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Secondary Metabolites from a Marine-Derived Endophytic Fungus Penicillium chrysogenum QEN-24S
Gao, Shu-Shan1,2; Li, Xiao-Ming1; Du, Feng-Yu1; Li, Chun-Shun1; Proksch, Peter3; Wang, Bin-Gui1
2011
发表期刊MARINE DRUGS
ISSN1660-3397
卷号9期号:1页码:59-70
文章类型Article
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.; 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.
关键词Marine Endophyte Penicillium Chrysogenum Secondary Metabolites
学科领域Pharmacology & Pharmacy
DOI10.3390/md9010059
URL查看原文
收录类别SCI
语种英语
WOS记录号WOS:000288892000004
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被引频次:75[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/11937
专题实验海洋生物学重点实验室
作者单位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
第一作者单位实验海洋生物学重点实验室
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Gao, Shu-Shan,Li, Xiao-Ming,Du, Feng-Yu,et al. Secondary Metabolites from a Marine-Derived Endophytic Fungus Penicillium chrysogenum QEN-24S[J]. MARINE DRUGS,2011,9(1):59-70.
APA Gao, Shu-Shan,Li, Xiao-Ming,Du, Feng-Yu,Li, Chun-Shun,Proksch, Peter,&Wang, Bin-Gui.(2011).Secondary Metabolites from a Marine-Derived Endophytic Fungus Penicillium chrysogenum QEN-24S.MARINE DRUGS,9(1),59-70.
MLA Gao, Shu-Shan,et al."Secondary Metabolites from a Marine-Derived Endophytic Fungus Penicillium chrysogenum QEN-24S".MARINE DRUGS 9.1(2011):59-70.
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