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采用凝集素对须毛癣菌和其他嗜角质丝状真菌的真菌细胞壁表面糖缀合物进行碳水化合物分析。

Carbohydrate profiling of fungal cell wall surface glycoconjugates of Trichophyton tonsurans and other keratinophilic filamentous fungi using lectins.

机构信息

Department of Mycology, Federal University of Pernambuco, Recife, PE, Brazil.

出版信息

Mycoses. 2011 Nov;54(6):e789-94. doi: 10.1111/j.1439-0507.2011.02026.x. Epub 2011 May 25.

Abstract

Various researchers have concluded that lectins are useful reagents for the study of fungal cell wall surface glycoconjugates. In this study, we evaluated the expression of N-acetyl-D-glucosamine, L-fucose, D-galactose and glucose/mannose on the cell wall surface of Trichophyton tonsurans and other keratinophilic filamentous fungi, using a simple lectin-binding protocol. The fungal cultures used were isolated from soils obtained from public parks by the hair-bait technique. The lectin assays used concanavalin A (Con A), wheat germ agglutinin (WGA), Ulex europeus agglutinin I (UEA-I) and peanut agglutinin (PNA), all conjugated with horseradish peroxidase. Adhesive tape was placed sticky-side down over the fungal colony, gently pressed and then removed. The fungal-tape samples were incubated with the lectin for 1 h at 4 °C. Lectin binding was visualised using 3,3-diaminobendizine (DAB) and hydrogen peroxidase. There was a high expression of N-acetyl-D-glucosamine on the cell wall surface of all fungi species tested, whereas the expression of L-fucose, D-galactose and glucose/mannose demonstrated inter-specific variations. The lectin-binding assay presented in this article eliminates many of the laborious steps involved in other protocols. The amount and quality of the mycelium and spores immobilised by the adhesive tapes were suitable for obtaining the carbohydrate profile in glycoconjugates of the cell wall surface of filamentous fungi.

摘要

多位研究人员得出结论,凝集素是研究真菌细胞壁表面糖缀合物的有用试剂。在这项研究中,我们使用简单的凝集素结合方案评估了糠秕马拉色菌和其他嗜角质丝状真菌细胞壁表面的 N-乙酰-D-葡萄糖胺、L-岩藻糖、D-半乳糖和葡萄糖/甘露糖的表达。使用的真菌培养物是通过毛发诱饵技术从公共公园的土壤中分离出来的。使用的凝集素检测有伴刀豆球蛋白 A(Con A)、麦胚凝集素(WGA)、荆豆凝集素 I(UEA-I)和花生凝集素(PNA),均与辣根过氧化物酶结合。粘性面向下将胶带贴在真菌菌落上,轻轻按压后取下。将真菌-胶带样品在 4°C 下与凝集素孵育 1 小时。使用 3,3-二氨基联苯胺(DAB)和过氧化物酶使凝集素结合可视化。所有测试的真菌物种的细胞壁表面都高度表达 N-乙酰-D-葡萄糖胺,而 L-岩藻糖、D-半乳糖和葡萄糖/甘露糖的表达则表现出种间差异。本文介绍的凝集素结合测定法消除了其他方案中许多繁琐的步骤。胶带固定的菌丝体和孢子的数量和质量适合获得丝状真菌细胞壁表面糖缀合物中的碳水化合物图谱。

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