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  • 1
    ISSN: 1365-2958
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: A 7.3 kbp DNA fragment, encompassing the erythromycin (Em) resistance gene (ermE) and a portion of the gene cluster encoding the biosynthetic genes for erythromycin biosynthesis in Saccharopolyspora erythraea (formerly Streptomyces erythraeus) has been cloned in Streptomyces lividans using the plasmid vector pIJ702, and its nucleotide sequence has been determined using a modified dideoxy chain-termination procedure. In particular, we have examined the region immediately 5′ of the resistance determinant, where the tandem promoters for ermE overlap the promoters for a divergently transcribed coding sequence (ORF). Disruption of this ORF using an integrational pIJ702-based plasmid vector gave mutants which were specifically blocked in erythromycin biosynthesis, and which accumulated 3-O-α-L-mycarosylerythronolide B: this behaviour is identical to that of previously described eryC1 mutants. The eryC1-gene product, a protein of subunit Mr 39200, is therefore involved either as a structural or as a regulatory gene in the formation of the deoxyamino-sugar desosamine or in its attachment to the macro-lide ring.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant pathology 44 (1995), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Didymella rabiei grew saprophytically on pieces of infested chickpea stems and pods, and formed pycnidia and pseudothecia. The extent of saprophytic growth and production of viable spores were determined by the incubation conditions. On debris left on the soil surface under natural conditions, the fungus rapidly colonized the tissues, formed abundant pseudothecia and pycnidia, and remained viable throughout the 2 years of the study. When plant debris was buried, D, rabiei was restricted to the original lesions, in which it formed new pycnidia and was viable for 2 to 5 months. Under controlled conditions in the laboratory, D. rabiei extensively colonized plant debris spread over the soil surface. On the other hand, the fungus did not grow on buried debris, or showed only very limited development when the artificially infested debris was buried between two layers of sterilized soil. Incubation temperature was the principal factor associated with the production of conidia and especially ascospores.
    Type of Medium: Electronic Resource
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