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首页> 外文期刊>Journal of bacteriology >Mini-Tn5 transposon derivatives for insertion mutagenesis, promoter probing, and chromosomal insertion of cloned DNA in gram-negative eubacteria.
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Mini-Tn5 transposon derivatives for insertion mutagenesis, promoter probing, and chromosomal insertion of cloned DNA in gram-negative eubacteria.

机译:Mini-Tn5转座子衍生物,用于革兰氏阴性真细菌中的插入诱变,启动子探测和克隆DNA的染色体插入。

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摘要

A collection of Tn5-derived minitransposons has been constructed that simplifies substantially the generation of insertion mutants, in vivo fusions with reporter genes, and the introduction of foreign DNA fragments into the chromosome of a variety of gram-negative bacteria, including the enteric bacteria and typical soil bacteria like Pseudomonas species. The minitransposons consist of genes specifying resistance to kanamycin, chloramphenicol, streptomycin-spectinomycin, and tetracycline as selection markers and a unique NotI cloning site flanked by 19-base-pair terminal repeat sequences of Tn5. Further derivatives also contain lacZ, phoA, luxAB, or xylE genes devoid of their native promoters located next to the terminal repeats in an orientation that affords the generation of gene-operon fusions. The transposons are located on a R6K-based suicide delivery plasmid that provides the IS50R transposase tnp gene in cis but external to the mobile element and whose conjugal transfer to recipients is mediated by RP4 mobilization functions in the donor.
机译:已经构建了Tn5衍生的微型转座子的集合,该集合大大简化了插入突变体的产生,与报告基因的体内融合以及将外源DNA片段引入多种革兰氏阴性细菌(包括肠杆菌和幽门螺杆菌)的染色体中的过程。典型的土壤细菌,如假单胞菌。小型转座子由指定对卡那霉素,氯霉素,链霉素-壮观霉素和四环素的抗性作为选择标记的基因和一个独特的NotI克隆位点,侧接Tn5的19个碱基对的末端重复序列组成。其他衍生物还包含lacZ,phoA,luxAB或xylE基因,这些基因缺少其天然启动子,其定位于末端重复序列的末端,能够产生基因-操纵子融合体。转座子位于基于R6K的自杀传递质粒上,该质粒顺式提供IS50R转座酶tnp基因,但在移动元件外部,其向受体的结合转移是通过供体中的RP4动员功能介导的。

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