Abstract
A rapid DNA extraction method utilizing a bead-beating machine is described. High molecular weight DNA could be extracted from up to 24 samples in less than 2 h. The DNA was suitable for direct use in the polymerase chain reaction (PCR). Both prokaryotic and eukaryotic cells were successfully lysed by the method, established using primers specific for these groups. The small subunits ribosomal RNA (rRNA) spacer region from both eukaryotes and eubacteria could be readily amplified with DNA from different soils generating different amplification patterns.
Original language | English |
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Pages (from-to) | 49-53 |
Number of pages | 5 |
Journal | Letters in Applied Microbiology |
Volume | 27 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jul 1998 |