Construction of Double Cross-over Expression Vector for Chloroplast Multicistron in Brassica napus L.  

油菜叶绿体多顺反子双交换表达载体的构建(英文)

作　　者：武玉永[1] 姚庆收[1] 马立新[2] 

机构地区：[1]滨州医学院医学遗传学教研室,山东烟台264003 [2]湖北大学生命科学学院分子微生物学与基因工程实验室,湖北武汉430062

出　　处：《Agricultural Science & Technology》2013年第3期402-406,共5页农业科学与技术（英文版）

基　　金：Supported by National 863 Project of China (2002AA227011);Natural Science Foundation of Hubei Province (2003ABAI18);Natural Science Foundation of Shandong Province (ZR2010HQ054)~~

摘　　要：[Objective] This study aimed to construct Brassica napus chloroplast multi- cistron double cross-over expression vector, to lay the foundation for the genetic engi- neering research of Brassica napus chloroplast. [Method] Two primers were designed based on the known Brassica napus chloroplast DNA sequences AF267640 and Z50868 in GenBank. By using PCR method, two Brassica napus L. chloroplast DNA fragments were obtained, which were named RbcL and ACCD. The two Brassica na- pus chloroplast DNA homologous fragments were then cloned into plasmid pMD18-T to obtain recombinant plasmid pHBM715. Tandem expression cassette harboring spectinomycin-resistant gene aadA, mannanase gene man and green fluorescent pro- tein gene gfp was cloned into the plasmid pHBM715, thereby constructing Brassica napus chloroplast multicistron double cross-over expression vector pHBM716, which was transformed into Escherichia coil for expression and identification. [Result] Plate qualitative analysis was conducted for the functional identification of expression cas- sette in the constructed Brassica napus chloroplast multicistron double cross-over ex- pression vector, results showed that the three genes of the same multicistron were all expressed in E. coil [Conclusion] This study successfully constructed Brassica napus chloroplast multicistron double cross-over expression vector, which laid the foundation for the genetic engineering of Brassica napus chloroplast.[目的]构建甘蓝型油菜叶绿体多顺反子表达载体,以期为油菜叶绿体基因工程研究奠定基础。[方法]根据GenBank中已知的油菜叶绿体DNA序列AF267640和Z50868,设计两对引物,用PCR方法获得了两段甘蓝型油菜叶绿体DNA片段,分别命名为RbcL和ACCD。将这两段甘蓝型油菜叶绿体DNA同源片段克隆到质粒pMD18-T中得到质粒pHBM715,然后再将由壮观霉素抗性基因aadA、甘露聚糖酶基因man和绿色荧光蛋白基因gfp这3个基因串联的表达盒克隆到质粒pHBM715中,从而构建成甘蓝型油菜叶绿体多顺反子表达载体pHBM716,并将该载体在大肠杆菌中进行表达鉴定。[结果]通过平板定性分析对所构建的油菜叶绿体表达载体上的表达盒进行了功能鉴定,表明同一多顺反子的3个基因在大肠杆菌中均得到了表达。[结论]该研究成功构建了甘蓝型油菜叶绿体多顺反子表达载体,为油菜叶绿体基因工程研究奠定了基础。

关 键 词：Brassica napus L. Chloroplast DNA Multicistron Double cross-over Expression vector Functional identification 

分 类 号：S565.4[农业科学—作物学]