摘要
目的从猪带绦虫六钩蚴总RNA中扩增45WB2基因,并在甲醇酵母分泌表达载体pPIC9K中获得高效表达。方法采用逆转录-聚合酶链反应(RT-PCR),从孵化激活的六钩蚴克隆获得459bp的基因,亚克隆至酵母分泌表达载体pPIC9K中,经测序验证读码框正确后,重组质粒电转化毕赤酵母SMD1168菌株。用PCR方法检测结果表明,目的基因整合进毕赤酵母染色体DNA中。重组菌株用1%甲醇诱导,分别取诱导72和96h的上清和沉淀进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质印迹(Westernblotting)分析。结果重组菌株在毕赤酵母中的表达蛋白分子量为Mr16000,表达产物占上清总蛋白量的32.8%,且能被猪囊尾蚴病患者血清识别。结论基因在毕赤酵母中成功表达,表达产物有望作为免疫原用于猪囊尾蚴病的免疫预防。
Objective To amplify and express the gene from Taenia solium oncosphere in Pichia pastoris system. Methods Total RNA was extracted from hatched and activated oncospheres. A 459bp specific fragment was amplified by RT-PCR. It was subcloned into the secreted expression vector pPIC9K, and identified by sequencing and then transformed into P. pastoris SMD1168 by electroporation. PCR analysis showed that 45WB2 was integrated into the genomic DNA of yeast. The recombinants were induced by 1% methanol and the culture supernatant was collected and tested by SDS-PAGE and Western blotting. Results 45WB2 gene was expressed successfully in P. pastoris and the product was recognized by human positive serum against cysticercosis. Conclusion The recombinant 45WB2 expressed in P. pastoris may be used to prevent pigs from the infection of Taenia solium.
出处
《中国寄生虫学与寄生虫病杂志》
CAS
CSCD
北大核心
2005年第3期171-174,共4页
Chinese Journal of Parasitology and Parasitic Diseases
基金
国家重大基础研究发展规划项目(No.G1999011906)~~
