摘要:为研究和缓艾美尔球虫(Eimeria mitis)的1A蛋白基因的免疫原性,根据GenBank中1A蛋白基因序列设计1对特异性引物,采用RT-PCR技术扩增出和缓艾美尔球虫的1A蛋白基因,并将其与原核表达载体pSmart-I连接,构建原核表达载体pSmart-I-1A,然后转化入大肠杆菌BL21中,IPTG诱导表达,经SDS-PAGE 鉴定表达产物。结果显示,成功克隆出了和缓艾美耳球虫的1A蛋白基因,构建的重组原核表达质粒经双酶切及测序鉴定结果正确。IPTG诱导后,1A蛋白分子质量单位约为44.9kD,蛋白在菌体上清和沉淀中均有存在,主要存在于上清中。并进一步对其免疫原性进行了分析,为1A蛋白的免疫保护性研究提供了基础。 26599 毕业论文关键词:和缓艾美尔球虫;1A蛋白基因;原核表达
Cloning and expression of the 1A protein genes of Eimeria mitis
Abstract:Studying the immunogenicity of 1A protein gene of Eimeria mitis, a pairs of specific primers were designed by the sequence of 1A protein gene in GenBank. 1A gene of Eimeria mitis amplified using RT-PCR technology, and constructed the expression vector pSmart-I-1A, then transformed into E. coli BL21, induced expression by IPTG,identified by SDS-PAGE. The results showed that the 1A protein gene of Eimeria mitis was successfully cloned, and the sequence and vector were verified correctly by double restriction enzyme digestion, sequence analysis. After IPTG induction, the molecular weight unit of 1A protein was about 44.9kD, the protein existed in supernatant and precipitation, mainly in supernatant. The immunogenicity of the 1A protein was further analyzed, which provided the basis for the study of the immune protection of the 1A protein.
Key words: Eimeria mitis; 1A protein gene; prokaryotic expression
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