Madoń J, Hütter R
Institute of Microbiology, Swiss Federal Institute of Technology, Zürich.
J Bacteriol. 1991 Oct;173(20):6325-31. doi: 10.1128/jb.173.20.6325-6331.1991.
A new procedure for transformation of Amycolatopsis (Nocardia) mediterranei LBG A3136 was developed. The method makes use of polyethylene glycol and alkaline cations and enables direct transformation of the A. mediterranei mycelium with high efficiency: more than 10(6) transformants per microgram of DNA were obtained. Transformation of A. mediterranei is stimulated by the ionophore antibiotic valinomycin and abolished by arsenate and p-chloromercuribenzenesulfonate. pMEA123, a vector based on the indigenous plasmid pMEA100 and containing the erythromycin resistance gene, was constructed.
开发了一种新的地中海拟无枝酸菌(诺卡氏菌)LBG A3136转化程序。该方法利用聚乙二醇和碱性阳离子,能够高效地直接转化地中海拟无枝酸菌的菌丝体:每微克DNA可获得超过10⁶个转化子。离子载体抗生素缬氨霉素可刺激地中海拟无枝酸菌的转化,而砷酸盐和对氯汞苯磺酸盐则可消除这种转化。构建了基于天然质粒pMEA100并含有红霉素抗性基因的载体pMEA123。