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Appl. Environ. Microbiol., Apr 1995, 1201-1207, Vol 61, No. 4
TD Leser, M Boye and NB Hendriksen
Genetically engineered Pseudomonas sp. strain B13(FR1) was released into
laboratory-scale marine ecosystem models (microcosms). Survival of the
introduced population in the water column and the sediment was determined
by plating on a selective medium and by quantitative competitive PCR. The
activity of the released bacteria was determined by in situ hybridization
of single cells with a specific rRNA-targeting oligonucleotide probe. Two
microcosms were inoculated with 10(6) cells ml-1, while an uninoculated
microcosm served as a control. The number of Pseudomonas sp. strain
B13(FR1) cells decreased rapidly to ca. 10(2) cells ml-1 within 2 days
after the release, which is indicative of grazing by protozoa. Three days
after the introduction into seawater, cells were unculturable, but PCR
continued to detect cells in low numbers. Immediately after the release,
the ribosomal content of Pseudomonas sp. strain B13(FR1) corresponded to a
generation time of 2 h. The growth rate decreased to less than 0.04 h-1 in
5 days and remained low, probably because of carbon limitation of the
cells. Specific amendment of the microcosms with 10 mM 4-chlorobenzoate
resulted in a rapid increase of the growth rate and an exponentially
increasing number of cells detected by PCR, but not in resuscitation of the
cells to a culturable state. The release of Pseudomonas sp. strain B13(FR1)
into the microcosms seemed to affect only the indigenous bacterioplankton
community transiently. Effects on the community were also apparent from the
handling of water during filling of the microcosms and the amendment with
4-chlorobenzoate.
Copyright © 1995, American Society for Microbiology
Survival and activity of Pseudomonas sp. strain B13(FR1) in a marine microcosm determined by quantitative PCR and an rRNA-targeting probe and its effect on the indigenous bacterioplankton
Department of Marine Ecology and Microbiology, National Environmental Research Institute, Roskilde, Denmark.
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