【摘要】 根据猪链球菌2型溶菌酶释放蛋白基因(mrp)的序列,设计并合成了1对特异性引物,以青海株的基因组DNA为模板扩增了mrp基因ORF1序列。将PCR产物进行了T/A克隆,转化大肠杆菌,鉴定成功获得目的片段后,将其定向亚克隆到pET-28a(+)中,构建了原核表达质粒pET-28a-mrp,并将其转化至大肠杆菌BL21感受态细胞中,经1 mmol/L IPTG诱导和SDS-PAGE分析,出现了与预期目的蛋白一致的外源蛋白带(27.0 ku)。Western-blot分析表明,该融合蛋白具有MRP的抗原表位。研究结果为今后开展该病的免疫学研究奠定了一定基础。更多还原

【Abstract】 The ORF1 sequence of gene mrp encoding muramidase-released protein(MRP) was amplified from genomic DNA of Streptococcus suis type 2 Qinghai strain by PCR with specific primers.The PCR product was cloned into pMD18-T vector and transformed into host strain Escherichia coli,and the plasmid of positive clone was extracted,digested with enzymes and purified.Then the fragment was sub-cloned into expression vector pET-28a(+) and the prokaryotic expression vector pET-28a-mrp was constructed.The recombinant plasmid was transformed into E.coli BL21 competent cells and then induced by 1 mmol/L IPTG.SDS-PAGE analysis revealed that a band of approximately 27.0 ku in molecular weight was expressed from the induced E.coli BL21 component cells.Western-blot analysis indicated that the protein possessed antigenic epitopes of MRP.The result provided foundation for immunological studies of MRP.更多还原