期刊文献+

提高外源基因在巴斯德毕赤酵母中表达量的研究进展 被引量:5

The Study on Improving Expression Levels of Heterologous Gene in Pichia pastoris
下载PDF
导出
摘要 巴斯德毕赤酵母 (Pichiapastoris)表达系统是基因工程研究中广泛使用的真核表达系统 ,与现有的其它表达系统相比 ,巴斯德毕赤酵母在表达产物的糖基化修饰、折叠、加工、外分泌及表达量等方面有明显的优势。外源基因在该系统中表达时 ,由于受基因内部的结构、分泌信号、甲醇诱导的浓度及诱导时间、培养温度、启动子、表达环境的 pH值等诸多因素的影响 ,一些外源蛋白的表达也存在着表达不够稳定、表达量较低 ,甚至不表达的情况。对影响巴斯德毕赤酵母表达的各种可能因素进行了分析 ,结合具体实践经验 ,就如何提高外源基因在巴斯德毕赤酵母中表达量的问题进行了综述。 As a eukaryote expression system, Pichia pastoris has been widely used in genetic engineering, which has many merits in the gene expression, protein process and secretion. The gene expression is influenced by a number of factors, such as the structure of gene, secretion signal peptides, methanol concentration, induction phase, temperature, PH, and promoter etc. These factors make some heterologous genes express unstably or express a little. This article analyzes these factors and reviews how to improve expression levels of heterologous genes in Pichia pastoris.
出处 《生物技术通报》 CAS CSCD 2004年第2期23-26,30,共5页 Biotechnology Bulletin
关键词 外源基因 巴斯德毕赤酵母 表达量 基因工程 真核表达系统 表达产物 Pichia pastoris Yeast expression system Gene expression
  • 相关文献

参考文献9

二级参考文献76

  • 1[1]Sreekrishna K, Brankamp R G, Kropp K E, et al. Strategies for optimal synthesis and secretion of heterologous proteins in the methylotrophic yeast Pichia pastoris. Gene, 1997, 190: 55~62.
  • 2[2]Clare J J, Scorer C A, Buckholz R G, et al. Expression of EGF and HIV envelope glycoprotein. Methods Mol Biol, 1998, 103: 209.
  • 3[3]Scorer C A, Buckholz R G, Clare J J, et al. The intracellular production and secretion of HIV-1 envelope protein in the methylotrophic yeast Pichia pastoris. Gene, 1993, 136:111~119.
  • 4[4]Zhang Y J, Jin N Y, Jiang W Z, et al. Cloning and expression of the external-glycoprotein gene mutant from HIV-2 in the methylotrophic yeast Pichia pastoris and identification of the glycoprotein. Biotechnol Appl Biochem, 2001, 34:1~4.
  • 5[5]Withers-Martinez C, Carpenter E P, Hackett F, et al. PCR-based gene synthesis as an efficient approach for expression of the A+T-rich malaria genome.Protein Eng, 1999, 12:1113~1120.
  • 6[6]Cregg J M, Cereghino J L, Shi J Y, et al. Recombinant protein expression in Pichia pastoris. Mol Biotechnol, 2000, 16: 23~52.
  • 7[7]Waterham H R, Digan M E, Koutz P J, et al. Isolation of the Pichia pastoris glyceraldehyde-3-phosphate dehydrogenase gene and regulation and use of its promoter. Gene, 1997, 186: 37~44.
  • 8[8]Shen S, Sultar G, Jeffries T W, et al. A strong nitrogen source-regulated promoter for controlled expression of foreign genes in the yeast Pichia pastoris. Gene, 1998, 216: 93~102.
  • 9[9]Thill G P, Dark G R, Stillman G R, et al. Proceedings of the Sixth International Symposium on Genetics of Industrial Microorganisms. 1990,477~490.
  • 10[10]Brierley R A. Secretion of recombinant human insulin-like growth factor I (IGF-I). Methods Mol Biol, 1998, 103: 149~177.

共引文献159

同被引文献45

引证文献5

二级引证文献10

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