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BNYVV CP基因的克隆及载体构建
Cloning of cDNA for BNYVV CP Gene and Construction of Transforming Vector
【摘要】 以甜菜丛根病根或病叶总RNA为模板,经反转录PCR扩增合成编码BNYVV CP的全长cDNA,将其克隆于pUCm-T载体上,获得了重组质粒pUCm-T/CP。经序列分析,此cDNA为一个567 bp长的开放阅读框架,编码由188个氨基酸组成的病毒外壳蛋白。又将CP基因构建到植物双元载体pROKⅡ中。最后通过三亲融合,得到了融合农杆菌LB4404。
【Abstract】 Identification and characterization of a full-length cDNA encoding for BNYVV coat protein was described. The cDNA was 567 bp in length with open reading frame of 188 amino acids. The CP gene was inserted into the plant binary vector pROKII. And finally the recombinant vector pROKII was infused into Agrobac-terium tumefactions.
【关键词】 甜菜丛根病;
CP cDNA;
克隆;
转化载体;
【Key words】 Rhizomania of sugar beet; CP cDNA; Cloning; Transforming vector;
【Key words】 Rhizomania of sugar beet; CP cDNA; Cloning; Transforming vector;
- 【文献出处】 华北农学报 ,Acta Agriculturae Boreali—Sinica , 编辑部邮箱 ,2004年02期
- 【分类号】S566.3
- 【被引频次】3
- 【下载频次】97