A simple procedure for isolating yeast DNA suitable for use ns a template f
or PCR amplification is described. SDS treatment alone is sufficient for ex
traction of chromosomal DNA from yeast cells. Cells of a yeast colony are s
uspended in a small volume (about 20 mu L) of a 0.25% SDS solution, mixed v
igorously and centrifuged. The supernatant cart be directly used as a templ
ate after dilution to give nn SDS concentration of less than 0.01% in the f
inal PCR mixture.