Hannecart-Pokorni E, Godard C, Beumer J
Ann Microbiol (Paris). 1976 Jul;127(1):15-24.
Receptor sites for phages FP3, V, P1kcvir, H+, C21, T4, T3, T7 and 6SR have been investigated, by comparing the lytic activity of these phages on R mutants of strain F6 (F6R) and of various serotypes (FH) of Shigella flexneri with their inhibition by the lipopolysaccharides isolated from these mutants. The results suggest the following localizations for the receptor sites: phage FP3: lipid A-KDO; phage V: heptose or glucose; phage C21: heptose-glucose; phages H+, P1kcvir, T4 and T3: glucose; phage T7: glucose-galactose; phage 6SR: complete core structure.
通过比较噬菌体FP3、V、P1kcvir、H+、C21、T4、T3、T7和6SR对福氏志贺氏菌F6菌株的R突变体(F6R)和各种血清型(FH)的裂解活性以及从这些突变体中分离出的脂多糖对它们的抑制作用,对这些噬菌体的受体位点进行了研究。结果表明受体位点的定位如下:噬菌体FP3:脂质A-酮脱氧辛糖酸;噬菌体V:庚糖或葡萄糖;噬菌体C21:庚糖-葡萄糖;噬菌体H+、P1kcvir、T4和T3:葡萄糖;噬菌体T7:葡萄糖-半乳糖;噬菌体6SR:完整的核心结构。