Suppr超能文献

用于鉴定猪肉和马肉的重组酶聚合酶扩增检测方法。

Recombinase polymerase amplification assays for the identification of pork and horsemeat.

机构信息

Department of Animal Science, Division of Microbiology and Animal Hygiene, Georg-August-University of Goettingen, Goettingen, Germany.

TwistDx(TM) Limited, Cambridge, United Kingdom.

出版信息

Food Chem. 2020 Aug 30;322:126759. doi: 10.1016/j.foodchem.2020.126759. Epub 2020 Apr 6.

Abstract

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.

摘要

检测肉类产品中的动物物种对于防止加工过程中的掺假和不必要的污染至关重要。金标准是实时聚合酶链反应(PCR)检测方法,可以在高度配备的实验室中进行。为了开发现场即时检测方法,我们建立了两种基于重组酶聚合酶扩增(RPA)的快速分子检测方法,用于检测猪肉和马 DNA。目标基因是猪线粒体 ND2 和马 ATP6-8 基因。猪肉和马_RPA 检测方法分别在 11 到 6 分钟内检测到 16 个和 1 个 DNA 分子/µl。肉中的肌红蛋白不会影响检测方法的性能,而高背景 DNA 的存在会使灵敏度降低一个对数级。两种检测方法都具有高度特异性,可在肉混合物中识别出低至 0.1%的目标 DNA。两种 RPA 检测方法都可以现场使用,作为一种快速、移动的检测系统,用于确定肉类产品的污染情况。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验