Hether N W, Jackson L L
J Bacteriol. 1983 Nov;156(2):809-17. doi: 10.1128/jb.156.2.809-817.1983.
A lipoteichoic acid (LTA) was extracted from Listeria monocytogenes (serotype 1) by phenol-water partition and isolated by gel-filtration chromatography. The LTA exhibited amphiphilic properties by changes in gel-filtration mobility in the presence of detergent buffers and after mild base hydrolysis. In a hemagglutination assay, Listeria LTA bound antibody prepared against a known LTA from Streptococcus spp. Listeria LTA inhibited the binding of anti-LTA antibody to a Lactobacillus LTA in a hemagglutination inhibition assay. The Listeria LTA contained glucose, galactose, fatty acids, glycerol, and phosphate with molar ratios of 0.05, 0.07, 0.21, 0.94, and 1.0 to phosphate, respectively. Adjacent glycerols were linked between the C-1 and C-3 positions by phosphodiesters (structural type 1). The average chain length was 19 +/- 2 (standard deviation) glycerol-phosphate repeating units. Approximately one glycosyl side chain was present per LTA molecule. The side chain was a galactose-containing disaccharide. The lipid portion of the LTA was a galactose- and glucose-containing glycolipid which may have been a phosphoglycolipid, but the structure was not confirmed. Major fatty acids of LTA and the glycolipid were 17:anteiso, 15:anteiso, 16:iso, 16:n, and 18:n. L. monocytogenes contained cell wall products typical of gram-positive bacteria which is in contrast to the reports by others of the presence of lipopolysaccharides from L. monocytogenes.
通过酚-水分配法从单核细胞增生李斯特菌(血清型1)中提取脂磷壁酸(LTA),并通过凝胶过滤色谱法进行分离。在存在去污剂缓冲液时以及轻度碱水解后,LTA通过凝胶过滤迁移率的变化表现出两亲性。在血凝试验中,李斯特菌LTA与针对已知链球菌属LTA制备的抗体结合。在血凝抑制试验中,李斯特菌LTA抑制抗LTA抗体与乳酸杆菌LTA的结合。李斯特菌LTA含有葡萄糖、半乳糖、脂肪酸、甘油和磷酸盐,其与磷酸盐的摩尔比分别为0.05、0.07、0.21、0.94和1.0。相邻的甘油通过磷酸二酯在C-1和C-3位之间相连(结构类型1)。平均链长为19±2(标准差)个甘油磷酸重复单元。每个LTA分子大约存在一个糖基侧链。侧链是含半乳糖的二糖。LTA的脂质部分是含半乳糖和葡萄糖的糖脂,可能是磷酸糖脂,但结构未得到证实。LTA和糖脂的主要脂肪酸为17:anteiso、15:anteiso、16:iso、16:n和18:n。单核细胞增生李斯特菌含有革兰氏阳性菌典型的细胞壁产物,这与其他关于单核细胞增生李斯特菌存在脂多糖的报道形成对比。