Bioinspired Cu/Zn-ZIF nanozyme with excellent laccase-like activity for selective colorimetric detection of phenolic pollutants

被引:0
|
作者
Wei, Wenyu [1 ]
Wang, Han [1 ]
Su, Ping [1 ]
Song, Jiayi [1 ]
Yang, Yi [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem, Beijing Key Lab Environmentally Harmful Chem Anal, Beijing 100029, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Cu/Zn-ZIF; Laccase mimetic; Selectivity; Colorimetric detection; Phenolic pollutants; METAL-ORGANIC FRAMEWORK; PEROXIDASE-LIKE; COPPER; CONSTRUCTION; DEGRADATION; CLUSTER; SITE;
D O I
10.1016/j.talanta.2025.127862
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The ingenious design of active sites in mimetic enzymes is crucial for developing enzyme-like functional materials with high activity and selectivity. Inspired by the N-ligand-rich copper centers of natural laccase, a novel laccase-like nanozyme was developed by loading copper ions into zeolite imidazolate framework-8 (Cu/Zn-ZIF). Benefiting from the precise mimicry of the catalytic center and the high dispersion of catalytic sites which were supported by the MOF backbone, Cu/Zn-ZIF manifested superior laccase-like activity. Notably, its substrate affinity and catalytic efficiency were substantially higher compared to those of natural laccase. More importantly, experimental results proved that the catalytic mechanism of Cu/Zn-ZIF was similar to that of natural laccase. In addition, Cu/Zn-ZIF nanozyme presented commendable stability under various harsh conditions compared to natural laccase. Surprisingly, limited by the pore size, Cu/Zn-ZIF exhibited the selectivity for different sizes substrates which was not found in natural laccase. As a proof of concept application, a colorimetric detection platform for 4-methoxyphenol was constructed with a broad linear range (1-150 mu g/mL) and a low limit of detection (0.33 mu g/mL). This study provides a novel approach for the rational design of nanozymes and serves as a feasible reference for enriching the application scenarios of laccase-like nanozymes.
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页数:10
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