Umelo E, Trust T J
Department of Biochemistry and Microbiology and Canadian Bacterial Diseases Network, University of Victoria, British Columbia, Canada.
J Bacteriol. 1997 Sep;179(17):5292-9. doi: 10.1128/jb.179.17.5292-5299.1997.
Two tandemly located flagellin genes, flaA and flaB, with 79% nucleotide sequence identity were identified in Aeromonas salmonicida A449. The fla genes are conserved in typical and atypical strains of A. salmonicida, and they display significant divergence at the nucleotide level from the fla genes of the motile species Aeromonas hydrophila and Aeromonas veronii biotype sobria. flaA and flaB encode unprocessed flagellins with predicted Mrs of 32,351 and 32,056, respectively. When cloned under the control of the Ptac promoter, flaB was highly expressed when induced in Escherichia coli DH5alpha, and the FlaB protein was detectable even in the uninduced state. In flaA clones containing intact upstream sequence, FlaA was barely detectable when uninduced and poorly expressed on induction. The A. salmonicida flagellins are antigenically cross-reactive with the A. hydrophila TF7 flagellin(s) and evolutionarily closely related to the flagellins of Pseudomonas aeruginosa and Vibrio anguillarum. Electron microscopy showed that A. salmonicida A449 expresses unsheathed polar flagella at an extremely low frequency under normal laboratory growth conditions, suggesting the presence of a full complement of genes whose products are required to make flagella; e.g., immediately downstream of flaA and flaB are open reading frames encoding FlaG and FlaH homologs.
在杀鲑气单胞菌A449中鉴定出两个串联排列的鞭毛蛋白基因flaA和flaB,其核苷酸序列同一性为79%。fla基因在杀鲑气单胞菌的典型菌株和非典型菌株中保守,并且它们在核苷酸水平上与运动性嗜水气单胞菌和维氏气单胞菌sobria生物型的fla基因存在显著差异。flaA和flaB分别编码预测分子量为32,351和32,056的未加工鞭毛蛋白。当在Ptac启动子控制下克隆时,flaB在大肠杆菌DH5α中诱导时高表达,甚至在未诱导状态下也可检测到FlaB蛋白。在含有完整上游序列的flaA克隆中,未诱导时FlaA几乎检测不到,诱导时表达不佳。杀鲑气单胞菌鞭毛蛋白与嗜水气单胞菌TF7鞭毛蛋白存在抗原交叉反应,并且在进化上与铜绿假单胞菌和鳗弧菌的鞭毛蛋白密切相关。电子显微镜显示,在正常实验室生长条件下,杀鲑气单胞菌A449以极低频率表达无鞘极鞭毛,这表明存在一组完整的基因,其产物是形成鞭毛所必需的;例如,在flaA和flaB的紧邻下游是编码FlaG和FlaH同源物的开放阅读框。