4.7 Article

Bioactive polyketides from the pathogenic fungus of Epicoccum sorghinum

期刊

PLANTA
卷 253, 期 6, 页码 -

出版社

SPRINGER
DOI: 10.1007/s00425-021-03635-y

关键词

Sorghum; Epicoccum sorghinum; Polyketide; Cytotoxicity; Structure-activity relationship

资金

  1. Ministry of Science and Technology, Taiwan [MOST 108-2320-B-037-022-MY3, 109-2811-B-037-517, 109-2927-I-037-502]
  2. Drug Development and Value Creation Research Center, Kaohsiung Medical University
  3. Department of Medical Research, Kaohsiung Medical University Hospital [KMU-TC108A03-11]
  4. National Sun Yat-sen University

向作者/读者索取更多资源

The study identified Epicoccum sorghinum as a major fungal contaminant of sorghum grains capable of producing toxic mycotoxins. Through chemical investigation, a new polyketide compound, epicorepoxydon B, was discovered along with known polyketides that exhibited potential inhibitory activities against human cancer cells.
Main conclusion We discovered and identified a series of characteristic substances, including one new polyketide, epicorepoxydon B, of the important pathogenic fungus, Epicoccum sorghinum, of sorghum. The fungal extract and some isolated polyketides are sensitive to a malignant triple-negative breast cancer cell line, MDA-MB-231. Sorghum (Kaoliang) grain is an important crop with high economic value and several applications. In Taiwan, sorghum has been used in the wine industry, and Kinmen Kaoliang Liquor is a well-known Asian brand. Fungal contamination is one of the major threats affecting the production of sorghum grain resulting in economic losses as well as human and animal health problems. Several fungal species can infect sorghum grain and generate some toxic secondary metabolites. Epicoccum sorghinum is one of the major fungal contaminants of sorghum grains and a potent producer of mycotoxins such as tenuazonic acid (TeA). However, except for TeA, few studies focused on chemical compounds produced by this fungus. To explore the potential biological and toxic effects of E. sorghinum, a chemical investigation was carried out on the ethyl acetate extract of the fungus because it showed cytotoxic activity against a triple-negative breast cancer cell line, MDA-MB -231 (54.82% inhibition at 20 mu g/mL). One new polyketide, epicorepoxydon B (1), along with six known compounds including 4,5-dihydroxy-6-(6'-methylsalicyloxy)-2-hydroxymethy1-2-cyclohexenl-one (2), epicorepoxydon A (3), 3-hydroxybenzyl alcohol (4), 6-methylsalicylic acid (5), gentisyl alcohol (6), and 6-(hydroxymethyl)benzene-1,2,4-triol (7) were obtained, and their structures were established by the interpretation of their MS and NMR spectroscopic data. The cytotoxic activity of all isolated polyketides 1-7 was evaluated, and compounds 2, 6, and 7 exhibited potent activities against A549, HepG2, and MDA-MB-231 human cancer cell lines with IC50 value ranging from 1.86 to 18.31 mu M. The structure-activity relationship of the isolated compounds was proposed. [GRAPHICS] .

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