Kessler A C, Brown P K, Romana L K, Reeves P R
Department of Microbiology, University of Sydney, NSW, Australia.
J Gen Microbiol. 1991 Dec;137(12):2689-95. doi: 10.1099/00221287-137-12-2689.
The rfb region of Yersinia pseudotuberculosis serogroup IIA has been cloned and expression of O antigen in Escherichia coli K12 was demonstrated. Transposon mutagenesis analysis confined the DNA region required for O antigen expression to a 19.3 kb fragment, and the O antigen expressed was visualized by SDS-PAGE and silver staining. Southern hybridization analysis demonstrated significant levels of similarity between the Yersinia rfb region and the 3,6-dideoxyhexose pathway genes rfbF and rfbG, previously isolated from Salmonella enterica LT2, but no similarity to the abequose synthase gene rfbJ of the same strain or the paratose synthase gene rfbS isolated from S. enterica Ty2. The evolutionary relationship between the abequose biosynthetic genes of the two species of Salmonella and Yersinia is discussed.
对假结核耶尔森氏菌血清群IIA的rfb区域进行了克隆,并证实了其O抗原在大肠杆菌K12中的表达。转座子诱变分析将O抗原表达所需的DNA区域定位到一个19.3 kb的片段,通过SDS-PAGE和银染可视化所表达的O抗原。Southern杂交分析表明,耶尔森氏菌rfb区域与先前从肠炎沙门氏菌LT2分离的3,6-二脱氧己糖途径基因rfbF和rfbG之间存在显著的相似性,但与同一菌株的阿比可糖合酶基因rfbJ或从肠炎沙门氏菌Ty2分离的副糖合酶基因rfbS没有相似性。讨论了两种沙门氏菌和耶尔森氏菌的阿比可糖生物合成基因之间的进化关系。