首页> 外文期刊>Molecular Microbiology >First evidence for gene replacement in Leptospira spp. Inactivation of L. biflexa flaB results in non-motile mutants deficient in endoflagella.
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First evidence for gene replacement in Leptospira spp. Inactivation of L. biflexa flaB results in non-motile mutants deficient in endoflagella.

机译:钩端螺旋体属中的基因替换的第一个证据。双弯曲乳杆菌flaB的失活导致内鞭毛缺陷的非运动性突变体。

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Leptospira spp. offer many advantages as model bacteria for the study of spirochaetes. However, homologous recombination between introduced DNA and the corresponding chromosomal loci has never been demonstrated. A unique feature of spirochaetes is the presence of endoflagella between the outer membrane sheath and the cell cylinder. We chose the flaB flagellin gene, constituting the flagellar core, as a target for gene inactivation in the saprophyte Leptospira biflexa. The amino acid sequence of the FlaB protein of L. biflexa was most similar to those of spirochaetes Brachyspira hyodysenteriae (agent of swine dysentery), Leptospira interrogans (agent of leptospirosis) and Treponema pallidum (agent of syphilis). A suicide vector containing the L. biflexa flaB gene disrupted by a kanamycin marker was UV irradiated or alkali denatured before electroporation. This methodology allowed the selection of many kanamycin-resistant colonies resulting from single and double cross-over events at the flaB locus. The double recombinant mutants are non-motile, as visualized in both liquid and semi-solid media. In addition, a flaB mutant selected for further analysis was shown to be deficient in endoflagella by electron microscopy. However, most of the transformants had resulted from a single homologous recombination event, giving rise to the integration of the suicide vector. We evaluated the effect of the sacB and rpsL genes in L. biflexa as potential counterselectable markers for allelic exchange, and then used the rpsL system for the positive selection of flaB double recombinants in a streptomycin-resistant strain. Like the flaB mutant studied above, the Strr double cross-over mutant was non-motile and deficient in endoflagella. Our results demonstrate that FlaB is involved in flagella assembly and motility. They also show the feasibility of performing allelic replacement in Leptospira spp. by homologous recombination.
机译:钩端螺旋体作为研究螺旋藻的模型细菌,具有许多优势。然而,从未证明引入的DNA和相应的染色体基因座之间的同源重组。螺旋藻的独特特征是在外膜鞘和细胞圆柱之间存在鞭毛。我们选择了构成鞭毛核心的flaB鞭毛蛋白基因作为腐生腐生钩端螺旋体中基因失活的目标。双弯曲乳杆菌FlaB蛋白的氨基酸序列与螺旋体猪痢疾短螺旋体(猪痢疾的病原体),问号钩端螺旋体(钩端螺旋体病的病原体)和苍白螺旋体(梅毒的体征)最相似。在电穿孔前,对含有被卡那霉素标记破坏的双弯曲乳杆菌flaB基因的自杀载体进行紫外线照射或对其进行碱变性。这种方法可以选择由于flB位点的一次和两次交叉事件而产生的许多卡那霉素抗性菌落。如在液体和半固体培养基中所见,双重重组突变体是不运动的。另外,通过电子显微镜显示,选择用于进一步分析的flaB突变体在鞭毛内膜中缺乏。然而,大多数转化体是由单个同源重组事件产生的,从而导致自杀载体的整合。我们评估了双弯曲乳杆菌中sacB和rpsL基因作为等位基因交换的潜在反选择标记的作用,然后将rpsL系统用于链霉素抗性菌株中flaB双重重组体的阳性选择。像上面研究的flaB突变体一样,Strr双交换突变体也没有运动能力,并且鞭毛内膜缺陷。我们的结果表明,FlaB参与鞭毛的组装和运动。他们还显示了在钩端螺旋体中进行等位基因置换的可行性。通过同源重组。

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