TABLE 3.
Amount of DNA extracted from different soils after lysis treatments according to protocols 1 to 5a
| Soil no. (origin)b | Amt of DNA (μg/g [dry wt] of soil) ± SD extracted after lysis protocol:c
|
||||||
|---|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4a | 4b | 5a | 5b | |
| 1. (Australia) | 17 ± 2 | 52 ± 2 | 32 ± 5 | 16 ± 3 | 33 ± 2 | 59 ± 1 | 27 ± 0 |
| 2. (Peyrat) | 29 ± 2 | 58 ± 1 | 40 ± 2 | 29 ± 2 | 18 ± 3 | 56 ± 1 | 15 ± 1 |
| 3. (Côte St André) | 36 ± 7 | 60 ± 6 | 148 ± 10 | 94 ± 7 | 38 ± 6 | 73 ± 5 | 47 ± 6 |
| 4. (Chazay) | 9 | 16 | NDd | 32 | 15 | 15 | 70 |
| 6. (Dombes) | 4 ± 2 | 26 ± 3 | 43 ± 1 | 61 ± 1 | 66 ± 1 | 160 ± 7 | 102 ± 5 |
Quantification was performed by phosphorimaging after dot blot hybridization with the universal probe FGPS431 (Table 2).
For soils 1, 2, 3, and 6, n = 3; for soil 4, n = 1.
Protocols: 1, no treatment; 2, dry soil grinding; 3, dry soil grinding plus Ultraturrax homogenization; 4a, dry soil grinding, homogenization, and microtip sonication; 4b, dry soil grinding, homogenization, and Cup Horn sonication; 5a, dry soil grinding, homogenization, microtip sonication, and chemical and enzymatic lysis; 5b, dry soil grinding, homogenization, Cup Horn sonication, and chemical and enzymatic lysis. See also Fig. 1.
ND, not determined.