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减蛋综合征病毒纤维蛋白和六邻体蛋白可溶性表达条件的优化

李嘉宁 高张珊 张美华 黄茜 宋素泉 闫丽萍 刘建柱

动物医学进展2026,Vol.47Issue(8):34-43,10.
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动物医学进展2026,Vol.47Issue(8):34-43,10.

减蛋综合征病毒纤维蛋白和六邻体蛋白可溶性表达条件的优化

Optimisation of Conditions for Soluble Expression of Egg Drop Syndrome Virus Fiber and Hexon Proteins

李嘉宁 1高张珊 2张美华 2黄茜 2宋素泉 2闫丽萍 2刘建柱1

作者信息

  • 1. 山东农业大学动物医学院,山东泰安 271018
  • 2. 南京农业大学动物医学院,江苏南京 210095
  • 折叠

摘要

Abstract

To achieve soluble prokaryotic expression of Fiber,Penton and Hexon proteins of Egg Drop Syn-drome Virus(EDSV)strain AV127,the genes encoding these proteins were cloned into the multiple clo-ning site of the prokaryotic expression vector pET-32a(+),generating recombinant plasmids pET-32a(+)-Fiber,pET-32a(+)-Hexon,and pET-32a(+)-Penton.Then,these three recombinant plasmids were transformed into Rosetta(DE3)for induction expression,and the soluble expression conditions of Fiber and Hexon proteins were further optimized to achieve the maximum soluble expression level.The SDS-PAGE i-dentification results showed that Penton protein had the highest soluble expression level,accounting for 95.30%of the total bacterial protein.Hexon protein increased its soluble expression level from 63.29%to 83.73%by optimizing the concentration of IPTG.For Fiber protein,by optimizing the expression vector,in-duction temperature,time,and expression strain,the soluble expression level was increased from 28.54%to 75.04%,achieving the maximum soluble expression of Fiber,Penton,and Hexon proteins.This study suc-cessfully established an efficient expression system for the major structural protein of EDSV,laid a solid foundation for subsequent protein purification and functional studies,and also had important reference val-ue for the prokaryotic expression of other viral structural proteins.

关键词

减蛋综合征病毒/六邻体蛋白/五邻体蛋白/纤维蛋白/可溶性表达

Key words

Egg drop syndrome virus/Fiber protein/Penton protein/Hexon protein/Soluble expression

分类

农业科技

引用本文复制引用

李嘉宁,高张珊,张美华,黄茜,宋素泉,闫丽萍,刘建柱..减蛋综合征病毒纤维蛋白和六邻体蛋白可溶性表达条件的优化[J].动物医学进展,2026,47(8):34-43,10.

基金项目

国家自然基金面上项目(32272994) (32272994)

国家重点研发子课题(2022YFC2601600) (2022YFC2601600)

动物医学进展

1007-5038

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