Ferchichi M, Valcheva R, Prévost H, Onno B, Dousset X
UMR INRA-1014 SECALIM, ENITIAA, rue de la Géraudière BP 82225, 44322 Nantes cedex 3, France.
Int J Food Microbiol. 2008 Apr 30;123(3):269-76. doi: 10.1016/j.ijfoodmicro.2008.02.014. Epub 2008 Feb 23.
Based on the 16S-23S ribosomal DNA (rDNA) intergenic spacer region (ISR), an identification tool for rapid differentiation of Lactobacillus nantensis, Lactobacillus spicheri and Lactobacillus hammesii, species isolated recently from French sourdough was developed. The DNA fragments containing ISRs were amplified with primers pairs 16S/p2 and 23S/p7. Clone libraries of the PCR-amplified rDNA with these primers were constructed using a pCR2.1 TA cloning kit and sequenced. The DNA sequences obtained were analyzed and species-specific primers were designed from these sequences. Two PCR amplicons, which were designated small ISR (S-ISR) and large ISR (L-ISR), were obtained for all Lactobacillus species studied. The L-ISR sequence reveale2d the presence of two tRNA genes, tRNAAla and tRNAIle. Species-specific primers designed allowed rapid identification of these species. The specificity of these primers was positively demonstrated as no response was obtained for more than 200 other species tested.
基于16S - 23S核糖体DNA(rDNA)基因间隔区(ISR),开发了一种用于快速区分南特乳杆菌、斯氏乳杆菌和哈氏乳杆菌的鉴定工具,这些菌种是最近从法国酸面团中分离出来的。用引物对16S/p2和23S/p7扩增包含ISR的DNA片段。使用pCR2.1 TA克隆试剂盒构建用这些引物PCR扩增的rDNA克隆文库并进行测序。对获得的DNA序列进行分析,并从这些序列中设计物种特异性引物。对所有研究的乳杆菌物种都获得了两个PCR扩增子,分别命名为小ISR(S - ISR)和大ISR(L - ISR)。L - ISR序列显示存在两个tRNA基因,即tRNAAla和tRNAIle。设计的物种特异性引物能够快速鉴定这些物种。这些引物的特异性得到了肯定的证明,因为对测试的200多种其他物种均未产生反应。