Behnke D, Ferretti J J
J Bacteriol. 1980 Nov;144(2):806-13. doi: 10.1128/jb.144.2.806-813.1980.
The erythromycin resistance determinant of plasmid pDB102, a derivative of plasmid pSM19035, was cloned into the single HindIII site of the 3.6-megadalton cryptic Streptococcus mutans plasmid pVA318 and introduced into Streptococcus sanguis strain Challis by transformation. Plasmid pDB201, which was isolated from one of the transformants, consisted of the vector plasmid and the 1.15-megadalton HindIII fragment D of pSM19035. HindIII fragment D contained within it one of the two unique "spacer" sequences of pSM19035. Electron micrographs of self-annealed molecules of the recombinant plasmid revealed classical stem-loop structures, and the resistance determinant of pSM19035 appeared as a transposon-like structure. No differences were observed in either the type or the level of erythromycin resistance by pSM19035 or pDB201. The availability of a cloned erythromycin resistance determinant should be useful for future comparative studies of macrolide, lincosamide, and streptogramin B resistance plasmids in streptococci.
质粒pDB102是质粒pSM19035的衍生物,其红霉素抗性决定子被克隆到3.6兆道尔顿的变形链球菌隐蔽性质粒pVA318的单一HindIII位点,并通过转化导入血链球菌Challis菌株。从其中一个转化子中分离出的质粒pDB201由载体质粒和pSM19035的1.15兆道尔顿HindIII片段D组成。HindIII片段D包含pSM19035两个独特“间隔区”序列中的一个。重组质粒自身退火分子的电子显微照片显示出典型的茎环结构,pSM19035的抗性决定子呈现为转座子样结构。pSM19035或pDB201在红霉素抗性的类型或水平上均未观察到差异。克隆的红霉素抗性决定子的可得性对于未来链球菌中大环内酯类、林可酰胺类和链阳菌素B抗性质粒的比较研究应是有用的。