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| 鹅副粘病毒NP基因的原核表达及表达产物抗原性检测 | |
| 引用本文： | 杨玉菊,王君伟,李曦,杨志,何海娟.鹅副粘病毒NP基因的原核表达及表达产物抗原性检测[J].中国兽医杂志,2005,41(12):3-6. |
| 作者姓名： | 杨玉菊 王君伟 李曦 杨志 何海娟 |
| 作者单位： | 1. 哈尔滨学院生化学院,黑龙江,哈尔滨,150086 2. 东北农业大学动物医学院,黑龙江,哈尔滨,150030 3. 中国农业科学院哈尔滨兽医研究所,黑龙江,哈尔滨,150001 |
| 基金项目： | 黑龙江省“十五“攻关课题（GB01B503-02） |
| 摘 要： | 根据GenBank中发表的GPMVSF02株的NP基因的核苷酸序列设计合成一对引物，通过RT-PCR扩增JS／1／97／Go株的NP基因，将其克隆人pMDl8-T载体，序列测定和分析表明：所扩增的NP基因的核苷酸长为1470bp，共编码490个氨基酸。再将NP基因定向亚克隆至原核表达载体pGEX-6P的多克隆位点，经酶切鉴定后将含有NP基因的阳性亚克隆重组质粒转化到大肠杆菌BL21中，用诱导荆IPTG分别以不同的浓度进行诱导，并在不同的诱导时间进行采样，样品经处理后通过SDS-PAGE、Westernblot和Dot-ELISA进行分析。结果显示：以终浓度为1mmol／LIPTG进行诱导4h表达可达到高峰。表达的融合蛋白大小约为80kD，并具有良好的抗原性。 |
| 关 键 词： | 鹅副粘病毒 NP基因 克隆 原核表达 抗原性检测 |
| 文章编号： | 0529-6005（2005）12-0003-04 |
| 收稿时间： | 2004-10-28 |
| 修稿时间： | 2004年10月28 |
Prokaryotic expression of NP gene from goose paramyxovirus and detection of antigenicity of the expressed product |
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| YANG Yu-ju,WANG Jun-wei,LI Xi,YANG Zhi,HE Hai-juan.Prokaryotic expression of NP gene from goose paramyxovirus and detection of antigenicity of the expressed product[J].Chinese Journal of Veterinary Medicine,2005,41(12):3-6. | |
| Authors: | YANG Yu-ju WANG Jun-wei LI Xi YANG Zhi HE Hai-juan |
| Institution: | Department of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, China |
| Abstract: | According to the sequence of NP gene of goose paramyxovirus (GPMV) SF02 isolate strain which published on Genebank, A pair of primers was designed and synthesized, The NP gene of JS/1/97/Go strain was amplified by means of RT-PCR and cloned into pMD18-T vector, The positive recombinant clone was characterized by enzyme digestion and was sequenced. The sequence analysis showed that NP gene consisted of 1 470 bp nucleotides and encoded 490 amino acids. The NP gene of JS/1/97/Go strain was subcloned into prokaryotic expression vector pGEX-6P, The recombinant plasmid carrying NP gene was characterized by enzyme analysis, The positive recombinant plasmid was then transformed into E.coli. BL21strain, Samples were collected at different induction time and different concentration after induced by IPTG. The specificity of the expressed protein was identified with SDS-PAGE, Western-blot and Dot-ELISA. The result shows: The optimal amount of expressed protein is induced with IPTG at 1 mmol/L concentration for 4 hours. The fusion protein is about 80 kD in size. and has very good antigenicity. |
| Keywords: | goose paramyxovirus NP gene cloning prokaryotic expression detection of antigenicity |
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