We describe a simple and efficient procedure for transformation of Schizosaccharomyces pombe. Sz. pombe colonies grown on minimal (SD) plates were directly removed and suspended in a 100 μl reaction mixture containing 70 μl PLATE solution (50% polyethylene glycol-4000, 100 mM lithium acetate, 10 mM Tris-HCl, pH 4.9, and 1 mM EDTA), 10 μl plasmid DNA (1 μg), 10 μl carrier DNA (100 μg) and 10 μl sterile distilled water. After incubation at 30°C for 1 h followed by heat shock treatment at 42°C for 15 min, the reaction mixture was spread on a selection plate. The transformation efficiency obtained using the procedure was approximately 8000 transformants/μg DNA. The method is simple and time-saving, making it especially useful for a large number of samples and when a high transformation efficiency is not required.
|出版ステータス||出版済み - 6月 2004|
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