Detection of Hazelnut and Almond Adulteration in Olive Oil: An Approach by qPCR

被引:5
|
作者
Ramos-Gomez, Sonia [1 ]
Busto, Maria D. [1 ]
Ortega, Natividad [1 ]
机构
[1] Univ Burgos, Dept Biotechnol & Food Sci, Area Biochem & Mol Biol, Plaza Misael Banuelos S-N, Burgos 09001, Spain
来源
MOLECULES | 2023年 / 28卷 / 10期
关键词
authenticity; Corylus avellana; melting curve analysis; Olea europaea; olive oil adulteration; Prunus dulcis; qPCR; REAL-TIME PCR; ALLERGEN CODING SEQUENCES; H-1-NMR SPECTROSCOPY; PROCESSED FOODS; DNA EXTRACTION; PRUNUS-DULCIS; SOYBEAN OIL; EDIBLE OILS; AUTHENTICATION; TOOL;
D O I
10.3390/molecules28104248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Virgin olive oil (VOO), characterized by its unique aroma, flavor, and health benefits, is subject to adulteration with the addition of oils obtained from other edible species. The consumption of adulterated olive oil with nut species, such as hazelnut or almond, leads to health and safety issues for consumers, due to their high allergenic potential. To detect almond and hazelnut in olive oil, several amplification systems have been analyzed by qPCR assay with a SYBR Green post-PCR melting curve analysis. The systems selected were Cora1F2/R2 and Madl, targeting the genes coding the allergenic protein Cor a 1 (hazelnut) and Pru av 1 (almond), respectively. These primers revealed adequate specificity for each of the targeted species. In addition, the result obtained demonstrated that this methodology can be used to detect olive oil adulteration with up to 5% of hazelnut or almond oil by a single qPCR assay, and with a level as low as 2.5% by a nested-qPCR assay. Thus, the present research has shown that the SYBR-based qPCR assay can be a rapid, precise, and accurate method to detect adulteration in olive oil.
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页数:15
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