Nishitani Yosuke, Sasaki Eiki, Fujisawa Tomohiko, Osawa Ro
Department of Bioscience, Graduate School of Science and Technology, Kobe University, Kobe, Japan.
Syst Appl Microbiol. 2004 Feb;27(1):109-17. doi: 10.1078/0723-2020-00262.
A total of 77 tannase producing lactobacilli strains isolated from human feces or fermented foods were examined for their genotypic profiles and intensities of tannase production. With a PCR-based assay targeting recA gene, all strains except one isolate were assigned to either Lactobacillus plantarum, L. paraplantarum, or L. pentosus whereas a 16/23S rDNA targeted PCR-based assay identified all except 6 isolates (inclusive of the above one isolate) as one of the closely related species. Subsequent DNA/DNA hybridization assays revealed that these 6 exceptional isolates showed low homology (between 1.2% and 55.8% relative DNA binding) against type strains of the three species. Supplemental carbohydrate fermentation profiles on the 6 isolates indicated that two of them were identified as L. acidophilus, one as Pediococcus acidilactici, one as P. pentosaceus, and two remained unidentifiable. The evidence suggests that the 16/23S rDNA targeted PCR assay can be used as a reliable identification tool for the closely related lactobacilli, and that the tannase gene is widely distributed within members of the Lactobacillaceae family. Meanwhile, a randomly amplified polymorphism DNA (RAPD) analysis revealed that all except 8 isolates were well allocated in 4 major RAPD clusters, though not species specific, consisting of two L. plantarum predominant clusters, one L. paraplantarum predominant, and one L. pentosus predominant. The RAPD patterns of the 8 non-clustered isolates, which consisted of the 6 unidentifiable isolates and 2 isolates identified as L. pentosus, were <40% similarity to those belonging to the 4 clusters. A quantitative assay of the tannase activities showed that there was a marked variation in the activities among the strains, which did not correlate with either species identification or clustering by RAPD.
对从人类粪便或发酵食品中分离出的77株产单宁酶的乳酸杆菌菌株进行了基因型分析和单宁酶产生强度检测。通过基于PCR的针对recA基因的检测方法,除了一个分离株外,所有菌株都被归类为植物乳杆菌、副植物乳杆菌或戊糖乳杆菌,而基于16/23S rDNA靶向的PCR检测方法将除6个分离株(包括上述一个分离株)之外的所有菌株鉴定为密切相关的物种之一。随后的DNA/DNA杂交检测表明,这6个特殊的分离株与这三个物种的模式菌株显示出低同源性(相对DNA结合率在1.2%至55.8%之间)。对这6个分离株的补充碳水化合物发酵谱分析表明,其中两个被鉴定为嗜酸乳杆菌,一个为嗜酸片球菌,一个为戊糖片球菌,还有两个无法鉴定。证据表明,基于16/23S rDNA靶向的PCR检测方法可作为密切相关乳酸杆菌的可靠鉴定工具,并且单宁酶基因在乳杆菌科成员中广泛分布。同时,随机扩增多态性DNA(RAPD)分析表明,除8个分离株外,所有菌株都很好地分配在4个主要的RAPD簇中,尽管不是物种特异性的,其中包括两个以植物乳杆菌为主的簇、一个以副植物乳杆菌为主的簇和一个以戊糖乳杆菌为主的簇。这8个未聚类的分离株(包括6个无法鉴定的分离株和2个被鉴定为戊糖乳杆菌的分离株)的RAPD模式与属于这4个簇的分离株的相似性<40%。单宁酶活性的定量检测表明,菌株之间的活性存在显著差异,这与物种鉴定或RAPD聚类均无相关性。