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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Marine biology 72 (1982), S. 7-15 
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The uptake of several species of bacteria by the common mussel Mytilus edulis (L.) and the subsequent fate of some polymers of the bacteria have been investigated in a study carried out during 1981. Bacteria (Escherichia coli, Micrococcus luteus, M. roseus, Bacillus cereus, Staphylococcus aureus and a marine pseudomonad, 1-1-1) were radiolabelled by growth in medium containing 3H-thymidine and the uptake of bacteria by Mytilus edulis was monitored. Labelled and unlabelled bacteria, at initial concentrations of 0.5 to 1x107 bacteria ml-1, were cleared at similar, exponential rates with no significant difference in the rates for different bacteria: 90% of bacteria were cleared in a mean time of 1.93±0.12 h (SEM, n=63). Those bacteria with cell walls which were sensitive to M. edulis lysozyme were rapidly degraded by the mussel and 3H-labelled DNA was released in a form not precipitable by 10% trichloroacetic acid. Lysozyme-resistant bacteria (Micrococcus roseus and S. aureus) were cleared from suspension by Mytilus edulis but most were rejected intact. By measuring the rate of release of 3H-thymidine-labelled material from the mussel the rate of degradation of lysozyme-sensitive bacteria by M. edulis was found. For different bacteria the degradation rate varied from approx 2x108 to 27x108 bacteria h-1 with an overall mean of 10x108 bacteria h-1. A thymidine- and diaminopimelicacid-requiring auxotroph of E. coli was radiolabelled with 3H-thymidine, 3H-diaminopimelic acid or 14C-glucose and fed to M. edulis. Bacteria were cleared and degraded by the mussel; 3H-diaminopimelic acid-labelled or 14C-glucose-labelled polymers were retained, whereas 3H-thymidine-labelled polymers were released into the surrounding water. Extracts of the digestive gland of M. edulis degraded lysozyme-sensitive bacteria to release 3H-thymidine-labelled material, but did not release 3H-thymidine-labelled material from lysozyme-resistant bacteria. It is concluded that M. edulis can select lysozymesensitive bacteria for subsequent processing and discriminate between bacterial polymers to reject DNA. Also, bacteria could provide a substantial fraction of the carbon requirement of the mussel.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Marine biology 75 (1983), S. 57-61 
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Changes in mean style weight and in lysozyme activity of the style, digestive gland, gill and mantle of Mytilus edulis and Tellina tenuis from the Clyde Sea area, Scotland, were investigated over tidal cycles in March and August, 1981. For M. edulis, significant changes occurred in the style weight, style lysozyme activity and digestive gland lysozyme activity during a 22 h period. These appear to be related to a diurnal cycle rather than a tidal cycle. Changes in the weight of the style of M. edulis may be caused by dissolution during feeding, and style lysozyme may be secreted independently of the style matrix. The activity of lysozyme in T. tenuis is unaffected by the tide, suggesting that this intertidal bivalve can feed throughout the tidal cycle.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 250 (1974), S. 236-238 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] HeLa cells were infected with vaccinia virus and collected 48 h after infection; soluble virus-free preparations (HVSA) containing both viral and hostspecific precipitinogens were prepared5. Preliminary work confirmed previous observations1,6 that HVSA had no effect on its own when added to ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish diseases 19 (1996), S. 0 
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish diseases 15 (1992), S. 0 
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: Abstract. Ten strains of Vibrio anguillarum produced three different types of iron-binding compounds when cultured under different conditions. These were (1) a common phenolate siderophore produced by all strains. (2) a hydroxamate siderophore produced by three strains and (3) a second phenolate siderophore, tentatively identified as anguibactin, produced by V. anguillarum strain 775 and two other strains, all of which contained a plasmid of 45–50 Md. The relative affinities of these siderophores, determined by competition for 55Fe was: anguibactin 〈 hydroxamate siderophore 〈 common phenolate siderophore. However, under these conditions, none removed iron from purified aerobactin. Experimental infection of rainbow trout. Oncorhynchus mykiss (Walbaum), showed that only the common phenolate siderophore was detected in the kidney and spleen of fish infected with strains 91079 and NCIMB6. The hydroxamate siderophore produced in vitro by strain NCIMB6 was not detected in vivo. However, in the kidney of fish infected with strain 775, both the common phenolate siderophore and anguibactin were detected, showing that a second uptake system is required by strain 775 in vivo and that the iron-uptake system based on the common phenolate siderophore is defective.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish diseases 10 (1987), S. 0 
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: Abstract. A proteinase produced by the bivalve pathogen Vibrio alginolyticus NCMB 1339 was purified by preparative isoelectric focusing and gel filtration. Proteinase activity was associated with two components of molecular weights 43000 and 41000 and was toxic to larval Ostrea edulis. Production of this enzyme was maximal during the late exponential phase of growth and it remained stable throughout the stationary phase of growth. At 37°C, activity against azocasein was optimal at pH 7–5. The enzyme was inhibited by mercuric chloride, dithiothreitol and ethylene diamine tetra-acetic acid, but not by pepstatin-A, phenylmethylsulphonyl-fluoride or tosyl-L-lysine chloromethylketone.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Journal of fish diseases 23 (2000), S. 0 
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: Abstract. Seven marine Vibrio strains pathogenic for fish or shellfish (including strains of Vibrio alginolyticus, V. anguillarum, V. tubiashi and V. ordalii) were categorized into three groups on the basis of their extracellular proteinases. Antiserum raised against purified Vibrio alginolyticus NCMB 1339 proteinase neutralized the enzymes produced by all seven Vibrio strains and, on immunodiffusion, the V. alginolyticus proteinase gave a reaction of partial antigenic identity with the other Vibrio strains. In experimental infections of Ostrea edulis larvae with V. alginolyticus, the production of proteinase was demonstrated by immunofluorescence with fluorescein-labelled anti-serum. The toxicity of purified proteinase to larval O. edulis was significantly reduced by preincubation with antiserum but, when larvae were challenged with V. alginolyticus culture supernate containing a similar proteinase concentration, preincubation with antiserum had no protective effect.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish diseases 9 (1986), S. 0 
    ISSN: 1365-2761
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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