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Analysis of Lipooligosaccharide Biosynthesis in theNeisseriaceae

机译:奈瑟菌科中脂寡糖生物合成的分析

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Neisserial lipooligosaccharide (LOS) contains three oligosaccharide chains, termed the α, β, and γ chains. We used Southern hybridization experiments on DNA isolated from variousNeisseria spp. to determine if strains considered to be nonpathogenic possessed DNA sequences homologous with genes involved in the biosynthesis of these oligosaccharide chains. The presence or absence of specific genes was compared to the LOS profiles expressed by each strain, as characterized by their mobilities on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel and their reactivities with various LOS-specific monoclonal antibodies. A great deal of heterogeneity was seen with respect to the presence of genes encoding glycosyltransferases in Neisseria. All pathogenic species were found to possess DNA sequences homologous with the lgtgene cluster, a group of genes needed for the synthesis of the α chain. Some of these genes were also found to be present in strains considered to be nonpathogenic, such as Neisseria lactamica, N. subflava, and N. sicca. Some nonpathogenicNeisseria spp. were able to express high-molecular-mass LOS structures, even though they lacked the DNA sequences homologous withrfaF, a gene whose product must act before gonococcal and meningococcal LOS can be elongated. Using a PCR amplification strategy, in combination with DNA sequencing, we demonstrated that N. subflava 44 possessed lgtA, lgtB, andlgtE genes. The predicted amino acid sequence encoded by each of these genes suggested that they encoded functional proteins; however, structural analysis of LOS isolated from this strain indicated that the bulk of its LOS was not modified by these gene products. This suggests the existence of an additional regulatory mechanism that is responsible for the limited expression of these genes in this strain.
机译:奈瑟球菌低聚糖(LOS)包含3条寡糖链,分别称为α,β和γ链。我们对分离自各种 Neisseria spp的DNA进行了Southern杂交实验。确定被认为是非致病性的菌株是否具有与参与这些寡糖链生物合成的基因同源的DNA序列。将特定基因的存在与否与每个菌株表达的LOS谱进行比较,以它们在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳凝胶上的迁移性以及它们与各种LOS特异性单克隆抗体的反应性为特征。关于奈瑟氏菌中编码糖基转移酶的基因,存在很大的异质性。发现所有病原体都具有与 lgt 基因簇同源的DNA序列,这是合成α链所需的一组基因。还发现其中一些基因存在于被认为是非致病性的菌株中,例如乳酸奈瑟氏菌,枯草芽孢杆菌 N。干燥剂。一些非致病性奈瑟菌 spp。即使它们缺乏与 rfaF 同源的DNA序列,该分子仍能表达大分子LOS结构,该基因的产物必须在淋球菌和脑膜炎球菌LOS延长之前起作用。使用PCR扩增策略,结合DNA测序,我们证明了 N。 subflava 44具有 lgtA,lgtB lgtE 基因。这些基因各自编码的预测氨基酸序列表明,它们编码功能蛋白。然而,从该菌株分离的LOS的结构分析表明,其大部分LOS没有被这些基因产物修饰。这表明存在另外的调节机制,其负责这些基因在该菌株中的有限表达。

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