IN-SITU PROBING OF GRAM-POSITIVE BACTERIA WITH HIGH DNA G+C CONTENT USING 235-RIBOSOMAL-RNA-TARGETED OLIGONUCLEOTIDES

被引:451
作者
ROLLER, C [1 ]
WAGNER, M [1 ]
AMANN, R [1 ]
LUDWIG, W [1 ]
SCHLEIFER, KH [1 ]
机构
[1] TECH UNIV MUNICH, LEHRSTUHL MIKROBIOL, D-80290 MUNICH, GERMANY
来源
MICROBIOLOGY-UK | 1994年 / 140卷
关键词
OLIGONUCLEOTIDE PROBES; 23S RIBOSOMAL-RNA; IN SITU HYBRIDIZATION; GRAM-POSITIVE BACTERIA; INSERTION;
D O I
10.1099/00221287-140-10-2849
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
23S-rRNA-targeted oligonucleotide probes were designed far 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(T), 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.
引用
收藏
页码:2849 / 2858
页数:10
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