首页> 外国专利> immunoglobulin a1 proteases (iga1 proteases)procedure in the field of manufacture of such enzymes as well as vaccine containing enzymes and fragments thereof for immunisation against bacterial meningitis and other diseases caused by iga1 - protease producing bacteria

immunoglobulin a1 proteases (iga1 proteases)procedure in the field of manufacture of such enzymes as well as vaccine containing enzymes and fragments thereof for immunisation against bacterial meningitis and other diseases caused by iga1 - protease producing bacteria

机译:免疫球蛋白a1蛋白酶(iga1蛋白酶)在此类酶以及含该酶的酶及其片段的生产领域中的程序,用于针对细菌性脑膜炎和其他由iga1-蛋白酶产生的细菌引起的疾病进行免疫

摘要

Secretion of IgA1 proteases is a characteristic of Haemophilus influenzae and several other bacterial pathogens causing infectious diseases, including meningitis. Indirect evidence suggests that the proteases are important virulence factors. The iga gene encoding IgA1 protease, especially that from H. influenzae serotype b, has been cloned into Escherichia coli in which the recombinant iga gene was expressed and the resulting protease secreted. Sequencing a part of a 7.5 kb DNA fragment containing the iga gene revealed a large open reading frame (ORF) with a strongly biased codon usage and having the potential of encoding a protein of 1541 amino acids and a molecular mass of 169 kd. Putative promoter and terminator elements flanking the ORF have been identified. Comparing the deduced amino acid sequence of the produced H. influenzae IgA1 protease with that of a similar protease from Neisseria gonorrhoeae reveals several domains with a high degree of homology. Analogous to mechanisms known from the N. gonorrhoeae IgA protease secretion, there is proposed a scheme of post-translational modifications of the H. influenzae IgA1 protease precursor leading to a secreted protease with a molecular mass of 108 kd which is close to the Mr 100 kd estimated for the mature IgA1 protease.
机译:IgA1蛋白酶的分泌是流感嗜血杆菌和其他引起感染性疾病(包括脑膜炎)的细菌病原体的特征。间接证据表明蛋白酶是重要的毒力因子。已将编码IgA1蛋白酶的iga基因,特别是来自流感嗜血杆菌血清型b的iga基因克隆到大肠杆菌中,在其中表达了重组iga基因,并分泌了所得的蛋白酶。对包含iga基因的7.5 kb DNA片段的一部分进行测序,揭示了一个巨大的开放阅读框(ORF),其密码子使用严重偏向,并且具有编码1541个氨基酸和169 kd分子量的蛋白质的潜力。已经鉴定出ORF侧翼的推定启动子和终止子元件。将产生的流感嗜血杆菌IgA1蛋白酶的推导氨基酸序列与淋病奈瑟氏球菌的相似蛋白酶的推导氨基酸序列进行比较,发现了几个具有高度同源性的域。类似于淋病奈瑟氏球菌IgA蛋白酶分泌的已知机制,提出了流感嗜血杆菌IgA1蛋白酶前体的翻译后修饰方案,导致分泌的蛋白酶分子质量为108 kd,与Mr 100接近估计成熟IgA1蛋白酶的kd。

著录项

  • 公开/公告号NO913665L

    专利类型

  • 公开/公告日1991-11-18

    原文格式PDF

  • 申请/专利权人 KILIAN MOGENS;POULSEN KNUD;

    申请/专利号NO19910003665

  • 发明设计人 KILIAN MOGENS;POULSEN KNUD;

    申请日1991-09-17

  • 分类号C12N9/00;

  • 国家 NO

  • 入库时间 2022-08-22 05:34:42

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