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作 者:何诚[1] 唐辉滨[1] 田昱[1] 宋后燕[1] 朱运松[1]
机构地区:[1]上海医科大学分子遗传学研究室
出 处:《中国生物化学与分子生物学报》1998年第5期547-552,共6页Chinese Journal of Biochemistry and Molecular Biology
摘 要:将编码379个氨基酸残基的PAI-1cDNA插入到含AOX1启动子和PHO1分泌信号肽序列的甲醇营养型酵母载体中,构建成表达质粒pYIS-1.表达质粒转化P.pastoris甲醇营养型酵母细胞,筛选His+Mut-表型的转化子,经低密度摇瓶培养,1%甲醇诱导表达7d后,培液经SDS-PAGE分析,PAI-1生物活性测定和Westernblot证实表达出分子量为43~51kD的4条PAI-1条带.表达的PAI-1能有效地分泌到培液中,占培液总蛋白的26%左右,达4mg/L培液;其比活性为1.16×104AU/mg.By inserting PAI 1 cDNA coding 379 amino acid residues into the methylotrophic yeast expression vector pHIL S1 containing AOX1 promotor and the sequences of PHO1 secreting signal peptides,the expression plasmid pYIS 1 was constructed and then transformed into P.pastoris GS115.The His + Mut - transformants were selected and fermentated in flasks with low density.After 7 days of 1% methanol induction,the expression media were analyzed and the expressed protein was verified to be recombinant human PAI 1(rh PAI 1) in different molecular weights of 43—51 kD by SDS PAGE,bioactivity and Western blot detection.The expressed rhPAI 1 could be effectively secreted into media,and its highest quantity was estimated to be 26% of total proteins or 4 mg/L in media.The specific activity of rhPAI 1 was 1.16×10 4 AU/mg.The non homogeneity of M r of expressed rhPAI 1 may be related to the length of its oligosaccharide chains.The PAI 1 expressed in P.pastoris was very helpful to further study its structure and physiological function.
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