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Synthesis, cloning, and expression of Mycoplasma suis inorganic pyrophosphatase gene using PCR-based accurate synthesis and overlap-extension PCR, and its immunogenicity analysis.

机译:猪支原体无机焦磷酸酶基因的合成,克隆和表达基于PCR的精确合成和重叠延伸PCR及其免疫原性分析。

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摘要

Mycoplasma suis (M. suis), a hemotrophic pathogen of pigs, causes economic losses in swine production throughout the world. Inorganic pyrophosphatase (ppa) is a very important gene in M. suis. The ppa gene of M. suis was synthesized by PCR-based accurate synthesis (PAS) and overlapextension PCR, inserted into vector pMD18-T, and then subcloned to the prokaryotic expression vector pET28c.The recombinant plasmid pET28c_ppa was transformed to E. coli BL21 for expression under induction of isopropyl thiogalactoside. The expressed product was identified by SDS-PAGE and Western blot, which suggested that the recombinant protein has good antigenicity. Piglets were immunised with purified recombinant protein, and specific antibodies to the recombinant protein were detected in piglet serum. The results show that the ppa gene can be efficiently expressed in E. coli and that the expressed recombinant protein can elicit a specific serum antibody response in piglets. PAS and overlap-extension PCR were first used to synthesize the ppa of M. suis. They provide simple, rapid, reliable and relatively inexpensive methods to synthesize, clone, and express genes. The experiment conducted in this paper will enable future research into the role and function of the ppa gene
机译:猪支原体(猪支原体)是一种猪的营养病原体,在全世界范围内造成了猪生产的经济损失。无机焦磷酸酶(ppa)是猪链球菌中非常重要的基因。通过基于PCR的精确合成(PAS)和重叠延伸PCR合成猪链球菌的ppa基因,将其插入载体pMD18-T中,然后亚克隆到原核表达载体pET28c中,将重组质粒pET28c_ppa转化到大肠杆菌BL21中在异丙基硫代半乳糖苷的诱导下表达。通过SDS-PAGE和Western blot鉴定表达产物,表明重组蛋白具有良好的抗原性。用纯化的重组蛋白免疫仔猪,并在仔猪血清中检测到针对重组蛋白的特异性抗体。结果表明,ppa基因可以在大肠杆菌中有效表达,并且表达的重组蛋白可以在仔猪中引发特定的血清抗体反应。首先使用PAS和重叠延伸PCR合成猪莫拉氏杆菌的ppa。它们提供了简单,快速,可靠且相对便宜的方法来合成,克隆和表达基因。本文所进行的实验将使未来对ppa基因的作用和功能的研究成为可能。

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