Dobritsa A P, Mikhaĭlova T G, Dubovaia V I
Genetika. 1985 May;21(5):748-55.
The conjugative IncN plasmid R15 (SmrSurHgr, 62.3 kb) is cleaved by the hexanucleotide-specific endonucleases BglII, HindIII, EcoRI, BamHI, SmaI, SalI, PstI and XhoI into 9, 9, 6, 5, 4, 4, 4 and 2 fragments, respectively. The restriction sites were located on the physical map of the R15 genome. Distribution of the cleavage sites is strongly asymmetric. 28 of 32 sites for BamHI, EcoRI, HindIII, SalI, SmaI and PstI were located close to or within the sequences of transposable elements Tn2353 and Tn2354. According to the results of analysis of R15::Tn1756 deletion derivatives and recombinant plasmids harboring fragments of R15, the genetic determinants for resistance to Sm, Su and Hg were mapped, as well as the regions necessary for EcoRII restriction--modification and for plasmid replication and conjugation. The features of physical and genetic structures of R15 and other IncN plasmids are discussed.
接合型IncN质粒R15(SmrSurHgr,62.3 kb)被六核苷酸特异性内切酶BglII、HindIII、EcoRI、BamHI、SmaI、SalI、PstI和XhoI分别切割成9、9、6、5、4、4、4和2个片段。这些限制酶切位点位于R15基因组的物理图谱上。切割位点的分布极不对称。BamHI、EcoRI、HindIII、SalI、SmaI和PstI的32个位点中有28个位于转座元件Tn2353和Tn2354的序列附近或内部。根据对R15::Tn1756缺失衍生物和携带R15片段的重组质粒的分析结果,绘制了对链霉素、磺胺和汞的抗性遗传决定簇图谱,以及EcoRII限制修饰、质粒复制和接合所必需的区域。讨论了R15和其他IncN质粒的物理和遗传结构特征。