Secondary Metabolites from a Marine-Derived Endophytic Fungus Penicillium chrysogenum QEN-24S

被引:76
作者
Gao, Shu-Shan [1 ,2 ]
Li, Xiao-Ming [1 ]
Du, Feng-Yu [1 ]
Li, Chun-Shun [1 ]
Proksch, Peter [3 ]
Wang, Bin-Gui [1 ]
机构
[1] Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] Univ Dusseldorf, Inst Pharmaceut Biol & Biotechnol, D-40225 Dusseldorf, Germany
基金
美国国家科学基金会;
关键词
marine endophyte; Penicillium chrysogenum; secondary metabolites; ASPERGILLUS-NIGER EN-13; ENANTIOSELECTIVE SYNTHESIS; CHAETOMIUM-GLOBOSUM; NATURAL-PRODUCTS; A-C; ALKALOIDS;
D O I
10.3390/md9010059
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Penicillium chrysogenum QEN-24S, an endophytic fungus isolated from an unidentified marine red algal species of the genus Laurencia, displayed inhibitory activity against the growth of pathogen Alternaria brassicae in dual culture test. Chemical investigation of this fungal strain resulted in the isolation of four new (1-3 and 5) and one known (4) secondary metabolites. Their structures were identified as two polyketide derivatives penicitides A and B (1 and 2), two glycerol derivatives 2-(2,4-dihydroxy-6-methylbenzoyl)-glycerol (3) and 1-(2,4-dihydroxy-6-methylbenzoyl)-glycerol (4), and one monoterpene derivative penicimonoterpene (5). Penicitides A and B (1 and 2) feature a unique 10-hydroxy-or 7,10-dihydroxy-5,7-dimethylundecyl moiety substituting at C-5 of the alpha-tetrahydropyrone ring, which is not reported previously among natural products. Compound 5 displayed potent activity against the pathogen A. brassicae, while compound 1 exhibited moderate cytotoxic activity against the human hepatocellular liver carcinoma cell line.
引用
收藏
页码:59 / 70
页数:12
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