Leitao Eduardo A, Bittencourt Vera C B, Haido Rosa M T, Valente Ana P, Peter-Katalinic Jasna, Letzel Matthias, de Souza Lauro M, Barreto-Bergter Eliana
Instituto de Microbiologia Professor Paulo de Góes, CCS Universidade Federal do Rio de Janeiro, 21944-970, Rio de Janeiro, RJ, Brasil.
Glycobiology. 2003 Oct;13(10):681-92. doi: 10.1093/glycob/cwg089. Epub 2003 Jul 8.
O-linked oligosaccharide groups ranging from di- to hexasaccharide were beta-eliminated by mild alkaline treatment under reducting conditions from the peptidogalactomannan of Aspergillus fumigatus mycelial cell wall. The resulting reduced oligosaccharides, which were the minor components of the peptidogalactomannan fraction, were fractionated to homogeneity by successive gel filtration and high-performance liquid chromatography. Their primary structures were determined based on a combination of techniques including gas chromatography, ESI-QTOF-MS, 1H COSY and TOCSY, and 1H-13C HMQC NMR spectroscopy and methylation analysis, to be: alpha-Glcp-(1 --> 6)-Man-ol, beta-Galf-(1 --> 6)-alpha-Manp-(1 --> 6)-Man-ol, beta-Galf-(1 --> 5)-beta-Galf-(1 --> 6)-alpha-Manp-(1 --> 6)-Man-ol and beta-Galf-(1 --> 5)-[beta-Galf-(1 --> 5]3-beta-Galf-(1 --> 6)-Man-ol. The beta-Galf containing oligosaccharides have not been previously described as fungal O-linked oligosaccharides. The peptidogalactomannan is antigenic and was recognized by human sera of patients with aspergillosis when probed by ELISA, but de-O-glycosylation rendered a 50% decrease in its reactivity. Furthermore, when tested in a hapten inhibition test, the isolated oligosaccharide alditols were able to block, on a dose-response basis, recognition between human sera and the intact peptidogalactomannan. The immunodominant epitopes were present in the tetra- and hexasaccharide, which contain a beta-Galf-(1 --> 5)-beta-Galf terminal group. These results suggest that the O-glycosidically linked oligosaccharide chains, despite being the less abundant carbohydrate component of the A. fumigatus peptidogalactomannan, may account for a significant part of its antigenicity, other than the known activity associated with the galactomannan component.
在还原条件下,通过温和的碱性处理,从烟曲霉菌丝细胞壁的肽聚糖甘露聚糖中β-消除了二糖至六糖的O-连接寡糖基团。所得的还原寡糖是肽聚糖甘露聚糖组分的次要成分,通过连续的凝胶过滤和高效液相色谱法将其分离至同质。基于气相色谱、电喷雾电离-四极杆飞行时间质谱、1H COSY和TOCSY、1H-13C HMQC NMR光谱以及甲基化分析等技术的组合,确定了它们的一级结构为:α-Glcp-(1→6)-Man-ol、β-Galf-(1→6)-α-Manp-(1→6)-Man-ol、β-Galf-(1→5)-β-Galf-(1→6)-α-Manp-(1→6)-Man-ol和β-Galf-(1→5)-[β-Galf-(1→5)]3-β-Galf-(1→6)-Man-ol。含β-Galf的寡糖以前未被描述为真菌O-连接寡糖。肽聚糖甘露聚糖具有抗原性,通过ELISA检测时,被曲霉病患者的人血清识别,但去O-糖基化使其反应性降低了50%。此外,在半抗原抑制试验中进行测试时,分离出的寡糖糖醇能够基于剂量反应阻断人血清与完整肽聚糖甘露聚糖之间的识别。免疫显性表位存在于四糖和六糖中,其含有β-Galf-(1→5)-β-Galf末端基团。这些结果表明,尽管O-糖苷连接的寡糖链是烟曲霉肽聚糖甘露聚糖中含量较少的碳水化合物成分,但除了与半乳甘露聚糖成分相关的已知活性外,它可能在其抗原性中占很大一部分。