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基于tuf基因的引物的开发与应用,用于多重PCR检测市售乳制品中的嗜酸乳杆菌、干酪乳杆菌群、德氏乳杆菌和长双歧杆菌。

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.

作者信息

Sheu Sen-Je, Hwang Wen-zhe, Chen Hsin-Chih, Chiang Yu-Cheng, Tsen Hau-Yang

机构信息

Department of Food Science and Biotechnology, National Chung Hsing University, No. 250, Kuo Kuang Road, Taichung City, Taiwan 402, Republic of China.

出版信息

J Food Prot. 2009 Jan;72(1):93-100. doi: 10.4315/0362-028x-72.1.93.

DOI:10.4315/0362-028x-72.1.93
PMID:19205469
Abstract

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 X 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.

摘要

基于延伸因子Tu基因(tuf)设计了用于检测嗜酸乳杆菌、干酪乳杆菌属、德氏乳杆菌和长双歧杆菌的PCR引物。通过对88株乳酸杆菌、肠球菌、双歧杆菌及其他细菌进行PCR,确认了这四组引物的特异性。结果表明,这些引物组分别为嗜酸乳杆菌、德氏乳杆菌、干酪乳杆菌属和长双歧杆菌产生了预测的397、230、202和161 bp的PCR产物。所测试的目标生物以外的细菌物种未产生假阳性结果。当将这四组引物组合用于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这些产品标签上列出的LAB物种。采用这种多重PCR方法,牛奶样品中每种LAB菌株的鉴定限为N×10³CFU/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检测以及使用API 50 CHL试剂盒进行生化试验得到了证实。当这种多重PCR方法用于测定LAB和双歧杆菌的总活菌数时,可以确保商业发酵乳制品的质量。

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