Lindberg A A, Holme T, Hellerqvist C G, Svensson S
J Bacteriol. 1970 May;102(2):540-7. doi: 10.1128/jb.102.2.540-547.1970.
The formation of complete cell wall core lipopolysaccharide (LPS) and O-antigenic side chains after addition of d-galactose to the uridine diphosphate-galactose-4-epimeraseless mutant, Salmonella typhimurium LT2-M1, has been studied by (i) determination of adsorption rates of smooth and rough specific bacteriophages, (ii) passive hemagglutination inhibition, and (iii) qualitative and quantitative determination of the polysaccharide composition and structure. A rapid synthesis of the complete core LPS and O side chains occurred in bacteria in the log phase and the early stationary phase. Phage C21, which attaches to unsubstituted Rc structures, was adsorbed by the bacteria for only 10 min after the addition of d-galactose. Unsubstituted Rc structures, however, could still be detected after 160 min by immunological and chemical assays. Attachment of the P22 phage, which requires O-specific side chains with more than one repeating unit for adsorption, was demonstrated 10 min after the addition of d-galactose. Attachment of the Felix O-1 phage, which requires a complete core, was observed between 20 and 80 min after the addition of d-galactose. The rough specific phages 6SR and Br2 did not adsorb to the bacteria at any time after the addition of d-galactose. By passive hemagglutination inhibition, the presence of O-specific structures could be demonstrated after 10 min. No antigenic activity of the Ra and Rb structures was observed in the LPS preparations isolated at any time after the addition of d-galactose. Methylation analysis of LPS preparations isolated at 10 and 160 min after the addition of d-galactose showed that the O-specific side chains contained an average of 11 and 15 repeating units, respectively. In the 10-min sample, every 25th "Rc structure" carried a side chain, compared to every 3rd residue in the 160-min sample.
在向尿苷二磷酸半乳糖-4-差向异构酶缺陷型鼠伤寒沙门氏菌LT2-M1添加d-半乳糖后,完整细胞壁核心脂多糖(LPS)和O抗原侧链的形成已通过以下方法进行研究:(i)测定光滑型和粗糙型特异性噬菌体的吸附率;(ii)被动血凝抑制;(iii)多糖组成和结构的定性及定量测定。在对数期和早期稳定期的细菌中,完整核心LPS和O侧链迅速合成。附着于未取代Rc结构的噬菌体C21,在添加d-半乳糖后仅10分钟就被细菌吸附。然而,通过免疫和化学分析,在160分钟后仍可检测到未取代的Rc结构。需要具有多个重复单元的O特异性侧链才能吸附的P22噬菌体,在添加d-半乳糖后10分钟就显示出吸附。需要完整核心的Felix O-1噬菌体在添加d-半乳糖后20至80分钟之间被观察到吸附。粗糙型特异性噬菌体6SR和Br2在添加d-半乳糖后的任何时间都不吸附到细菌上。通过被动血凝抑制,在10分钟后可证明存在O特异性结构。在添加d-半乳糖后的任何时间分离的LPS制剂中均未观察到Ra和Rb结构的抗原活性。对添加d-半乳糖后10分钟和160分钟分离的LPS制剂进行甲基化分析表明,O特异性侧链分别平均含有11个和15个重复单元。在10分钟的样品中,每25个“Rc结构”带有一条侧链,而在160分钟的样品中,每3个残基带有一条侧链。