diacetyl production. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1388 / 1393
页数:6
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