首页 | 本学科首页   官方微博 | 高级检索  
     

酿酒酵母丙酮酸脱羧酶基因的克隆及表达
引用本文:蒋雅红,游松,任杰,谢兰漪. 酿酒酵母丙酮酸脱羧酶基因的克隆及表达[J]. 沈阳药科大学学报, 2002, 19(4): 291-293,307
作者姓名:蒋雅红  游松  任杰  谢兰漪
作者单位:1. 沈阳药科大学制药工程学院,辽宁,沈阳,110016
2. 沈阳大学生物与环境工程学院,辽宁,沈阳,110044
摘    要:目的酿酒酵母 (Saccharomycescerevisiae)丙酮酸脱羧酶 (PDC)基因的克隆和表达。方法利用PCR技术从酿酒酵母的总cDNA中钓取出PDCsc基因 ,构建其高效表达质粒 ,利用Ion和ompT蛋白酶缺陷株EscherichiacoliBL2 1 (DE3)进行表达。结果扩增出长约 1 7kb的PDCsc基因 ,成功构建其表达质粒pSC -2 2b ,对转化菌株的SDS -PAGE分析结果显示 :该基因获得高效表达 ,表达蛋白占细胞总蛋白的 1 8 6 %。结论成功构建高效表达PDCsc基因的工程菌株 ,为实现利用PDCsc进行的生物转化奠定基础

关 键 词:酿酒酵母  丙酮酸脱羧酶  克隆  高效表达
文章编号:1006-2858(2002)04-0291-03

Molecular cloning and expression of pyruvate decarboxylase cDNA from Saccharomyces cerevisiae
JIANG Ya-hong ,YOU Song ,REN Jie ,XIE Lan-yi. Molecular cloning and expression of pyruvate decarboxylase cDNA from Saccharomyces cerevisiae[J]. Journal of Shenyang Pharmaceutical University, 2002, 19(4): 291-293,307
Authors:JIANG Ya-hong   YOU Song   REN Jie   XIE Lan-yi
Affiliation:JIANG Ya-hong 1,YOU Song 1,REN Jie 1,XIE Lan-yi 2
Abstract:Objective To clone and express the pyruvate decarboxylase(PDCsc) from Saccharomyces cerevisiae.Methods To clone PDCsc gene from its cDNA mixture by PCR, construct its expressing plasmid and express its encoding protein by using the Ion and ompT protease deficient strain Escherichia coli BL21(DE3). Results PDCsc gene (ca. 1.7 kb) was obtained,and its expressing plasmid pSC-22b was successfully constructed. The SDS-PAGE result showed that the overexpression of PDCsc was achieved and the target protein reached 18.6% among the total soluble proteins in its host strain.Conclusions The engineering strain for overexpression PDCsc was successfully constructed, which set up a base for the biotransformation using PDCsc as a catalyst.
Keywords:Saccharomyces cerevisiae  pyruvate decarboxylase  clone  overexpression
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号