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德氏假单胞菌(Pseudomonas delafieldii)R-8脱硫基因启动子的克隆与鉴定
引用本文:余志坚,李焕杰,王海胜,李信.德氏假单胞菌(Pseudomonas delafieldii)R-8脱硫基因启动子的克隆与鉴定[J].江苏农业学报,2009,25(3).
作者姓名:余志坚  李焕杰  王海胜  李信
作者单位:1. 中国农业科学院研究生院生物化学与分子生物学实验室,北京100081;东华理工大学生物系,江西抚州344000
2. 中国农业科学院研究生院生物化学与分子生物学实验室,北京,100081
基金项目:国家"863"计划项目 
摘    要:利用PCR方法,从专一性脱硫菌德氏假单胞菌(Pseudomonas delafieldii)R-8中克隆了脱硫基因启动子系列缩短的片段,连接至启动子探测型表达载体pPR9TT,电转原始菌R-8,并测定重组菌R-8-P中的报告基因LacZ表达量.结果表明脱硫基因核心启动子区缩短至300 bp,并对启动子序列进行了预测.

关 键 词:德氏假单胞菌  脱硫基因  启动子

Cloning and Characterization of the dsz Promoter Region from Pseudomonas delafieldii R-8
YU Zhi-jian,LI Huan-jie,WANG Hai-sheng,LI Xin.Cloning and Characterization of the dsz Promoter Region from Pseudomonas delafieldii R-8[J].Jiangsu Journal of Agricultural Sciences,2009,25(3).
Authors:YU Zhi-jian  LI Huan-jie  WANG Hai-sheng  LI Xin
Institution:1.Laboratory of Biochemical and Molecular Biology;Graduate School of Chinese Academy of Agricultural Sciences;Beijing 100081;China;2.Department of Biology;East China Institute of Technology;Fuzhou 344000;China
Abstract:The dsz promoter serial deletion fragments were cloned by PCR from strain Pseudomonas delafieldii R-8 which can convert dibenzothiophene into 2-hydroxybiphenyl and sulfate.Series fragments were cloned into the detection of expression vector pPR9TT,then reintroduced into strain R-8 to obtain engineering strains R-8-P,and the expression of reporter gene,LacZ,in R-8-P was determined.The results showed that the size of the dsz core promoter region was 300 bp,and regulation region was forecasted.
Keywords:Pseudomonas delafieldii R-8  desulfurization gene  promoter  pPR9TT  
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