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The bacterial strain Vibrio cholerae KM 207 classic biovar Serovar Inaba - producer of protective antigens

机译:细菌霍乱弧菌KM 207经典生物变种Serovar Inaba-保护性抗原的产生者

摘要

FIELD: biotechnology, microbiology. SUBSTANCE: invention relates to preparing the strain Vibrio cholerae KM 207 of classic biovar serovar Inaba as a producer of protective antigens (subunit B as component of choleraic toxin, the main colonizing factor of choleraic vibrio, toxin-coregulated adhesion pili, protective and immunogenic protein OmpU of external membrane). Method involves conjugative incorporation to cells the natural toxigenic strain Vibrio cholerae 569B of classic biovar serovar Inaba recombinant plasmid pCT105 (KmrTcr) with cloned genes of choleraic toxin and the following elimination of plasmid. The level of choleraic toxin production in the strain is increased by 2.6 times (23.4 mcg/ml), synthesis of toxin- -coregulated adhesion pili is elevated also and protein OmpU appeared. In culturing the strain addition of antibiotics to medium is not required as in the case of plasmid strains. Using the strain allows the enhancement of choleraic toxin production level, toxin-coregulated adhesion pili (this causes self-agglutination of cells in broth) and synthesizes protein OmpU of external membrane. Invention can be used for preparing vaccines and diagnostic test-systems. EFFECT: valuable properties of strain. 2 ex
机译:领域:生物技术,微生物学。发明内容本发明涉及制备经典的生物变种血清型Inaba的霍乱弧菌KM 207菌株作为保护性抗原的生产者(B亚基作为霍乱毒素的成分,霍乱弧菌的主要定居因子,毒素复合的粘附菌毛,保护性和免疫原性蛋白外膜的OmpU)。该方法涉及将霍乱弧菌经典的生物变种Inaba重组Inaba重组质粒pCT105(KmrTcr)的天然产毒菌株霍乱弧菌569B与霍乱毒素的克隆基因结合掺入细胞中,然后去除质粒。该菌株中的霍乱毒素产生水平增加了2.6倍(23.4 mcg / ml),毒素-核心复合粘附菌毛的合成也提高了,蛋白OmpU出现了。在培养菌株中,与质粒菌株的情况一样,不需要向培养基中添加抗生素。使用该菌株可以提高霍乱毒素的产生水平,毒素为核心的粘附菌毛(这会导致肉汤中细胞的自凝集)并合成外膜蛋白OmpU。本发明可用于制备疫苗和诊断测试系统。效果:菌株的宝贵特性。 2前

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