Bonamy Celine, Labarre Jean, Cazaubon Laurent, Jacob Christiane, Le Bohec Françoise, Reyes Oscar, Leblon Gérard
Laboratoire de Biologie Moléculaire des Corynébactéries, Institut de Génétique et de Microbiologie, Université de Paris-Sud, Bâtiment 409, 91405 Orsay cedex, France.
J Biotechnol. 2003 Sep 4;104(1-3):301-9. doi: 10.1016/s0168-1656(03)00150-0.
IS1207 is the insertion most frequently found among the spontaneous mutations that abolish the activity of an Escherichia coli phage lambda cI gene integrated in the Corynebacterium Brevibacterium lactofermentum ATCC21086 genome. We examined the transposition of transposon-like structures composed of a selective kanamycin resistance gene (aph3), and one or two IS1207 sequences. One of these, the Tn5531 transposon, transposed efficiently in Corynebacterium glutamicum. A replicative and a non-replicative Tn5531 delivery vector were used in Tn5531 mutagenesis. As IS1207, transposon Tn5531 shows a high frequency of transposition and mutagenesis, and a low target specificity. These features make of Tn5531 an adequate choice for gene identification and gene tagging experiments.
IS1207是在自发突变中最常发现的插入序列,这些自发突变会使整合在短乳杆菌ATCC21086基因组中的大肠杆菌噬菌体λ cI基因失活。我们研究了由选择性卡那霉素抗性基因(aph3)以及一个或两个IS1207序列组成的类转座子结构的转座情况。其中之一,即Tn5531转座子,能在谷氨酸棒杆菌中高效转座。在Tn5531诱变中使用了复制型和非复制型Tn5531递送载体。与IS1207一样,转座子Tn5531显示出高频率的转座和诱变,以及低靶标特异性。这些特性使Tn5531成为基因鉴定和基因标签实验的合适选择。