Induced production of the novel glycolipid ustilagic acid C in the plant pathogen Ustilago maydis

被引:14
|
作者
Yang, Xiao-Long [1 ,2 ]
Awakawa, Takayoshi [1 ]
Wakimoto, Toshiyuki [1 ]
Abe, Ikuro [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Hebei Univ, Coll Pharmaceut Sci, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
Epigenetic modifier; Ustilago maydis; Glycolipid; Ustilagic acid; PSEUDOZYMA-FLOCCULOSA; GENE-CLUSTER;
D O I
10.1016/j.tetlet.2013.04.131
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Glycolipids have attracted interest from the pharmaceutical, cosmetic, and food industries, due to their unique chemical properties and interesting biological activities. The phytopathogenic fungus Ustilago maydis, a well-known producer of glycolipids, reportedly secretes large amounts of the glycolipid biosurfactant ustilagic acid under special culture conditions. Thus, we utilized chemical epigenetic modifiers, DNA methyltransferase (DNMT) inhibitors and/or histone deacetylase (HDAC) inhibitors, to induce the expression of silent biosynthetic pathways for isolating novel glycolipids produced by this fungus. HPLC analyses revealed that supplementations of the DNMT inhibitor 5-azacytidine and the HDAC inhibitor SBHA to the liquid culture of U. maydis induced the production of the novel glycolipid ustilagic acid C (1), along with the known ustilagic acid B (2). Glycolipids 1 and 2 displayed weak antifungal activities against Aspergillus terreus and Candida albicans. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3655 / 3657
页数:3
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