1.Centrifuge 2-3ml bacteria liquid with 8000rpm and remove the supernatant; resuspense the liquid with lysyme(10mg/ml)~200ul and then leave it at temperature 37℃ for 0.5-1 hour. 2.Centrifuge the liquid with 8000rpm and remove the supernatant; resuspense it with 250uL buffer P1. 3.Add 250uL buffer P2 (Alkaline lysis buffer), make it clear (reverse the tube evenly for several times) and leave it at room temperature for 2-4 minutes. 4.Add 350uL buffer P3 and reverse the tube evenly until it layers. 5.Centrifuge the tube for 10 minutes and extract plasmid extraction column from the upper water phase. 6.The following steps are identical with those of Escherichia coli.
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