Tronchin G, Poulain D, Biguet J
Arch Microbiol. 1979;123(3):245-9. doi: 10.1007/BF00406657.
The ultrastructural localization of polysaccharides in the cell wall of Candida albicans was carried out by means of Concanavalin A on glycol methacrylate ultrathin sections. The sections were incubated successively with horseradish peroxydase, 3-3' diaminobenzidine and H2O2, for revealing the binding sites of the lectin. This method allowed us to localize mannan, since Concanavalin A does not react with other polysaccharides of the C. albicans cell wall. In these conditions mannan was found to be located in two continuous reactive layers at the periphery of blastospores cell wall. The results are discussed in relation with those obtained by another method using the polysaccharide detection technique described by Thiery (PATAg).
通过伴刀豆球蛋白A对甲基丙烯酸乙二醇酯超薄切片进行白色念珠菌细胞壁多糖的超微结构定位。切片先后与辣根过氧化物酶、3,3'-二氨基联苯胺和过氧化氢孵育,以显示凝集素的结合位点。由于伴刀豆球蛋白A不与白色念珠菌细胞壁的其他多糖反应,该方法使我们能够定位甘露聚糖。在这些条件下,发现甘露聚糖位于芽生孢子细胞壁外围的两个连续反应层中。结合使用蒂埃里(PATAg)描述的多糖检测技术的另一种方法所获得的结果对这些结果进行了讨论。