Detection Contaminant DNA of a Pig on a Sample Meat Mills in Some City Markets Bengkulu, Using a Genetic Marker DNA Mitochondria Cytochrome B

C. Muslim, Iin Isnaini, Sipriyadi
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Abstract

The purpose of the study was to find out if there was a mixture of pork in ground beef samples in some Bengkulu city markets using the molecular Genetic DNA mitochondrial cytochrome b. The research was conducted from December 2019 to May 2020. Sampling was conducted at 10 meat mills in Bengkulu City (Pasar Panorama, Pasar Minggu, Pasar Barukoto, and Sungai Serut Fish Market). DNA isolation, DNA amplification, and electrophoresis are carried out in the biotechnology laboratory, Department of Biology, University of Bengkulu. The meat samples that had been milled were then performed genome DNA isolation following the Qiagen DNeasy for Food Kit protocol. PCR (Polymerous Chain Reaction) is carried out as many as 30 cycles with Primer Forward referring to and primary Reverse Mix (pork, cow, and chicken), Reverse Pork for pigs and Reverse cow for cows. PCR products are electrophobic on 1% agarose gel and then visualized under UV light using Gel Document System Axygen. As a result of the study, on the primary use of Rcow all samples contained cow DNA. In primary use reverse pork, no DNA tape is amplified. In the primary use of Reverse mix from ten samples all containing cow DNA, one sample is thought to contain pig DNA i.e. s7 samples, and six of them contain chicken DNA (S1, S4, S5, S6, S7, and S8). Generally, meat milling in Bengkulu city located in Pasar Panorama, Pasar Minggu, Pasar Barukoto, and Sungai Serut Fish Market is not tainted with pork even though one sample is found, this is because it is influenced by the amount of meat that is milled still too much.
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利用遗传标记DNA线粒体细胞色素B检测蚌库鲁市一些城市市场肉类加工厂样品中猪的污染DNA
该研究的目的是利用分子遗传DNA线粒体细胞色素b来确定明古鲁一些城市市场的碎牛肉样本中是否含有猪肉混合物。该研究于2019年12月至2020年5月进行。在明古鲁市的10个肉类加工厂(Pasar Panorama、Pasar Minggu、Pasar Barukoto和Sungai Serut鱼市场)进行了抽样。DNA分离、DNA扩增和电泳在Bengkulu大学生物系生物技术实验室进行。将研磨后的肉类样品按照Qiagen DNA for Food Kit协议进行基因组DNA分离。PCR (Polymerous Chain Reaction)进行多达30个循环,引物正向参照和初级反向混合(猪肉、牛和鸡),猪为反向猪肉,牛为反向奶牛。PCR产物在1%琼脂糖凝胶上电泳,然后在紫外灯下使用gel Document System oxygen进行可视化。研究结果表明,在首次使用Rcow时,所有样品都含有奶牛的DNA。在主要使用反向猪肉时,没有DNA磁带被扩增。在对10个全部含有牛DNA的样本进行反向混合的初步使用中,一个样本被认为含有猪DNA,即s7个样本,其中6个含有鸡DNA (S1, S4, S5, S6, s7和S8)。一般来说,在明古鲁市,位于帕萨尔Panorama,帕萨尔Minggu,帕萨尔Barukoto和Sungai Serut鱼市场的肉类加工中,即使发现一个样本,也不会受到猪肉污染,这是因为加工的肉量仍然过多。
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