Raabe T, Jenny E, Meyer J
Department of Microbiology, Biozentrum, University of Basel, Switzerland.
Mol Gen Genet. 1988 Dec;215(1):176-80. doi: 10.1007/BF00331322.
We present a method that allows positive selection and rapid analysis of mutations in Enterobacteriaceae. Mutations are detected in a 2630 bp selection cartridge inserted in two different bacterial multicopy plasmid vectors. Spontaneous mutations in Escherichia coli, Enterobacter cloacae and Citrobacter freundii include insertions, deletions and point mutations. The small size of the target sequence facilitates rapid analysis of DNA rearrangements by cleavage with restriction enzymes and of any type of mutation by DNA sequence analysis. While in E. coli insertions of the mobile elements IS1, IS2 and IS5 were readily found, insertions of putative new transposable elements were detected in Enterobacter cloacae. The selection cartridge can thus serve as a tool for studying the spectrum of insertion mutations in Enterobacteriaceae and probably other Gram-negative bacteria, and the dependency of this spectrum on physiological and environmental factors and the host's genetic background can be investigated.
我们提出了一种方法,可对肠杆菌科细菌中的突变进行阳性选择和快速分析。突变是在插入两种不同细菌多拷贝质粒载体的2630 bp选择盒中检测到的。大肠杆菌、阴沟肠杆菌和弗氏柠檬酸杆菌中的自发突变包括插入、缺失和点突变。目标序列的小尺寸便于通过限制性内切酶切割快速分析DNA重排,并通过DNA序列分析快速分析任何类型的突变。虽然在大肠杆菌中很容易发现移动元件IS1、IS2和IS5的插入,但在阴沟肠杆菌中检测到了假定的新转座元件的插入。因此,该选择盒可作为研究肠杆菌科细菌以及可能其他革兰氏阴性细菌中插入突变谱的工具,并且可以研究该谱对生理和环境因素以及宿主遗传背景的依赖性。