Suppr超能文献

开发并验证了一种用于检测肉类产品中鼠肉真实性的快速试剂盒,该试剂盒采用了一种物种特异性的 PCR 检测方法。

Development and validation of a rapid kit for authenticity of murine meat in meat products with a species-specific PCR assay.

机构信息

School of Laboratory Medicine, Beihua University, Jilin, Jilin, China.

Deptartment of Molecular Diagnosis, Innovation Center for Detection Technology on DNA Fingerprint of Traditional Chinese Medicine, Jilin, Jilin Province, China.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2020 Apr;37(4):552-560. doi: 10.1080/19440049.2020.1718218. Epub 2020 Feb 10.

Abstract

Adulteration of meat products with murine meat poses a huge threat to consumer health and leads to serious disruption in food markets. Species authentication of murine meat is still technically challenging. We, therefore, developed a species-specific PCR kit consisting of murine meat DNA extraction, PCR reaction and identifying systems. We designed novel universal primers targeting highly conserved region on mitochondrial cytochrome b gene ( b) from four murines (lab rats, lab mice, wild rat and wild mice), as well as specific primers for meat from four widely consumed animal species, cattle, sheep, duck and donkey. Simultaneously, pasmid inserted specific b fragment was cloned and used as the internal positve control in the kit. The kit parameters of specificity, sensitivity, stability and validity were determined using mimic counterfeiting meatball. The specificity of the DNA detection kit was 100% in authentication of the four fraudulent meats of cattle, sheep, duck and donkey mixed murine meat. The minimum detection limit of the sample DNA was 0.1 μg. The kit, which had freeze-thawed up to 20 times and stored for 1 year, also was powerful in detecting an amount of 0.1 mg in artificial counterfeited cattle, sheep, duck and donkey meat products. The murine-species DNA detection kit proposed in this study has proved to be a simple, accurate and effective assay, and can be applied to the identification of murine meat traces in common edible meat, to ensure the realisable implementation of meat product market supervision.

摘要

肉类掺假鼠肉对消费者健康构成巨大威胁,并导致食品市场严重混乱。鼠肉的物种鉴定仍然具有技术挑战性。因此,我们开发了一种由鼠肉 DNA 提取、PCR 反应和鉴定系统组成的物种特异性 PCR 试剂盒。我们设计了针对线粒体细胞色素 b 基因(b)上高度保守区域的新型通用引物,该基因来自四种鼠类(实验大鼠、实验小鼠、野鼠和野鼠),以及四种广泛食用动物物种(牛、羊、鸭和驴)的特异性引物。同时,将插入特异性 b 片段的质粒克隆并用作试剂盒中的内部阳性对照。使用模拟假冒肉丸确定了试剂盒的特异性、灵敏度、稳定性和有效性参数。该 DNA 检测试剂盒在鉴定牛、羊、鸭和驴肉混合鼠肉的四种欺诈性肉类方面具有 100%的特异性。样品 DNA 的最小检测限为 0.1 μg。该试剂盒可进行多达 20 次的冻融,并且在 1 年内也可以有效地检测出 0.1 mg 的人工假冒牛肉、羊肉、鸭肉和驴肉产品。本研究中提出的鼠种 DNA 检测试剂盒已被证明是一种简单、准确和有效的检测方法,可用于鉴定常见食用肉中的鼠肉痕迹,以确保实现对肉类产品市场的监管。

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