Jones R T, Koeltzow D E, Stocker B A
J Bacteriol. 1972 Sep;111(3):758-70. doi: 10.1128/jb.111.3.758-770.1972.
Escherichia coli K-12 varkappa971 was crossed with a smooth Salmonella typhimurium donor, HfrK6, which transfers early the ilv-linked rfa region determining lipopolysaccharide (LPS) core structure. Two ilv(+) hybrids differing in their response to the LPS-specific phages FO and C21 were then crossed with S. typhimurium HfrK9, which transfers early the rfb gene cluster determining O repeat unit structure. Most recombinants selected for his(+) (near rfb) were agglutinated by Salmonella factor 4 antiserum. Transfer of an F' factor (FS400) carrying the rfb-his region of S. typhimurium to the same two ilv(+) hybrids gave similar results. LPS extracted from two ilv(+),his(+), factor 4-positive hybrids contained abequose, the immunodominant sugar for factor 4 specificity. By contrast, his(+) hybrids obtained from varkappa971 itself by similar HfrK9 and F'FS400 crosses were not agglutinated by factor 4 antiserum, indicating that the parental E. coli varkappa971 does not have the capacity to attach Salmonella O repeat units to its LPS core. It is concluded that the Salmonella rfb genes are expressed only in E. coli varkappa971 hybrids which have also acquired ilv-linked genes (presumably rfa genes affecting core structure or O-translocase ability, or both) from a S. typhimurium donor. When E. coli varkappa971 was crossed with a smooth E. coli donor, Hfr59, of serotype O8, which transfers his early, most his(+) recombinants were agglutinated by E. coli O8 antiserum and lysed by the O8-specific phage, Omega8. This suggests that, although the parental E. coli K-12 strain varkappa971 cannot attach Salmonella-specific repeat units to its LPS core, it does have the capacity to attach E. coli O8-specific repeat units.
将大肠杆菌K-12 κ971与光滑型鼠伤寒沙门氏菌供体HfrK6进行杂交,HfrK6会早期转移决定脂多糖(LPS)核心结构的ilv连锁rfa区域。然后将两个对LPS特异性噬菌体FO和C21反应不同的ilv(+)杂种与鼠伤寒沙门氏菌HfrK9进行杂交,HfrK9会早期转移决定O重复单位结构的rfb基因簇。大多数为his(+)(靠近rfb)筛选出的重组体被沙门氏菌4型抗血清凝集。将携带鼠伤寒沙门氏菌rfb-his区域的F'因子(FS400)转移到相同的两个ilv(+)杂种中,得到了相似的结果。从两个ilv(+)、his(+)、4型因子阳性杂种中提取的LPS含有阿比可糖,这是4型特异性的免疫显性糖。相比之下,通过类似的HfrK9和F'FS400杂交从κ971自身获得的his(+)杂种未被4型抗血清凝集,这表明亲本大肠杆菌κ971没有能力将沙门氏菌O重复单位连接到其LPS核心上。得出的结论是,沙门氏菌rfb基因仅在大肠杆菌κ971杂种中表达,这些杂种还从鼠伤寒沙门氏菌供体获得了ilv连锁基因(推测是影响核心结构或O-转位酶能力或两者的rfa基因)。当大肠杆菌κ971与血清型为O8的光滑型大肠杆菌供体Hfr59杂交时,Hfr59会早期转移his,大多数his(+)重组体被大肠杆菌O8抗血清凝集,并被O8特异性噬菌体Omega8裂解。这表明,虽然亲本大肠杆菌K-12菌株κ971不能将沙门氏菌特异性重复单位连接到其LPS核心上,但它确实有能力连接大肠杆菌O8特异性重复单位。