首页> 外国专利> GLYCEROALDEHYDE TRIPHOSPHATE DEHYDROGENASE GENE PROMOTER AND USE THEREOF

GLYCEROALDEHYDE TRIPHOSPHATE DEHYDROGENASE GENE PROMOTER AND USE THEREOF

机译:甘油醛酸三磷酸脱氢酶基因启动子及其用途

摘要

PURPOSE:To improve the productivity of cephalosporins by integrating a glyceroaldehyde triphosphate dehydrogenase gene(GLDG) originated from Acremonium chrysogenum(ACG) into a plasmid. CONSTITUTION:(A) A DNA fragment having e.g. the base sequence of formula containing the GLDG promoter active part of ACG is cut from the chromosome DNA of ATCC 11550 strain, etc., of ACG. The GLDG promoter of ACG is integrated to obtain a plasmid (B). A plasmid (C) is produced by integrating a GLDG translation initiation site at the downstream of the GLDG promoter site of ACG. A GLDG structure gene is integrated to the downstream of the promoter or translation initiation site of the components B and C to obtain (D) a plasmid such as pGH2. A transformant capable of synthesizing cephalosporins and obtained by the transformation with the component D is aerobically cultured in a medium containing glucose, etc., at pH5-9 and 20-30 deg.C for 4-14 days to obtain cephalosporins.
机译:目的:通过将源自产黄顶孢霉(ACG)的甘油醛三磷酸脱氢酶基因(GLDG)整合到质粒中,以提高头孢菌素的生产率。宪法:(A)具有例如从ACG的ATCC 11550株等的染色体DNA切出含有ACG的GLDG启动子活性部分的式子的碱基序列。整合ACG的GLDG启动子以获得质粒(B)。通过在ACG的GLDG启动子位点的下游整合GLDG翻译起始位点来产生质粒(C)。将GLDG结构基因整合到组分B和C的启动子或翻译起始位点的下游,以获得(D)质粒,例如pGH2。通过用组分D转化而获得的能够合成头孢菌素的转化体在含有葡萄糖等的培养基中在pH5-9和20-30℃下需氧培养4-14天,以获得头孢菌素。

著录项

  • 公开/公告号JPH02265494A

    专利类型

  • 公开/公告日1990-10-30

    原文格式PDF

  • 申请/专利权人 TAKEDA CHEM IND LTD;

    申请/专利号JP19890342278

  • 申请日1989-12-27

  • 分类号C12N15/80;C12N1/15;C12P35/00;

  • 国家 JP

  • 入库时间 2022-08-22 06:24:47

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