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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 149 (1989), S. 24-30 
    ISSN: 1615-6102
    Keywords: Adhesion ; Calcium ; Lectins ; Phytophthora cinnamomi ; Secretion ; Zoospore
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary During encystment,Phytophthora cinnamomi zoospores bind firmly to the host surface. We have developed a microassay to study adhesion of the zoospores to solid surfaces, both biological and non-biological. The results show that timing of the acquisition of adhesiveness during encystment correlates closely with the secretion of high molecular weight glycoproteins. The adhesive phase is short lived, occurring between 1 and 4 min after induction of encystment. During this period, cells that come into contact with a variety of surfaces (glass, plastic, and onion epidermis) become firmly attached, while cells that come into contact with one of these substrata after this period are unable to bind. Our results also show that EGTA inhibits cyst adhesion, while addition of calcium promotes cyst adhesion, especially of cysts more than 4 min old. To help identify the cyst surface component involved in adhesion we tested a number of lectins for their ability to block cyst adhesion. Soybean agglutinin andHelix pomatia agglutinin, lectins which bind to the secreted high molecular weight glycoproteins, both inhibit adhesion in the presence and absence of the hapten sugar, indicating that inhibition was non-specific. Wheatgerm agglutinin, a lectin which does not bind to the cyst surface, also blocked adhesion non-specifically.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 191 (1996), S. 79-83 
    ISSN: 1615-6102
    Keywords: Cytoplasmic pH ; pH-sensitive carboxyfluorescein ; Zoospore ; Fungus ; Intracellular alkalinisation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Changes in intracellular pH (pHi) have been examined during zoosporogenesis inPhytophthora cinnamomi in order to elucidate the molecular mechanisms that bring about initiation of the orderly cleavage of the sporangium. By microinjecting a dextranconjugated pH-sensitive fluorescent indicator, 2′,7′-bis(2-carboxyethyl)-5(6)-carboxyfluorescein (BCECF dextran), and using fluorescence ratio image analysis, the pHi of a sporangium was monitored throughout the process of zoosporogenesis. The pHi of mature sporangia was found to remain constant at pH 6.84 ± 0.05 (mean ± SE, n=6) at room temperature (24 °C), but increased to 7.04 ± 0.04 (p 〈 0.001) during a 20 min cold treatment at 19 °C. As the process of zoosporogenesis proceeded, the increased level of pHi was maintained for 30–40 min after initiation of the cold shock. Zoosporogenesis was blocked when the pHi of the sporangium was held constant by microinjecting with 10 mM HEPES buffer (pH 7.0) before cytoplasmic cleavage was induced by a cold shock. In contrast, no inhibitory effect was observed when sporangia were microinjected with HEPES buffer after the cold shock. These results indicate that initiation of cytoplasmic cleavage requires a rise in pHi.
    Type of Medium: Electronic Resource
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