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首页> 外文期刊>Applied and Environmental Microbiology >A direct PCR detection method for Clostridium tyrobutyricum spores in up to 100 milliliters of raw milk.
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A direct PCR detection method for Clostridium tyrobutyricum spores in up to 100 milliliters of raw milk.

机译:一种直接PCR检测方法,可检测多达100毫升原奶中的酪丁酸梭菌孢子。

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A direct detection method for Clostridium tyrobutyricum spores in up to 100 ml of raw milk is presented. The bacterial spores are concentrated by centrifugation after chemical extraction of the milk components. The vegetative cells are selectively lysed, and their DNA is digested and washed away. Afterwards, the DNA is liberated from the spores by microwave treatment. For the identification of the C. tyrobutyricum DNA, a two-step PCR method with two nested pairs of primers is used. The primers were derived from the 16S-23S rRNA spacer region of C. tyrobutyricum, and the specificity of each of them for C. tyrobutyricum is demonstrated. The detection limit can be estimated to be between 3 and 30 spores in 100 ml of raw milk.
机译:提出了一种直接检测方法,可检测多达100 ml的原料奶中的酪丁酸梭菌孢子。化学提取牛奶成分后,通过离心浓缩细菌孢子。营养细胞被选择性裂解,其DNA被消化并洗去。然后,通过微波处理将DNA从孢子中释放出来。为了鉴定酪丁酸梭菌DNA,使用了具有两个嵌套引物对的两步PCR方法。引物来自酪丁酸梭菌的16S-23S rRNA间隔区,并证明了它们各自对酪丁酸梭菌的特异性。在100毫升原料奶中,检出限估计为3至30个孢子。

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