首页> 外国专利> A method of high cell-density culture of Escherichia coli by overproducing Mlc protein

A method of high cell-density culture of Escherichia coli by overproducing Mlc protein

机译:通过过量生产Mlc蛋白进行大肠杆菌高细胞密度培养的方法

摘要

The invention relates to a method for over-expressing a regulator of the carbohydrate metabolism Mlc protein of Escherichia coli. More specifically, the present invention provides a Mlc overexpressing mutant strain produced by the method of over-expressing the Mlc protein by inducing a mutation to the transcription control region of the mlc gene in the E. coli -10 region and SD sequence a ribosome binding site, the method comprising. Can be by lowering the metabolic rate and specific growth rate per E. coli in the glucose added culture medium due doemeuro Mlc protein over-expression by suppressing the production of acetate toxic metabolic by-product of glucose metabolism in the culture of E. coli at a high concentration according to the invention, Mlc overexpressing mutant strain produced by the present invention can increase the production of recombinant proteins are used as the foreign gene, expression host cells.
机译:本发明涉及过表达大肠杆菌的碳水化合物代谢Mlc蛋白的调节剂的方法。更具体地,本发明提供了通过在大肠杆菌-10中诱导 mlc 基因的转录控制区的突变来过表达MLC蛋白的方法而产生的MLC过表达突变株。区域和SD序列具有核糖体结合位点,该方法包括。可以通过抑制大肠杆菌中葡萄糖代谢的乙酸有毒代谢副产物的产生来降低doemeuro Mlc蛋白过度表达,从而降低添加葡萄糖的培养基中每个大肠杆菌在葡萄糖添加培养基中的代谢速率和比生长速率。根据本发明的高浓度,通过本发明产生的Mlc过表达突变株可以增加重组蛋白的产量,用作外源基因,表达宿主细胞。

著录项

  • 公开/公告号KR100485614B1

    专利类型

  • 公开/公告日2005-04-27

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20010006274

  • 发明设计人 지근억;조상희;신동우;유상렬;

    申请日2001-02-08

  • 分类号C12N15/09;

  • 国家 KR

  • 入库时间 2022-08-21 22:03:54

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