首页> 美国卫生研究院文献>other >Four different integrative recombination events involved in the mobilization of the gonococcal 5.2 kb beta-lactamase plasmid pSJ5.2 in Escherichia coli
【2h】

Four different integrative recombination events involved in the mobilization of the gonococcal 5.2 kb beta-lactamase plasmid pSJ5.2 in Escherichia coli

机译:大肠杆菌中淋球菌5.2 kbβ-内酰胺酶质粒pSJ5.2的动员涉及四个不同的整合重组事件

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We identified and characterized four different recombination mechanisms involved in the cointegrative transfer of the Neisseria gonorrhoeae beta-lactamase plasmid pSJ5.2 by the gonococcal 41 kb tet(M) and the Gram negative self-transmissible plasmids N3 and R64 drd-33 using an Escherichia coli recA- background. Mobilization of pSJ5.2 by the tet(M) plasmid occurred by cointegration through a replicative transposition of two IS1 elements inserted upstream from the beta-lactamase gene of pSJ5.2 and creating a IS1::beta-lactamase hybrid promoter. Two types of recombinational events occurred within the 1.8 kb BamH1-HindIII fragment of pSJ5.2 with the N3 and R64 plasmids. A non-homologous recombination was found at coordinates 1817 and 2849 of pSJ5.2 with sequences from R64. A non-homologous recombination combined with an IS26-mediated one-ended transposition was found at coordinates 1817 and 3010 of pSJ5.2 with N3. In both recombinational events, a deletion of over 1 kb of pSJ5.2 occurred. The fourth recombination event was detected in the 1.0 kb BamH1-HindIII fragment of pSJ5.2 by homologous recombination between DNA from the truncated Tn3 resolvase gene of pSJ5.2 and the resolvase sequences from R64 and N3.
机译:我们鉴定和表征了淋病球菌41 kb tet(M)和淋巴球菌N3和R64 drd-33使用淋球菌共同感染淋病奈瑟氏球菌β-内酰胺酶质粒pSJ5.2的四种整合机制大肠杆菌recA-背景。 tet(M)质粒对pSJ5.2的动员是通过将两个IS1元件在pSJ5.2的β-内酰胺酶基因上游插入复制性转位并产生IS1 ::β-内酰胺酶杂合启动子的共整合而实现的。在带有N3和R64质粒的pSJ5.2的1.8 kb BamH1-HindIII片段中发生了两种类型的重组事件。在pSJ5.2的坐标1817和2849处发现非同源重组,具有来自R64的序列。在pSJ5.2与N3的坐标1817和3010处发现非同源重组与IS26介导的单端转座结合。在两个重组事件中,均发生了超过1 kb的pSJ5.2缺失。通过截短的pSJ5.2的Tn3分离酶基因的DNA与R64和N3的分离酶序列之间的同源重组,在pSJ5.2的1.0 kb BamH1-HindIII片段中检测到第四个重组事件。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号