Ceratocystis ulmi in Finland

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منابع مشابه

Ca(II)-calmodulin regulation of fungal dimorphism in Ceratocystis ulmi.

We have shown that Ca(II) ions, ethylene glycol-bis(beta-aminoethyl ether)-N,N-tetraacetic acid, LaCl3, and six known calmodulin inhibitors shift the yeast-mycelium dimorphic potential of Ceratocystis ulmi. Our data are consistent with the conclusions that Ca(II)-calmodulin interaction is necessary for mycelial growth in C. ulmi and that the absence of this interaction leads to the yeast phase.

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Lipoxygenase inhibitors shift the yeast/mycelium dimorphism in Ceratocystis ulmi.

The yeast-mycelium dimorphism in Ceratocystis ulmi, the causative agent of Dutch elm disease, was switched by gossypol, nordihydroguaiaretic acid, and propylgallate. In each case the mycelial form was converted to the yeast form. These compounds are recognized lipoxygenase inhibitors. Inhibitors of cyclooxygenase and thromboxane synthetase did not cause mycelia to shift to the yeast form. We su...

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Phytotoxin Isolated from Liquid Cultures of Ceratocystis ulmi.

Phytotoxic material has been isolated from liquid cultures of Ceratocystis ulmi. One component of the material has been obtained in pure form and has proved to be a rather thermostable glycoprotein. This compound induced disease symptoms, similar to those produced by the fungus itself, in elm sprouits and trees.

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Inoculum size effect in dimorphic fungi: extracellular control of yeast-mycelium dimorphism in Ceratocystis ulmi.

We studied the inoculum size effect in Ceratocystis ulmi, the dimorphic fungus that causes Dutch elm disease. In a defined glucose-proline-salts medium, cells develop as budding yeasts when inoculated at > or = 10(6) spores per ml and as mycelia when inoculated at <10(6) spores per ml. The inoculum size effect was not influenced by inoculum spore type, age of the spores, temperature, pH, oxygen...

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Calmodulin levels in the yeast and mycelial phases of Ceratocystis ulmi.

The calmodulin content of the yeast and mycelial phases of Ceratocystis ulmi was determined by radioimmunoassay. Calmodulin levels increased at the G1-S boundary of the cell cycle, coinciding with the first visible appearance of buds or germ tubes. However, in both phases the cellular calmodulin levels were equivalent. No differential synthesis was observed.

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ژورنال

عنوان ژورنال: Karstenia

سال: 1974

ISSN: 0453-3402

DOI: 10.29203/ka.1974.87