Pichia pastoris and as recombinant DNA for the transformation thereof an integrative vector which contains a functional selection marker of Saccharomyces cerevisiae, the promotor of the alcohol oxidase gene (AOX₁) of the yeast itself, as the transcription terminator that of glyceraldehyde 3-phosphate dehydrogenase (GAP) of S. cerevisiae, or that which is carried by the heterologous gene to be expressed, and another sequence homologous to the genome of Pichia pastoris which serves for the integration thereof. The expression vectors used further contain a heterologous gene bound to the signal peptide of the sucrose invertase gene (SUC2) of S. cerevisiae. This method guarantees that the polypeptide products are recoverable under controllable conditions and with high yields. The strains according to the present invention can be used for the large-scale production of pharmaceutical products or of enzymes of industrial interest."/> A method for the expression of hetero logical genes in the yeast pichia pastoris, expression method and transformed microorganisms
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A method for the expression of hetero logical genes in the yeast pichia pastoris, expression method and transformed microorganisms

机译:在酵母毕赤酵母中表达异源基因的方法,表达方法和转化的微生物

摘要

The present invention provides a highly efficient method for the expression of heterologous genes, using as the host an auxotrophic his3 mutant of strain BKM-90 of Pichia pastoris and as recombinant DNA for the transformation thereof an integrative vector which contains a functional selection marker of Saccharomyces cerevisiae, the promotor of the alcohol oxidase gene (AOX₁) of the yeast itself, as the transcription terminator that of glyceraldehyde 3-phosphate dehydrogenase (GAP) of S. cerevisiae, or that which is carried by the heterologous gene to be expressed, and another sequence homologous to the genome of Pichia pastoris which serves for the integration thereof. The expression vectors used further contain a heterologous gene bound to the signal peptide of the sucrose invertase gene (SUC2) of S. cerevisiae. This method guarantees that the polypeptide products are recoverable under controllable conditions and with high yields. The strains according to the present invention can be used for the large-scale production of pharmaceutical products or of enzymes of industrial interest.
机译:本发明提供了一种高效表达异源基因的方法,使用 Pichia pastoris 的菌株BKM-90的营养缺陷型his3突变体作为宿主,并用作重组DNA进行转化。作为其整合载体,其包含酵母自身的醇氧化酶基因(AOX₁)的启动子酿酒酵母的功能选择标记,作为甘油醛3-的转录终止子。 S 的磷酸脱氢酶(GAP)。 酿酒酵母,或由待表达的异源基因携带的,以及与毕赤酵母的基因组同源的另一个序列,用于其集成。所使用的表达载体还包含与 S 的蔗糖转化酶基因(SUC2)的信号肽结合的异源基因。 啤酒。该方法保证了多肽产物在可控条件下可以高收率回收。根据本发明的菌株可用于大规模生产药物产品或工业上感兴趣的酶。

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