首页> 外文会议>International Forum on Progress on Post-Genome Technologies(5'IFPT); 20070910-11; Suzhou(CN) >Identification of an Alga-Lysing bacteria isolated from TaiHu Lake by the analysis of 16S rRNA and 16S-23S rRNA intergenic spacer region
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Identification of an Alga-Lysing bacteria isolated from TaiHu Lake by the analysis of 16S rRNA and 16S-23S rRNA intergenic spacer region

机译:通过16S rRNA和16S-23S rRNA基因间隔区分析鉴定从太湖分离的溶藻细菌。

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To characterize and identify a Alga-Lysing bacteria isolated from TaiHu Lake by the analysis of 16S rRNA and 16S-23S rRNA intergenic spacer region, genomic DNA were extracted from alga-lysing bacterial colonies isolated from TaiHu Lake. Two pairs of primer were used to amplify the sequences of 16S rRNA gene and 16S-23S rRNA intergenic spacer region. The PCR products were subcloned into pGEM?-T Easy vectors and transformed into Dh5α. Positive clones were randomly selected for sequencing. The alignment of nucleotide sequence, evolutionary distances and phylogenetic trees were analyzed by software CLUSTAL X and PHYLIP version 3.6. 16S rRNA sequence of the isolated strain showed the strain isolated from TaiHu Lake was not clustered on the same evolution branch with the most type-strains except for Pseudomonas aeruginosa strain LMG 1242T. The blast result between strain isolated and Pseudomonas aeruginosa strain LMG 1242T showed that there were three different base pairs lied in the sites of 398, 1094, and 1302. The homology of the two strains reached 99.8%. ISR sequence of the isolated strain showed the highest homology with Pseudomonas aeruginosa strain UCBPP-PA14 as to 95.6%. Compared with sequences in the GenBank nucleotide database, the bacterial strains isolated was primarily identified as Pseudomonas sp. By the 16S rRNA gene and 16S-23S rRNA intergenic spacer region analysis.
机译:为了通过分析16S rRNA和16S-23S rRNA基因间间隔区来鉴定和鉴定从太湖分离的溶藻细菌,从太湖分离的溶藻细菌菌落中提取基因组DNA。使用两对引物扩增16S rRNA基因和16S-23S rRNA基因间隔区的序列。将PCR产物亚克隆到pGEMβ-TEasy载体中,并转化到Dh5α中。随机选择阳性克隆进行测序。通过软件CLUSTAL X和PHYLIP 3.6版分析核苷酸序列的比对,进化距离和系统发育树。分离株的16S rRNA序列显示,除铜绿假单胞菌LMG 1242T外,从太湖分离出的菌株没有与大多数类型菌株在同一进化分支上聚类。分离株与铜绿假单胞菌LMG 1242T的爆炸结果表明,在398、1094和1302位点存在3个不同的碱基对,两个菌株的同源性达到99.8%。分离出的菌株的ISR序列与铜绿假单胞菌菌株UCBPP-PA14具有最高的同源性,为95.6%。与GenBank核苷酸数据库中的序列相比,分离出的细菌菌株主要鉴定为假单胞菌。通过16S rRNA基因和16S-23S rRNA基因间隔区的分析。

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