Direct immobilization of glucose oxidase in magnetic mesoporous bioactive glasses

被引:13
|
作者
Min, Dandan [1 ]
Zhang, Xudong [1 ]
He, Wen [1 ]
Zhang, Yang [2 ]
Li, Piwu [3 ]
Zhang, Meimei [1 ]
Liu, Jianan [1 ]
Liu, Shujiang [1 ]
Xu, Fengxiu [1 ]
Du, Yi [1 ]
Zhang, Zhilong [1 ]
机构
[1] Shandong Polytech Univ, Shandong Prov Key Lab Proc & Testing Technol Glas, Jinan 250353, Peoples R China
[2] Ocean Univ China, Coll Engn, Qingdao 266100, Peoples R China
[3] Shandong Polytech Univ, Shandong Key Lab Fermentat Engn, Jinan 250353, Peoples R China
关键词
NONHEME IRON ENZYME; FORCE MICROSCOPY; DRUG-DELIVERY; NANOPARTICLES; FE3O4; BEHAVIOR; SUPPORT; SYSTEM; PH;
D O I
10.1039/c3tb20480d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Direct immobilization of enzymes on the bioactive glasses is conceptually a completely new strategy. We find that the Fe2O3-CaO-SiO2-P2O5 magnetic mesoporous bioactive glass (MMBG) is an ideal immobilization matrix for glucose oxidase (GOD). Its unique chemical surface properties and open mesopores enhance the catalytic activity of directly immobilized GOD. In this paper, MMBG was synthesized using the sol-gel approach and polyethylene glycol (PEG) as template at 700 degrees C. GOD molecules were spontaneously entrapped inside the open mesoporous structure and onto the surface of MMBG via iron ion binding, their activity was not impaired. The substrates and products can access and diffuse freely through the open mesoporous structure in MMBG. This study is focused on understanding the formation mechanism of MMBG, the immobilized mechanism of GOD and the magnetic separation mechanism of MMBG from the reaction medium. The MMBG can be utilized in the design of a solid support for any enzyme for bioconversion, bioremediation, and biosensors.
引用
收藏
页码:3295 / 3303
页数:9
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