Moreno E, Pitt M W, Jones L M, Schurig G G, Berman D T
J Bacteriol. 1979 May;138(2):361-9. doi: 10.1128/jb.138.2.361-369.1979.
In an attempt to obtain pure and well characterized smooth lipopolysaccharide (S-LPS) and rough lipopolysaccharide (R-LPS), smooth and rough strains of Brucella abortus were extracted by two different modifications of the phenol-water method. S-LPS was obtained in the phenol phase, and R-LPS was obtained in the aqueous phase. Further purification was accomplished by treatment with enzymes, detergents, NaI as a chaotropic agent to separate non-covalently bound contaminants, and by gel filtration. The degree of purity of the molecules was determined by chemical and immunological analysis and by electrophoresis in sodium dodecyl sulfate-polyacrylamide gels. Lipid identification by gas-liquid chromatography showed seven major fatty acids. Palmitic acid accounts for about 50%, stearic acid accounts for about 10%, and hydroxylated fatty acids account for less than 5% of total fatty acids. 2-Keto-3-deoxyoctonate but not heptose was detected in the sugar analysis. Protein was found to be firmly bound to S-LPS but not to R-LPS.
为了获得纯净且特征明确的光滑型脂多糖(S-LPS)和粗糙型脂多糖(R-LPS),采用两种不同改进的酚水法提取流产布鲁氏菌的光滑型菌株和粗糙型菌株。S-LPS在酚相中获得,R-LPS在水相中获得。通过用酶、去污剂、作为离液剂的碘化钠处理以分离非共价结合的污染物,并通过凝胶过滤进一步纯化。通过化学和免疫学分析以及在十二烷基硫酸钠-聚丙烯酰胺凝胶中的电泳来确定分子的纯度。气液色谱法鉴定脂质显示有七种主要脂肪酸。棕榈酸约占50%,硬脂酸约占10%,羟基化脂肪酸占总脂肪酸的比例不到5%。在糖分析中检测到2-酮-3-脱氧辛酸,但未检测到庚糖。发现蛋白质与S-LPS紧密结合,但与R-LPS不结合。