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刘玉江, 戴佳琳, 黄江, 王宇. 猪带绦虫成虫EF-1基因生物信息分析及原核表达[J]. 中国公共卫生, 2011, 27(1): 83-84. DOI: 10.11847/zgggws2011-27-01-40
引用本文: 刘玉江, 戴佳琳, 黄江, 王宇. 猪带绦虫成虫EF-1基因生物信息分析及原核表达[J]. 中国公共卫生, 2011, 27(1): 83-84. DOI: 10.11847/zgggws2011-27-01-40
LIU Yu-jiang, DAI Jia-lin, HUANG Jiang, . Bioinformatics analysis of function and prokaryotic expression of elongation factor-1 in Taenia. solium[J]. Chinese Journal of Public Health, 2011, 27(1): 83-84. DOI: 10.11847/zgggws2011-27-01-40
Citation: LIU Yu-jiang, DAI Jia-lin, HUANG Jiang, . Bioinformatics analysis of function and prokaryotic expression of elongation factor-1 in Taenia. solium[J]. Chinese Journal of Public Health, 2011, 27(1): 83-84. DOI: 10.11847/zgggws2011-27-01-40

猪带绦虫成虫EF-1基因生物信息分析及原核表达

Bioinformatics analysis of function and prokaryotic expression of elongation factor-1 in Taenia. solium

  • 摘要: 目的 分析和预测猪带绦虫成虫延伸因子(elongation factor-1,EF-1)基因及其编码蛋白的结构域特性,并进行原核表达.方法 利用在线生物信息学网站及工具进行序列分析、预测其编码的延伸因子的理化特性、抗原表位、翻译后的修饰、功能域、亚细胞定位、拓扑结构、二级结构、三维空间构象等,将其编码区序列克隆岛原核表达载体pET-28 a(+)上,测序鉴定重组质粒.结果 该基因全长1 657 bp,编码区为186~1 533 bp,编码448个氨基酸,为全长基因;无跨膜区,具有多个磷酸化位点,蛋白的理化性质稳定,理论分子量为49 011.5 Da;没有质体、线粒体定位序列;十二烷基-聚丙烯酰胺凝胶电泳(SDS-PAGE)结果表明,目的基因在大肠埃希菌BL21~DE3中表达成功.结论 发现猪带绦虫成虫延伸因子基因,成功构建重组原核表达质粒.

     

    Abstract: Objective To analyze and predict structural charac teristics of elongation factor1 in Teania.solium with bio informatics and to detectits prokaryotic expression.Methods Byonline analysis with bioinformatics websites and soft ware package, the physical chemical charac teristics, modification sites after translation, domains, subcelluar location,topological structure, second structure, and 3D structure of elong ation factor 1(EF1) were ana lyzed.The EF1 gene was inserted in to the prokaryotic expression vector pET 28a(+) and then was am plified with PCR and sequenced.Results Anovel cDNA sequence EF1 with 1657 pbcoding 488 aminoacids and a molecular weight of 49011.5 was identified.PCR,double enzyme digestion and DNA sequencing indicated that pET 28a(+) and EF 1 recom binant plasmid were succe ssfully constructed.Sodium dodecyl sulfate poly aery lamide gelelectrophoresis(SDS PAG E) results showed that the gene was expressed in E scherichia coli BL21/DE3.Conclusion A novelgene of Taenia.solium is successfully identified and expressed with prokaryotic vector.

     

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