首页> 外文期刊>Poljoprivreda (Osijek) >COMPARISON OF COMMERCIAL DNA KITS AND TRADITIONAL DNA EXTRACTION PROCEDURE IN PCR DETECTION OF PORK IN DRY/FERMENTED SAUSAGES
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COMPARISON OF COMMERCIAL DNA KITS AND TRADITIONAL DNA EXTRACTION PROCEDURE IN PCR DETECTION OF PORK IN DRY/FERMENTED SAUSAGES

机译:PCR法检测干/发酵香肠中猪肉中商业DNA试剂盒和传统DNA提取方法的比较

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In the present study four commercially available DNA extraction kits (Wizard? Genomic DNA Purification Kit, High Pure PCR Template Kit, DNeasy mericon Food and GeneJET PCR Purification Kit), as well as standard phenol/chloroform isolation technique have been evaluated regarding their concentration, purity and suitability for amplification of porcine DNA in dry/fermented sausages. The isolates were assessed for quantity and quality using spectrophotometer (IMPLEN GmbH, Germany). To verify template usability and quality of isolated DNA, the polymerase chain reaction (PCR) targeting at porcine cytochrome b by species specific primers was used. The comparison of extraction methods revealed satisfactory efficiency and purity of all extraction kits, while with standard phenol/chloroform isolation method high concentrations of DNA with low A260/280 were obtained. However, all the investigated techniques proved to be suitable for identification of porcine DNA in dry/fermented sausage. Thus, the standard phenol/chloroform DNA extraction method, as the cost-effective one, can be recommended as a good alternative to more expensive isolation kits when investigating the presence of pork DNA in dry/ fermented meat products.
机译:在本研究中,已经评估了四种市售的DNA提取试剂盒(Wizard?基因组DNA纯化试剂盒,高纯度PCR模板试剂盒,DNeasy mericon Food和GeneJET PCR纯化试剂盒)以及标准的苯酚/氯仿分离技术,干/发酵香肠中猪DNA的纯度和扩增性。使用分光光度计(IMPLEN GmbH,德国)评估分离物的数量和质量。为了验证模板的可用性和分离的DNA的质量,使用了通过物种特异性引物靶向猪细胞色素b的聚合酶链反应(PCR)。提取方法的比较表明,所有提取试剂盒均具有令人满意的效率和纯度,而采用标准苯酚/氯仿分离方法,可获得高浓度,低A260 / 280的DNA。但是,所有研究的技术均证明适用于鉴定干/发酵香肠中的猪DNA。因此,在研究干/发酵肉制品中猪肉DNA的存在时,可以建议使用标准的苯酚/氯仿DNA提取方法,是一种经济高效的方法,可以替代更昂贵的分离试剂盒。

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