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Modified Yeast with lactate dehydrogenase encoding Gene of human origin with deletion of the gene encoding pyruvate decarboxylase

机译:乳酸脱氢酶编码的酵母修饰人源基因,丙酮酸脱羧酶编码基因缺失

摘要

Yeast that can produce lactic acid with High Productivity without Neutralization with Alkali, characterized by a capability of lactic acid production and an excellent Growth capacity to produce, process and Method for production Go lactic acid in which it is used.Guest in the Yeast Schizosaccharomyces pombe have been introduced between 3 and 5 copies of a Gene that encodes a lactate dehydrogenase of human origin and has been deleted or Inactivated a Gene which is part of a group of genes encoding a pyruvate decarboxylase.Yeast which can be developed to reach a concentration of cells of at least 4.0 G (based on dry weight of cells / L) when it was cultivated in a Culture medium which was prepared by inoculating the cells at an initial concentration of 0,04 G (based on dry weight of cells / L) in a 500 ml Sakaguchi Flask containing 100 ml of Culture Broth Liquid comprising 1% Yeast Extract, 2% peptone and glucose 6% over a period of 20 hours at a temperature of 90 degrees, with agitation to go Speed of 110 rpm and at a depth of 7 cm.And can produce lactic acid in a concentration of at least 80 g / l when it is grown in a Culture medium which was prepared by inoculating the cells at an initial concentration of 0.04 G (based on dry weight of cells / L) in a 500 ml Flask containing Sakaguchi 100 ml of Culture Broth Liquid comprising 1% Yeast Extract,2% peptone and glucose 6% over a period of 20 hours at a temperature of 90 degrees, with stirring at a Speed of 110 rpm and at a depth of 7 cm, then inoculate the cells thus obtained at an initial concentration of 36 g (based on dry weight of algal cells. Cells / L) in a test tube with a diameter of 18 mm.And a length of 150 mm and contains 4.5 ml of an aqueous solution comprising 11.1% Glucose and carry out fermentation for a period of 3 hours at a temperature of 90 degrees, with an agitation with an angle of 43,5u00ba, at a Speed of 110 rpm and at a depth of 7 cm. Method for producing lactic acid which is used as a Yeast that has been described.
机译:可以在不与碱中和的情况下高效生产乳酸的酵母,其特征在于具有生产乳酸的能力以及出色的生产,生产方法和生产方法的生产能力。使用乳酸的酵母是裂殖酵母的客体。已被引入3至5个拷贝的基因编码人类起源的乳酸脱氢酶,并已被删除或灭活了一个基因,该基因是编码丙酮酸脱羧酶的一组基因的一部分。在培养基中培养的细胞至少为4.0 G(基于细胞的干重/ L),该培养基是通过以0.04 G的初始浓度接种细胞(基于细胞的干重// L)在90摄氏度的温度下于20个小时内放入500毫升Sakaguchi烧瓶中,该烧瓶中含有100毫升包含1%酵母提取物,2%蛋白ept和6%葡萄糖的培养液,并在90度搅拌继续以110 rpm的速度和7 cm的深度运行,并且在以初始浓度接种细胞而制备的培养基中生长时可以产生至少80 g / l的乳酸在500毫升装有Sakaguchi的烧瓶中,在100毫升的温度下于20个小时内,在100毫升的Sakaguchi 100毫升培养液中加入0.04 G(基于细胞的干重/升),其中含有1%的酵母提取物,2%的蛋白ept和6%的葡萄糖。在以110 rpm的速度和7 cm的深度搅拌的情况下,以90度旋转,然后以36 g的初始浓度(基于藻类细胞的干重)接种由此获得的细胞。直径为18毫米,长度为150毫米的试管中的细胞(/ L),其中装有4.5毫升含11.1%葡萄糖的水溶液,并在90度的温度下发酵3小时,以43.5°的角度以110 rpm的速度和7 cm的深度进行搅拌。已经描述了生产用作酵母的乳酸的方法。

著录项

  • 公开/公告号AR102238A1

    专利类型

  • 公开/公告日2017-02-15

    原文格式PDF

  • 申请/专利权人 JMTC ENZYME CORPORATION;

    申请/专利号AR2015P103283

  • 申请日2015-10-09

  • 分类号C12N1/19;C12N15/81;C12P7/56;C12R1/645;

  • 国家 AR

  • 入库时间 2022-08-21 13:40:59

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