Li Jian-Rong, Yu Ping
College of Food Science, Biotechnology and Environmental Engineering, Zhejiang Gongshang University, Hangzhou, 310035, People's Republic of China.
Appl Biochem Biotechnol. 2007 Jan;136(1):127-39. doi: 10.1007/BF02685943.
The gene for the Cu, Zn-superoxide dismutase (SOD) from the yeast Saccharomyces cerevisiae was cloned, characterized, and overexpressed in the methylotrophic Pichia pastoris. The sod gene sequence obtained is 465 bp and encodes 154 amino acid residues. The sod gene sequence was cloned into the pPIC9K vector, yielding pAB22. The linearized pAB22 DNA, digested with restriction enzyme SacI, was transformed into the genome of the GS115 strain of the yeast P. pastoris. The SOD was purified from the cultured yeast by ammonium sulfate precipitation and DEAE-cellulose column chromatography. This relatively simple purification method produced a single band on analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The overexpressed SOD protein was shown to have immunologically biologic activity and to be enzymatically active. The yeast overexpressing Cu, Zn- SOD appeared to be more resistant to oxidative stress such as paraquat, menadione, and heat shock.
克隆、鉴定了来自酿酒酵母的铜锌超氧化物歧化酶(SOD)基因,并在甲基营养型巴斯德毕赤酵母中进行了过量表达。获得的sod基因序列为465 bp,编码154个氨基酸残基。将sod基因序列克隆到pPIC9K载体中,得到pAB22。用限制性内切酶SacI消化线性化的pAB22 DNA,将其转化到巴斯德毕赤酵母GS115菌株的基因组中。通过硫酸铵沉淀和DEAE-纤维素柱色谱法从培养的酵母中纯化SOD。这种相对简单的纯化方法在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析中产生了一条单一的条带。过量表达的SOD蛋白显示具有免疫生物学活性和酶活性。过量表达铜锌SOD的酵母似乎对百草枯、甲萘醌和热休克等氧化应激更具抗性。