首页> 外国专利> Manufacturing method null of transformation microbe and heat-resistant gurukoshidaze which include the rearrangement body plasmid and the said plasmid which include heat-resistant gurukoshidaze gene DNA and said

Manufacturing method null of transformation microbe and heat-resistant gurukoshidaze which include the rearrangement body plasmid and the said plasmid which include heat-resistant gurukoshidaze gene DNA and said

机译:包括重排体质粒的转化微生物和耐热古鲁克达兹的制造方法无效,以及包括耐热古鲁克达兹基因DNA的所述质粒和所述质粒。

摘要

PURPOSE:To mass produce heat-resistant beta-glucosidase through the cultivation at a temperature near the room one and purification by introducing the DNA which originates from a microorganism in Thermus and participates heat- resistant beta-glucosidase into Escherichia coli. CONSTITUTION:When the gene DNA participating the heat-resistant beta- glucosidase is isolated from a microorganism in Thermus, e.g., ZK-001 (FERM P-9184), a DNA having 4 recognition sites by restriction enzyme, BamH I; 2 sites by the restriction enzyme, Sac I, and 1 site by Kpn I. The DNA is bonded to a vector plasmid and introduced into Escherichia coli, then the microorganism is cultured to mass produce heat-resistant beta-glucosidase.
机译:目的:通过在室温附近的温度下进行培养,大量生产耐热性β-葡萄糖苷酶,然后通过将来源于微生物的DNA引入耐热性β-葡萄糖苷酶中进行纯化。组成:当从嗜热菌中的微生物中分离出参与耐热β-葡糖苷酶的基因DNA时,例如ZK-001(FERM P-9184),该DNA具有限制性酶BamHI的4个识别位点。限制性内切酶Sac I有2个位点,Kpn I有1个位点。DNA结合到载体质粒上并导入大肠杆菌,然后培养微生物以大量生产耐热性β-葡萄糖苷酶。

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