Liesack W, Pitulle C, Stackebrandt E
Institut für Allgemeine Mikrobiologie, Christian-Albrechts-Universität, Kiel, FRG.
Lett Appl Microbiol. 1990 Aug;11(2):96-9. doi: 10.1111/j.1472-765x.1990.tb01285.x.
A 21-mer DNA oligonucleotide probe targeting the 23S rRNA of Mycobacterium leprae was developed and its high specificity demonstrated by dot-blot hybridization. Even under relaxed hybridization and washing conditions (20 degrees C below Tm) the probe was highly selective in that positive signals were only detected with M. leprae, about half of the slow-growing and one of the fast-growing reference mycobacteria and Gordona bronchialis. At more stringent washing temperatures (6 degrees C below Tm) only the rRNA of Mycobacterium leprae was detectable.
开发了一种靶向麻风分枝杆菌23S rRNA的21聚体DNA寡核苷酸探针,并通过斑点杂交证明了其高特异性。即使在宽松的杂交和洗涤条件下(低于解链温度20℃),该探针仍具有高度选择性,因为仅在麻风分枝杆菌、约一半的缓慢生长型和一种快速生长型参考分枝杆菌以及支气管戈登菌中检测到阳性信号。在更严格的洗涤温度下(低于解链温度6℃),仅可检测到麻风分枝杆菌的rRNA。