Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/23208
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    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/23208


    Title: Activation of the promoter of fengycin synthetase operon by the UP element
    Authors: Wan-Ju Ke
    Ban-Yang Chang
    Tsuey-Pin Lin
    Shih-Tung Liu
    Contributors: 保健營養系
    Date: 2009-07
    Issue Date: 2010-11-12 16:11:18 (UTC+8)
    Abstract: Bacillus subtilis F29-3 produces an anti-fungal peptidic antibiotic that is synthesized nonribosomally by fengycin synthetases. Our earlier work established that the promoter of the fengycin synthetase operon is located 86 nucleotides upstream of the translational initiation codon of fenC. This investigation involves transcriptional fusions with a DNA fragment that contains the region between -105 and +80 and determines that deleting the region between -55 and -42 reduces the promoter activity by 64.5%. Transcriptional fusions on the B. subtilis DB2 chromosome also indicate that mutating the sequence markedly reduces the promoter activity. An in vitro transcription analysis confirms that the transcription is inefficient when the sequence in this region is mutated. The electrophoretic mobility shift and footprinting analyses demonstrate that the C-terminal domain of the RNA polymerase subunit binds to the region between -55 and -39. These results indicated that the sequence is an UP element. Finally, this UP element is critical to the production of fengycin, since mutating the UP sequence on the chromosome of B. subtilis F29-3 reduces the transcription of the fen operon by 85% and prevents the cells from producing enough fengycin to suppress the germination of Paecilomyces variotii spores on agar plates.
    Relation: Journal of Bacteriology191(14):p.4615-4623
    Appears in Collections:[Dept. of Health and Nutrition (including master's program)] Periodical Articles

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