Brogden K A, Rimler R B, Cutlip R C, Lehmkuhl H D
Am J Vet Res. 1986 Apr;47(4):727-9.
Lipopolysaccharides (LPS) were extracted from a serotype of each of 2 species of Pasteurella isolated from sheep with respiratory tract infections. Lipopolysaccharides from P haemolytica 82-25 (serotype 1A) or P multocida P-1573 (serotype 12) were mixed with sheep lung surfactant and were incubated for 6 hours at 37 C. After incubation, LPS-surfactant mixtures were centrifuged overnight in sucrose density gradients, and fractions were analyzed. Binding occurred between LPS and surfactant vesicles resulting in a stable complex with densities greater than those with the surfactant alone. The surfactant alone had a density of 1.052 to 1.060 g/ml. Diffuse bands of surfactant had a density of 1.075 to 1.092 when incubated with P haemolytica LPS and a density of 1.069 to 1.105 when incubated with P multocida LPS.
从患有呼吸道感染的绵羊身上分离出的2种巴斯德氏菌的各血清型中提取脂多糖(LPS)。将溶血巴斯德氏菌82 - 25(血清型1A)或多杀巴斯德氏菌P - 1573(血清型12)的脂多糖与绵羊肺表面活性剂混合,并在37℃下孵育6小时。孵育后,将LPS - 表面活性剂混合物在蔗糖密度梯度中过夜离心,并对各组分进行分析。LPS与表面活性剂囊泡之间发生结合,形成了密度高于单独表面活性剂的稳定复合物。单独的表面活性剂密度为1.052至1.060 g/ml。与溶血巴斯德氏菌LPS孵育时,表面活性剂的弥散带密度为1.075至1.092,与多杀巴斯德氏菌LPS孵育时,密度为1.069至1.105。