Santos M, Vallejo I, Rebordinos L, Gutiérrez S, Collado I G, Cantoral J M
Laboratorio de Genética y Microbiología, Facultad de Ciencias del Mar, Universidad de Cádiz, Polígono del Río San Pedro, Puerto Real, Spain.
FEMS Microbiol Lett. 1996 Apr 1;137(2-3):153-8. doi: 10.1111/j.1574-6968.1996.tb08098.x.
A transformation system has been developed for the pathogen fungus Botrytis cinerea, based on the utilization of the wide host plasmid pUT737 that contains the Sh ble gene, conferring resistance to phleomycin. Transformed protoplasts were regenerated at 10-25 micrograms ml(-1) of phleomycin, at a frequency of 25-40 transformants per microgram of DNA, and they were resistant up to 50 micrograms ml(-1). Southern hybridization using undigested and digested total DNA showed the presence of circular autonomously replicating plasmid pUT737 in the transformants. Reisolated plasmid from transformed fungus transformed E. coli and rescued plasmid was identified as PUT737. Transformants were grown for four generations under non-selective conditions and replicative plasmids were still detected. Plasmids present in all transformants at this stage had been modified from native pUT737 and showed the same size and configuration indicating that selection through stabilizing plasmid forms has happened.
基于对含有赋予博来霉素抗性的Sh ble基因的广宿主质粒pUT737的利用,已开发出一种针对病原菌灰葡萄孢的转化系统。转化的原生质体在10 - 25微克/毫升的博来霉素浓度下再生,每微克DNA的转化频率为25 - 40个转化体,并且它们在高达50微克/毫升的浓度下仍具有抗性。使用未消化和消化的总DNA进行的Southern杂交显示,转化体中存在环状自主复制质粒pUT737。从转化真菌中重新分离的质粒转化了大肠杆菌,拯救的质粒被鉴定为PUT737。转化体在非选择性条件下培养四代,仍能检测到复制型质粒。此时所有转化体中存在的质粒已从天然pUT737修饰而来,显示出相同的大小和构型,表明通过稳定质粒形式进行了选择。