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作 者:梁爱华[1] 苏智广[1] 李晓玲[1] 王伟[1]
机构地区:[1]山西大学生物工程实验室
出 处:《中国生物化学与分子生物学报》1999年第2期205-210,共6页Chinese Journal of Biochemistry and Molecular Biology
基 金:国家自然科学基金;山西省自然科学基金
摘 要:以山西风陵渡东亚钳蝎(ButhusmartensiKarsch)的尾腺总RNA为模板,根据已知的蝎神经毒素保守氨基酸序列设计引物,利用PCR技术,扩增并克隆了两个蝎神经毒素基因.序列分析表明,由两个基因导出的氨基酸序列(BmKMm1和BmKMm2)与已知的蝎神经毒素BmKⅠ、BmKⅡ、BmKⅢ、BmKM1、BmKM9有很高的同源性.将BmKMm2基因重组到大肠杆菌分泌型表达载体pExSec1中进行表达.SDS-PAGE证明表达产物被分泌到细胞周间质及培养液中.The total RNA was isolated from the venom gland of scorpion Buthus martensii Karsch.According to the reported amino acid sequences of the scorpion neurotoxins BmKⅠ,BmKⅡ,two primers were designed and synthesized.By means of RT PCR one PCR fragment was obtained.The PCR products were cloned into pGEM T vector.Four clones were sequenced.Analysis of the nucleotide sequences showed that they belonged to two genes encoding the anti mammalian neurotoxins (named BmK Mm1 and Bmk Mm2).The deduced amino acid sequences shared a high homology with the known sequences of the anti mammalian neurotoxins BmKⅠ,BmKⅡ,BmKⅢ,BmKM1 and BmKM9.To express the BmKMm2 gene in Escherichia coli a novel expression secretion vector ,pExSec1,had been chosen.This vector contained a strong and tightly regulated T7 promoter.Translation started at the protein A leader sequence followed by the synthetic IgG binding domains (ZZ sequence) of protein A.The BmKMm2 gene was inserted into the multiple cloning site in the correct reading frame.The produced fusion protein ZZ BmK Mm2 was secreted into the culture medium of the host cell.It was isolated by affinity chromatography on IgG Sepharose.The biological activity of the fusion protein was tested on mice.
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