Marx Christopher J, Lidstrom Mary E
University of Washington, Seattle, USA.
Biotechniques. 2002 Nov;33(5):1062-7. doi: 10.2144/02335rr01.
Complete genome sequences are now available for many bacterial species that lack sophisticated genetic tools. We describe the development of a broad-host-range cre-lox system that allows antibiotic marker recycling in a variety of gram-negative bacteria. This system consists of an allelic exchange vector bearing a kanamycin cassette flanked by loxP sites and a tetracycline-resistant IncP plasmid that provides expression of the Cre recombinase. We demonstrate this system by generating unmarked deletions of genes in two different bacteria, Methylobacterium extorquens AM1 and Burkholderia fungorum LB400. This new antibiotic marker recycling system offers the possibility of creating unmarked mutants in a wide variety of gram-negative bacteria. Furthermore, marker recycling allows the generation of strains bearing multiple genetic manipulations in organisms for which few antibiotic markers are currently available.
现在已有许多缺乏精密遗传工具的细菌物种的完整基因组序列。我们描述了一种广宿主范围的cre-lox系统的开发,该系统允许在多种革兰氏阴性细菌中回收抗生素标记。该系统由一个等位基因交换载体和一个四环素抗性的IncP质粒组成,等位基因交换载体带有一个两侧为loxP位点的卡那霉素盒,IncP质粒提供Cre重组酶的表达。我们通过在两种不同的细菌,即嗜甲基甲基杆菌AM1和真菌伯克霍尔德氏菌LB400中产生基因的无标记缺失来证明该系统。这种新的抗生素标记回收系统提供了在多种革兰氏阴性细菌中创建无标记突变体的可能性。此外,标记回收允许在目前可用抗生素标记很少的生物体中产生携带多种基因操作的菌株。