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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 712 (1994), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 712 (1994), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 276 (1978), S. 498-500 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Table 1 Effect of agrocin 84 on in vitro transformation of habituated tobacco cells by A. tumefaciens Nopaline content of extracts Tumour development on tobacco plants Callus tissue Cell medium Strain (% dry wt) (µgml-1) C58 0.35 〈 0.04 + C58 〈 0.01 〈 0.04 - ...
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  • 4
    ISSN: 1432-2048
    Keywords: Gibberellin metabolism (enzymes) ; Phaseolus (GA metabolism) ; Seed development (GA metabolism)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A time-course study is described relating the enzyme activities for GA20 metabolism with seed development in Phaseolus vulgaris L. Enzyme activity for the 3β-hydroxylation of GA20 to GA1, and for the 2,3-desaturation of GA20 to GA5, was confined to the cotyledons and showed maximal specific activity at 21 d after anthesis. These enzyme activities co-occurred, together with a much lower level of activity for the 2β-hydroxylation of GA20 to GA29. The observed rates of GA1, GA5 and GA29 formation from GA20 were constant under a range of incubation conditions. Enzyme activity for the conversion of GA1 to GA8 was detected only in embryos of seed from 40 d after anthesis. By deuterium-labelling and analysis of the products by gas chromatography-selected ion monitoring it was shown that 2β-hydroxylation of GA1 to GA8 and 3β-hydroxylation of GA20 to GA1 occur with retention of configuration and that the conversion of GA20 to GA5 occurs with loss of the 2β- and 3β-hydrogens. These results establish that GA1 is not formed from GA20 via GA5.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Planta 191 (1993), S. 158-165 
    ISSN: 1432-2048
    Keywords: Gibberellin translocation ; Mutant (dwarf pea) ; Pisum (dwarf mutant) ; Stem elongation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The physiological and biochemical consequences of treating Le (tall) and le (dwarf) pea seedlings with varying quantities of the gibberellins [3H]GA20 and GA1 have been investigated. Although the percentage uptake of these compounds from the site of application on the 3∘ stipules was low and most of the applied GA remained unmetabolised in situ, the quantitative relationship between GA translocation and GA dosage was found to be linear for GA1 but saturating for GA20. The movement of the GAs and their subsequently produced metabolites was mainly acropetal. They accumulated in greatest quantity in the apical extremities of the shoot. Overall, the extent to which GA20 was metabolished in le seedlings was considerably less than in Le pea seedlings. Although all le tissues contained significantly less [3H]GA1 than their Le counterparts, phenotypic effects of the le mutation were apparent only on internode and tendril development. Increased tissue growth, consequent upon GA treatment, was also apparent only in the internodes and tendrils of le plants. For internodes, GA1 content determined the mid-logarithmic-phase growth rate and, consequently, final length. For tendrils, GA20 rather than GA1 may be the primary stimulatory agent.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of plant growth regulation 2 (1983), S. 251-264 
    ISSN: 1435-8107
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A gibberellin 2β-hydroxylase has been purified from mature seeds ofPhaseolus vulgaris. The enzyme is of molecular weight 36,000 and has the characteristics of a dioxygenase; the cofactors areα-ketoglu-tarate, Fe2+ and ascorbate, and activity is stimulated by catalase. The Vmax of the enzyme is 6.86 nmole h−1 mg−1, and the Km values for [1,2-3H2]GA1 andα-ketoglutarate are 0.085 μM and 21 μM, respectively. The purified enzyme preparation catalyzes hydroxylation of GA1, GA4, GA9, and GA20 but exhibits a marked preference for the 3-hydroxylated gibberellins as substrate.
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  • 7
    ISSN: 1573-5192
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The technique of sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) has been evaluated as a method for the characterization of trypanosomes. 2. Twenty-five populations, including seven clones, isolated from bats in Europe, Canada and Latin America could be grouped into eight subpopulations having similar polypeptide profiles. We propose to designate such subpopulations by the term ‘peptideme’. 3. Our peptidemes were compared with the previous classification, obtained by DNA buoyant density (Newton, 1976), isoenzym electrophoresis and morphological studies (Baker et al., 1976, 1978; Baker & Miles, 1979) as follows: 4. Peptideme 1 corresponded with Trypanosoma dionisii dionisii and peptideme 2 with T. d. breve and T. Hedricki. However, peptidemes 1 and 2 had some common shared characters. 5. Peptideme 3 corresponded with T. myoti and peptideme 4 with strain Z of T. cruzi marinkellei. Again, peptidemes 3 and 4 had some shared characters and these also shared some characters with peptidemes 1 and 2. 6. Peptideme 5 contained strains N2 and N6 of T. vespertilionis; the other strains of this species (482 and 482 clone 1), although sharing some common characters, were sufficiently different to enable us to group them as peptideme 6. 7. The remaining T. c. marinkellei strains were grouped into peptidemes 7 (B7, M1116, M1117, M1117X) and 8 (B34, M1909), although once again, these two peptidemes had some shared characters. Thus the peptideme method of classification of these trypanosomes corresponds well with the classification proposed previously but it is a more sensitive method and can recognize more subtle variation between the strains.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Parasitology research 72 (1986), S. 573-576 
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A method of cloning leishmanial promastigotes is described in which mid-exponential phase cultures are diluted to contain approximately 3×103 promastigotes per ml. Hanging-drop preparations made from 0.2–0.4 μl volumes of the diluted culture seen to contain a single promastigote are picked-up in glass capillary tubes. Additional culture medium is taken into the capillaries which are then heat-sealed and incubated at 22° C. Growth of leishmanial promastigotes inside the sealed capillary tubes is followed by direct microscopic observation through the walls of the tubes. When active promastigotes are seen the contents of the tubes are inoculated into small volumes of culture medium. The method is extremely easy to use, requires no specialised apparatus, and has been successfully used with different strains and species ofLeishmania, with up to 100 percent of the cloned organisms growing.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0878
    Keywords: Exocytosis ; Phagocytosis ; Cell cooperation ; Prophenoloxidase ; Invertebrate immunity ; Pacifastacus leniusculus ; Carcinus maenas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The role of exocytosis in the cellular defence reactions of arthropods was investigated using in vitro cultures of isolated haemocytes (blood cells) from the freshwater crayfish Pacifastacus leniusculus, and the shore crab Carcinus maenas. In both species, activated lysates of those cell types that contain the prophenoloxidase activating system (granular cells of crab and crayfish and semigranular cells of crayfish) were found to induce degranulation (exocytosis) of semigranular and granular cells. A cell lysate, in which the prophenoloxidase system was kept inactive, did not have this effect. Limited degranulation of granular cells of crab was also induced by lipopolysaccharides as has earlier been shown for crayfish semigranular cells. The phagocytic capability of semigranular cells from crayfish was lost after exocytosis induced by the Ca2+ ionophore A23187, and under no conditions were the granular cells of crabs or crayfish seen to ingest bacteria in vitro. An opsonic function for the attaching proteins of a β1,3-glucan-activated haemocyte lysate was demonstrated using the phagocytic hyaline cells from crabs. Phenoloxidase appeared to lack opsonic properties. We suggest that, in crustaceans, opsonization takes place through hierarchically stimulated exocytotic release, and biochemical activation of the prophenoloxidase activating system: first from lipopolysaccharide-sensitive cells (semigranular cells of crayfish or granular cells of crabs) and then from granular cells, triggered by the initially released and activated prophenoloxidase system. Finally, “sticky” proteins of the activated prophenoloxidase system coat the invader, rendering it susceptible to the phagocytes (hyaline cells in both crab and crayfish and, to a lesser extent, semigranular cells of crayfish). These processes would, together, constitute a cellular communication pathway not previously demonstrated for invertebrates.
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  • 10
    ISSN: 1432-0878
    Keywords: Prophenoloxidase ; Haemocytes ; Degranulation ; Phagocytosis ; Opsonins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary To study the role of the prophenoloxidase activating system, an enzyme cascade located in the haemocytes of crustaceans, in the cellular defences of the freshwater crayfish, Astacus astacus in vitro, monolayer cultures of mixed or separated haemocyte populations, isolated by density gradient centrifugation, were challenged with the bacterium, Moraxella sp. pre-coated with phenoloxidase and the other attaching proteins in crayfish haemocyte lysate (HLS), or in the case of controls, with saline or Moraxella sp. pre-incubated in saline alone. Examination of the coverslips 1 h after inoculation revealed that, in the mixed haemocyte cultures, most of the cells had undergone profound degranulation and lysis following exposure to the HLS-coated bacteria. Cell lysis was also evident in the experimental semigranular cell monolayers, but not in the controls, although in those controls treated with the saline-incubated bacteria, the semigranular haemocytes had undergone degranulation without lysis. In contrast, the granular cells appeared to be unaffected by the saline-incubated Moraxella sp., and with the HLS-coated bacteria displayed only marked degranulation. Greater numbers of bacteria were always associated with the cells or cell remnants in the experimental cultures compared to the controls. We suggest that the attaching proteins of the prophenoloxidase cascade are strong nonself signals for the haemocytes, causing them to degranulate and release previously cell-bound recognition factors into the haemolymph, where they are free to trigger activation of adjacent haemocytes.
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