Roller C, Wagner M, Amann R, Ludwig W, Schleifer K H
Lehrstuhl für Mikrobiologie, Technische Universität München, Germany.
Microbiology (Reading). 1994 Oct;140 ( Pt 10):2849-58. doi: 10.1099/00221287-140-10-2849.
23S-rRNA-targeted oligonucleotide probes were designed for the phylogenetic group 'Gram-positive bacteria with high G + C content of DNA' (GPBHGC). A sequence idiosyncrasy in two adjacent base pairs in the stem of helix 69 in domain IV of the 23S rRNA is present in all hitherto analysed strains of GPBHGC. An oligonucleotide probe targeted to this region hybridized only with strains of GPBHGC and was successfully used for in situ monitoring of these cells in activated sludge. Another unique feature of the 23S rRNA molecules of GPBHGC is a large insertion in domain III. Fluorescent oligonucleotides targeted to the highly variable regions of the rRNA within the insertions of Corynebacterium glutamicum DSM 20300, Aureobacterium testaceum DSM 20166 and Brevibacterium sp. DSM 20165 hybridized specifically to their target strains, whereas probing with oligonucleotides complementary to the rRNA-coding strand of the 23S rDNA and to the spacer between 16S and 23S rRNA of C. glutamicum did not result in detectable fluorescence. This confirmed that the large 23S insertions are indeed present in 23S rRNAs of GPBHGC and provide potential target sites for highly specific nucleic acid probes.
针对“DNA中G + C含量高的革兰氏阳性菌”(GPBHGC)这一系统发育组设计了靶向23S - rRNA的寡核苷酸探针。在GPBHGC所有迄今分析的菌株中,23S rRNA结构域IV中螺旋69茎部的两个相邻碱基对存在序列特异性。靶向该区域的寡核苷酸探针仅与GPBHGC菌株杂交,并成功用于活性污泥中这些细胞的原位监测。GPBHGC的23S rRNA分子的另一个独特特征是结构域III中有一个大的插入片段。靶向谷氨酸棒杆菌DSM 20300、睾丸金色杆菌DSM 20166和短杆菌属DSM 20165插入片段内rRNA高变区的荧光寡核苷酸与它们的目标菌株特异性杂交,而用与谷氨酸棒杆菌23S rDNA的rRNA编码链以及16S和23S rRNA之间的间隔区互补的寡核苷酸进行探测未产生可检测到的荧光。这证实了GPBHGC的23S rRNA中确实存在大的23S插入片段,并为高度特异性核酸探针提供了潜在的靶位点。