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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : Munksgaard International Publishers
    Physiologia plantarum 102 (1998), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: In ectomycorrhizae auxins are proposed to attenuate elicitor-induced defence reactions in the host plant. To examine this hypothesis we compared the elicitor-induced accumulation of peroxidase isoforms between suspension-cultured spruce (Picea abies[L.] Karst.) cells incubated in media with and without auxins. In spruce cells changes in ionically and covalently wall-bound as well as symplasmic peroxidase (EC 1.11.1.7) activities were observed when elicitors from the following fungal species were applied: (1) Hebeloma crustuliniforme, an ectomycorrhizal partner of spruce; (2) Suillus variegatus, an ectomycorrhizal fungus incompatible with spruce; (3) Heterobasidion annosum, a spruce pathogen. Activity staining after SDS-PAGE and western blotting showed an accumulation of an ionically wall-bound 38-kDa peroxidase isoform. In addition, two covalently wall-bound isoforms (34 and 53 kDa) that could be released from spruce cell walls by cellulase and pectinase treatment were also induced by elicitors from these fungi. Moreover, in cells cultured without auxins all the elicitors triggered a rapid and transient accumulation of ionically wall-bound peroxidases, which reached a maximum activity 48 h after elicitor application. This early and transient peroxidase accumulation was diminished and delayed in cells cultured in the presence of auxins. In contrast, activity of peroxidases released into the culture medium of spruce cells or into the medium of protoplasts was suppressed by the elicitors of Hebeloma crustuliniforme. However, this suppression was attenuated by the action of auxins. It is suggested that under natural conditions, in infected spruce roots, the elicitors of the compatible fungus cause both suppression of the peroxidase (which is secreted to the free space of the roots), and induction of wall-bound and symplasmic peroxidases. On the other hand, auxins synthesized by the fungus could weaken these different elicitor-mediated effects.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2285
    Keywords: Parasitic angiosperm ; Succulence ; Cations ; Organic osmolytes ; Cyclitols
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The inorganic ion and organic solute composition of Tapinanthus oleifolius (Loranthaceae) and Viscum rotundifolium (Viscaceae) growing on various host trees in Namibia were investigated. Organic osmolytes accounted for 22.8–45.1% of the total solutes determined in leaves of the mistletoes parasitizing Acacia nebrownii, Catophractes alexandri, Grewia flava and Ziziphus mucronata. On other hosts (Acacia karroo, Euphorbia virosa, Salvadora persica and Tamarix usneoides) T. oleifolius showed distinct succulence with increasing leaf age, with leaves more than 3 mm thick on E. virosa. In the more succulent leaves (〉 1.1 kg H2O m−2 leaf area) organic solutes were only of minor importance. Water content per leaf area was significantly correlated with chloride content per leaf area, suggesting that succulence served as a means to keep ion concentration at a physiological tolerable level. At whole plant levels 93.7% of the total sodium of the mistletoe bush was located in leaves thicker than 1 mm for T. oleifolius parasitizing Tamarix usneoides. This pronounced sequestration of sodium in older leaves as well as the high variability of the K/Na ratio in various parts of the parasite-host system point to highly selective ion distribution processes in this association.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 1995-09-01
    Print ISSN: 0931-1890
    Electronic ISSN: 1432-2285
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Published by Springer
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