Melo S C O, Pungartnik C, Cascardo J C M, Brendel M
Departamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brasil.
Genet Mol Res. 2006 Dec 14;5(4):851-5.
DNA isolation from some fungal organisms is difficult because they have cell walls or capsules that are relatively unsusceptible to lysis. Beginning with a yeast Saccharomyces cerevisiae genomic DNA isolation method, we developed a 30-min DNA isolation protocol for filamentous fungi by combining cell wall digestion with cell disruption by glass beads. High-quality DNA was isolated with good yield from the hyphae of Crinipellis perniciosa, which causes witches' broom disease in cacao, from three other filamentous fungi, Lentinus edodes, Agaricus blazei, Trichoderma stromaticum, and from the yeast S. cerevisiae. Genomic DNA was suitable for PCR of specific actin primers of C. perniciosa, allowing it to be differentiated from fungal contaminants, including its natural competitor, T. stromaticum.
从某些真菌生物体中分离DNA很困难,因为它们具有相对不易被裂解的细胞壁或荚膜。我们从一种酵母酿酒酵母基因组DNA分离方法开始,通过将细胞壁消化与玻璃珠细胞破碎相结合,开发了一种用于丝状真菌的30分钟DNA分离方案。从引起可可树扫帚病的有害刺盘孢菌的菌丝、其他三种丝状真菌香菇、姬松茸、层状木霉以及酵母酿酒酵母中,以良好的产量分离出了高质量的DNA。基因组DNA适用于有害刺盘孢菌特异性肌动蛋白引物的PCR,使其能够与包括其天然竞争者层状木霉在内的真菌污染物区分开来。