Ionic Liquid-Mediated Dynamic Polymerization for Facile Aqueous-Phase Synthesis of Enzyme-Covalent Organic Framework Biocatalysts

被引:15
|
作者
Gao, Rui [1 ]
Kou, Xiaoxue [1 ]
Tong, Linjing [1 ]
Li, Zhi-Wei [1 ]
Shen, Yujian [1 ]
He, Rongwei [1 ]
Guo, Lihong [1 ]
Wang, Hao [1 ]
Ma, Xiaomin [5 ]
Huang, Siming [2 ,3 ,4 ]
Chen, Guosheng [1 ]
Ouyang, Gangfeng [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Peoples R China
[2] Guangzhou Med Univ, Guangzhou Municipal & Guangdong Prov Key Lab Mol T, NMPA, Guangzhou 511436, Peoples R China
[3] Guangzhou Med Univ, Sch Pharmaceut Sci, State Key Lab Resp Dis, Guangzhou 511436, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou 511436, Peoples R China
[5] Southern Univ Sci & Technol, Cryo EM Ctr, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Covalent Organic Frameworks; Enzyme Immobilization; Ionic Liquid; Pollutants Degradation; IMMOBILIZATION; CRYSTALLINE;
D O I
10.1002/anie.202319876
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Utilizing covalent organic framework (COF) as a hypotoxic and porous scaffold to encapsulate enzyme (enzyme@COF) has inspired numerous interests at the intersection of chemistry, materials, and biological science. In this study, we report a convenient scheme for one-step, aqueous-phase synthesis of highly crystalline enzyme@COF biocatalysts. This facile approach relies on an ionic liquid (2 mu L of imidazolium ionic liquid)-mediated dynamic polymerization mechanism, which can facilitate the in situ assembly of enzyme@COF under mild conditions. This green strategy is adaptive to synthesize different biocatalysts with highly crystalline COF "exoskeleton", as well evidenced by the low-dose cryo-EM and other characterizations. Attributing to the rigorous sieving effect of crystalline COF pore, the hosted lipase shows non-native selectivity for aliphatic acid hydrolysis. In addition, the highly crystalline linkage affords COF "exoskeleton" with higher photocatalytic activity for in situ production of H2O2, enabling us to construct a self-cascading photo-enzyme coupled reactor for pollutants degradation, with a 2.63-fold degradation rate as the poorly crystalline photo-enzyme reactor. This work showcases the great potentials of employing green and trace amounts of ionic liquid for one-step synthesis of crystalline enzyme@COF biocatalysts, and emphasizes the feasibility of diversifying enzyme functions by integrating the reticular chemistry of a COF. We herein report an ionic liquid-mediated dynamic polymerization for designing highly crystalline enzyme-covalent organic framework (COF) biocatalysts. The highly crystalline COF "exoskeleton" affords the hosted lipase with non-native catalytic selectivity for aliphatic acid hydrolysis. While the high photocatalytic activity of crystalline COF enables us to construct a self-cascading photo-enzyme coupled nanoreactor for pollutants degradation.+image
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页数:13
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