Butler M J, Gardiner R B, Day A W
Department of Biology, University of Western Ontario, London, Ontario, N6A 5B7 Canada.
Mycologia. 2005 Mar-Apr;97(2):312-9. doi: 10.3852/mycologia.97.2.312.
Silver-staining procedures were investigated for their effectiveness in identifying cell wall-based fungal melanins in live and fixed plastic embedded samples, particularly 1,8-dihydroxynaphthalene (DHN) based polyketide melanins. We developed a simple and reliable melanin-staining technique based on a silver accumulation method originally published for histological demonstration of heavy metal sulfides in mammalian tissues. Copper is bound to fungal melanin followed by formation of the copper sulfide at melanin sites in fungal cell walls, which then are amplified into vivid black stains using a silver enhancement step. The method demonstrates patterns of melanization in a range of fungal hyphae and is suitable for light and electron microscopy. Albino mutant fungi and normally nonmelanized fungi do not stain with the sulfide-silver technique. Mammalian melanocytes also were labeled by the technique, indicating its universality as a melanin probe.
研究了银染程序在识别活的和固定的塑料包埋样本中基于细胞壁的真菌黑色素,特别是基于1,8 - 二羟基萘(DHN)的聚酮黑色素方面的有效性。我们基于最初发表的用于组织学显示哺乳动物组织中重金属硫化物的银积累方法,开发了一种简单可靠的黑色素染色技术。铜与真菌黑色素结合,随后在真菌细胞壁的黑色素位点形成硫化铜,然后通过银增强步骤将其放大为鲜明的黑色污渍。该方法展示了一系列真菌菌丝中的黑色素化模式,适用于光学显微镜和电子显微镜。白化突变真菌和通常无黑色素的真菌不会被硫化银技术染色。该技术也标记了哺乳动物黑色素细胞,表明其作为黑色素探针的通用性。