Enzyme embedded metal organic framework (enzyme-MOF): De novo approaches for immobilization

被引:190
作者
Nadar, Shamraja S. [1 ]
Vaidya, Leena [1 ]
Rathod, Virendra K. [1 ]
机构
[1] Inst Chem Technol, Dept Chem Engn, Mumbai 400019, Maharashtra, India
关键词
Metal organic frameworks; Enzyme; Immobilization; Biomineralization; Co-precipitation; Encapsulation; ZEOLITIC IMIDAZOLATE FRAMEWORKS; RECENT PROGRESS; BIOMIMETIC MINERALIZATION; FACILE SYNTHESIS; MAGNETIC NANOPARTICLES; ENHANCED ACTIVITY; ENCAPSULATION; COIMMOBILIZATION; GLUCOAMYLASE; BIOCATALYSTS;
D O I
10.1016/j.ijbiomac.2020.01.240
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
The porous material has been considered as a potential candidate for immobilizing enzymes. Recently, metal organic framework (MOF) has been emerged as a hybrid organic inorganic material with unique intrinsic properties such as well-defined pore structure, excellent chemico-thermal stability, and extremely high surface areas which make them as a suitable scaffold for enzyme immobilization. The outstanding improvement in catalytic performance, high enzyme loading capacity, remarkable interaction between enzyme and MOF are the key features of the novel enzyme-MOF biocomposites. Amongst different immobilization approaches of enzyme-MOF composite development, de novo strategy received immense attention due to rapid, facile, mild immobilization procedure which exhibits potentially superior catalytic activity and extraordinary operational stability. This review presents a holistic insight of two different de novo strategies i.e. co-precipitation and biomineralization with state-of-art examples. Further, the recent developments in enzyme-MOF composites along with their potential features and characteristics are exploited in terms of catalytic activity, thermal/chemical stability, Michaelis-Menten kinetics, recyclability and storage stability. The advanced de novo strategies such as multienzyme catalytic system and magnetic enzyme-MOF are explored in the latter part of highlights. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:861 / 876
页数:16
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