Two FAST multiplex real-time PCR reactions to assess the presence of genetically modified organisms in food

被引:31
作者
Cottenet, Geoffrey [1 ]
Blancpain, Carine [1 ]
Sonnard, Veronique [1 ]
Chuah, Poh Fong [2 ]
机构
[1] Nestec Ltd, Inst Food Safety & Analyt Sci, Nestle Res Ctr, Lausanne, Switzerland
[2] Nestle Qual Assurance Ctr, Qual Rd, Singapore, Singapore
关键词
Genetically modified organisms; Screening; Detection; Real-time PCR; QUANTIFICATION; VALIDATION; GMOS;
D O I
10.1016/j.foodchem.2018.09.050
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Methods to detect the presence of genetically modified organisms (GMOs) are evolving constantly to comply with legislation and include new transgenic traits developed by biotechnology companies. Since traditional screening methods target only a limited number of markers, not all GM-events can be detected easily. To cover a broader range, a new GMO screening method was developed, based on two real-time PCR reactions, targeting i) six major GM-markers and ii) six GM-events that do not contain these markers. This method used the FAST PCR technology and allowed a further reduction in time-to-result. Using a wide array of reference materials and proficiency test samples, the method showed a broad screening capacity and the absolute limit of detection was consistently below 20 copies, thereby demonstrating the method is fit-for-purpose.
引用
收藏
页码:760 / 765
页数:6
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