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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 29 (1995), S. 2535-2540 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-184X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Seawater samples from a variety of locations contained viable luminous bacteria, but luminescence was not detectable although the system used to measure light was sensitive enough to measure light from a single, fully induced luminous bacterial cell. When the symbiotically luminous fishCleidopus gloriamaris was placed in a sterile aquarium, plate counts of water samples showed an increase in luminous colony-forming units. Luminescence also increased, decreasing when the fish was removed. Light measurements of water samples from a sterile aquarium containingPhotoblepharon palpebratus, another symbiotically luminous fish, whose bacterial symbionts have not been cultured, showed a similar pattern of increasing light which rapidly decreased upon removal of the fish. These experiments suggest that symbiotically luminous fishes release brightly luminous bacteria from light organs into their environment and may be a source of planktonic luminous bacteria. Although planktonic luminous bacteria are generally not bright when found in seawater, water samples from environments with populations of symbiotically luminous fish may show detectable levels of light.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 129 (1981), S. 299-304 
    ISSN: 1432-072X
    Keywords: Bioluminescence ; Marine bacteria ; Autoinduction ; Continuous culture ; Chemostat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Several strains of four species of luminous marine bacteria were maintained in a chemostat at a constant dilution rate and a variety of steady state densities by carbon (glycerol) limitation in order to study the relationship between culture density and bioluminescence activity. In general, luminescence per cell was constant at high culture density, and decreased dramatically at low culture density. For Vibrio fischeri, luminescence decreased to nondectable levels when the culture was maintained at low density; such dark cells were stimulated to synthesize luciferase and became luminous within minutes when purified autoinducer was added to the chemostat. Two strains, Photobacterium phosphoreum NZ11D and Photobacterium leiognathi S1, did not show the decrease in light intensity at low culture density that was characteristic of all other strains tested; they appeared to be constitutive for bioluminescence.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 112 (1977), S. 73-79 
    ISSN: 1432-072X
    Keywords: Induction ; Bioluminescence ; Luciferase ; Luminous bacteria ; Photobacterium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The synthesis of the luminous system of the marine luminous bacterium Photobacterium fischeri is subject to a complex, self-regulated control system called autoinduction. The bacteria produce an autoinducer which accumulates in the medium at a constant rate (as a function of cell growth). When autoinducer reaches a critical concentration it stimulates, at the level of transcription, the synthesis of the luminous system. Autoinduction is thus viewed as an environmental sensing mechanism, which curtails the synthesis of the luminous system under dilute conditions. For several isolates of P. fischeri it was found that variations in luminescence intensity could be accounted for by correlated variations in autoinducer production.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 112 (1977), S. 9-16 
    ISSN: 1432-072X
    Keywords: Oxygen ; Bioluminescence ; Induction ; Bacterial symbiosis ; Fish luminescence ; Luminous bacteria ; Photobacterium ; Beneckea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The synthesis of the bioluminescent systems in many strains of two species of the genus Photobacterium which were isolated as symbionts is greater at low oxygen concentrations, where aerobic growth is blocked. In strains of two other species, one Photobacterium of symbiotic orgin, and one (genus Beneckea) whose luminous members are not known to be involved in symbiotic associations, a different response is observed. At low oxygen concentrations, where there is an inhibition of growth, there is also a similar decrease in the synthesis, of the luminescent system. These species-specific differences may indicate important ecological differences along with distinctive differences in the molecular control mechanisms involved in the synthesis of luciferase.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Ligh emitted by the bioluminescent bacterium, Xenorhabdus luminescens (isolated from a nematode host), can be measured to monitor reductions of these bacteria in the presence of phagotrophs. X. luminescens is relatively large (0.6 ? 3 μm), but comparable in size to many cyanobacteria. We used the light emission method to examine phagotroph feeding on X. luminescens using uni-specific cultures of two chrysomonads, Ochromonas sp. and Spulemma sp. From light decay rates in control and experimental vials, we computed an apparent filtration rate (FR); then, for a concentration (C) of 1 ? 106 bacteria ml−1, we estimated capture rate (CR) as FR ? C. The Ochromonas sp. did not ingest the bacterium. The maximum estimated FR for Spumella, observed at 6.0 ? 103 flagellates ml−1 (medium density), was 0.37 ml h−1, for a volume-specific clearance rate (FR/cell volume) of 7.9 ? 105 h−1 and a CR of 62 bacteria ? flagellate−1 h−1. Video microscopy indicated these were accurate estimates of capture rates.Microscopic counts were used to monitor growth of a flagellate, Spumella sp., on X. luminescens as the sole food supply. The flagellate doulbed in number every 3.2, while consuming bacteria at a rate of 23 bacteria flagellate−1 h−1. The Spumella grazed the bacteria to a minimum of 5 ? 105 cells ml−1, a concentration comparable to observed field densities of other bacteria.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 53 (1988), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Cultures of the primary form of Xenorhabdus luminescens strain Hm gave rise to secondary forms after prolonged static incubation in two broth media. The secondary forms were deficient in pigmentation and extracellular antibiotic, protease and lipase activities, and were about 100-fold less luminous than the primary form in vivo. Secondary forms isolated on two separate occasions from two different media were identical in their deficiencies. Cultures of the secondary form in defined broth media produced no detectable secondary metabolites, unlike the primary form, and grew more rapidly than the primary form. A protocol for screening primary cultures of X. luminescens for secondary forms is presented.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 19 (1983), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We report the successful cultivation and partial characterization of novel members of ɛ-Proteobacteria, which have long been recognized solely as genetic signatures of small subunit ribosomal RNA genes (rDNA) from a variety of habitats occurring in deep-sea hydrothermal fields. A newly designed microhabitat designated ‘in situ colonization system’ was used for enrichment. Based on phylogenetic analysis of the rDNA of the isolates, most of these represent the first cultivated members harboring previously uncultivated phylotypes classified into the Uncultivated ɛ-Proteobacteria Groups A, B, F and G, as well as some novel members of Group D. Preliminary characterization of the isolates indicates that all are mesophilic or thermophilic chemolithoautotrophs using H2 or reduced sulfur compounds (elemental sulfur or thiosulfate) as an electron donor and O2, nitrate or elemental sulfur as an electron acceptor. The successful cultivation will enable the subsequent characterization of physiological properties and ecological impacts of a diversity of ɛ-Proteobacteria in the deep-sea hydrothermal environments.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 139 (1996), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Cytoplasmic inclusions surrounded by a bilayer membrane were seen in thin sections, negatively stained and freeze-fractured preparations of Shewanella putrefaciens. Cells harvested from the late exponential and early stationary phase showed a higher number of these vesicles than bacteria isolated from early exponential or late stationary phase. Chemical dyes for polyphosphate or poly-β-hydroxybutyrate did not stain the material enclosed within these vesicles. Elemental analysis of the material indicated that the content was organic in nature and might be a protein. HPLC analysis of the material showed that it was probably not a carbon source, nor an electron acceptor used by S. putrefaciens.
    Type of Medium: Electronic Resource
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