Anderson D G, Moseley S L
Department of Microbiology, School of Medicine, University of Washington, Seattle 98195.
J Bacteriol. 1988 Oct;170(10):4890-6. doi: 10.1128/jb.170.10.4890-4896.1988.
The genetic organization of the polypeptides required for the biosynthesis of the F41 adhesin of enterotoxigenic Escherichia coli strains was investigated. Maxicell analysis demonstrated that a recombinant plasmid which mediated mannose-resistant hemagglutination and F41 antigen production encoded four polypeptides of 29, 30, 32, and 86 kilodaltons. The 29-kilodalton protein was identified as the F41 antigen, and the nucleotide sequence of the gene was determined. Extensive homology was observed between the region encoding the putative signal sequences of the F41 and K88 antigens and in the region immediately upstream of the antigen genes. The nucleotide sequence homology between F41 and K88 determinants was further investigated by Southern blot hybridization. A K88 probe hybridized at high stringency to all fragments shown to be essential for F41 production except for fragments internal to the F41 antigen gene.
对产肠毒素大肠杆菌菌株F41黏附素生物合成所需多肽的基因组织进行了研究。最大细胞分析表明,介导甘露糖抗性血凝和F41抗原产生的重组质粒编码四种分子量分别为29、30、32和86千道尔顿的多肽。29千道尔顿的蛋白质被鉴定为F41抗原,并测定了该基因的核苷酸序列。在编码F41和K88抗原假定信号序列的区域之间以及抗原基因紧邻上游的区域观察到广泛的同源性。通过Southern印迹杂交进一步研究了F41和K88决定簇之间的核苷酸序列同源性。K88探针在高严谨度下与所有显示对F41产生至关重要的片段杂交,但F41抗原基因内部的片段除外。