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首页> 外文期刊>International Journal of Food Microbiology >Rapid identification of Lactobacillus nantensis, Lactobacillus spicheri and Lactobacillus hammesii species using species-specific primers
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Rapid identification of Lactobacillus nantensis, Lactobacillus spicheri and Lactobacillus hammesii species using species-specific primers

机译:使用物种特异性引物快速鉴定南乳杆菌,spicheri乳杆菌和hammesii hammesii菌种

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摘要

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 reveale(2)d the presence of two tRNA genes, tRNA Ala and tRNAl(lc). 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. (C) 2008 Elsevier B.V. All rights reserved.
机译:基于16S-23S核糖体DNA(rDNA)基因间隔区(ISR),开发了一种鉴定工具,用于快速区分南洋乳杆菌,spicheri乳杆菌和hammesii乳杆菌,它们是最近从法国酵母中分离出的物种。用引物对16S / p2和23S / p7扩增含有ISR的DNA片段。使用pCR2.1 TA克隆试剂盒构建带有这些引物的PCR扩增rDNA的克隆文库并进行测序。分析获得的DNA序列,并从这些序列设计物种特异性引物。对于所有研究的乳杆菌属物种,获得了两个PCR扩增子,分别称为小ISR(S-ISR)和大ISR(L-ISR)。 L-ISR序列揭示(2)d两个tRNA基因tRNA Ala和tRNA1(lc)的存在。设计的物种特异性引物可以快速鉴定这些物种。这些引物的特异性得到了积极的证明,因为对200多种其他受试物种没有反应。 (C)2008 Elsevier B.V.保留所有权利。

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