Monack D M, Falkow S
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305.
Mol Microbiol. 1993 Nov;10(3):545-53. doi: 10.1111/j.1365-2958.1993.tb00926.x.
The genes encoding urease were cloned from Bordetella bronchiseptica and the 5.2 kb of DNA essential for expression analysed in a T7 RNA polymerase transcription-translation system. At least four polypeptides with predicted molecular weights of 69,000, 26,000, 12,200 and 11,000 were found. Partial DNA sequence of the gene encoding the 69,000 Da polypeptide revealed high amino acid identity to the alpha-subunit of Proteus mirabilis urease, UreC and jack bean urease. A stable, unmarked deletion was constructed in this gene to create a urease-negative mutant of B. bronchiseptica. To assess colonization in a guinea-pig model, the urease-negative strain was inoculated with the urease-positive parental strain in a mixed infection. The urease-negative strain out competed the urease-positive strain in the trachea, lungs and caecum. We demonstrate that urease is not essential for B. bronchiseptica colonization of the guinea-pig respiratory and digestive tracts.
从支气管败血波氏杆菌中克隆出编码脲酶的基因,并在T7 RNA聚合酶转录-翻译系统中分析了表达所需的5.2 kb DNA。发现了至少四种预测分子量分别为69,000、26,000、12,200和11,000的多肽。编码69,000 Da多肽的基因的部分DNA序列显示与奇异变形杆菌脲酶的α亚基、UreC和刀豆脲酶具有高度氨基酸同一性。在该基因中构建了一个稳定的、无标记的缺失,以产生支气管败血波氏杆菌的脲酶阴性突变体。为了评估在豚鼠模型中的定植情况,将脲酶阴性菌株与脲酶阳性亲代菌株进行混合感染接种。脲酶阴性菌株在气管、肺和盲肠中比脲酶阳性菌株更具竞争力。我们证明脲酶对于支气管败血波氏杆菌在豚鼠呼吸道和消化道中的定植不是必需的。