期刊文献+

设计表达兔防御素基因NP1

Design and Expression of Rabbit Gene Defensin NP1
下载PDF
导出
摘要 利用计算机软件对在将大肠杆菌中表达的兔防御素NP -1基因进行分析。消除宿主菌不表达或低效表达的密码子。同时对NP -1基因与质粒 pGEX -4T -1中融合基因GST进行RNA二级结构预测 ,通过对RNA二级结构进行分析 ,消除可能影响基因表达的二级结构 ,设计了有利于今后对目的基因的表达的兔防御素基因 ,并在大肠杆菌高效表达。结果表明 :合成基因可以在大肠杆菌中高效表达。 The rabbit defensin NP-1 gene which will be expressed in E.coli was analyzed by software.The codon with little no expression(was eliminated).At the same time,the RNA and TIR secondary structure of GST gene and GST-defensin fusion gene in pGEX-4t-1 vector was pridicted,and the secondary structure which will affect the expression was eliminated.
作者 徐文生 许杨
出处 《江西农业大学学报》 CAS CSCD 2003年第3期418-422,共5页 Acta Agriculturae Universitatis Jiangxiensis
关键词 兔防御素基因NPl 融合基因 质粒 pGEx表达 secondary structure fuse gene vector pGEX expression
  • 相关文献

参考文献16

  • 1Nagpal S, Gupta V, Kaur K J, ct al. Structure- function analysis of tritrypticin, an antibacterial peptide of innate immune origin[J]. J Biol Chem, 1999, 274(33) :23 296 -23 304.
  • 2Bikshapathy E, Sitaram N, Nagaraj R. Addition and omission analogs of the 13 -residue antibacterial and hemolytic peptide PKLLKTFLSKWIG: structural preferences, model membrane binding and biological activities[ J]. J Pept Res, 1999, 53 (1) :47 -55.
  • 3Olins P O, Lee S C. Recent advances in heterologous gene expression in Escherichia coli[ J]. Current Opinion in Biotechnology, 1993,4:520 - 525.
  • 4Barrick D, Villanueba K, Childs J, et al. Quantitative analysis of ribosome binding sites in E. coil[ J]. Nucleic Acids Res, 1994,22 1 287- 1 295.
  • 5Chen H, Bjerknes M. Kumar R, et al. Determination of the optiomal aligned spacing between the Shine - Dalgarno sequence and the traslation initiation codon of Escherichia coll. mRNAs[ J]. Nucleic Acids Res, 1994,22:4 953 -4 957.
  • 6Gurevieh A I, Esipov R S, Kachalina T A, et al. Relation between the level of E. coli gene expression and the structure of translation initiation region (TIR). Ⅲ. Sites of complementary interaction of TIR with 16S rRNA[ J]. Bioorg Khim, 1997, 23 ( 11 ) : 888 - 894.
  • 7Helke A, Geisen R M,Vollmer M, et al. An unstructured mRNA region and a 5'hairpin represent important elements of the E. coli translation initiation signal determined by using the bacteriophage T7 gene 1 translation start site[ J]. Nucleic Acids Res, 1993, 21(24) :5 705 -5 711.
  • 8Rex G, Surin B, Besse G, et al. The mechanism of translational coupling in Escherichia coli. higher order structure in the atpHA mRNA acts as a conformational switch regulating the access of de novo initiating ribosomes[ J]. J Biol Chem, 1994, 269(27):18 118- 18 127.
  • 9Kamath - Loeb A s, Gross C a. Translational regulation of σ32 synthesis: requirement for an internal control element. J Bacteriol, 1991,173:3 904 - 3 906.
  • 10Nagai H, Yuzawa H, Yura Ti. Interplay of two cis - acting mRNA region in translational control of σ^32 synthesis during the heat shock response of Escherichia coli[ J ]. Proc Natl Acad Sci ( USA ), 1991,88 : 10 515 - 10 519.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部