Hamada W, Reignault P, Bompeix G, Boccara M
Laboratoire de biochimie et de pathologie végétales, UPMC, Paris, France.
Curr Genet. 1994 Sep;26(3):251-5. doi: 10.1007/BF00309556.
A transformation method has been developed for the phytopathogenic fungus Botrytis cinerea. Protoplasts were transformed with pAN7-1 plasmid carrying the Escherichia coli hygromycin phosphotransferase gene (hph), conferring hygromycin B resistance, downstream from an Aspergillus nidulans promoter. Molecular analysis, showed that transformation resulted in an integration of the plasmid into different regions of the B. cinerea genome and occurred through non-homologous recombination. The frequency was 2-10 transformants per micrograms of DNA. Transformants expressed phosphotransferase activity confirming that the hph gene conferred the hygromycin-resistance phenotype. All transformants analysed so far proved to be stable after several subcultures without any selective pressure.
已开发出一种用于植物致病真菌灰葡萄孢的转化方法。用携带大肠杆菌潮霉素磷酸转移酶基因(hph)的pAN7 - 1质粒对原生质体进行转化,该基因赋予潮霉素B抗性,位于构巢曲霉启动子下游。分子分析表明,转化导致质粒整合到灰葡萄孢基因组的不同区域,且通过非同源重组发生。转化频率为每微克DNA产生2 - 10个转化体。转化体表达磷酸转移酶活性,证实hph基因赋予了潮霉素抗性表型。到目前为止,所有分析的转化体在无任何选择压力的情况下经过几次传代培养后都证明是稳定的。