一种多拷贝毕赤酵母表达载体的构建及人脑源性神经营养因子的表达

利用PCR技术扩增出pPIC9K载体的HIS4 Kan序列片段 ,与pPICZα重组 ,构建结合了两个载体特点的适合体外构建多拷贝基因表达盒的毕赤酵母表达载体pPICZα1,改造后的载体含HIS4 Kan序列 ,能整合到酵母染色体上 ,具有筛选方便、外源基因多拷贝组建迅速、蛋白产物分泌表达和易纯化等优点。将人脑源性神经营养因子(hBDNF)的cDNA(35 7bp)克隆入载体pPICZα1,利用同尾酶BglⅡ、BamHⅠ不可逆连接方式 ,分别构建含有 1、2、3、6个拷贝hBDNF表达盒的重组表达载体 ,电击法转化毕赤酵母GS115菌株 ,用G4 18和Zeocin筛选转化子 ,筛选到的阳性转化子用 0 5 %甲醇诱导 ,获得分泌型表达。表达产物类似于天然神经营养因子单体大小、分子量约 14kD。多拷贝hBDNF表达盒的表达水平亦高于单拷贝hBDNF表达盒 ,ELISA和Westernblot检测表明 :表达的蛋白能与鸡抗人脑源性神经营养因子抗体特异结合 ,证实该表达蛋白具有hBDNF的免疫原性

Construction of a multi-copy Pichia expression vector and expression of human brain-derived neurotrophic factor in Pichia pastoris

A pPICZ alpha1 vector was reconstructed with pPICZ alpha vector and PCR product of His4-Kan sequence from pPIC9K vector. The sequence encoding human brain-derived neurotrophic factor (hBDNF) was inserted into pPICZ alpha1. The expression vectors carrying 1, 2, 3, 6 copies of expression cassettes were constructed and transformed into Pichia pastoris GS115 respectively. The transformants were screened with G418/Zeocin and induced by 0.5% methanol, and the results of SDS-PAGE confirmed that the expression protein was about 14 kD and the percentage of the protein was about 20% of the total secreted protein. ELISA and Western blot analysis demonstrated that the protein could be specifically combined with chicken antibodies to human-BDNF.