首页 | 本学科首页   官方微博 | 高级检索  
     

腐蹄病节瘤拟杆菌纤毛蛋白与绵羊白细胞介素-2融合基因表达载体的构建及表达
引用本文:王克坚,Om Dhungyel,余兴龙,冯书章,赵宝华,J R Egerton,朱平,殷震. 腐蹄病节瘤拟杆菌纤毛蛋白与绵羊白细胞介素-2融合基因表达载体的构建及表达[J]. 中国兽医学报, 2002, 22(2): 131-133
作者姓名:王克坚  Om Dhungyel  余兴龙  冯书章  赵宝华  J R Egerton  朱平  殷震
作者单位:1. 中国农业科学院吉林特产研究所,吉林,吉林市,132109
2. 澳大利亚悉尼大学
3. 解放军军需大学军事兽医研究所,吉林,长春,130062
基金项目:国家“九五”科技攻关项目 ( 96 -0 0 5 -0 2 -0 3-0 9),国家科技部科研院所技术开发研究专项资金项目
摘    要:

关 键 词:腐蹄病  节瘤拟杆菌  纤毛蛋白基因  绵羊白细胞介素2基因
文章编号:1005-4545(2002)02-0131-03
修稿时间:2000-10-06

Construction of a Plasmid pmPili IL-2 Expressing a Fusion Construct of D.no dosus Pili Gene and Ovine IL-2 Gene
Om Dhungyel,J R Egerton. Construction of a Plasmid pmPili IL-2 Expressing a Fusion Construct of D.no dosus Pili Gene and Ovine IL-2 Gene[J]. Chinese Journal of Veterinary Science, 2002, 22(2): 131-133
Authors:Om Dhungyel  J R Egerton
Abstract:A fusion expression plasmid was constructed by inserting the ovine IL-2 gene into PME290-Pili in the Pili gene at downstream 619 bp.The plasmid harbouring ovine IL-2 sequence was designated pmPili IL-2.The fusion protein was expressed by transforming the pmPili IL-2 into the competent host cell BL-21(DE3).Specific reaction between PiliIL-2 fusion protein and the antiserum of D.nodosus serotype E Pili was observed by cross electrophoresis.The molecular weight of the recombinant fusion protein was about 33 000 by SDS-PAGE and analyzed with thin layer.The recombinant Pili IL-2 fusion gene was expressed at higher level with about 5.49% of the total proteins of the transformant host cell BL-21(DE3).
Keywords:footrot  D.nodosus  Pili gene  OviIL-2 gene
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号