Department of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel, London, WC1E 7HT, UK.
Methods Mol Biol. 2020;2075:223-233. doi: 10.1007/978-1-4939-9877-7_16.
In this chapter, a highly sensitive method to measure plasmid stability in Gram-negative bacteria is described. This procedure is based on the counterselection of plasmid-containing cells using an aph-parE cassette. When bacteria carrying the aph-parE module in the plasmid of interest are grown in media containing rhamnose as the only carbon source, the P promoter is induced, ParE is synthesized, and plasmid-containing cells are eliminated; bacteria that have lost the plasmid survive. The absence of the kanamycin resistance marker (aph) can be used to confirm the loss of the plasmid in rhamnose grown bacteria.
在本章中,描述了一种用于测量革兰氏阴性菌中质粒稳定性的高灵敏度方法。该方法基于使用 aph-parE 盒对含有质粒的细胞进行反选择。当携带感兴趣质粒中 aph-parE 模块的细菌在含有鼠李糖作为唯一碳源的培养基中生长时,P 启动子被诱导,ParE 被合成,含有质粒的细胞被消除;失去质粒的细菌存活下来。卡那霉素抗性标记(aph)的缺失可用于确认在鼠李糖生长的细菌中质粒的丢失。