Development and validation of sensitive and rapid CRISPR/Cas12-based PCR method to detect hazelnut in unlabeled products

被引:7
作者
Yin, Xinying [1 ,2 ]
Yang, Lili [1 ]
Sun, Xiuyan [1 ]
Zheng, Qiuyue [1 ]
Piao, Yongzhe [1 ]
Hu, Bing [1 ]
Zhang, Xiaobo [1 ]
Cao, Jijuan [1 ]
机构
[1] Dalian Minzu Univ, Key Lab Biotechnol & Bioresources Utilizat, Minist Educ, Dalian 116600, Peoples R China
[2] Sichuan Univ, Coll Biomass Sci & Engn, Hlth Food Evaluat Res Ctr, Chengdu 610065, Sichuan, Peoples R China
关键词
Food authenticity; Food allergen; Hazelnut; CRISPR/Cas12a; Real-time PCR; Processed food; REAL-TIME PCR; SEQUENCES; FOOD;
D O I
10.1016/j.foodchem.2023.137952
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Hazelnut, one of the most popular tree nuts, is widely found in processed food and even very small amounts can trigger severe allergic reactions in susceptible people. Herein, we developed a sensitive and rapid method based on CRISPR and qPCR capable of detecting low-abundance hazelnut in processed food. The assay, known as CRISPR-based nucleic acid test method (Crinac) can detect 1 % of hazelnut in a mixture and allows the species to be identified in a complex processed sample. The detection process can be completed within 60 min. Contributed to amplification via PCR and CRISPR/Cas12a, enables end-fluorescence measurement for the quantification of hazelnut, thus reducing assay time and eliminating the need for costly real-time fluorescence PCR instruments. The assay based on CRISPR/Cas12 and PCR has potential as a sensitive and reliable analytical tool for the detection of food authenticity.
引用
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页数:8
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