Huang Chien-Hsun, Chang Mu-Tzu, Huang Lina
Bioresource Collection and Research Center, Food Industry Research and Development Institute, 331 Shih-Pin Road, Hsinchu 30062, Taiwan.
National Health Research Institutes, Institute of Biotechnology and Pharmaceutical Research, 35 Keyan Road, Zhunan, Miaoli County 35053, Taiwan.
Mol Cell Probes. 2014 Aug;28(4):192-4. doi: 10.1016/j.mcp.2014.03.003. Epub 2014 Mar 24.
Identifying Lactobacillus species using only phenotypic and genotypic (16S rDNA sequence analysis) techniques yields inaccurate results. The objective of this study was to develop species-specific primers based on randomly amplified polymorphic DNA (RAPD) fingerprinting to distinguish species within the closely related Lactobacillus plantarum group. One of these primers, OPD-3, produced a species-specific band that was found only in the tested Lactobacillus pentosus. This specific fragment was isolated from agarose gel and ligated into a vector for DNA sequencing. A pair of primers, SpOPD3Lpen-F1/R1, that were highly specific sequence-characterized-amplified-regions (SCARs) were designed according to the nucleotide sequences of the specific RAPD marker. These primers were used for PCR analysis of the template DNA of the Lactobacillus strains, and a single 542 bp species-specific band was found only in L. pentosus. Using PCR, a novel species-specific primer pair is shown to rapidly, accurately and effectively distinguish L. pentosus from other species in the L. plantarum group of probiotic bacteria.
仅使用表型和基因型(16S rDNA序列分析)技术鉴定乳酸杆菌属物种会产生不准确的结果。本研究的目的是基于随机扩增多态性DNA(RAPD)指纹图谱开发物种特异性引物,以区分密切相关的植物乳杆菌组内的物种。其中一个引物OPD-3产生了一个物种特异性条带,该条带仅在测试的戊糖乳杆菌中发现。从琼脂糖凝胶中分离出这个特定片段,并连接到载体中进行DNA测序。根据特定RAPD标记的核苷酸序列设计了一对高度特异性的序列特征性扩增区域(SCAR)引物SpOPD3Lpen-F1/R1。这些引物用于对乳酸杆菌菌株的模板DNA进行PCR分析,并且仅在戊糖乳杆菌中发现了一条542 bp的物种特异性单一条带。通过PCR,显示出一对新的物种特异性引物能够快速、准确且有效地将戊糖乳杆菌与植物乳杆菌组中的其他益生菌物种区分开来。