首页> 外国专利> RECOMBINANT PLASMID DNA PZAT1 USED FOR PREPARING DNA-PROBE WHICH IS USED FOR IDENTIFICATION OF TOXIGENIC STRAINS OF ANTHRAX PATHOGEN, METHOD OF CONSTRUCTION OF PLASMID DNA PZAT1 AND A STRAIN OF BACTERIUM ESCHERICHIA COLI USED FOR PREPARING RECOMBINANT PLASMID DNA PZAT1 AND DNA-PROBE WHICH IS USED FOR IDENTIFICATION OF TOXIGENIC STRAINS OF ANTHRAX PATHOGEN

RECOMBINANT PLASMID DNA PZAT1 USED FOR PREPARING DNA-PROBE WHICH IS USED FOR IDENTIFICATION OF TOXIGENIC STRAINS OF ANTHRAX PATHOGEN, METHOD OF CONSTRUCTION OF PLASMID DNA PZAT1 AND A STRAIN OF BACTERIUM ESCHERICHIA COLI USED FOR PREPARING RECOMBINANT PLASMID DNA PZAT1 AND DNA-PROBE WHICH IS USED FOR IDENTIFICATION OF TOXIGENIC STRAINS OF ANTHRAX PATHOGEN

机译:用于鉴定DNA探针的重组质粒DNA PZAT1,其用于鉴定产炭疽病原菌的毒力菌株,质粒DNA PZAT1的构建方法以及用于制备重组质粒的大肠杆菌DNA菌株炭疽病原菌毒性菌株的鉴定

摘要

FIELD: medicinal biotechnology. SUBSTANCE: method involves construction of recombinant plasmid DNA carrying species-specific fragment of anthrax plasmid pXOI which is used for DNA-probe. Synthesis level of recombinant plasmid in cells of strain is 1.5-2 mg per 1 l nutrient medium. DNA-probe prepared on the basis of plasmid DNA pZAT1 is hybridized only with toxigenic strains of anthrax pathogen that ensures to differentiate their from other bacteria including closely related bacilli and avirulent strains Bacillus anthracis no containing plasmid pXOI. EFFECT: construction of plasmid DNA indicated above. 4 cl, 1 dwg, 1 tbl
机译:领域:药物生物技术。物质:该方法涉及构建携带炭疽质粒pXOI物种特异性片段的重组质粒DNA,该片段用于DNA探针。菌株细胞中重组质粒的合成水平为每1升营养培养基1.5-2mg。仅将基于质粒DNA pZAT1制备的DNA探针与炭疽病原体的产毒菌株杂交,以确保将其与其他细菌区分开,包括紧密相关的杆菌和无毒力的炭疽芽孢杆菌菌株,不含质粒pXOI。效果:构建上述质粒DNA。 4厘升,1载重吨,1桶

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