首页> 外国专利> RECOMBINANT PLASMID DNA ECO 1831RI ENCODING SYNTHESIS OF RESTRICTION ENDONUCLEASE ECO 1831RI, STRAIN OF BACTERIUM ESCHERICHIA COLI - A PRODUCER OF RESTRICTION ENDONUCLEASE ECO 1831RI

RECOMBINANT PLASMID DNA ECO 1831RI ENCODING SYNTHESIS OF RESTRICTION ENDONUCLEASE ECO 1831RI, STRAIN OF BACTERIUM ESCHERICHIA COLI - A PRODUCER OF RESTRICTION ENDONUCLEASE ECO 1831RI

机译:重组质粒DNA ECO 1831RI编码限制性内切酶ECO 1831RI,大肠杆菌的菌株-限制性内切酶ECO 1831RI的生产者

摘要

FIELD: genetic engineering. SUBSTANCE: new recombinant plasmid pECO 1831RI (size is 8.1 thousand nucleotide pairs) has genes of restriction-modification system Eco 1831RI and consists of Bam HI-fragment of vector pUC19 and BglII-fragment of the natural plasmid p1831, three recognition sites by restrictase Eco RI, two sites - StyI, and one site for restrictases: KpnI, SalI, HindIII, PstI, SmaI, and resistance determinant to ampicillin also. Obtained plasmid provides increased synthesis of restrictase Eco 1831RI. Proposed strain E. coli BKM CR - 3680D prepared by transformation with plasmid DNA pECO 1831RI into the strain E. coli R802 provides the high level of enzyme content, 2500000 U/1 g wet bimass, not less. The yield of purified enzyme is 350000 U/g biomass. EFFECT: increased yield of enzyme. 3 cl
机译:领域:基因工程。物质:新的重组质粒pECO 1831RI(大小为8.1千个核苷酸对)具有限制性修饰系统Eco 1831RI的基因,由载体pUC19的Bam HI片段和天然质粒p1831的BglII片段组成,三个限制性酶切位点RI,两个位点-StyI和一个限制性酶切位点:KpnI,SalI,HindIII,PstI,SmaI和氨苄青霉素的抗性决定子。获得的质粒提供了限制性酶Eco 1831RI的增加的合成。通过用质粒DNA pECO 1831RI转化到大肠杆菌R802中而制备的拟议的大肠杆菌BKM CR-3680D菌株提供了高水平的酶含量,为2500000 U / 1 g湿重质量。纯化的酶的产量为350000 U / g生物质。效果:增加酶的产量。 3厘升

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