Development of a rapid on-site detection method for pork in processed meat products using real-time loop-mediated isothermal amplification

被引:58
作者
Lee, Shin-Young [1 ]
Kim, Mi-Ju [1 ]
Hong, Yeun [1 ]
Kim, Hae-Yeong [1 ]
机构
[1] Kyung Hee Univ, Grad Sch Biotechnol, Yongin 446701, South Korea
关键词
Direct real-time LAMP; Meat authentication; Pork; On-site detection; HIGHLY-SPECIFIC PCR; SPECIES IDENTIFICATION; MULTIPLEX PCR; DNA; ADULTERATION; ASSAY; CHICKEN; TURKEY; GENE; BEEF;
D O I
10.1016/j.foodcont.2016.01.041
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
On-site detection with minimal equipment and no risk of contamination of samples is crucial for the rapid and sensitive identification of pork in processed meat products. To resolve this issue, a reliable loop-mediated isothermal amplification (LAMP) method was developed to detect pork in meat using a portable real-time fluorometer without the need for DNA extraction. Pork-specific primers for the LAMP assay were designed based on the mitochondrial D-loop regions, and eukaryotic primers based on the 18S rRNA gene were used for the endogenous control. The adoption of an endogenous control prevented false-negative results. The detection level was 1 pg for raw pork DNA and 0.1% of pork in a beef-meat mixture. The applicability of the developed method was demonstrated in commercially processed meat products. Forty-two meat products were successfully verified for labeling compliance using this method within 30 min without the need for nucleic acid extraction. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:53 / 61
页数:9
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