Stackebrandt E, Smida J, Kazda J
Institut für Algemeine Mikrobiologie, Chritian-Albrechts-Universität, Kiel, FRG.
Acta Leprol. 1989;7 Suppl 1:222-5.
Two long stretches of the 16S from Mycobacterium leprae were sequenced using reverses transcriptase and the chain termination technique. Homology values were calculated for 11 cultivable mycobacteria and a phylogenetic tree constructed from evolutionary distance values (Knuc). Slow and fast growing mycobacteria used in this study form a taxonomic unit but were phylogenetically well separated. It could be confirmed that M. leprae is a true member of the slowly growing pathogenic mycobacteria branching off intermediate to other members of this subgroup. Comparison of the 16 rRNA primary structures reveals that the nucleotide sequence of M. leprae contains regions of sufficient variation to serve as potential target sites for DNA probes. Here we describe the designation of a DNA oligonucleotide and its use in dot blot hybridization experiments were it was directed against bulk RNA isolated from several mycobacteria.
利用逆转录酶和链终止技术对麻风分枝杆菌16S的两段长序列进行了测序。计算了11种可培养分枝杆菌的同源性值,并根据进化距离值(Knuc)构建了系统发育树。本研究中使用的生长缓慢和生长快速的分枝杆菌形成一个分类单元,但在系统发育上有很好的区分。可以确认,麻风分枝杆菌是生长缓慢的致病性分枝杆菌的真正成员,在该亚组的其他成员中间分支出来。对16 rRNA一级结构的比较表明,麻风分枝杆菌的核苷酸序列包含足够变异的区域,可作为DNA探针的潜在靶位点。在此,我们描述了一种DNA寡核苷酸的命名及其在斑点印迹杂交实验中的应用,该实验针对从几种分枝杆菌中分离的总RNA。