Lobophorin C and D, New Kijanimicin Derivatives from a Marine Sponge-Associated Actinomycetal Strain AZS17
Wei, Rong-Bian1,2,3; Xi, Tao3; Li, Jing4; Wang, Ping2; Li, Fu-Chao1; Lin, Yong-Cheng4; Qin, Song1
刊名MARINE DRUGS
2011-03-01
卷号9期号:3页码:359-368
关键词Marine Sponge Actinomycete Lobophorin c And d Cytotoxic Activity
ISSN号1660-3397
DOI10.3390/md9030359
文献子类Article
英文摘要Marine sponge Hymeniacidon sp. was collected from coastal waters of the East China Sea to isolate symbiotic microorganisms. The resulting sponge-associated actinomycete, Streptomyces carnosus strain AZS17, was cultivated in a 20 L volume of medium for production of bioactive secondary metabolites. Bioassay-guided isolation and purification by varied chromatographic methods yielded two new compounds of kijanimicin derivatives, AS7-2 and AS9-12. Their structures were elucidated by spectroscopy and comparison with literatures. Results showed these two compounds were structurally similar to the previously reported compounds lobophorin A and B, yet differed in specific bond forms, stereochemistry and optical activities. The two novel compounds were named lobophorin C and D. In vitro cytotoxicity investigation by MTT assay indicated their selective activities. Lobophorin C displayed potent cytotoxic activity against the human liver cancer cell line 7402, while lobophorin D showed significant inhibitory effect on human breast cancer cells MDA-MB 435.; Marine sponge Hymeniacidon sp. was collected from coastal waters of the East China Sea to isolate symbiotic microorganisms. The resulting sponge-associated actinomycete, Streptomyces carnosus strain AZS17, was cultivated in a 20 L volume of medium for production of bioactive secondary metabolites. Bioassay-guided isolation and purification by varied chromatographic methods yielded two new compounds of kijanimicin derivatives, AS7-2 and AS9-12. Their structures were elucidated by spectroscopy and comparison with literatures. Results showed these two compounds were structurally similar to the previously reported compounds lobophorin A and B, yet differed in specific bond forms, stereochemistry and optical activities. The two novel compounds were named lobophorin C and D. In vitro cytotoxicity investigation by MTT assay indicated their selective activities. Lobophorin C displayed potent cytotoxic activity against the human liver cancer cell line 7402, while lobophorin D showed significant inhibitory effect on human breast cancer cells MDA-MB 435.
学科主题Pharmacology & Pharmacy
URL标识查看原文
语种英语
WOS记录号WOS:000288892900006
公开日期2012-07-03
内容类型期刊论文
源URL[http://ir.qdio.ac.cn/handle/337002/11892]  
专题海洋研究所_实验海洋生物学重点实验室
作者单位1.Chinese Acad Sci, Inst Oceanol, Open Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
2.Zhejiang Ocean Univ, Coll Marine Sci, Zhoushan 316004, Peoples R China
3.China Pharmaceut Univ, Marine Drugs Res Ctr, Nanjing 210018, Peoples R China
4.Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
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Wei, Rong-Bian,Xi, Tao,Li, Jing,et al. Lobophorin C and D, New Kijanimicin Derivatives from a Marine Sponge-Associated Actinomycetal Strain AZS17[J]. MARINE DRUGS,2011,9(3):359-368.
APA Wei, Rong-Bian.,Xi, Tao.,Li, Jing.,Wang, Ping.,Li, Fu-Chao.,...&Qin, Song.(2011).Lobophorin C and D, New Kijanimicin Derivatives from a Marine Sponge-Associated Actinomycetal Strain AZS17.MARINE DRUGS,9(3),359-368.
MLA Wei, Rong-Bian,et al."Lobophorin C and D, New Kijanimicin Derivatives from a Marine Sponge-Associated Actinomycetal Strain AZS17".MARINE DRUGS 9.3(2011):359-368.
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