利用rflp-pcr技术对部分动物生肉进行分子检测

K. Taha
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引用次数: 0

摘要

线粒体细胞色素b基因在肉类掺假研究中起着重要作用。本研究采用通用型cyt b基因359bp的RFLP-PCR技术对绵羊、山羊、牛和驴的生肉品种进行了鉴别。从每只动物身体的不同部位收集了10个本地样本。所有样品均进行DNA分离处理,并采用聚合酶链反应(PCR)扩增。用HinfI酶和RsaI酶切扩增子,酶切产物得到每个物种的特异特征带,然后琼脂糖电泳分析。hini RE为绵羊、山羊和牛创造了三个片段,它们之间有一些相似之处,而为驴创造了两个片段。除了绵羊和山羊长度相同外,RsaI RE在所有不同长度的物种中均产生两条条带。因此,HinfI和RsaI结合的RFLP-PCR技术是一种快速、简便、易操作的动物物种鉴定方法,在动物肉种检测中具有重要的应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MOLECULAR DETECTION OF RAW MEAT FOR SOME ANIMAL SPECIES USING RFLP-PCR TECHNIQUE
Mitochondrial cytochrome b gene plays a serious role in studying adulteration of meat species. This research study designed to distinguish the raw meat species of sheep, goat, cattle and donkey using RFLP-PCR technique of a universal cyt b gene 359bp. Ten indigenous samples were collected from each animal in different parts of the body. All the samples were processed for DNA isolation and amplified with a Polymerase chain reaction (PCR). The amplicons were cleavage with HinfI and RsaI restriction enzymes, digestion of PCR product resulted in production of specific characterization bands for each species then analyzed by agarose electrophoresis. HinfI RE created three fragments for sheep, goat and cattle, with some similarities in a few bands between them, while yielded two bands for donkey. RsaI RE produced two bands for all species with different length except sheep and goats have the same length. Thus, results recommend that the RFLP-PCR technique with HinfI and RsaI play an important role to detect the animal meat species, since it is a fast, simple and easily handle method for identification of animal species.
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CiteScore
0.20
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16
审稿时长
20 weeks
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