首页> 外国专利> RECOMBINANT PLASMID DNA PROVIDING SYNTHESIS OF BORRELIA GARINII IMMUNODOMINANT PROTEIN FOR LYME-BORRELIOSIS DIAGNOSIS

RECOMBINANT PLASMID DNA PROVIDING SYNTHESIS OF BORRELIA GARINII IMMUNODOMINANT PROTEIN FOR LYME-BORRELIOSIS DIAGNOSIS

机译:重组质粒DNA合成博氏鲍氏菌免疫诊断的蛋白质。

摘要

FIELD: gene engineering, biotechnology, medicine.;SUBSTANCE: invention relates to production of polypeptides bearing specific antigen determinants of OspC protein and FlaB flagellin fragment appropriate to genus Borrelia garinii being prevalent in Russia. Recombinant plasmid pREB9-H6-F7 DNA providing synthesis of B.garnii FlaB protein fragment contains: fragment with size of 100 b.p. encoding signal amino acid sequence of Staphylococcus aureus -toxin (CAT) and eight N-terminated amino acid residues of mature CAT; B.garnii flaB gene fragment with size of 500 b.p; nucleotide sequence in flaB gene reading frame encoding amino acid residues of glycin and 6 histidins; pIL-2/21 plasmid BamHI - EcoR1 DNA fragment with internal unique Xmal restriction site, containing -lactamase bla gene and regulatory region of Proteus mirabilis recA gene; unique Xmal, EcoR I, BstEII and BamHI restriction sites. Recombinant plasmid pREB9-H6-C25 DNA providing synthesis of B.garnii OspC protein contains fragment with size of 660 b.p. encoding B.garnii OspC protein; nucleotide sequence in ospC gene reading frame encoding amino acid residues of glycin and 6 histidins; pIL-2/21 plasmid BamHI - EcoR1 DNA fragment with internal unique Xmal restriction site, containing -lactamase bla gene and regulatory region of Proteus mirabilis recA gene; unique Xmal, EcoR I, BstEII and BamHI restriction sites.;EFFECT: high specific diagnosis method with improved accuracy.;2 cl, 2 dwg, 5 ex
机译:技术领域:本发明涉及带有OspC蛋白和FlaB鞭毛蛋白片段的特定抗原决定簇的多肽的生产,该多肽适合于在俄罗斯流行的鲍氏疏螺旋体属。提供甘蓝芽孢杆菌FlaB蛋白片段合成的重组质粒pREB9-H6-F7 DNA包含:大小为100b.p的片段。金黄色葡萄球菌毒素(CAT)的信号氨基酸序列和成熟CAT的八个N末端氨基酸残基; B.garnii flaB基因片段,大小为500 b.p; flaB基因阅读框中的核苷酸序列,编码甘氨酸和6种组蛋白的氨基酸残基; pIL-2 / 21质粒BamHI-EcoR1 DNA片段,具有内部独特的XmaI限制性位点,含有-内酰胺酶bla基因和变形杆菌procus mirabilis recA基因的调控区;独特的Xmal,EcoR I,BstEII和BamHI限制位点。重组质粒pREB9-H6-C25 DNA提供了B.garnii OspC蛋白的合成,其片段大小为660b.p。编码B.garnii OspC蛋白; ospC基因阅读框中的核苷酸序列,编码甘氨酸和6种组蛋白的氨基酸残基; pIL-2 / 21质粒BamHI-EcoR1 DNA片段,具有内部独特的XmaI限制性位点,含有-内酰胺酶bla基因和变形杆菌procus mirabilis recA基因的调控区;独特的Xmal,EcoR I,BstEII和BamHI限制性酶切位点;效果:具有更高准确性的高特异性诊断方法; 2 cl,2 dwg,5 ex

著录项

  • 公开/公告号RU2260047C2

    专利类型

  • 公开/公告日2005-09-10

    原文格式PDF

  • 申请/专利权人

    申请/专利号RU20030131242

  • 发明设计人 BEKLEMISHEV A.B. (RU);IVANOV I.D. (RU);

    申请日2003-10-23

  • 分类号C12N15/09;C12N15/31;C12Q1/68;

  • 国家 RU

  • 入库时间 2022-08-21 22:01:55

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