首页> 外文期刊>Journal of applied microbiology >Identification of Lactobacillus alimentarius and Lactobacillus farcinimis with 16S-23S rDNA intergenic spacer region polymorphism and PCR amplification using species-specific oligonucleotide
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Identification of Lactobacillus alimentarius and Lactobacillus farcinimis with 16S-23S rDNA intergenic spacer region polymorphism and PCR amplification using species-specific oligonucleotide

机译:利用16S-23S rDNA基因间隔区多态性鉴定食品乳杆菌和杆状乳杆菌,并使用种特异性寡核苷酸进行PCR扩增

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Aims: The restriction fragment length polymorphism (RFLP) method was used to differentiate Lactobacillus species having closely related identities in the 16S-23S rDNA intergenic spacer region (ISR). Species-specific primers for Lact. farciminis and Lact. alimentarius were designed and allowed rapid identification of these speices. Methods and Results: The 16S-23S rDNA spacer region was amplified by primers tAla and 23S/p10, then digested by HinfI and TaqI enzymes and analysed by electrophoresis. Digestion by HinfI was not sufficient to differentiate Lact. sakei, Lact. curvatus, Lact. farciminis, Lact. alimentarius, Lact. plantarum and Lact. paraplantarum. In contrast, digestion carried out by TaqI revealed five different patterns allowing these species to be distinguished, except for Lact. plantarum from Lact. paraplantarum. The 16S-23S rDNA spacer region of Lact. farciminis and Lact. alimentarius were amplified and then cloned into vector pCR 2.1 and sequenced. The DNA sequences obtained were analysed and species-specific primers were designed from these sequences. The specificity of these primers was positively demonstrated as no response was obtained for 14 other species tested. Results and Conclusions: The species-specific primers for Lact. farciminis and Lact. alimentarius were shown to be useful for identifying these species among other lactobacilli. The RFLP profile obtained upon digestion with HinfI and TaqI enzymes can be used to discriminate Lact. farciminis, Lact. alimentarius, Lact. sakei, Lact. curvatus and Lact. plantarum. Significance and Impact of the Study: In this paper, we have established the first species-specific primer for PCR identification of Lact. farciminis and Lact. alimentarius. Both species-specific primer and RFLP, could be used as tools for rapid identification of lactobacilli up to species level.
机译:目的:使用限制性片段长度多态性(RFLP)方法区分在16S-23S rDNA基因间隔区(ISR)中具有密切相关的身份的乳酸杆菌。乳酸菌种特异性引物。 farciminis和Lact。设计了食品饮料,并可以快速鉴定这些香料。方法和结果:用引物tAla和23S / p10扩增16S-23S rDNA间隔区,然后用HinfI和TaqI酶消化,并进行电泳分析。 HinfI消化不足以区分乳酸。莱西,乳酸。弯曲,乳酸。 farciminis,乳酸。 alimentarius,乳酸。车前草和乳酸。 plant旁。相比之下,由TaqI进行的消化揭示了五个不同的模式,可以区分这些物种,除了乳酸。乳酸菌的植物。 plant旁。 Lact的16S-23S rDNA间隔区。 farciminis和Lact。扩增食品,然后克隆到载体pCR 2.1中并测序。分析获得的DNA序列,并从这些序列设计物种特异性引物。这些引物的特异性得到了积极的证明,因为对其他14个物种没有反应。结果与结论:乳酸菌种特异性引物。 farciminis和Lact。业已证明在其他乳杆菌中,alimentarius可用于鉴定这些物种。用HinfI和TaqI酶消化后获得的RFLP谱可用于区分乳酸。 farciminis,乳酸。 alimentarius,乳酸。莱西,乳酸。弯曲和乳酸。车前草。研究的意义和影响:在本文中,我们建立了第一个用于PCR鉴定乳杆菌的物种特异性引物。 farciminis和Lact。 alimentarius。物种特异性引物和RFLP都可以用作快速鉴定乳酸菌直至物种水平的工具。

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