Rossignol M, Basset A, Espéli O, Boccard F
Centre de génétique moléculaire du CNRS, UPR 2167, Gif-sur-Yvette, France.
Res Microbiol. 2001 Jun;152(5):481-5. doi: 10.1016/s0923-2508(01)01221-9.
We have constructed an R6K-based suicide vector that permits the random insertion of a mini-transposon named NKBOR into the chromosome of Gram-negative bacteria and the subsequent rapid cloning of sequences flanking the insertion site in Escherichia coli. This mini-transposon contains a conditional R6K plasmid origin of replication, a kanamycin resistance gene and unique restriction sites between the IS10 inverted repeats. NKBOR can be propagated by replication in an E. coli strain containing the R6K replicase pi protein. Alternatively the mini-transposon can be replicated in a pSC 101 derivative that is thermosensitive for its replication so that the mini-transposon acts as a suicide plasmid at nonpermissive temperatures. Efficient NKBOR transposition is ensured by expression of an adjacent transposase gene and has been demonstrated in E. coli, Klebsiella pneumoniae, and Erwinia carotovora. Sequences flanking the insertion sites in these strains can be rapidly recovered and identified in E. coli strains expressing the R6K pi protein.
我们构建了一种基于R6K的自杀载体,它能使一个名为NKBOR的微型转座子随机插入革兰氏阴性菌的染色体中,并随后在大肠杆菌中快速克隆插入位点两侧的序列。这个微型转座子包含一个条件性R6K质粒复制起点、一个卡那霉素抗性基因以及位于IS10反向重复序列之间的独特限制性酶切位点。NKBOR可通过在含有R6K复制酶π蛋白的大肠杆菌菌株中复制来增殖。或者,该微型转座子也可以在对其复制具有温度敏感性的pSC 101衍生物中复制,这样在非许可温度下微型转座子就作为自杀质粒起作用。相邻转座酶基因的表达确保了NKBOR的高效转座,并且已在大肠杆菌、肺炎克雷伯菌和胡萝卜软腐欧文氏菌中得到证实。在表达R6K π蛋白的大肠杆菌菌株中,可以快速回收并鉴定这些菌株中插入位点两侧的序列。