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用于革兰氏阴性真细菌中插入诱变、启动子探测及克隆DNA染色体插入的Mini-Tn5转座子衍生物。

Mini-Tn5 transposon derivatives for insertion mutagenesis, promoter probing, and chromosomal insertion of cloned DNA in gram-negative eubacteria.

作者信息

de Lorenzo V, Herrero M, Jakubzik U, Timmis K N

机构信息

GBF-National Research Centre for Biotechnology, Braunschweig, Federal Republic of Germany.

出版信息

J Bacteriol. 1990 Nov;172(11):6568-72. doi: 10.1128/jb.172.11.6568-6572.1990.

Abstract

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.

摘要

构建了一组Tn5衍生的微型转座子,极大地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片段导入多种革兰氏阴性细菌的染色体,包括肠道细菌和典型的土壤细菌如假单胞菌属。微型转座子由指定对卡那霉素、氯霉素、链霉素-壮观霉素和四环素抗性的基因作为选择标记,以及一个独特的NotI克隆位点,两侧是Tn5的19个碱基对的末端重复序列。进一步的衍生物还包含lacZ、phoA、luxAB或xylE基因,它们没有位于末端重复序列旁边的天然启动子,其方向有利于产生基因-操纵子融合。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,其向受体的接合转移由供体中的RP4动员功能介导。

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