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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Mobilization of the gonococcal 5.2kb beta-lactamase plasmid pSJ5.2 into Escherichia coli by cointegration with several gram-conjugative plasmids
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Mobilization of the gonococcal 5.2kb beta-lactamase plasmid pSJ5.2 into Escherichia coli by cointegration with several gram-conjugative plasmids

机译:通过与几种革兰氏结合质粒共整合,将淋球菌5.2kbβ-内酰胺酶质粒pSJ5.2转移到大肠杆菌中

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We report the mobilization by cointegration of the gonococcal 5.2 kb beta-lactamase plasmid pSJ5.2 in an Escherichia coli background. Transfer of pSJ5.2 was measured by filter mating assays with five different conjugative plasmids from Enterobacteriaceae and the gonococcal 41 kb tet(M). Plasmid pSJ5.2 was mobilized to E. coli at frequencies of 1.7 x 10(-6), 9.3 x 10(-8) and 2.7 x 10(-5) by the tet(M), R64 drd-33 and N3 conjugative plasmids, respectively. Mobilization of pSJ5.2 by the 41 kb tet(M) conjugative plasmid resulted in stable Amp R E. coli transconjugants consisting of pSJ5.2 plasmid with an insertion located in the 2.4 kb BamHI-BamHl fragment. Mobilization of pSJ5.2 by R64drd-33 and N3 conjugative plasmids involved stable cointegrates as detected by Southern Blot with a DIG-labelled PstI-digested pSJ5.2 probe. Restriction analysis of the R64:: pSJ5.2 and N3:: pSJ5.2 cointegrates and Southern Blot with the pSJ5.2 probe showed that cointegrates formed by deletion of DNA regions within the 1.8 kb BamHI-HindIII fragment of pSJ5.2. The plasmid thus appears to use multiple recombination mechanisms for cointegration with different conjugative plasmids. The complete nucleotide sequence of pSJ5.2 was determined, and will be a useful tool to further investigate the molecular mechanisms leading to its cointegrative transfer. (c) 2006 Elsevier Inc. All rights reserved.
机译:我们报告了在大肠杆菌背景下淋球菌5.2 kbβ-内酰胺酶质粒pSJ5.2的整合动员。用五个不同的肠杆菌科细菌和41 kb淋球菌的tet(M)结合质粒通过过滤器交配测定法测量pSJ5.2的转移。通过tet(M),R64 drd-33和N3结合剂将质粒pSJ5.2以1.7 x 10(-6),9.3 x 10(-8)和2.7 x 10(-5)的频率动员到大肠杆菌质粒,分别。 41 kb tet(M)接合质粒对pSJ5.2的动员产生稳定的Amp R大肠杆菌转接合子,由pSJ5.2质粒组成,插入片段位于2.4 kb BamHI-BamH1片段中。 R64drd-33和N3结合质粒对pSJ5.2的动员涉及稳定的共整合,如Southern blot用DIG标记的PstI消化的pSJ5.2探针检测到的。对R64 :: pSJ5.2和N3 :: pSJ5.2的限制性酶切分析以及用pSJ5.2探针进行的Southern印迹分析显示,通过缺失pSJ5.2的1.8 kb BamHI-HindIII片段中的DNA区域形成了共整合。因此,该质粒似乎使用多种重组机制与不同的接合质粒共整合。确定了pSJ5.2的完整核苷酸序列,它将是进一步研究导致其共整合转移的分子机制的有用工具。 (c)2006 Elsevier Inc.保留所有权利。

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