首页> 外文期刊>Journal of food protection >Development And Use Of Tuf Gene-based Primers For The Multiplex Pcr Detection Of Lactobacillus Acidophilus,lactobacillus Casei Group, Lactobacillus Delbrueckii, And Bifidobacterium Longum In Commercial Dairy Products
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Development And Use Of Tuf Gene-based Primers For The Multiplex Pcr Detection Of Lactobacillus Acidophilus,lactobacillus Casei Group, Lactobacillus Delbrueckii, And Bifidobacterium Longum In Commercial Dairy Products

机译:基于Tuf基因的引物的开发和用于商业乳制品中嗜酸乳杆菌,干酪乳杆菌组,德氏乳杆菌和长双歧杆菌多重PCR检测

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PCR primers specific for the detection of Lactobacillus acidophilus, Lactobacillus casei group, Lactobacillus delbrueckii, and Bifidobacterium longum were designed based on the elongation factor Tu gene (tuf). The specificity of these four primer sets were confirmed by PCR with 88 bacterial strains of Lactobacillus, Enterococcus, Bifidobacterium, and other bacterial species. Results indicated that these primer sets generated predicted PCR products of 397, 230, 202, and 161 bp for L. acidophilus, L. delbrueckii, L. casei group, and B. longum, respectively. Bacterial species other than the target organisms tested did not generate false-positive results. When these four primer sets were combined for the simultaneous detection of the lactic acid bacteria (LAB) in fermented milk products including yogurt, the LAB species listed on the labels of these products could be identified without the preenrichment step. The identification limit for each LAB strain with this multiplex PCR method was N×10~3 CFU/ml in milk samples. The results of our multiplex PCR method were confirmed by PCR assay using primers based on the 16S rDNA or the 16S-23S intergenic spacer region and by biochemical tests using the API 50 CHL kit. When this multiplex PCR method was used with the determination of counts of total viable LAB and bifidobacteria, the quality of commercial fermented milk products could be assured.
机译:基于延伸因子Tu基因(tuf)设计了用于检测嗜酸乳杆菌,干酪乳杆菌组,德氏乳杆菌和长双歧杆菌的PCR引物。这四种引物组的特异性通过88株乳酸杆菌,肠球菌,双歧杆菌和其他细菌种类的PCR确证。结果表明,这些引物组分别为嗜酸乳杆菌,德氏乳杆菌,干酪乳杆菌和长双歧杆菌产生了397、230、202和161 bp的预测PCR产物。除测试目标生物以外的细菌种类均未产生假阳性结果。当将这四个引物组合在一起以同时检测包括酸奶在内的发酵乳制品中的乳酸菌(LAB)时,无需预富集步骤即可鉴定出这些产品标签上列出的LAB种类。该多重PCR方法对牛奶样品中每个LAB菌株的鉴定极限为N×10〜3 CFU / ml。我们的多重PCR方法的结果通过使用基于16S rDNA或16S-23S基因间隔区的引物进行PCR分析以及使用API​​ 50 CHL试剂盒进行的生化测试得到了证实。当使用这种多重PCR方法测定总活菌LAB和双歧杆菌的计数时,可以确保商业发酵乳制品的质量。

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