McShan W M, Williams R P, Hull R A
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, Texas 77030.
Infect Immun. 1987 Dec;55(12):3017-22. doi: 10.1128/iai.55.12.3017-3022.1987.
A cosmid gene library was prepared from Neisseria gonorrhoeae JC1, a serum-resistant clinical isolate from a patient with disseminated gonococcal infection. From this library a recombinant molecule, pWM3, was isolated which had the ability to transform F62, a serum-sensitive strain of N. gonorrhoeae, to serum resistance. This plasmid contained 2.2 kilobases of insert gonococcal DNA that coded for two peptides, one of 29 kilodaltons (kDa) and one of 17.5 kDa. Deletion of the region coding for the 29-kDa peptide resulted in the loss of the ability of the plasmid to transform F62 to serum resistance. N. gonorrhoeae F62 acquired the ability to bind blocking antibody when transformed with pWM3 or subclones that code for only the 29-kDa protein. Although similar in size, the cloned 29-kDa protein and protein III are antigenically distinct.
用淋球菌(Neisseria gonorrhoeae)JC1构建了黏粒基因文库,JC1是从一名播散性淋球菌感染患者中分离出的血清抗性临床菌株。从该文库中分离出一个重组分子pWM3,它能够将血清敏感的淋球菌菌株F62转化为血清抗性。该质粒含有2.2千碱基的插入淋球菌DNA,编码两种肽,一种为29千道尔顿(kDa),另一种为17.5 kDa。缺失编码29 kDa肽的区域导致该质粒失去将F62转化为血清抗性的能力。当用pWM3或仅编码29 kDa蛋白的亚克隆进行转化时,淋球菌F62获得了结合封闭抗体的能力。尽管大小相似,但克隆的29 kDa蛋白和蛋白III在抗原性上是不同的。