重组酶聚合酶扩增
聚合酶链反应
DNA
生物
实时聚合酶链反应
分子生物学
线粒体DNA
重组酶
化学
基因
生物化学
重组
作者
Jonas Kissenkötter,Susanne Böhlken-Fascher,Matthew S. Forrest,Olaf Piepenburg,Claus‐Peter Czerny,Ahmed Abd El Wahed
出处
期刊:Food Chemistry
[Elsevier BV]
日期:2020-04-06
卷期号:322: 126759-126759
被引量:38
标识
DOI:10.1016/j.foodchem.2020.126759
摘要
Detection of animal species in meat product is crucial to prevent adulterated and unnecessary contamination during processing. Gold standard is the real-time PCR assays, which can be conducted at highly equipped laboratories. Toward the development of point-of-need test, two rapid molecular assays based on recombinase polymerase amplification (RPA) for the detection of pork and horse DNA were established. Target genes are the porcine mitochondrial ND2 and equine ATP 6–8 genes. The pork and horse_RPA assays detected 16 and one DNA molecules/µl in eleven to six minutes, respectively. The myoglobin in the meat did not influence the assays performances, while the presence of high background-DNA induced a one log decrease in the sensitivity. Both assays are highly specific and identify down to 0.1% of their target DNA in meat mixtures. Both RPA assays could be used on-site as a rapid and mobile detection system to determine contamination of meat products.
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