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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 39 (1994), S. 55-61 
    ISSN: 1573-5044
    Keywords: Anthurium andraeanum ; callus culture ; contaminants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Latent infections of tissue-cultured Anthurium andraeanum Lind. caused by the blight pathogen, Xanthomonas campestris pv. dieffenbachiae (McCulloch & Pirone) Dye, were examined. The pathogen survived in or on callus for over 4 months without producing symptoms in callus or turbidity in the medium. The pathogen survived for more than 1 year on or within stage II shoots without producing symptoms and was successively transferred three times as latently infected shoots were multiplied. The pathogen did not grow or survive for more than 2 weeks in Murashige and Skoog medium lacking plant material. The addition of coconut water enhanced bacterial growth and produced turbidity in culture media. Latently infected in vitro anthuriums may be inoculum sources for subsequent outbreaks of the disease.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Yeast 8 (1992), S. 39-45 
    ISSN: 0749-503X
    Keywords: Flow cytometry ; autolytic mutants ; protoplasts ; yeast ; viability assay ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Simple methods, based on the technique of flow cytometry, have been developed for the phenotypic characterization of yeast autolytic mutants and for the analysis of the formation and regeneration of the yeast protoplasts. The expression of lytic mutations determined uptake of the fluorescent dye propidium iodide, which could be carefully monitored by flow cytometry. Mixed populations of lysed and viable cells were precisely quantified and sorted, and the technique was also applied to demonstrate protection from lysis of mutant cells with cell wall defects, in the presence of osmotic stabilizers. Protoplast formation and regeneration was monitored by analysing relative cell size; this was facilitated by the preparation of homogeneous protoplast preparations. The technique of flow cytometry proved superior to other conventional methods for these types of study.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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