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作 者:程鹏[1] 张佃波[1] 王海防[1] 公茂庆[1]
机构地区:[1]山东省寄生虫病防治研究所,山东济宁272033
出 处:《实用医技杂志》2007年第20期2707-2708,共2页Journal of Practical Medical Techniques
摘 要:目的:构建弓形虫p30—Rop2复合基因大肠杆菌/分枝杆菌穿梭表达质粒。方法:利用PCR技术从已构建的pET30-p30-Rop2质粒扩增p30-Rop2复合基因片段,亚克隆于大肠杆菌/分枝杆菌穿梭质粒pSTM3,构建重组质粒pSTM3-p30-Rop2,并进行双酶切鉴定和测序分析。结果:成功构建pSTM3-p30-Rop2重组穿梭表达载体,测序结果发现有一个碱基发生突变,但没有改变开放阅读框。结论:pSTM3-p30—Rop2穿梭质粒的成功构建为弓形虫分枝杆菌疫苗的研制提供了前提条件。Objective To construct recombinant Escherichia coli/Mycobacterium shuttle plasmid pSTM3-p30-Rop2 of Toxoplasma gondii. Methods p30-Rop2 compound gene was amplified from pET30-p30-Rop2 and subcloned into the shuttle plasmid pSTM3 to attain a recombinant plasmid pSTM3-p30-Rop2. Results p30-Rop2 compound gene was subcloned into pSTM3 correctly identified by digestion . There was a mutation analyzed by sequencing but did not change the open reading frame. Conclusion The recombinant M. S-pSTM3-p30-Rop2 is constructed successfully which lay a foundation to the construct of new vaccine of Toxoplasma gondii.
关 键 词:弓形虫 p30-Rop2复合基因 穿梭表达载体
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