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High-level expression of the ORF6 gene of porcine reproductive and respiratory syndrome virus (PRRSV) in Pichia pastoris.

机译:猪繁殖与呼吸综合征病毒(PRRSV)ORF6基因在巴斯德毕赤酵母中的高水平表达。

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摘要

High-level expression of the ORF6 gene of porcine reproductive and respiratory syndrome virus (PRRSV) has been proved very difficult. In this work, we cloned and sequenced the ORF6 gene of PRRSV and found that it could not be expressed in Pichia pastoris strain GS115. Then, the ORF6 gene was modified and synthesized based on the codon bias, poly (A) signal of yeast expression system and secondary structure of 5'-end mRNA of foreign gene. The modified gene was inserted into the yeast expression vector pPICZalphaA, induced and expressed by the same methods. The recombinant protein with a molecular mass of approximately 23 kDa was screened by SDS-PAGE and identified by Western blot with convalescent sera of animals infected with CH-1a strain of PRRSV. The results indicated that it was similar to the native protein. The expression level of the recombinant protein could attain 2.0 g/L. In the meanwhile, the optimal conditions for expression were determined. It provides an additional means for studying the structural and functional characteristics of PRRSV ORF6 gene.
机译:猪繁殖与呼吸综合征病毒(PRRSV)的ORF6基因的高水平表达已被证明是非常困难的。在这项工作中,我们克隆并测序了PRRSV的ORF6基因,发现它不能在巴斯德毕赤酵母GS115中表达。然后,基于密码子偏倚,酵母表达系统的poly(A)信号和外源基因5'-端mRNA的二级结构,对ORF6基因进行了修饰和合成。将修饰的基因插入酵母表达载体pPICZalphaA,通过相同方法诱导和表达。通过SDS-PAGE筛选分子量约为23kDa的重组蛋白,并通过蛋白质印迹法用感染PRRSV的CH-1a株的动物的恢复期血清进行鉴定。结果表明它与天然蛋白相似。重组蛋白的表达水平可以达到2.0 g / L。同时,确定了表达的最佳条件。它为研究PRRSV ORF6基因的结构和功能特性提供了其他手段。

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