Abstract
The limitations of currently available antifungal agents and the rapid emergence of drug-resistant strains necessitate more efficient approaches to screening and developing novel antifungal drugs. The antifungal activity of the natural products of a series of plants was evaluated and wighteone, 5, 7, 4′–trihydroxy–6–(γ,γ-dimethylallyl)isoflavone showed excellent anti-yeast activity (MIC against Saccharomyces cerevisiae was 4 μg/ml). Transcriptome profiling of wighteone-treated S. cerevisiae indicated that wighteone is different from commonly used antifungal compounds in its mode of action.
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Received 17 June 2005; Revisions requested 4 July 2005 and 22 August 2005; Revisions received 8 August 2005 and 28 October 2005; Accepted 2 November 2005
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Yin, H., Zhao, Y., Zhang, Y. et al. Genome-wide Analysis of the Expression Profile of Saccharomyces cerevisiae in Response to Treatment with the Plant Isoflavone, Wighteone, as a Potential Antifungal Agent. Biotechnol Lett 28, 99–105 (2006). https://doi.org/10.1007/s10529-005-4954-0
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DOI: https://doi.org/10.1007/s10529-005-4954-0