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    Transformation of the nematode-trapping fungus Arthrobotrys oligospora

    Access Status
    Fulltext not available
    Authors
    Tunlid, A.
    Ahman, J.
    Oliver, Richard
    Date
    1999
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    TUNLID A, AHMAN J & OLIVER RP (1999) Transformation of the nematode-trapping fungus Arthobotrys oligospora. FEMS Microbiology Letters 173 111-116
    DOI
    10.1111/j.1574-6968.1999.tb13491.x
    Faculty
    Department of Environmental & Agriculture
    School of Agriculture and Environment
    Faculty of Science and Engineering
    Remarks

    A copy of this item may be available from Professor Richard Oliver

    Email: Richard.oliver@curtin.edu.au

    URI
    http://hdl.handle.net/20.500.11937/32750
    Collection
    • Curtin Research Publications
    Abstract

    The nematode-trapping fungus Arthrobotrys oligospora was transformed to hygromycin resistance using the hygromycin-B phosphotransferase gene from Escherichia coli under the control of various heterologous fungal promoters. Plasmid DNA was introduced into fungal protoplasts by polyethylene glycol/CaCl2 treatment. Transformation frequencies varied between 1–6 transformants per μg DNA. Seven out of 13 integration events analyzed from transformants were single copy integrations, whereas the remaining were multiple and more complex integrations. The addition of restriction enzymes during transformations increased the frequency of single copy integrations. Co-transformation, using the E. coli uidA gene encoding the β-glucuronidase reporter gene under the control of an Aspergillus nidulans promoter, occurred at frequencies of up to 63%.

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