|本期目录/Table of Contents|

[1]郭松林,王玉,冯建军,等.鳗鲡病原菌二联外膜蛋白基因工程表达载体的构建[J].集美大学学报(自然科学版),2014,19(5):330-338.
 GUO Song-lin,WANG Yu,FENG Jian-Jun,et al.Constrction of a Bivalent Expression Vector of Outer Membrane Protein of Two Pathogens Pathogenic to Eels[J].Journal of Jimei University,2014,19(5):330-338.
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鳗鲡病原菌二联外膜蛋白基因工程表达载体的构建()
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《集美大学学报(自然科学版)》[ISSN:1007-7405/CN:35-1186/N]

卷:
第19卷
期数:
2014年第5期
页码:
330-338
栏目:
水产、食品与生物工程
出版日期:
2014-09-25

文章信息/Info

Title:
Constrction of a Bivalent Expression Vector of Outer Membrane Protein of Two Pathogens Pathogenic to Eels
作者:
郭松林12王玉12冯建军12林鹏12
1.集美大学水产学院,福建 厦门 361021;2.鳗鲡现代产业技术教育部工程研究中心,福建 厦门 361021
Author(s):
GUO Song-lin12WANG Yu12FENG Jian-Jun12LIN Peng12
1.Fishery College,Jimei University,Jimei University,Xiamen 361021,China;2.Engineering Research Center of the Morden Industry Technology for Eel,Ministry of Education,Jimei University,Xiamen 361021,China
关键词:
嗜水气单胞菌迟钝爱德华氏菌鳗鲡二联外膜蛋白表达载体
Keywords:
Aeromonas hydrophilaEdwardsiella tardaeelbivalent outer membrane proteinexpression vector
分类号:
-
DOI:
-
文献标志码:
A
摘要:
根据鳗鲡病原性嗜水气单胞菌Ⅱ型孔蛋白(porinⅡ)和迟钝爱德华氏菌外膜蛋白S(ompS2)的基因全长序列,分别选取这两个全长序列中表达其蛋白质膜外部分且理论免疫原性较好的两个基因片段,通过融合PCR技术连接这两个外膜蛋白基因片段.根据表达载体(pGEX-2T-His)的限制性酶切位点在连接序列片段的两端引入限制性酶切位点BamHⅠ和EcoRⅠ,成功构建了双外膜蛋白基因片段重组表达载体(pGEX-2T-His-porinⅡ-ompS2).表达载体理论表达产物的蛋白质结构预测表明表达产物无信号肽和跨膜区,不存在三级结构;亲水性和免疫原性预测分析表明该表达蛋白理论上为可溶性蛋白并具有丰富的抗原决定簇,本研究为该表达载体的蛋白表达、纯化以及表达产物的免疫原性研究奠定了基础.
Abstract:
A fusion DNA that composed of fragments of two genes that,encoding outer region of the outer termembrane proteins which have good immunogenicity of Aeromonas hydrophila(porin Ⅱ) and Edwardsiella tarda(ompS2),were obtained by the “two-steps” fusion PCR.Cut sites of BamHⅠand EcoRⅠ were added at two 5’ end of two primers amplifying the fusion DNA respectively,The recombinant expression vector(pGEX-2T-His-porinⅡ-ompS2)expressing fused protein was constructed.Protein structure prediction showed that the fused protein(bivalent outer membrane protein) had no signal peptide,transmembrane region or three stage structure. Hydrophilic and immunogenicity analysis showed that the expressed fused protein is a soluble protein that is made up of many antigenic determinants.This study laid a foundation for the expression,purification and immunogenicity study of the protein expressed by the recombinant expression vector.

参考文献/References:

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备注/Memo

备注/Memo:
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更新日期/Last Update: 2014-12-04