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Appl. Environ. Microbiol., Nov 1997, 4360-4369, Vol 63, No. 11
C Wawer, MS Jetten and G Muyzer
The genetic diversity and expression of the [NiFe] hydrogenase large-
subunit gene of Desulfovibrio spp. in environmental samples were determined
in order to show in parallel the existing and active members of
Desulfovibrio populations. DNA and total RNA were extracted from different
anaerobic bioreactor samples; RNA was transcribed into cDNA. Subsequently,
PCR was performed to amplify a ca.-440-bp fragment of the [NiFe]
hydrogenase large-subunit gene and its mRNA. Denaturing gradient gel
electrophoresis analysis was used to separate the PCR products according to
their sequence and thereby to visualize the individual community members.
Desulfovibrio strains corresponding to amplified [NiFe] hydrogenase
transcripts were regarded as metabolically active, because in pure cultures
transcripts were detectable in exponentially growing cells but not in
cultures in the stationary phase. DNA sequencing and comparative sequence
analysis were used to identify the detected organisms on the basis of their
[NiFe] hydrogenase sequences. The genes of characterized Desulfovibrio spp.
showed a considerable extent of divergence (ca. 30%), whereas sequences
obtained from bacterial populations of the bioreactors showed a low level
of variation and indicated the coexistence of closely related strains
probably belonging to the species Desulfovibrio sulfodismutans. Under
methanogenic conditions, all detected populations were active; under
denitrifying conditions, no [NiFe] hydrogenase mRNA was visible. Changes in
activity and composition of Desulfovibrio populations caused by changes in
the environmental conditions could be monitored by using the approach
described in this study.
Copyright © 1997, American Society for Microbiology
Genetic diversity and expression of the [NiFe] hydrogenase large- subunit gene of Desulfovibrio spp. in environmental samples
Molecular Ecology Group, Max-Planck-Institute for Marine Microbiology, Bremen, Germany.
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