摘要
将染色体整合型糖多孢红霉菌表达载体pZMW-tsr转入大肠杆菌ET12567(pUZ8002);以其作为供体,采用接合转移的方法将硫链丝菌素抗性基因tsr转入4-羟基环孢菌素A衍生物[γHyMeLeu4]CyA生产菌野野村菌CYA4OH。PCR结果表明,tsr基因已经整合到CYA4OH基因组上。研究表明pZMW载体能够在稀有放线菌野野村菌中有效表达外源基因。
The recombinant vector pZMW-tsr, which could be integrated into S. erythraea chromosome,was transformed to Escherichia coli ET12567 (pUZ8002). Gene tsr was transformed to the [γHyMeLeu4]CyA-pro- ducing strain Nonomuraea sp. CYA4OH by conjugation method using Escherichia coli ET12567 (pUZS002, pZMW-tsr) as a conjugal donor. PCR Identification showed that gene tsr was integrated into the chromosome of CYA4OH. It was confirmed that pZMW could express exogenous genes effectively in rare actinomycete Nono- rnuraea sp..
出处
《化学与生物工程》
CAS
2013年第4期44-46,共3页
Chemistry & Bioengineering
基金
微生物药物技术创新与新药创制产学研联盟资助项目(2010ZX09401-403)