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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 250 (1996), S. 734-741 
    ISSN: 1617-4623
    Keywords: Key words Bacillus thuringiensis ; cry gene expression ; Encapsulation ; Sigma factors ; Sporulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  The sigE and sigK genes, encoding the sporulation-specific sigma factors σ35 and σ28 of Bacillus thuringiensis, were each disrupted by inserting a gene conferring resistance to kanamycin into their coding sequence. The B. thuringiensis SigE- and SigK- mutant strains were blocked at different sporulation stages and were unable to sporulate. The SigE- strain was blocked at stage II of sporulation, whereas the SigK- strain was blocked at stage IV. The expression of a cryIAa′-′lacZ transcriptional fusion was analysed in these genetic backgrounds and it was found that both sigma factors are involved in the in vivo transcription of this gene. However, the SigK- strain harbouring the cryIAa gene produced amounts of toxin similar to those produced by the B. thuringiensis Spo+ strain. The toxins accumulated in the mother cell compartment to form a crystal inclusion which remained encapsulated within the cell wall. Thus, transcription from the σE-dependent promoter alone (Bt I promoter) is sufficient to support high levels of toxin production in B. thuringiensis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 250 (1996), S. 734-741 
    ISSN: 1617-4623
    Keywords: Bacillus thuringiensis ; cry gene expression ; Encapsulation ; Sigma factors ; Sporulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract ThesigE andsigK genes, encoding the sporulation-specific sigma factorsσ 35 andσ 28 ofBacillus thuringiensis, were each disrupted by inserting a gene conferring resistance to kanamycin into their coding sequence. TheB. thuringiensis SigE− and SigK− mutant strains were blocked at different sporulation stages and were unable to sporulate. The SigE− strain was blocked at stage II of sporulation, whereas the SigK− strain was blocked at stage IV. The expression of acryIAa′-′lacZ transcriptional fusion was analysed in these genetic backgrounds and it was found that both sigma factors are involved in the in vivo transcription of this gene. However, the SigK− strain harbouring thecryIAa gene produced amounts of toxin similar to those produced by theB. thuringiensis Spo+ strain. The toxins accumulated in the mother cell compartment to form a crystal inclusion which remained encapsulated within the cell wall. Thus, transcription from theσ E-dependent promoter alone (Bt I promoter) is sufficient to support high levels of toxin production inB. thuringiensis.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
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