Hofstad T, Sveen K, Dahlén G
Acta Pathol Microbiol Scand B. 1977 Aug;85(4):262-70. doi: 10.1111/j.1699-0463.1977.tb01972.x.
Lipopolysaccharides (LPS) extracted from strains of Bacteroides fragilis, Bacteroides melaninogenicus and Bacteroides oralis with phenol-water, trichloroacetic acid, EDTA or liquid phenol-chloroform-petroleum ether (PCP) and isolated by ultracentrifugation, varied considerably in their quantitative chemical composition. Negligible yields of LPS were obtained by PCP-extraction. All preparations were more or less serologically active. All methods (except PCP) extracted the same O-antigenic determinants from B. fragilis. Endotoxic activity, as measured by primary skin inflammations in rabbits, was low but was present in all preparations. Proteins (and/or lipoproteins) co-precipitated with LPS in the ultracentrifuge.
用酚水、三氯乙酸、乙二胺四乙酸(EDTA)或液体苯酚 - 氯仿 - 石油醚(PCP)从脆弱拟杆菌、产黑色素拟杆菌和口腔拟杆菌菌株中提取并通过超速离心分离得到的脂多糖(LPS),其化学组成在数量上有很大差异。通过PCP提取获得的LPS产量可忽略不计。所有制剂或多或少都具有血清学活性。所有方法(除PCP外)从脆弱拟杆菌中提取相同的O抗原决定簇。通过兔原发性皮肤炎症测定的内毒素活性较低,但所有制剂中都存在。在超速离心机中,蛋白质(和/或脂蛋白)与LPS共沉淀。