嗜肺军团菌血清群-1常见质粒pLPG36的克隆、定位及偶联迁移

F López de Felipe
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引用次数: 4

摘要

从天然存在的嗜肺军团菌血清群-1中分离到一种命名为pLPG36的质粒,并通过CsCl浮力密度离心纯化。构建了该质粒的限制性内切图谱,为将4个BamHI片段克隆到pUC18独特的BamHI位点提供了基础。研究了四种重组质粒在大肠杆菌中的动员功能。其中只有pFLJ2能被IncP质粒RP4、pRK231和R702动员,而pSa、R40a、R387、pN3和R16质粒不能被动员。衍生质粒pFLJ2被R702比RP4和pRK231更有效地调动。通过遗传分析和缺失分析,将pLPG36的动员区定位在质粒的6kb EcoRI片段上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning, mapping and conjugal mobility of pLPG36, a common plasmid from Legionella pneumophila serogroup-1.
SUMMARY: A plasmid designated pLPG36 was isolated from the naturally occurring Legionella pneumophila serogroup-1 and purified by CsCl buoyant density centrifugation. A restriction map of this 58 kb plasmid was constructed and provided the basis for cloning four BamHI fragments into the unique BamHI site of pUC18. The four recombinant plasmids were investigated for the mobilization function in Escherichia coli strains. Only one of these, pFLJ2, was mobilized by the IncP plasmids RP4, pRK231 and R702, but not by plasmids pSa, R40a, R387, pN3 or R16. The derivative plasmid pFLJ2 was mobilized more efficiently by R702 than by RP4 or pRK231. By genetic and deletion analysis, the mobilization region of pLPG36 was located to a 6 kb EcoRI fragment of the plasmid.
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