Klee S R, Tzschaschel B D, Timmis K N, Guzman C A
Division of Microbiology, GBF-National Research Centre for Biotechnology, Braunschweig, Germany.
J Bacteriol. 1997 Apr;179(7):2421-5. doi: 10.1128/jb.179.7.2421-2425.1997.
Introduction of the rol genes of Shigella dysenteriae 1 and Escherichia coli K-12 into Shigella flexneri carrier strains expressing the heterologous S. dysenteriae type 1 lipopolysaccharide resulted in the formation of longer chains of S. dysenteriae 1 O antigen. In bacteria producing both homologous and heterologous O antigen, this resulted in a reduction of the masking of heterologous O antigen by homologous lipopolysaccharide and an increased immune response induced by intraperitoneal immunization of mice by recombinant bacteria. The rol genes of S. dysenteriae 1 and E. coli K-12 were sequenced, and their gene products were compared with the S. flexneri Rol protein. The primary sequence of S. flexneri Rol differs from both E. coli K-12 and S. dysenteriae 1 Rol proteins only at positions 267 and 270, which suggests that this region may be responsible for the difference in biological activities.
将痢疾志贺氏菌1型和大肠杆菌K-12的rol基因导入表达异源痢疾志贺氏菌1型脂多糖的弗氏志贺氏菌载体菌株中,导致形成了更长链的痢疾志贺氏菌1型O抗原。在同时产生同源和异源O抗原的细菌中,这导致同源脂多糖对异源O抗原的掩盖作用减弱,并且重组细菌腹腔免疫小鼠诱导的免疫反应增强。对痢疾志贺氏菌1型和大肠杆菌K-12的rol基因进行了测序,并将它们的基因产物与弗氏志贺氏菌Rol蛋白进行了比较。弗氏志贺氏菌Rol的一级序列仅在第267和270位与大肠杆菌K-12和痢疾志贺氏菌1型Rol蛋白不同,这表明该区域可能是生物活性差异的原因。