East A K, Collins M D
Department of Microbiology, AFRC Institute of Food Research, Reading Laboratory, UK.
FEMS Microbiol Lett. 1993 Jan 15;106(2):129-33. doi: 10.1111/j.1574-6968.1993.tb05947.x.
Amplification of the gene encoding 23S rRNA of Aeromonas hydrophila by polymerase chain reaction, with primers complementary to conserved regions of 16S and the 3'-end of 23S rRNA genes, resulted in a DNA fragment of approximately 3 kb. This fragment was cloned in Escherichia coli, and its nucleotide sequence determined. The region encoding 23S rRNA shows high homology with the published sequences of 23S rRNA from other members of the gamma division of Proteobacteria. The sequence of the intergenic spacer region, between the 16S and 23S rRNA genes, was determined in five clones. Three types of spacer were identified: two clones were identical and encoded tRNA(Ile) and tRNA(Ala) while the remaining three clones contained tRNA(Glu), only two had the same spacer sequences. This variation in sequence indicates that the different clones may be derived from different ribosomal RNA operons.
通过聚合酶链反应,用与16S和23S rRNA基因3'端保守区域互补的引物,扩增嗜水气单胞菌编码23S rRNA的基因,得到一个约3 kb的DNA片段。该片段克隆到大肠杆菌中,并测定其核苷酸序列。编码23S rRNA的区域与已发表的变形菌纲γ亚群其他成员的23S rRNA序列具有高度同源性。在五个克隆中测定了16S和23S rRNA基因之间的基因间隔区序列。鉴定出三种类型的间隔区:两个克隆相同,编码tRNA(Ile)和tRNA(Ala),而其余三个克隆仅含有tRNA(Glu),只有两个具有相同的间隔区序列。这种序列差异表明不同的克隆可能来自不同的核糖体RNA操纵子。