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Pisolithus tinctorius

T. Beguiristain, R. Cote, P. Rubini, C. Jayallemand, and F. Lapeyrie, Hypaphorine accumulation in hyphae of the ectomycorrhizal fungus Pisolithus tinctorius. Phytochemistry 40 1089 (1995). [Pg.291]

T. Beguiristain and F. Lapeyrie, Host plant stimulates hypaphorine accumulation in Pisolithus tinctorius hyphae during ectomycorrhizal infection while excreted fungal hypaphorine controls root hair development. New Phytol. 136 525 (1997). [Pg.291]

Rost FWD, Shepherd VA, Ashford AE. Estimation of the vacuolar pH in actively growing hyphae of the fungus Pisolithus tinctorius. Mycol Res 1995 99 549-553. [Pg.90]

Figure 2.5 Energy dispersive X-ray spectrum optained from a spherical electron-opaque granule of the fungus Pisolithus tinctorius, showing peaks for P and Ca (Orlovich and Ashford, 1993). Figure 2.5 Energy dispersive X-ray spectrum optained from a spherical electron-opaque granule of the fungus Pisolithus tinctorius, showing peaks for P and Ca (Orlovich and Ashford, 1993).
A. E. Ashford, P. A. Vesk, D. A. Orlovich, A. L. Markovina and W. G. Allaway (1999). Dispersed polyphosphate in fungal vacuoles in Eucalyptus pilularis/Pisolithus tinctorius ectomycorrhizas. [Pg.212]

D. A. Orlovich, and A. E. Ashford (1993). Polyphosphate granules are an artefact of specimen preparation in the ectomycorrhizal fungus Pisolithus tinctorius. Protoplasma, 173, 91-102. [Pg.248]

Two main acid phosphatases were purified from each extract of phosphate-supplied (la, Ila) or phosphate-starved (Ib, Ilb) cultures of the ectomycorrhizal fungus Pisolithus tinctorius (Berjaud and d Auzac, 1986). These soluble phosphatases could not he distinguished either hy their pH optimum (pH 5.0—5.5) or hy their optimal temperature (60°C). In contrast, the activation energy was lower in the case of the two phosphatases from starved mycelium (50.2—58.2 kj/mol) than those from phosphate-supplied mycelium (70.5-112.5 kJ/mol). Thus, their reaction rate was higher. [Pg.95]

Mousain, D. and Salsac, L. (1 985) Utilisation du phy-tate et activites phosphatases acides chez Pisolithus tinctorius, basidiomycete mycorh-izien. PhysiologieVegetale24, 193-200. [Pg.110]

Gill, M., and D.A. Lally A Naphthalenoid Pulvinic Acid Derivative from the Fungus Pisolithus tinctorius. Phytochem. 24, 1351 (1985). [Pg.266]

Cole, L. Hyde, G. J. Ashford, A. E. Uptake and compartmentalization of fluorescent probes by Pisolithus tinctorius hyphae evidence for an anion transport mechanism at the tonoplast but not for fluid-phase endocytosis. Protoplasma 1997,199, 18-29. [Pg.293]

Constit. of fungus Pisolithus tinctorius. Prisms (MeOH). [Pg.358]

Warrington S J, Black H D, Coons L B 1981 Entry of Pisolithus tinctorius hyphae into Pinus taeda roots. Can J Bot 59 2135-2139... [Pg.366]

TAN K.H. and NOPAMORNBODI V. 1979. Fulvic acid and the growth of the ectomycorrhizal fungus, Pisolithus tinctorius. Soil Biology and Biochemistry, 651-653. [Pg.73]


See other pages where Pisolithus tinctorius is mentioned: [Pg.268]    [Pg.82]    [Pg.186]    [Pg.188]    [Pg.25]    [Pg.25]    [Pg.43]    [Pg.106]    [Pg.35]    [Pg.100]    [Pg.102]    [Pg.108]    [Pg.110]    [Pg.243]    [Pg.252]    [Pg.322]    [Pg.93]    [Pg.93]    [Pg.103]    [Pg.71]    [Pg.4]    [Pg.271]    [Pg.290]    [Pg.348]    [Pg.965]    [Pg.306]   
See also in sourсe #XX -- [ Pg.188 ]

See also in sourсe #XX -- [ Pg.25 , Pg.43 , Pg.106 ]




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