The populations of N-2-fixing and denitrifying bacteria in an acid forest s
oil near Cologne were characterized by gene probing. The DNA isolated from
the soil for this purpose was suitable For DNA-DNA hybridization using 0.4-
0.7-kb probes targeting denitrification enzymes, dinitrogenase reductase (n
ifH) and eubacterial 16S rRNA. The densitometrical comparison of band inten
sities obtained in these Southern hybridizations indicated that the highest
number of total bacteria, of denitrifying and Nz-fixing microorganisms alw
ays occurred in the upper (similar to 5 cm) soil layer. The concentration o
f all these organisms decreased in parallel with the soil depth. The soil i
nvestigated was rich in nitrate in all layers, and the availability of nitr
ate apparently did not govern the distribution of denitrifying and N-2-fixi
ng bacteria in this soil. Soil cores investigated in the laboratory formed
N2O on addition of nitrate irrespective of the presence of C2H2. Hybridizat
ion intensities, with a gene probe for the 16S rRNA, and MPN numbers were g
enerally higher in soil samples taken from the roots of plants than in the
bulk soil. There was no selective enrichment of denitrifying or N-2-fixing
bacteria at the roots. The data obtained by hybridizing isolated soil DNA g
enerally matched previous results obtained with culturable bacteria. (C) 20
01 Federation of European Microbiological Societies. Published by Elsevier
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