Nanostructures for enzyme stabilization

被引:693
作者
Kim, J [1 ]
Grate, JW
Wang, P
机构
[1] Pacific NW Natl Lab, Richland, WA 99352 USA
[2] Univ Akron, Dept Chem Engn, Akron, OH 44325 USA
基金
美国国家科学基金会;
关键词
enzyme stabilization; nanostructures; enzyme adsorption; covalent attachment; nanoparticles; nanofibers; mesoporous silica; sol-gel; enzyme encapsulation; single enzyme nanoparticles;
D O I
10.1016/j.ces.2005.05.067
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Recent breakthroughs in nanotechnology have made various nanostructured materials more affordable for a broader range of applications. Although we are still at the beginning of exploring the use of these materials for biocatalysis, various nanostructures have been examined as hosts for enzyme immobilization via approaches including enzyme adsorption, covalent attachment, enzyme encapsulation, and sophisticated combinations of methods. This review discusses the stabilization mechanisms behind these diverse approaches; such as confinement, pore size and volume, charge interaction, hydrophobic interaction, and multipoint attachment. In particular, we will review recently reported approaches to improve the enzyme stability in various nanostructures such as nanoparticles, nanofibers, mesoporous materials, and single enzyme nanoparticles (SENs). In the form of SENs, each enzyme molecule is surrounded with a nanometer scale network, resulting in stabilization of enzyme activity without any serious limitation for the substrate transfer from solution to the active site. SENs can be further immobilized into mesoporous silica with a large surface area, providing a hierarchical approach for stable, immobilized enzyme systems for various applications, such as bioconversion, bioremediation, and biosensors. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1017 / 1026
页数:10
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