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棒状杆菌表达载体pJL23的构建
引用本文:陆军,唐炯,张文波,严维耀,郑兆鑫.棒状杆菌表达载体pJL23的构建[J].复旦学报(自然科学版),2000,39(3):292-296.
作者姓名:陆军  唐炯  张文波  严维耀  郑兆鑫
作者单位:1. 常熟高等专科学校生物系,常熟 215500
2. 生命科学学院,遗传工程国家重点实验室
摘    要:质粒pGA46-4带有从谷氨酸棒杆菌染色体上分离到的有启动功能的片段,用PCR技术从pGA46-4中扩增了该片段的关键区域;启动子PGL,将该启动子经EcoRⅠ-BamH Ⅰ双酶切后,与大肠杆菌质粒pJL01的EcoRⅠ-BamHⅠ大片段连接,再接入Xyl E gene和棒状杆菌质粒pXZ10142,构建成棒状杆菌-大肠杆菌穿梭表达载体pJL23。用邻苯二酚双加氧酶基因检测表明,该表达载体可在棒状

关 键 词:启动子  pXZ10142  pJL23  棒状杆菌  克隆表达载体
文章编号:0427-7104(2000)03-0292-05

Construction of a Expression Vector pJL23 in Corynebacteria
LU Jun,TANG Jiong,ZHANG Wen-bo,YAN Wei-yao,ZHENG Zhao-xin.Construction of a Expression Vector pJL23 in Corynebacteria[J].Journal of Fudan University(Natural Science),2000,39(3):292-296.
Authors:LU Jun  TANG Jiong  ZHANG Wen-bo  YAN Wei-yao  ZHENG Zhao-xin
Institution:LU Jun ,TANG Jiong ,ZHANG Wen-bo ,YAN Wei-yao ,ZHENG Zhao-xin (State Key Laboratory of Genetic Engineering, School of Life Sciences)
Abstract:Plasmid pGA46 4 contains a promoter function fragment isolated from the chromosome of Corynebacterium glutamicum . The essential part of this fragment promoter P GL is amplified from pGA46 4 by PCR. In order to construct a shuttle expression plasmid pJL23, this promoter was ligated with Escherichia coli plasmid pJL01, the Xyl E gene and the corynebacteria plasmid pXZ10142. According to the Catechol 2,3 dioxygenase expression results, the expression vector functions well in the expression of foreign genes in corynebacteria.
Keywords:promoter  PCR  Xyl  E gene  pXZ10142
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