Amano K, Fukushi K, Williams J C
J Gen Microbiol. 1985 Nov;131(11):3127-30. doi: 10.1099/00221287-131-11-3127.
Lipopolysaccharides from phase I (LPSI) Coxiella burnetii Ohio and Nine Mile strains and from phase II (LPSII) Nine Mile stain were negatively and positively and examined with the electron microscope. The ultrastructure of LPSI and LPSII positively stained with uranyl formate or uranyl acetate was ribbon-like. When negatively stained with uranyl acetate, LPSI was ribbon-like but LPSII exhibited hexagonal lattice structures. However, LPSII stained negatively with sodium phosphotungstate and ammonium molybdate exhibited hexagonal lattice ultrastructures which were not identical to those observed when negatively stained with uranyl acetate. The hexagonal lattice structures formed in vitro were due to the interactions of LPSII and the staining reagents rather than to protein-LPS interactions. The differences in the ultrastructures of LPSI and LPSII are undoubtedly based on variations in their chemical composition.
对来自第一相(LPSI)的伯纳特立克次体俄亥俄株和九里株以及来自第二相(LPSII)的九里株的脂多糖进行了负染和正染,并用电镜检查。用甲酸铀或醋酸铀正染的LPSI和LPSII的超微结构呈带状。用醋酸铀负染时,LPSI呈带状,但LPSII呈现六边形晶格结构。然而,用磷钨酸钠和钼酸铵负染的LPSII呈现出六边形晶格超微结构,与用醋酸铀负染时观察到的不同。体外形成的六边形晶格结构是由于LPSII与染色试剂的相互作用,而不是蛋白质-LPS相互作用。LPSI和LPSII超微结构的差异无疑基于它们化学组成的变化。