Meier U, Mayer H
J Bacteriol. 1985 Aug;163(2):756-62. doi: 10.1128/jb.163.2.756-762.1985.
A new rff mutation (rff-726) of Escherichia coli is described which affects the biosynthesis of the enterobacterial common antigen. This mutation was detected in an rfe-defective strain. A Tn10 insertion near the rfe locus was isolated to facilitate further mapping. Both mutations rfe and rff were mapped by transduction with bacteriophage P1, giving the gene order ilv rfe rff uvrD metE. The F' factor F14 was able to complement both mutations rfe and rff, whereas the F' factor F16 could complement the rfe but not the rff mutation. The rff mutation did not affect the biosynthesis of N-acetyl-D-mannosaminuronic acid, as the previously described rff mutations in Salmonella typhimurium do (H. C. Lew, H. Nikaido, and P. H. Mäkelä, J. Bacteriol. 136:227-233, 1978), and also did not affect the biosynthesis of other enterobacterial common antigen components; however, the biosynthesis of the complete enterobacterial common antigen molecule was blocked.
描述了一种影响肠道细菌共同抗原生物合成的大肠杆菌新rff突变(rff-726)。该突变是在一株rfe缺陷型菌株中检测到的。在rfe基因座附近分离到一个Tn10插入片段,以利于进一步定位。通过用噬菌体P1转导对rfe和rff这两个突变进行定位,得到基因顺序ilv rfe rff uvrD metE。F'因子F14能够互补rfe和rff这两个突变,而F'因子F16能够互补rfe突变,但不能互补rff突变。与先前在鼠伤寒沙门氏菌中描述的rff突变不同(H.C. Lew、H. Nikaido和P.H. Mäkelä,《细菌学杂志》136:227-233,1978),rff突变不影响N-乙酰-D-甘露糖醛酸的生物合成,也不影响其他肠道细菌共同抗原成分的生物合成;然而,完整的肠道细菌共同抗原分子的生物合成被阻断。