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CYTOCHROME P-450 HFLA PROTEIN, ITS DNA SEQUENCE AND A PROCESS FOR PRODUCING SAID PROTEIN

机译:细胞色素P-450 HFLA蛋白质,其DNA序列和生产唾液蛋白质的方法

摘要

PURPOSE:To make it possible to obtain the title protein in large quantities without containing a human-derived other protein by culturing a recombinant host cell in a culture medium. CONSTITUTION:A human fetal lever is purified by homogenizing in a buffer to afford a cytochrome P-450HFLa protein (A) having about 51000 molecular weight. Then a rabbit, etc., is immunized with the ingredient A to give an anti-P-450HFLa antibody (B). On the other hand, a fetal lever is treated with guanidinethiocyanate to extract total RNA, which is then chromatographed to afford mRNA (C). Then the ingredient C is translated to a protein and subjected to screening with the ingredient B to provide the desired mRNA fraction (D). Then the ingredient D is synthesized to a single-stranded cDNA, which is then treated with ligase to give a double-stranded cDNA (E). Then a recombinant DNA obtained by adding a linker to the ingredient E and introducing into a plasmid is introduced into escherichia coli and the resultant transformed strain is cultured in a culture medium and DNA sequence such as DNA expressed by formula I is expressed to produce cytochrome P-450HFLa protein containing an amino acid sequence expressed by formula II.
机译:目的:通过在培养基中培养重组宿主细胞,可以在不包含人源其他蛋白质的情况下大量获得标题蛋白质。组成:通过在缓冲液中匀浆纯化人胎儿杠杆,得到分子量约为51000的细胞色素P-450HFLa蛋白(A)。然后,用成分A免疫兔子等,得到抗P-450HFLa抗体(B)。另一方面,用硫氰酸胍处理胎儿杠杆以提取总RNA,然后对其进行色谱分离以提供mRNA(C)。然后将成分C翻译成蛋白质,并用成分B进行筛选以提供所需的mRNA部分(D)。然后将成分D合成为单链cDNA,然后将其用连接酶处理,得到双链cDNA(E)。然后,通过向成分E中添加接头并引入质粒而获得的重组DNA被引入大肠杆菌,并且将所得的转化菌株在培养基中进行培养,并且表达诸如式I所示的DNA的DNA序列以产生细胞色素P。 -450HFLa蛋白,含有式II表示的氨基酸序列。

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