摘要
利用聚球藻7942热休克基因groESL的启动子和报告基因egfp,构建了表达载体pUC-Tegfp并转化集胞藻6803,并通过所制备抗体对转基因藻进行蛋白免疫印迹检测.结果发现,在转基因藻株T-egfp的细胞粗提液中含有能与eGFP抗体特异结合的蛋白质,表明外源增强型绿色荧光蛋白基因(egfp)在集胞藻6803中成功表达.
The groESL gene promoter,originated from Synechococcus sp.PCC 7942,and the reporter gene egfp coding region were ligated into pUC19 vector to generate the shuttle expression plasmid,pUC-Tegfp,which was subsequently transferred into Synechocystis sp.PCC6803.Immunoblotting analysis showed the presence of eGFP protein in transgenic cells harboring pUC-Tegfp.This indicated that eGFP protein was cloned and overexpressed in transgenic cells.
出处
《西北植物学报》
CAS
CSCD
北大核心
2009年第2期229-233,共5页
Acta Botanica Boreali-Occidentalia Sinica
基金
上海市高等学校科技基金重点项目(05ZZ15)
上海师范大学校基金(SK200837)
关键词
集胞藻6803
增强型绿色荧光蛋白
转基因藻
Synechocystis sp.PCC6803
eGFP
transgenic Synechocystis sp.PCC6803 harboring pUC-Tegfp