Validasi Metode Analisis Cemaran DNA Babi pada Bakso Sapi Menggunakan Primer Mitokondria D-Loop22 dengan Metode Polymerase Chain Reaction (PCR)

Sri Wahyuni, S. Maryam, Aminah Aminah
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引用次数: 1

Abstract

The frequency of non-halal ingredient mixing, such as porkin on the food processed products of meatballs, has become an issue to the public, especially for moslems. Therefore, a reliable and valid method with high sensitivity is needed to specifically detect the pig contamination. This research aims to obtain a valid and reliable method by proposing polymerase chain reaction (PCR)  using mitochondrial D-Loop22 primer as a method in handing halal food authentication. The sample consisted of beef as a negative control, pork and pork meatballs as a positivecontrol, and five samples of meat balls found in Makassar for halal inspection.The method validation assay was conducted by testing the primary specificity on the fresh tissue (beef and pork) and testing the sensitivity by making a series of pig DNA dilution (1:10;  1:102;   1:103;   1:104)   and the variations of contaminated pig:cow (%b/b) : 0.05% , 0.1%, 1%, and 5%. The result of PCR amplification on agarose gel electrophoresis of 0.8% showed that method was able to detect the pig DNA contamination specifically in pigs and not amplify other DNA, and could still be detected up to pig contamination specifically in pigs and not amplify the other DNAs and could still be detected up to pig contamination of 0.05% and on DNA dilution of 1:103. Meanwhile, on the five samples analyzed, there were  not found pig DNA contamination characterized by no formed amplification bands.
猪肉豆蔻DNA分析方法的验证方法是采用线粒体D-Loop22与多位酶链反应(PCR)方法
非清真成分混合的频率,如猪肉在肉丸的食品加工产品中,已经成为公众,特别是穆斯林的一个问题。因此,需要一种可靠、有效、灵敏度高的方法来专门检测猪的污染。本研究提出利用线粒体D-Loop22引物进行聚合酶链反应(PCR)作为清真食品认证的方法,旨在获得一种有效可靠的方法。该样本包括牛肉作为阴性对照,猪肉和猪肉肉丸作为阳性对照,以及在望加锡发现的五个肉丸样品进行清真检查。该方法通过对新鲜组织(牛肉和猪肉)进行初级特异性测试,并通过一系列猪DNA稀释(1:10;1:102;1:103;1:104)和污染猪的变异:牛(%b/b): 0.05%, 0.1%, 1%和5%。琼脂糖凝胶电泳0.8%的PCR扩增结果表明,该方法能够特异性检测出猪的DNA污染而不扩增出其他DNA;对猪的DNA污染仍然能够特异性检测出猪的DNA污染而不扩增出其他DNA;对猪的DNA污染仍然能够特异性检测出0.05%的猪污染,DNA稀释为1:103。同时,在分析的5份样品中,未发现猪DNA污染未形成扩增带。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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