A barcode-DNA analysis method for the identification of plant oil adulteration in milk and dairy products

被引:24
|
作者
Uncu, Ayse Ozgur [1 ]
Uncu, Ali Tevfik [2 ]
机构
[1] Necmettin Erbakan Univ, Dept Biotechnol, TR-42090 Meram, Konya, Turkey
[2] Necmettin Erbakan Univ, Dept Mol Biol & Genet, TR-42090 Meram, Konya, Turkey
关键词
Chloroplast genome; DNA barcode; Food authenticity; Organelle genome; PCR; RAPID DETECTION; VEGETABLE-OILS; FAT ADULTERATION; HRM ANALYSIS; GHEE; AUTHENTICATION; AMPLIFICATION; PRIMERS; REGION; FOOD;
D O I
10.1016/j.foodchem.2020.126986
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present work, a barcode-DNA analysis method is described for the detection of plant oil adulteration in milk and dairy products. The method relies on the fact that plant DNA should not be present in readily detectable amounts in a dairy product unless it contains undeclared plant material. Thus, a universal plant barcode is chosen as the target to be amplified from dairy samples. Accordingly, barcode PCR-CE (PCR-capillary electrophoresis) assays are described, which do not require preliminary information on the species source of the adulterant oil type. Two PCR-CE assays, one operating on the plastid trnL (UAA) intron and the other targeting its inner P6 loop in nested format, were shown to detect corn, soybean, rapeseed and sunflower oils in clarified butter, milk and yogurt. Both barcodes are robustly amplified with extremely conserved primers. While the intron provides the species discrimination ability, the P6 loop provides superior detection sensitivity.
引用
收藏
页数:8
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