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Rapid identification of binary and ternary adulteration in camellia oil by CRISPR/Cas12a assay
Ting Shi1, Tenghui Dai2, Jing Zhou1
1State Key Laboratory of Genome and Multi-omics Technologies, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China; Key Laboratory of Edible Oil Quality and Safety, State Administration for Market Regulation, Wuhan Institute for Food and Cosmetic Control, Wuhan, 430040, China.
Abstract:
Camellia oil adulteration, bring about a serious potential threat to consumer health and food safety, yet current chromatography-based techniques require costly instruments and trained personnel, limiting their on-site detection. In this study, CRISPR/Cas12a was used for rapid identification of binary and ternary adulteration in camellia oil. On the basis of our screened RPA primer and crRNAs from corresponding rbcL genes, the CRISPR/Cas12a reaction, was completed within 40 min at a detection limit of 5% (w/w) in camellia oil adulterated with soybean oil, rapeseed oil, corn oil, and peanut oil, by visual naked-eye readout. Referring to the traditional gas chromatography technology, our constructed CRISPR/Cas12a method achieved 100% accuracy, highlighting its potential for routine market surveillance, especially for those oil samples at adulterated ratio ≤ 10%. This cost-effective and equipment-minimal assay, provide a promising tool for adulterated camellia oil on site detection, thus strengthening food quality control and consumer protection.

