Kaur Jasmine, Sharma Anshul, Lee Sulhee, Park Young-Seo
Department of Food Science and Biotechnology, Gachon University, Seongnam 13120, Republic of Korea.
J Microbiol Biotechnol. 2017 Oct 28;27(10):1778-1782. doi: 10.4014/jmb.1705.05022.
To identify and discriminate the bacterial species at the subspecific level, rep-PCR is a reliable genomic fingerprinting tool. Fourteen strains of bacteria were isolated from different food sources, identified as using 16S rRNA gene sequencing, and amplified using rep-primers (REP, ERIC, and (GTG)). Fingerprinting patterns generated bands in the range of 300-6,000 bp with REP, 150-6,000 bp with ERIC, and 200-1,700 bp with (GTG) primers. In UPGMA dendrogram analysis, 14 strains were clustered into three clades (I, II, and III) with all the primers, thus differentiating them at the molecular level. The present study revealed the differentiation of strains using rep-PCR.
为了在亚种水平上鉴定和区分细菌种类,重复聚合酶链反应(rep-PCR)是一种可靠的基因组指纹识别工具。从不同食物来源分离出14株细菌,通过16S rRNA基因测序进行鉴定,并使用重复引物(REP、ERIC和(GTG))进行扩增。指纹图谱模式显示,REP引物产生的条带范围为300-6000 bp,ERIC引物产生的条带范围为150-6000 bp,(GTG)引物产生的条带范围为200-1700 bp。在非加权组平均法(UPGMA)聚类分析中,所有引物都将14株细菌聚为三个分支(I、II和III),从而在分子水平上对它们进行了区分。本研究揭示了使用rep-PCR对菌株进行区分的情况。