Lin Jingwei, Jia Jia, Zhong Ming, Chen Lijing, Li Haoge, Guo Zhifu, Qi Mingfang, Liu Lixia, Li Tianlai
Sheng Wu Gong Cheng Xue Bao. 2014 Mar;30(3):464-71.
We transformed the fip-fve gene into Pichia pastoris GS115 for inducible and constitutive expression to obtain feasible bioactvie recombinant Fip-fve. The fip-fve gene was cloned from Flammulina velutipes fruting body by PCR and ligated to pPIC9 to construct inducible expression vector pPIC9-FIP-fve, and promotor pgap was used to replace the paox1 to construct constitutive expression vector pPIC9-PGAP-FIP-fve. These two vectors were used to transform P. pastoris by PEG method. The fip-fve was expressed after histamine-absence screening and yeast colony PCR. The inducible expression level reached 158.2 mg/L at the fourth day and the constitutive expression level was 46.3 mg/L and 29.5 mg/L using glucose and glycerol, respectively. The SDS-PAGE and Western blotting both proved the correctness of rFip-fve, and the hemagglutination test indicats the rFip-fve's bioactivity.
我们将fip - fve基因转化到毕赤酵母GS115中进行诱导型和组成型表达,以获得可行的具有生物活性的重组Fip - fve。通过PCR从金针菇子实体中克隆fip - fve基因,并连接到pPIC9上构建诱导型表达载体pPIC9 - FIP - fve,使用启动子pgap替换paox1构建组成型表达载体pPIC9 - PGAP - FIP - fve。通过PEG方法使用这两个载体转化毕赤酵母。经过无组胺筛选和酵母菌落PCR后,fip - fve得以表达。在第四天时,诱导型表达水平达到158.2 mg/L,使用葡萄糖和甘油时,组成型表达水平分别为46.3 mg/L和29.5 mg/L。SDS - PAGE和蛋白质免疫印迹均证明了rFip - fve的正确性,血凝试验表明了rFip - fve的生物活性。