摘要
以 p Bch质粒为基础 ,构建了分别由 35 s启动子、 rd2 9A启动子调控的 DREB1A基因双子叶植物表达载体p BD35 s、p BD2 9A,其植物选择标记为新霉素磷酸转移酶基因 (N PT ) ,适用于双子叶植物的遗传转化。以 p CU质粒为基础 ,构建了分别由 E12启动子、 rd2 9A启动子调控的 DREB1A基因单子叶植物表达载体 p CDE12、p CD2 9A,其植物选择标记为乙酰 Co A转移酶基因 (bar) ,适用于单子叶植物的遗传转化。并分别通过三亲本杂交法和冻融法将重组质粒导入根癌农杆菌 L BA4 4 0 4中 ,为通过农杆菌介导法将
Four plant transformation vector were constructed in this experiment.Plasmid pBD35s and pBD29A,which derived from pBch,including DREB 1A gene controlled by CaMV35s promoter and rd29A promoter respectively.Plasmid pCDE12 and pCD29A were derived from pCU,in which the DREB1A gene were regulated by E12 promoter and rd29A promoter respectively.Then the recombination plasmids were introduced into agrobacterium LBA4404 by tri parental conjugation and direct entering ways.$$$$
出处
《东北农业大学学报》
CAS
CSCD
2003年第2期199-204,共6页
Journal of Northeast Agricultural University