首页> 外国专利> YEAST STRAIN PASTORIS PS107(pPIC9HAbIL-2), WHICH IS THE PRODUCER OF HYBRID PROTEIN, CONSISTING OF ALBUMIN OF HUMAN PLASMA AND HUMAN INTERLEUKIN-2, RECOMBINANT PLASMID pPIC9HAbIL-2 AND THE METHOD FOR DESIGNING THEREOF

YEAST STRAIN PASTORIS PS107(pPIC9HAbIL-2), WHICH IS THE PRODUCER OF HYBRID PROTEIN, CONSISTING OF ALBUMIN OF HUMAN PLASMA AND HUMAN INTERLEUKIN-2, RECOMBINANT PLASMID pPIC9HAbIL-2 AND THE METHOD FOR DESIGNING THEREOF

机译:酵母PASTORIS PS107(pPIC9HAbIL-2),是混合蛋白的生产者,由人血浆和人白介素2的白蛋白组成,重组质粒pPIC9HAbIL-2及其设计方法

摘要

The invention relates to a pPIC9HAblL-2 recombinant plasmid, providing for biosynthesis and release of hybrid protein, which consists of albumin of human plasma and human IL-2, by the yeast cells, transformed by it, having the size of 10148 b.p., and which consists of the following elements: 1) EcoR1-Xho1 - fragment of plasmid DNA bifunctional bacterial-yeast vector pPIC9 with the size of 8.00 kb., bonded with restriction sites EcoR1-Xho1, and which comprises bacterial ampicillin resistance gene; bacterial region of inintiation of replication; yeast gene HIS4; fragment of 5'-noncoding region of yeast gene AOX1 having the size of 0.95 kb, which contains region, providing for activization of trenscription of this gene in the presence of methanol as a carbon source in cultural medium; preproregion of gene MF EMBED Equation.3 of yeast Saccharomyces cerevisiae having the size of 0.27 kb, which provides for release of hybrid protein, which consists of albumin of human plasma and human IL-2, into cultural medium; fragment of gene AOX1, having the size of 0.33 kb, containing the region of termination of transcription of this gene; and the fragment of 3'- noncoding region of gene AOX1 having the size of 0.76 kb; 2) Xho1-Bsu36l –fragment, having the size of 1749 b.p., containing the coding part of gene of albumin of human plasma with the exception of the region coding signal peptide, and stop codon; 3) Bsu36l-EcoR1 -, having the size of 399 b.p., containing the coding part of gene of human IL-2 with the exception of the region coding signal peptide. Also the invention relates to the yeast strain Pichia pastoris PS107(pPIC9HAblL-2, which is the producer of the mentioned hybrid protein, and which is the strain of Pichia pastoris PS99 (his4 pep4::PHO85), transformed by the mentioned plasmid. Also the invention relates to the method for designing of the mentioned recombinant plasmid pPIC9HAblL-2, which comprises a) gene of albumin of human plasma with the exception of the region coding signal peptide, and stop codon, is obtained by means of reverse PCL using of mRNA array, obtained from human hepatocytes, direct primer SEQ ID NO: 1, containing the site for restriction nuclease Xho1, reverse primer SEQ ID NO: 2, containing the site for restriction nuclease Mstll; b) gene of human IL-2 with the exception of the region coding signal peptide, obtained by means of PCR using of plasmid pJDB(MSIL) array, direct primer SEQ ID NO: 3, containing the site for restriction nuclease Bsu36l, reverse primer SEQ ID NO: 4, containing the site for restriction nuclease EcoR1; c) the obtained gene of albumin of human plasma is treated by restriction nucleases Xho1 and Mstll; d) the obtained gene of human IL-2 is treated by restriction nucleases Bsu36l and EcoR1; the genes of albumin of human plasma and human IL-2 are joined by ligase, and treated, as mentioned above, with plasmid pPIC9, preliminary treated by the restriction nucleases Xho1 and EcoR1; e) the cells of Escherichia coli are transformed by the prepared ligase mixture and clones, containing recombinant plasmid pPIC9HAblL-2 are selected.
机译:本发明涉及一种pPIC9HAblL-2重组质粒,其通过酵母细胞经人转化,大小为10148 bp的酵母细胞的合成和释放,由人血浆和人IL-2的白蛋白组成。其由以下元件组成:1)EcoR1-Xho1-质粒DNA双功能细菌-酵母载体pPIC9的片段,其大小为8.00kb,与限制性酶切位点EcoR1-Xho1结合,并包含细菌氨苄青霉素抗性基因;复制的细菌区域;酵母基因HIS4;酵母基因AOX1的5′-非编码区的片段,其大小为0.95kb,该片段含有在培养基中存在作为甲醇的甲醇作为碳源的情况下该基因的转录激活的区域;基因MF EMBED的前区大小为0.27 kb的酿酒酵母酵母,可将由人血浆白蛋白和人IL-2组成的杂合蛋白释放到培养基中;基因AOX1的片段,大小为0.33kb,含有该基因转录的终止区。以及基因AOX1的3'非编码区的片段,其大小为0.76kb; 2)Xho1-Bsu361-片段,大小为1749b.p。,含有人血浆白蛋白基因的编码部分,除了编码信号肽的区域外,还有终止密码子。 3)大小为399b.p.的Bsu361-EcoR1-,除编码信号肽的区域外,含有人IL-2基因的编码部分。本发明还涉及由所述质粒转化的酵母菌株巴斯德毕赤酵母PS107(pPIC9HAblL-2),其是所述杂合蛋白的生产者,并且是巴斯德毕赤酵母PS99(his4pep4 :: PHO85)的菌株。本发明涉及上述重组质粒pPIC9HAblL-2的设计方法,该重组质粒pPIC9HAblL-2包括:a)人乳清蛋白基因,除了编码信号肽的区域,以及终止密码子,是通过使用从人肝细胞中获得的mRNA阵列,含有限制性核酸酶Xho1位点的直接引物SEQ ID NO:1,含有限制性核酸酶MstII位点的反向引物SEQ ID NO:2; b)人IL-2基因,除区域编码信号肽外,使用质粒pJDB(MSIL)阵列通过PCR获得,直接引物SEQ ID NO:3,其包含限制性核酸酶Bsu36l的位点,反向引物SEQ ID NO:4,包含限制性核酸酶EcoR1的位点; c)用限制性核酸酶Xho1和MstII处理获得的人血浆白蛋白基因; d)用限制性核酸酶Bsu36l和EcoR1处理获得的人IL-2基因;用连接酶将人血浆白蛋白基因和人IL-2基因连接,并如上所述用质粒pPIC9处理,该质粒经限制性核酸酶Xho1和EcoR1初步处理。 e)通过制备的连接酶混合物转化大肠杆菌细胞,并选择含有重组质粒pPIC9HAblL-2的克隆。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号