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Process for the detection of insertion elements or transposons

机译:插入元件或转座子的检测方法

摘要

The invention relates to a process for the detection of insertion elements (IS elements) or transposons in coryneform bacteria, to a positive selection system suitable for this purpose, to the IS elements found in this way and to the use thereof. The process comprises: 1.1. the construction of a vector which is mobilisable from an E. coli mobiliser strain, is not self-transferable and is composed of 1.1.1 a DNA segment containing a replicon which is functional in E. coli, 1.1.2 a second DNA segment containing the DNA fragment coding for the mobilisation function (Mob site containing the oriT), 1.1.3 a third DNA segment which undergoes homologous recombination in Gram-positive bacteria and/or contains a replicon which is functional in coryneform bacteria 1.1.4 a DNA segment which contains the sacB gene and is derived from Bacillus subtilis, 1.2. transfer of this vector by conjugative transfer into the coryneform recipient strains, 1.3. cultivation of the transconjugants containing the vector in a nutrient medium containing 10 % sucrose, 1.4. lysis of the sucrose-resistant clones, cleavage of the plasmids with restriction endonucleases and analysis of the fragments.
机译:本发明涉及一种用于检测棒状细菌中的插入元件(IS元件)或转座子的方法,适合于此目的的阳性选择系统,以这种方式发现的IS元件及其用途。该过程包括:1.1。可从大肠杆菌动员菌株中动员的,不能自我转移的载体的构建,该载体由1.1.1包含在大肠杆菌中有功能的复制子的DNA片段,1.1.2包含编码动员功能的DNA片段(含有oriT的Mob位点),1.1.3在革兰氏阳性细菌中进行同源重组和/或在棒状细菌中有功能的复制子的第三个DNA片段1.1.4 DNA片段它包含sacB基因,源自枯草芽孢杆菌1.2。通过共轭转移到棒状受体菌株中,将该载体转移1.3。在含有10%蔗糖1.4的营养培养基中培养含有载体的转导结合体。裂解抗蔗糖的克隆,用限制性内切核酸酶切割质粒并分析片段。

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