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Genomic Dna Synthesis

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Genomic DNA was extracted from the fungal mat of Sclerotium rolfsii. Thirty mg of freeze-dried mycelium was ground to a fine powder in an Eppendorf tube in liquid nitrogen. The ground mycelium was resuspended and lysed in 500 µl of lysis buffer (40 mM Tris-acetate, 20 mM sodium acetate,1 mM EDTA, 1% w/v SDS pH 8) (Lerner and Model1981). RNase A (2 µl of 10 mg/ml; Sigma USA) was added and the mixture was incubated for 5 min at 37 °C. To facilitate the precipitation of most polysaccharides, protein and cell debris, 165 ml of 5 mol/l NaCl solution was added and the components mixed by inverting the tube several times. The suspension was centrifuged at 6700 x g for 20 min at 4 °C, the supernatant was immediately transferred to a fresh tube and

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