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In situ probing of Gram-positive bacteria with high DNA G + C content using 23S rRNA-targeted oligonucleotides

机译:使用23S rRNA靶向寡核苷酸的高DNA G + C含量的革兰氏阳性细菌的原位探测

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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 20300T, 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.
机译:为具有高G + C含量的DNA'(GPBHGC)设计了23s-RRNA靶向寡核苷酸探针。在23s rRNA结构域IV的螺旋69茎中的两个相邻碱基对的序列特质存在于GPBHGC的所有迄今为止分析的菌株中存在。靶向该区域的寡核苷酸探针仅涉及GPBHGC的菌株,并成功地用于在活性污泥中对这些细胞的原位监测。 23s rRNA分子的另一个独特特征是在结构域III中的大插入。荧光寡核苷酸靶向rRNA的高度可变区域,在谷氨酸杆菌DSM 20300T,AULEBACTACTACEUM DSM 20166和Brevibacterium SP的插入内。 DSM 20165特异性地杂交至其靶菌株,而用寡核苷酸与23s rdNA的RRNA编码链互补的寡核苷酸呼出,并且在C.谷氨酰胺的16s和23s RRNA之间的间隔物之间​​没有导致可检测的荧光。这证实,大23s插入确实存在于23s RRNA的GPBHGC中,并为高度特异性的核酸探针提供潜在的靶位点。

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