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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
来源:
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.
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页码:53 / 61
页数:9
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