1988
DOI: 10.1007/bf00425577
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A new purple sulfur bacterium from stratified freshwater lakes, Amoebobacter purpureus sp. nov.

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Cited by 74 publications
(66 citation statements)
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“…In contrast, the average N-based doubling time for C. clathratiforme (45 days) substantially exceeded the C-based growth rates, indicating that this anaerobic phototroph may indeed deposit C-rich storage products. The observed doubling times for all 3 species were significantly longer than those (0.5-1.5 days) reported for pure cultures of green and purple sulfur bacteria grown under ideal laboratory conditions (27)(28)(29) but were within the range (0.3-125 d) (20) of doubling times estimated from bulk in situ measurements of biomass or CO 2 fixation (20,30,31). Intriguingly, the C-and N-based doubling times (7 and 8 days) for bulk biomass from the Lake Cadagno chemocline were comparable with the doubling times for C. okenii and L. purpurea and substantially shorter than the doubling time for C. clathratiforme (Fig.…”
Section: Resultsmentioning
confidence: 56%
“…In contrast, the average N-based doubling time for C. clathratiforme (45 days) substantially exceeded the C-based growth rates, indicating that this anaerobic phototroph may indeed deposit C-rich storage products. The observed doubling times for all 3 species were significantly longer than those (0.5-1.5 days) reported for pure cultures of green and purple sulfur bacteria grown under ideal laboratory conditions (27)(28)(29) but were within the range (0.3-125 d) (20) of doubling times estimated from bulk in situ measurements of biomass or CO 2 fixation (20,30,31). Intriguingly, the C-and N-based doubling times (7 and 8 days) for bulk biomass from the Lake Cadagno chemocline were comparable with the doubling times for C. okenii and L. purpurea and substantially shorter than the doubling time for C. clathratiforme (Fig.…”
Section: Resultsmentioning
confidence: 56%
“…As described in detail previously (26), phototrophic sulfur bacteria were initially enriched in liquid medium containing 0. 5 g KH 2 (10). The medium was reduced with 0.3 g liter Ϫ1 Na 2 S · 9H 2 O (1.10 mM final concentration) and adjusted to a pH around 7.2 or 6.8 for Chromatiaceae (33) and Chlorobiaceae (23), respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Enrichments in liquid medium were resuspended in 5 ml liquid medium before inoculation into agar shake dilution series (1%, vol/vol) prepared by the Hungate technique (27,36). All cultures were incubated at room temperature (20 to 23°C) with a 6 h light/6 h dark photoperiod at light intensities of 4 to 8 and 5 to 20 E m Ϫ2 s Ϫ1 for Chlorobiaceae and Chromatiaceae, respectively, generated with an incandescent 40-W bulb placed at a distance of 60 cm from the cultures (10). Enrichments and resuspended colonies of the agar shake dilution series were analyzed for target organisms by in situ hybridization with Cy3-labeled oligonucleotide probes listed in Table 1 (31,32).…”
Section: Methodsmentioning
confidence: 99%
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“…In vivo-spectroscopy of water samples taken from 8-10 m and concentrated in the centrifuge indicated the presence of accessory pigments characteristic of phototrophic bacteria: phycoerythrin and phycocyanin (cyanobacteria), okenone (Chromatiaceae: Arnoebobacter purpureus, Eichler and Pfennig (1988)) and Isorenieratene/~-Isorenieratene (brown members of the Chlorobiaceae: Pelodictyon, Pelochrornatium). Epifluorescence microscopy revealed the presence of cyanobacteria by the orange autofluorescence of phycoerythrin (French and Young (1952)).…”
Section: Distribution Of Phytoplankton and Photosynthetic Pigmentsmentioning
confidence: 99%