Table 2.
Method/Kit |
Nicolaisen’s methoda |
MPb |
PMb |
PS + AKb |
Optimized method |
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TNA purification prior to digestc |
- |
+ |
- |
+ |
+ |
||||||||
Soils tested | FH | FL | Å | FH | FL | FH | FL | FH | FL | Å | FH | FL | Å |
Amplifiable DNAd | + | + | + | + | + | + | + | + | ±f | + | + | + | + |
Complete removal of DNA after 1st digestiond,e | + | - | - | + | - | + | - | + | - | - | + | + | - |
Complete removal of DNA after 2nd digestiond,e | + | - | - | + | ±f | + | - | + | - | + | + | + | + |
cDNA synthesis | + | NT | NT | + | ±f | + | NT | + | NT | + | + | + | + |
aMethod from Nicolaisen et al. (2008).
bSee Table 1 for list of kit abbreviations.
cTNA purification with the OPIR kit.
dSee text for details on DNA amplification and removal assessment.
eDNA was digested with TURBO DNase, and RCC kit was used for purification after each digestion.
fResults from replicates varied, likely due to the presence of inhibitory compounds.
gDNA, genomic DNA; NT, not tested because of residual gDNA.