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编码口蹄疫病毒VP1免疫活性肽基因片段的化学合成及克隆与表达

CLONING OF A GENE FRAGMENT CODING FOR THE IMMUNOGENIC DOMAIN OF VP1 OF FOOT AND MOUTH DISEASE VIRUS AND ITS EXPRESSION IN E. coli

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【作者】 郑兆鑫贺沛富严维耀王启松施文赵洪兴周智爱朱慈晖徐泉兴陈嘉棣李致勋施履吉

【Author】 Zheng Zhaoxin He Peifu Yan Weiyao Wang Qisong Shi Wen Zhao Hongxiug Zhou Zhiai Zhu Cihui Xu Quanxing Chen Jiali Li Zhixun Shi Luji Institute of Genetics, Fudan UniversityInstitute of Veterinary Science of Shanghai

【机构】 复旦大学遗传学研究所上海畜牧兽医研究所复旦大学遗传学研究所

【摘要】 口蹄疫病毒(FMDv)VP1蛋白质141~160位氨基酸的肽段,是免疫活性肽,含20个氨基酸,用DNA合成仪合成这段免疫活性肽基因片段,共72bp,5'端带有Eco RI切点,3'端带有BamHI切点,利用Eco RI和BamHI切点将兔疫活性肽基因片段克隆到带肴1ac启动子的基因表达载体pWR590质粒中,以O型FMDV抗体做为特异的IgG,检查FMDV抗原活性肽基因片段的表达,从210个菌落中选到有明显表达的菌株8株。

【Abstract】 The peptide corresponding to the 141-160 sequences of VP1 of foot and mouth disease virus is an immunogenic domain .It contains 20 amino acids. The gene fragment coding for this immunogenic peptide was chemically sy-thesized by DNA synthesizer. This fragment is 72bp long with Eco RI sites at the 5’ end and a Bam HI sites at the 3’ end.The synthetic nucleotide fragment was inserted into plasmid pWR590 which is an expression vector with lac promoter. Identification of the gene product was carried oat by using the antibody of O type of foot and mouth disease virus. 8 clones from 210 transformants were positive. The expressed product formed a fusion protein with β-galactosidase.

  • 【文献出处】 病毒学报 ,Chinese Journal of Virology , 编辑部邮箱 ,1989年01期
  • 【被引频次】11
  • 【下载频次】47
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