TABLE 3.
Procedure | Chemical treatmenta | Physical treatmentb | DNA yield (μg g [dry wt]−1)c
|
% Cell lysis with wetland sediment (mean ± SE)d | ||
---|---|---|---|---|---|---|
Agricultural soil | Forest soil | Wetland sediment | ||||
1 | SDS | B | 7.0 ± 0.5 | 26 ± 4 | 32 ± 1 | 68 ± 4 |
2 | SDS-phenol | B | 7.8 ± 0.2 | 31 ± 5 | 40 ± 4 | 77 ± 5 |
3 | SDS-chloroform | B | 7.9 ± 1.2 | 35 ± 7 | 53 ± 8 | 81 ± 4 |
4 | SDS-Chelex 100 | B | 6.2 ± 0.3 | 19 ± 5 | 32 ± 2 | 68 ± 7 |
5 | Lysozyme-SDS | FT | 1.5 ± 0.7 | 4 ± 3 | 6 ± 1 | 65 ± 4 |
6 | GTC | FT | <0.1 | <0.1 | 0.2 ± 0.3 | 64 ± 3 |
7 | SDS | FT | 2.7 ± 0.8 | 6 ± 3 | 6 ± 1 | 63 ± 6 |
8 | Lysozyme-SDS | B | 1.5 ± 1.2 | 9 ± 4 | 7 ± 4 | 69 ± 2 |
9 | GTC | B | <0.1 | <0.1 | <0.1 | 67 ± 4 |
See Table 2, footnotes a and b.
See Table 2, footnote c.
Calculated from the average density of ethidium bromide-stained DNA bands by using NIH Image software. The values are averages ± standard errors based on three or four independent extractions.
Estimated from the DAPI direct counts of bacterial cells per microscope field before and after DNA extraction. The values are average percentages of cells lysed ± standard errors based on three independent DNA extractions performed by using the same DNA extraction procedure.