首页> 外国专利> rekombinantisk, maenniskointerleukin - 2 - synthesis coding plasmid dna of ppr il2 - 19 - type, foerfarande foer otherwise construct of this plasmid dna and maenniskointerleukin - 2 - producer,naemnda plasmid dna innehaallande strain of bacteria culture of escherichia coli vniigenetika vl 903 (ppr il2 - 19)

rekombinantisk, maenniskointerleukin - 2 - synthesis coding plasmid dna of ppr il2 - 19 - type, foerfarande foer otherwise construct of this plasmid dna and maenniskointerleukin - 2 - producer,naemnda plasmid dna innehaallande strain of bacteria culture of escherichia coli vniigenetika vl 903 (ppr il2 - 19)

机译:rekombinantisk,maenniskointerleukin-2-ppr il2-19-型合成编码质粒dna,foerfarande foer否则构建该质粒dna和maenniskointerleukin-2-生产者,大肠杆菌质粒dna innehaallande菌株,大肠杆菌的细菌培养(v2) -19)

摘要

A recombinant plasmid DNA pPR-IL2-19, coding for synthesis of human interleukin-2 has a size of 3.85 k.b.p. and consists of the following elements: BamHI-BglII, a fragment of the size of 3.4 k.b.p. of vector plasmid pPR124B obtained on the basis of pPR40 and pML24; Cfr13-BglII, a fragment of the size of 0.45 k.b.p. of plasmid pAA1213-23B obtained by modifying plasmid pAA1213-23 constructed on the basis of plasmid pBR-322 containing the kDNA-copy of the gene of human interleukin-2. A method of construction of the above recombinant plasmid DNA consists in obtaining, by modifying plasmid pAA1213-23, plasmid pAA1213-23B, a fragment of which, together with the gene of interleukin-2, is integrated into vector plasmid pPR-IL2-19, and in transforming, by the thus obtained mixture, cells of E. coli C600 and in separating plasmid pPR-IL2-19 from the clones grown on a selective medium. A strain of bacteria E. coli VNIIGENETIKA VL 903 (pPR-IL2-19) as producer of human interleukin-2 deposited on 12.01.87 under No. 1869 at the culture collection of the USSR Research Institute for Antibiotics.
机译:编码人白介素-2合成的重组质粒DNA pPR-IL2-19的大小为3.85k.b.p。并由以下元素组成:BamHI-BglII,片段大小为3.4k.b.p。基于pPR40和pML24获得的载体质粒pPR124B; Cfr13-BglII,大小为0.45 k.b.p.通过修饰质粒pAA1213-23获得的质粒pAA1213-23B,所述质粒pAA1213-23基于包含人白介素2基因的kDNA拷贝的质粒pBR-322而构建。上述重组质粒DNA的构建方法是通过修饰质粒pAA1213-23获得质粒pAA1213-23B,其片段与白介素2的基因一起整合入载体质粒pPR-IL2-19中。然后,通过如此获得的混合物转化大肠杆菌C600的细胞,并从在选择性培养基上生长的克隆中分离质粒pPR-IL2-19。作为人白细胞介素2生产者的大肠杆菌VNIIGENETIKA VL 903(pPR-IL2-19)菌株,在1869年12月1日保藏在苏联抗生素研究所的培养物中,编号为1869.87。

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