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对铜绿假单胞菌中一个非接合性质粒上编码汞离子抗性的易位单元的表征。

Characterization of a translocation unit encoding resistance to mercuric ions that occurs on a nonconjugative plasmid in Pseudomonas aeruginosa.

作者信息

Stanisich V A, Bennett P M, Richmond M H

出版信息

J Bacteriol. 1977 Mar;129(3):1227-33. doi: 10.1128/jb.129.3.1227-1233.1977.

Abstract

The nonconjugative plasmid, pVS1, has a molecular weight of 18.5 X 10(6) and confers resistance to sulfonamides and to mercuric ions. In Pseudomonas aeruginosa PAO, the transfer can be mobilized by a variety of conjugative plasmids, and the process does not require a functional recombination system in the donor. Hybrid plasmids that arise by the relocation of the mer gene onto the mobilizing plasmid can be isolated readily, and, as far as can be determined, these hybrids retain the genome of the conjugative plasmid in toto. The relocation of mer occurs by a Rec-independent process and leads to a constant increase (about 6 X 10(6) daltons) in the size of the recipient plasmid. This suggests that the mer gene in pVS1 is located on a translocation unit, designated Tn501, of a molecular weight of about 6 X 10(6). The translocation of Tn501 into RP1 is not usually associated with the loss of any known plasmid-mediated function, but transfer-defective or tetracycline-sensitive derivatives do occur at frequencies of about 4%, whereas carbenicillin-sensitive or kanamycin-sensitive variants arise with a frequency of about 0.2% each. It seems therefore that the integration of Tn501 can occur at any one of a minimum of five sites in RP1.

摘要

非接合性质粒pVS1的分子量为18.5×10⁶,赋予对磺胺类药物和汞离子的抗性。在铜绿假单胞菌PAO中,该转移可被多种接合性质粒动员,且该过程在供体中不需要功能性重组系统。通过将mer基因重新定位到动员性质粒上产生的杂交质粒很容易分离出来,并且据测定,这些杂种质粒完全保留了接合性质粒的基因组。mer基因的重新定位通过一个不依赖Rec的过程发生,并导致受体质粒大小持续增加(约6×10⁶道尔顿)。这表明pVS1中的mer基因位于一个分子量约为6×10⁶的易位单元上,命名为Tn501。Tn501易位到RP1中通常与任何已知的质粒介导功能的丧失无关,但转移缺陷型或四环素敏感型衍生物确实以约4%的频率出现,而羧苄青霉素敏感型或卡那霉素敏感型变体出现的频率分别约为0.2%。因此,似乎Tn501的整合可以发生在RP1中至少五个位点中的任何一个位点。

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