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首页> 外文期刊>Infection and immunity >Structural modification of cell wall mannans of Candida albicans serotype A strains grown in yeast extract-Sabouraud liquid medium under acidic conditions.
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Structural modification of cell wall mannans of Candida albicans serotype A strains grown in yeast extract-Sabouraud liquid medium under acidic conditions.

机译:在酸性条件下在酵母提取物-Sabouraud液体培养基中生长的白色念珠菌血清A型菌株的细胞壁甘露聚糖的结构修饰。

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The cell wall mannans of two Candida albicans serotype A strains, NIH A-207 and J-1012 (abbreviated as A and J strains, respectively), cultured in yeast extract-Sabouraud liquid medium at pH 2.0, contained neither a phosphate group nor a beta-1,2-linked mannopyranose unit (H. Kobayashi, P. Giummelly, S. Takahashi, M. Ishida, J. Sato, M. Takaku, Y. Nishidate, N. Shibata, Y. Okawa, and S. Suzuki, Biochem. Biophys. Res. Commun. 175:1003-1009, 1991). In this study, the mannans obtained from A and J strains grown in pH 2.0 medium (abbreviated as mannans A2 and J2, respectively) exhibited quite different reactivities against rabbit anti-C. albicans and anti-Saccharomyces cerevisiae sera compared with those of mannans from the corresponding strains cultured in conventional medium at pH 5.9 (abbreviated as mannans A and J, respectively). Namely, mannans A2 and J2 lost reactivity against the former serum but reacted with the latter serum to a higher extent than mannans A and J. In order to account for these difference in more detail, mannans A2 and J2 were subjected to acetolysis. Elution profiles of the acetolysates were completely different from those of acetolysates obtained from mannans A and J reported in our previous papers. The 1H nuclear magnetic resonance spectra of the oligosaccharides from mannans A2 and J2 obtained by this procedure indicate that the side chains are composed of alpha-linked mannopyranose units densely linked to the alpha-1,6-linked backbone. The long side chains containing one alpha-1,3-linked mannopyranose unit are markedly increased.
机译:在pH 2.0的酵母提取物-Sabouraud液体培养基中培养的两种白色念珠菌血清型A菌株NIH A-207和J-1012(分别缩写为A和J菌株)的细胞壁甘露聚糖既不含磷酸基也不含磷酸氢根。 β-1,2-连接的甘露吡喃糖单元(H.Kobayashi,P.Giummelly,S。高桥,石田M.,佐藤J.M.Takaku,Yishidate,N.Shibata,Y.Okawa和S.Suzuki ,Biochem.Biophys.Res.Commun.175:1003-1009,1991)。在这项研究中,从在pH 2.0培养基中生长的A和J菌株(分别缩写为甘露聚糖A2和J2)获得的甘露聚糖对兔抗C的反应性完全不同。将白色念珠菌和抗酿酒酵母血清与在pH 5.9的常规培养基中培养的相应菌株的甘露聚糖血清(分别缩写为甘露聚糖A和J)进行比较。即,甘露聚糖A2和J2对前一种血清失去反应性,但是与后者血清反应的程度高于甘露聚糖A和J。为了更详细地说明这些差异,对甘露聚糖A2和J2进行了乙酰分解。乙酰水解产物的洗脱曲线与我们先前论文中报道的从甘露聚糖A和J获得的乙酰水解产物的洗脱曲线完全不同。通过该程序获得的来自甘露聚糖A2和J2的寡糖的1H核磁共振谱表明,侧链由紧密连接至α-1,6-连接的骨架的α连接的甘露吡喃糖单元组成。含有一个α-1,3-连接的甘露吡喃糖单元的长侧链显着增加。

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