Huang Zhi-Qing, Hu Hong-Yu, Chen Xiao-Ling, Ren Li-Ming, Lin Ai-Xing, Chen Yong-Fu
National Laboratory for Agrobiotechnology, College of Biology Science, China Agricultural University, Beijing 100094, China.
Sheng Wu Gong Cheng Xue Bao. 2005 Sep;21(5):731-6.
The porcine interferon-gamma (PoIFN-gamma) gene, in which the sequence encoding signal peptide was replaced by that of the alpha-factor of Saccharomyces cerevisiae, was cloned into Pichia pastoris expression vector pPIC9K. The recombinant plasmid pPIC9K-alpha-PoIFN-gamma was then transformed into Pichia pastoris GS115 cells by electroporation and stable multicopy recombinant Pichia pastoris strains were selected by G418 resistance. Two recombinants of multiple inserts were obtained. SDS-PAGE and Western blot assays of culture broth from a methanol-induced expression strain demonstrated that recombinant PoIFN-gamma, 17kD and 23kD proteins, were secreted into the culture medium. Target proteins, 60% of total proteins, were obtained in the culture medium at the concentration of 108 mg/L. This is the first secreted expression of porcine interferon-gamma gene in Pichia pastoris.
将猪干扰素-γ(PoIFN-γ)基因中编码信号肽的序列替换为酿酒酵母α-因子的序列后,克隆至毕赤酵母表达载体pPIC9K中。然后通过电穿孔法将重组质粒pPIC9K-α-PoIFN-γ转化至毕赤酵母GS115细胞中,并通过G418抗性筛选出稳定的多拷贝重组毕赤酵母菌株。获得了两个多插入片段的重组体。对甲醇诱导表达菌株的培养液进行SDS-PAGE和Western blot分析表明,重组PoIFN-γ(17kD和23kD蛋白)分泌到了培养基中。在培养基中获得了占总蛋白60%的目标蛋白,浓度为108 mg/L。这是猪干扰素-γ基因在毕赤酵母中的首次分泌表达。