杀虫剂
有机磷
乙酰胆碱酯酶
重组DNA
农药残留
大肠杆菌
色谱法
化学
酶
生物技术
生物化学
生物
食品科学
基因
农学
作者
Jing Cao,Miao Wang,Yongxin She,Lufei Zheng,Fen Jin,Yunling Shao,Jing Wang,A.M. Abd El‐Aty
标识
DOI:10.1021/acs.jafc.3c08618
摘要
Enabling the detection of organophosphate pesticide (OP) residues through enzyme inhibition-based technology is crucial for ensuring food safety and human health. However, the use of acetylcholinesterase, the primary target enzyme for OPs, isolated from animals in practical production poses challenges in terms of sensitivity and batch stability. To address this issue, we identified a highly sensitive and reproducible biorecognition element, TrxA-PvCarE1, derived from red kidney beans and successfully overexpressed it in Escherichia coli. The resulting recombinant TrxA-PvCarE1 exhibited remarkable sensitivity toward 10 OPs, surpassing that of commercial acetylcholinesterase. Additionally, this approach demonstrated the capability to simultaneously detect copper compounds with high sensitivity, expanding the range of pesticides detectable using the traditional enzyme inhibition method. Spiking recovery tests conducted on cowpea and carrot samples verified the suitability of the TrxA-PvCarE1-based technique for real-life sample analysis. In summary, this study highlights a promising comprehensive candidate for the rapid detection of pesticide residues.
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