aprE基因表达的分子生物学和微量热法分析  

Analysis of aprE Gene Expression Employing Microcalorimetric Technique and Molecular Biological Method

作　　者：李美菊[1] 陈向东[1] 刘国生[1] 杨洋[1] 王小娟[1] 耿晶[1] 梅运军[1] 刘义[2] 沈萍[1] 王金晶[1] 

机构地区：[1]武汉大学生命科学学院 [2]化学与分子科学学院,武汉430072

出　　处：《化学学报》2005年第18期1646-1650,共5页Acta Chimica Sinica

基　　金：国家自然科学基金(Nos.30070010;20373051)资助项目.

摘　　要：利用分子生物学方法(SDS-PAGE和酶活检测法)未检测到所克隆的aprE基因在大肠杆菌中的表达产物(碱性蛋白酶),而微量热法检测结果发现:重组菌株的生长代谢产热曲线之间存在明显的差异.根据这些差异,分析了该基因的上、下游调控序列对该基因在大肠杆菌中表达的重要作用,从而进一步对该基因进行了亚克隆,得到了生物学方法可检测到的表达产物.由此推测,微量热技术有可能为检测外源基因表达及其调控,以及为指导进一步基因工程操作提供一种新的快速灵敏的技术和方法.The expression product of the cloned aprE in E. coli failed to be detected by general molecular biological methods including SDS-PAGE and protease activity determination. However, the results obtained by microcalorimetric technique showed that there were obvious differences among their metabolism heat-out curves. Further analysis suggested that both up-stream and down-stream regulation sequences of the aprE gene could be the key factor for the expression of this gene in E. coli. Based on the information achieved by the analysis of metabolism heat-out curves, the aprE gene segments were sub-cloned again in another plasmid vector with a stronger promoter, and the gene expression product could be detected by general molecular biological method. The results suggested that microcalorimetric technique be a novel, fast and sensitive method to detect the foreign gene expression and regulation, furthermore to provide some suggestions for genetic engineering.

关 键 词：大肠杆菌 aprE基因 微量热技术 基因表达 分子生物学方法 外源基因表达 微量热法 表达产物 碱性蛋白酶 检测法 

分 类 号：Q786[生物学—分子生物学]