期刊文献+

分子伴侣过量表达对蛋白质分泌及可溶性的影响 被引量:10

The Effect of Over-expression of Chaperones on the Secretion and the Solubility of Proteins*
下载PDF
导出
摘要 通过过量表达大肠杆菌分子伴侣 Sec B和 Gro EL,研究了它们对靶蛋白的分泌及可溶性的影响 .在过量表达 Sec B的宿主菌中 ,周质空间分泌蛋白总量较对照组提高了约 71 % ,GL- 7- ACA酰化酶在周质空间酶的活力较对照组提高了约 1 .5倍 ,碱性磷酸酯酶在周质空间酶的活力较对照组提高了约 54% ;在过量表达 Gro EL的宿主菌中 ,周质分泌蛋白总量较对照组提高了约 52 % ,青霉素 G酰化酶在周质空间酶的活力较对照组提高了约 76% ,鲑鱼降钙素六聚体的可溶性组分的比例由原来的 45%增加到约 90 % ,而 MS2 -人白介素 - 3融合蛋白的包涵体有约 1 5%转变为可溶性组份 .上述结果表明 ,分子伴侣 Sec B和 Gro EL的过量表达促进了靶蛋白的分泌 ,Gro The effect of over expression of chaperones SecB and GroEL on the secretion and solubility of protein in Escherichia coli was examined,using a set of the proteins.A diverse range of effects on protein solubility and secretion was observed,and these effects were highly dependent on the particular chaperone.In the host strain over expressing chaperone SecB harboring pSecB,the amount of total periplasmic proteins was increased by about 71% and the activities of alkaline phosphatase(AP) and GL 7 ACA acylase(GL7A) were increased by about 54% and 1.5 fold respectively.In the host strain over expressing chaperone GroEL bearing pGroEL,the amount of total periplasmic proteins was increased by 52%,and the activity of penicillin G acylase(PA)was increased by about 76%;about 90% of Hexameric Calcitonin(Cal6)inclusion body and 15% of MS2 interleukin3(MS2 HIL3)inclusion body became soluble respectively.All the data were compared with the parental strains un bearing plasmids pSecB or pGroEL.In conclusion,the over expression of chaperones SecB and GroEL enhanced the secretion of the proteins,and GroEL also increased the solubility of recombinant proteins.
出处 《中国生物化学与分子生物学报》 CAS CSCD 2000年第3期382-387,共6页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家"8 6 3"生物技术项目资助 !(1 0 2 - 1 1 - 0 2 - 0 1 )
关键词 分子伴侣 分泌 可溶性表达 蛋白质 过量表达 Chaperone,Secretion,Soluble expression
  • 相关文献

参考文献13

  • 1[1]Gerhard Hanning,Sawas C Makrides. Strategies for optimizing heterologous protein expression in Escherichia coli. Tibtech,1998,16:54~60
  • 2[2]Laskey R A,Honda B M,Finch J T. Nucleosomes are assembled by an acidic protein which binds histones and transfers them to DNA. Nature,1978,275(5679):416~420
  • 3[3]Goloubinoff P,Christeller J T, Gatenhy A A, Lorimer G H. Reconstitution of active dimeric ribulose bisphosphate carboxylase from an unfolded state depends on two chaperonin proteins and Mg-ATP. Nature, 1989,342: 884~889
  • 4[4]Noriko kusukawa, Takashi Yura, Chiharu Ueguchi, Yoshinori Akiyama, Koreaki Ito. Effects of mutations in heat-shock genes groES and groEL on protein export in Escherichia coli. EMBO J,1989,8(11):3517~3521
  • 5[5]Collier D N. SecB:a molecular chaperone of Escherichia coli protein secretion pathway. Adv Protein Chem, 1993,44:151~193
  • 6[6]Gazen A, Levinthal C. A fine-structure genetic and chemical study of the ensyme alkaline phosphatase of E. coli I. Purification and characterization of alkaline phosphatase. Biochim Biophys Acta,1960,38:470~483
  • 7[7]Bomstein J, Evans W G. Automated colorimetric determination of 6-aminopenicillanic acid in fermentation media. Anal Chem,1965,37(4):576~578
  • 8[8]Akio Matsuda,Ken-Ichi Komatsu. Molecular cloning and structure of the gene for 7-(4-carboxybutanamido) cephalosporanic acid acylase form a Pseudomonas strain. J Bateriol, 1985,163(3):1222~1228
  • 9[9]Daniel M B, Stuart J E. Protein Methods. New York;Wiley-Liss Inc, 1991:27~42
  • 10[10]Kumamoto C A. Molecular chaperones and protein translocation across the Escherichia coli inner membrane. Mol Microbiol,1991,5(1):19~22

同被引文献75

引证文献10

二级引证文献39

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