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首页> 外文期刊>Applied Biochemistry and Biotechnology >Expression of Cu, Zn-superoxide dismutase gene from Saccharomyces cerevisiae in Pichia pastoris and its resistance to oxidative stress
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Expression of Cu, Zn-superoxide dismutase gene from Saccharomyces cerevisiae in Pichia pastoris and its resistance to oxidative stress

机译:酿酒酵母中铜,锌超氧化物歧化酶基因在毕赤酵母中的表达及其抗氧化性

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摘要

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.
机译:克隆,表征和酿酒酵母中的铜,锌超氧化物歧化酶(SOD)的基因,在甲基营养型毕赤酵母中过表达。获得的sod基因序列为465bp,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。用限制酶SacI消化的线性化的pAB22 DNA被转化到酵母巴斯德毕赤酵母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。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,这种相对简单的纯化方法产生了一条条带。超表达的SOD蛋白显示具有免疫生物学活性,并具有酶促活性。过表达Cu,Zn-SOD的酵母似乎对氧化应激(如百草枯,甲萘醌和热休克)更具抵抗力。

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