Cloning and Expression of 34kDa Protein Gene of Mycobacterium paratuberculosis in Escherichia coli
The gene encoding 34kDa protein gene from Mycobacterium paratuberculosis C-2, chromosomal DNA was amplified by using polymerase chain reaction (PCR), the PCR product was approximately 897bp DNA segment. The PCR product was cloned into pGEM-T vector and the cloning plasmid pGEM-T-34 was constructed successfully. The purified 34kDa protein gene was subcloned into the expression vector pET28a(+), and the prokaryotic expression Plasmid pET28a-34 was constructed. Plasmid containing pET28a-34 was transformed into competence Escherichia coli BL21 (DE3). The bacterium was induced by isopropyl-β-D-thiogalactopyranoside (IPTG) and its lysates were loaded directly onto sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), approximately 37kDa exogenous protein was observed on the SDS-PAGE. The protein was analyzed by using Western-blotting. The results indicated that the protein was of antigenic reactivity of M. paratuberculosis. The results were expected to lay foundation for further studies on the subunit vaccine, DNA vaccine and diagnostic reagents of 34kDa protein gene in their prevention against bovine paratuberculosis.
Xiu-Yun Jiang Chun-Fang Wang Fan-Li Zeng Yu-Qing Hu Xin-Yu Liu Hao-Ran Ning Zhao-Yang He
College of Life Sciences Jilin Agricultural University Changchun,China Animal Science College Jilin Agricultural University Changchun,China
国际会议
成都
英文
1-4
2010-06-18（万方平台首次上网日期，不代表论文的发表时间）