摘要
为探讨克隆有恶性疟原虫MSP1基因片断的重组pQEM1质粒在减毒鼠伤寒杆菌中的表达。使用转化和转导的方法构建减毒鼠伤寒杆菌X4064(pREP4/pQEM1);通过SDS-PAGE电泳检测减毒鼠伤寒杆菌X4064(pQEM1)和减毒鼠伤寒杆菌X4064(pREP4/pQEM1)的表达。实验结果成功地构建了减毒鼠伤寒杆菌X4064(pQEM1),X4064(pREP4/pQEM1)的诱导型表达量高于X4064(pQEM1)的组成型表达量。
To determine the expression of recombinant pQEM1 plasmid cloned the MSP1 No 1 fragment of P falciparum in attenuated Salmonella typhimurium X4064,transformation and transduction were used to construct attenuated S typhimurium X4064(pREP4/pQEM1) The expression level of S typhimurium X4064(pREP4/pQEM1) and S typhimurium X4064(pQEM1) was examined by the method of SDS PAGE The result showed that S typhimurium X4064(pREP4/pQEM1) was constructed successfully The inducible expression level of X4064(pREP4/pQEM1) was higher than that of S typhimurium X4064(pQEM1) whose expression was constitutive The experiment indicated that nonregulative expression could reduce the expression level of recombinant pQEM1 plasmid in attenuated S typhimurium X4064
出处
《实用寄生虫病杂志》
1998年第4期149-151,共3页
Journal of Practical Parasitic Diseases
基金
解放军总后勤部新高技术基金