Guerry P, Alm R A, Power M E, Logan S M, Trust T J
Enteric Diseases Program, Naval Medical Research Institute, Rockville, Maryland 20852.
J Bacteriol. 1991 Aug;173(15):4757-64. doi: 10.1128/jb.173.15.4757-4764.1991.
Campylobacter coli VC167 T2 has two flagellin genes, flaA and flaB, which share 91.9% sequence identity. The flaA gene is transcribed from a o-28 promoter, and the flaB gene from a o-54 promoter. Gene replacement mutagenesis techniques were used to generate flaA+ flaB and flaA flaB+ mutants. Both gene products are capable of assembling independently into functional filaments. A flagellar filament composed exclusively of the flaA gene product is indistinguishable in length from that of the wild type and shows a slight reduction in motility. The flagellar filament composed exclusively of the flaB gene product is severely truncated in length and greatly reduced in motility. Thus, while both flagellins are not necessary for motility, both products are required for a fully active flagellar filament. Although the wild-type flagellar filament is a heteropolymer of the flaA and flaB gene products, immunogold electron microscopy suggests that flaB epitopes are poorly surface exposed along the length of the wild-type filament.
空肠弯曲菌VC167 T2有两个鞭毛蛋白基因,flaA和flaB,它们的序列同一性为91.9%。flaA基因从σ-28启动子转录,flaB基因从σ-54启动子转录。利用基因置换诱变技术产生了flaA+flaB和flaA flaB+突变体。两种基因产物都能够独立组装成功能性细丝。仅由flaA基因产物组成的鞭毛细丝在长度上与野生型无法区分,并且运动性略有降低。仅由flaB基因产物组成的鞭毛细丝长度严重缩短,运动性大大降低。因此,虽然两种鞭毛蛋白对于运动性不是必需的,但两种产物对于完全活跃的鞭毛细丝都是必需的。虽然野生型鞭毛细丝是flaA和flaB基因产物的杂聚物,但免疫金电子显微镜显示,沿着野生型细丝的长度,flaB表位在表面的暴露情况较差。