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TnA转座子可被引入并维持在淋病奈瑟菌中。

TnA transposons can be introduced and maintained in Neisseria gonorrhoeae.

作者信息

Piffaretti J C, Soldati L

机构信息

Istituto Cantonale Batteriologico, Lugano, Switzerland.

出版信息

Res Microbiol. 1990 Jun;141(5):519-28. doi: 10.1016/0923-2508(90)90016-j.

Abstract

In Neisseria gonorrhoeae, all penicillinase-specifying plasmids isolated so far share homology with each other and carry a 60% deleted sequence of TnA. Plasmid pHD131, an element isolated from Haemophilus ducreyi and carrying an intact copy of the ampicillin resistance transposable element, was introduced from Escherichia coli into N. gonorrhoeae by both transformation and conjugative mobilization. Plasmids were recovered with no detectable deletion. After their transfer back into E. coli, transposition assays onto phage-lambda DNA demonstrated that the TnA elements were still functional. Plasmid pHD131 could be stably maintained in N. gonorrhoeae with or without the presence of penicillin. These results support the hypothesis that the absence in N. gonorrhoeae of plasmids carrying entire and functional TnA transposons cannot be ascribed to incompatibility between the genetic element and the host, but rather to a barrier to introduction of foreign DNA into gonococcus.

摘要

在淋病奈瑟菌中,迄今分离出的所有携带青霉素酶的质粒都彼此具有同源性,并且带有TnA的一个缺失了60%的序列。质粒pHD131是从杜克雷嗜血杆菌中分离出的一个元件,它携带完整的氨苄青霉素抗性转座元件拷贝,通过转化和接合转移从大肠杆菌导入到淋病奈瑟菌中。回收的质粒没有可检测到的缺失。将它们再转移回大肠杆菌后,在噬菌体λDNA上进行的转座分析表明,TnA元件仍然具有功能。质粒pHD131在有或没有青霉素存在的情况下都能在淋病奈瑟菌中稳定维持。这些结果支持这样一个假说,即淋病奈瑟菌中缺乏携带完整且有功能的TnA转座子的质粒不能归因于遗传元件与宿主之间的不相容性,而是归因于将外源DNA导入淋球菌存在障碍。

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