Wang Chuan, Zhang Chaowu, Pei Xiaofang, Liu Hengchuan
Department of Medical Technology, West China School of Public Health, Sichuan University, Chengdu 610041, China.
Wei Sheng Yan Jiu. 2007 Nov;36(6):713-5, 718.
For being further applied and studied, one strain of Lactobacillus delbrueckii subsp. bulgaricus (wch9901) separated from yoghourt which had been identified by phenotype characteristic analysis was identified by 16S rDNA and phylogenetic analyzed.
The 16S rDNA of wch9901 was amplified with the genomic DNA of wch9901 as template, and the conservative sequences of the 16S rDNA as primers. Inserted 16S rDNA amplified into clonal vector pGEM-T under the function of T4 DNA ligase to construct recombined plasmid pGEM-wch9901 16S rDNA. The recombined plasmid was identified by restriction enzyme digestion, and the eligible plasmid was presented to sequencing company for DNA sequencing. Nucleic acid sequence was blast in GenBank and phylogenetic tree was constructed using neighbor-joining method of distance methods by Mega3.1 soft.
Results of blastn showed that the homology of 16S rDNA of wch9901 with the 16S rDNA of Lactobacillus delbrueckii subsp. bulgaricus strains was higher than 96%. On the phylogenetic tree, wch9901 formed a separate branch and located between Lactobacillus delbrueckii subsp. bulgaricus LGM2 evolution branch and another evolution branch which was composed of Lactobacillus delbrueckii subsp. bulgaricus DL2 evolution cluster and Lactobacillus delbrueckii subsp. bulgaricus JSQ evolution cluster. The distance between wch9901 evolution branch and Lactobacillus delbrueckii subsp. bulgaricus LGM2 evolution branch was the closest.
wch9901 belonged to Lactobacillus delbrueckii subsp. bulgaricus. wch9901 showed the closest evolution relationship to Lactobacillus delbrueckii subsp. bulgaricus LGM2.
为进一步应用和研究,对从酸奶中分离得到的一株德氏保加利亚乳杆菌(wch9901)进行16S rDNA鉴定及系统发育分析,该菌株已通过表型特征分析鉴定。
以wch9901基因组DNA为模板,以16S rDNA保守序列为引物,扩增wch9901的16S rDNA。在T4 DNA连接酶作用下,将扩增得到的16S rDNA插入克隆载体pGEM-T中,构建重组质粒pGEM-wch9901 16S rDNA。通过限制性酶切鉴定重组质粒,将合格的质粒送交测序公司进行DNA测序。核酸序列在GenBank中进行比对,并使用Mega3.1软件采用距离法中的邻接法构建系统发育树。
blastn结果显示,wch9901的16S rDNA与德氏保加利亚乳杆菌菌株的16S rDNA同源性高于96%。在系统发育树上,wch9901形成一个独立分支,位于德氏保加利亚乳杆菌LGM2进化分支与由德氏保加利亚乳杆菌DL2进化簇和德氏保加利亚乳杆菌JSQ进化簇组成的另一进化分支之间。wch9901进化分支与德氏保加利亚乳杆菌LGM2进化分支的距离最近。
wch9901属于德氏保加利亚乳杆菌。wch9901与德氏保加利亚乳杆菌LGM2的进化关系最为密切。