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弓形虫多表位基因植物表达载体的构建
引用本文:周晓红,陈晓光,张晓东,杨培梁,习佳飞,胡建军,王亚楠,李林,沈树满. 弓形虫多表位基因植物表达载体的构建[J]. 中国寄生虫学与寄生虫病杂志, 2003, 21(2): 106-109
作者姓名:周晓红  陈晓光  张晓东  杨培梁  习佳飞  胡建军  王亚楠  李林  沈树满
作者单位:1. 第一军医大学寄生虫学教研室,广州,510515
2. 北京市农林科学院生物技术研究中心,北京,100089
3. 第一军医大学学员一旅五队,广州,510515
基金项目:国家自然科学基金(No.30080024),广东省自然科学基金(No.001052)
摘    要:目的构建弓形虫多表位基因(TGMG)植物表达载体。方法①将TGMG亚克隆人pBAC55构建中间载体pB35MG,再将其中E35S/TGMG/NOS3′结构单元亚克隆人pCAMBIA2300构建植物表达载体pC35MG。②将番茄果实特异性启动子E81.1插入pB35MG构建中间载体pB35E1MG,再将其中E35SE81.1/TGMG/NOS3′结构单元亚克隆人pCAMBIA2300构建植物表达载体pC35E1MG。③将番茄果实特异性启动子E82.2插入pB35MG构建中间载体pBE2MG,再将其中E82.2/TGMG/NOS3′结构单元亚克隆人pCAMBIA2300构建植物表达载体pCE2MG。测序鉴定pB35MG、pC35E1MG、pCE2MG中的TGMG序列。④pC35MG、pC35E1MG、pCE2MG转化根癌农杆菌LBA404。结果重组质粒用酶切鉴定均得到预期片段,pB35MG、pC35E1MG、pCE2MG测序结果正确。结论成功构建TGMG中间载体pB35MG、pB35E1MG、pBE2MG,以及植物表达载体pC35MG、pC35E1MG、pCE2MG。并将3种植物表达载体导入根癌农杆菌。

关 键 词:弓形虫  多表位基因  番茄果实特异性启动子  植物表达载体
文章编号:1000-7423(2003)-02-0106-04
修稿时间:2002-11-13

Construction of the Plant Expression Vectors Containing the Multiepitope Gene of Toxoplasma gondii
ZHOU Xiao-hong,CHEN Xiao-guang,ZHANG Xiao-dong,YANG Pei-liang,XI Jia-fei,HU Jian-jun,WANG Ya-nan,LI Lin,SHEN Shu-man. Construction of the Plant Expression Vectors Containing the Multiepitope Gene of Toxoplasma gondii[J]. Chinese Journal of Parasitology and Parasitic Diseases, 2003, 21(2): 106-109
Authors:ZHOU Xiao-hong  CHEN Xiao-guang  ZHANG Xiao-dong  YANG Pei-liang  XI Jia-fei  HU Jian-jun  WANG Ya-nan  LI Lin  SHEN Shu-man
Affiliation:Department of Parasitology, First Military Medical University, Guangzhou 510515.
Abstract:OBJECTIVE: To construct the plant expression vectors containing the multiepitope gene of Toxoplasma gondii (TGMG). METHODS: 1. TGMG was subcloned into pBAC55 vector to construct the intermediate plasmid pB35MG. The E35S/TGMG/NOS3' fragment was cleaved from pB35MG and ligated into the plant binary vector pCAMBIA2300 to construct the plant expression vector pC35MG. 2. Tomato fruit-specific E81. 1 promoter was introduced to pB35MG to construct pB35E1MG vector. The E35SE81. 1/TGMG/NOS3' fragment was subcloned into pCAMBIA2300 to construct the plant expression vector pC35E1MG. 3. Tomato fruit-specific E82.2 promoter was inserted to pB35MG to construct pBE2MG vector. The E82.2/TGMG/NOS3' fragment was subcloned into pCAMBIA2300 to construct the plant expression vector pCE2MG. The insert gene TGMG in the vectors pB35MG, pC35E1MG and pCE2MG were confirmed by sequencing. 4. pC35MG, pC35E1MG and pCE2MG were introduced into Agrobacterium tumefaciens strain LBA4404 competent cell. RESULTS: Digestion with restriction enzymes proved that all recombinant vectors had the inserts with expected length of the target fragments. And the sequencing results were confirmed correct. CONCLUSION: The TGMG intermediate vectors pB35MG, pB35E1MG and pBE2MG and the plant expression vectors pC35MG, pC35E1MG and pCE2MG were constructed successfully, and the three plant expression vectors were introduced into Agrobacterium tumefaciens.
Keywords:Toxoplasma gondii   multiepitope gene   tomato fruit-specific promoter   plant expression vector
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