幽门螺杆菌尿素酶B亚单位基因工程菌发酵工艺的研究  

Fermentable Study on the Gene Engineering E.coli of Helicobacter pylori Urease B

作　　者：曾浩[1] 邹全明[1] 张卫军[1] 鲁东水[1] 

机构地区：[1]第三军医大学临床微生物及免疫学教研室,重庆400038

出　　处：《微生物学杂志》2004年第5期20-22,共3页Journal of Microbiology

基　　金：国家 8 63计划资助课题 (No .2 0 0 1AA2 15 161);国家"九五"重点科技攻关项目 ( 96-90 1-0 1-5 4)

摘　　要：通过不同培养基、不同葡萄糖浓度、不同溶氧条件、补料与非补料对幽门螺杆菌尿素酶B亚单位(UreB)基因工程菌的菌体生长与外源蛋白表达量的影响的比较 ,建立了稳定、适宜的幽门螺杆菌尿素酶B亚单位基因工程菌发酵工艺。多批实验结果证明 ,菌体单产可达 86 g/L ,目的蛋白的表达率为 38.2 %。To investigate fermentation conditions of gene engineering E.coli strain for expression of Helicobacter pylori urease B, the influences of different kinds of media, the range of pH, induction time, glucose concentration and the fed batch on the growth of gene engineering E.coli strain and expression of UreB were compared, and, on the basis of this, the optimal fermentation conditions were studied. Under the optimal fermentation conditions, the cell output and expression rate of UreB reached 86 g/L and 38.2 % respectively.;

关 键 词：幽门螺杆菌 尿素酶B亚单位 大肠杆菌 发酵 

分 类 号：R379.9[医药卫生—病原生物学]