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. 2002 Jun;68(6):3067–3075. doi: 10.1128/AEM.68.6.3067-3075.2002

TABLE 1.

Detection of AOB and Nitrosomonas spp. in root, rhizosphere, and soil by PCR, DGGE, and FISHa

Sample AOB (Nitrosomonas) detected by:
amoA PCRb DGGEb FISHc (107 cells [cm3 of roots]−1)
KDML roots +++ (+) 5.0 ± 0.8 (1.2 ± 0.4)
Mahsuri roots +++ (−) 6.0 ± 1.0 (1.3 ± 0.4)
IR63087 roots +++ (+++) 6.8 ± 1.2 (4.0 ± 0.3)
KDML rhizosphere +++ (+) ND
Mahsuri rhizosphere +++ (−) ND
IR63087 rhizosphere +++ (++) ND
Unplanted soil +++ (+) ND
a

PCR was used to amplify the ammonium monooxygenase gene (amoA) which was subsequently resolved by DGGE. Cell densities were detected by FISH using group-specific oligonucleotide probes.

b

Symbols: +, ++, and +++, presence of amoA or (Nitrosomonas) PCR product in one, two, or three replicates, respectively; −, no product was detected in all replicates. Qualitative results from three replicates are presented.

c

Means (n = 15) of cell densities ± 95% confidence limits (all symbols and values in parentheses refer to Nitrosomonas).