纳米技术
封装(网络)
共价键
生化工程
材料科学
化学
计算机科学
工程类
有机化学
计算机网络
作者
Rui Gao,Xiaoxue Kou,Siming Huang,Siming Huang,Guosheng Chen,Gangfeng Ouyang
出处
期刊:ChemBioChem
[Wiley]
日期:2024-05-27
卷期号:25 (17): e202400339-e202400339
被引量:13
标识
DOI:10.1002/cbic.202400339
摘要
Utilizing covalent organic frameworks (COFs) as porous supports to encapsulate enzyme represents an advanced strategy for constructing COFs biocatalysts, which has inspired numerous interests across various applications. As the structural advantages including ultrastable covalent-bonded linkage, tailorable pore structure, and metal-free biocompatibility, the resultant enzyme-COFs biocatalysts showcase functional enhancement in catalytic activity, chemical stability, long-term durability, and recyclability. This Concept describes the recent advances in the methodological strategies for engineering the COFs biocatalysts, with specific emphasis on the pore entrapment and in situ encapsulation strategies. The structural advantages of the COFs hybrid biocatalysts for organic synthesis, environment- and energy-associated applications are also canvassed. Additionally, the remaining challenges and the forward-looking directions in this field are also discussed. We believe that this Concept can offer useful methodological guidance for developing active and robust COFs biocatalysts.
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