期刊文献+

南海沉积环境来源真菌Eurotium sp.SCSIO F452的次生代谢产物研究 被引量:4

Analysis of Secondary metabolites produced by Eurotium sp.SCSIO F452 isolated from the South China Sea Sediment
原文传递
导出
摘要 目的对1株南海沉积环境来源真菌的次生代谢产物进行分离、鉴定及活性研究。方法采用溶剂萃取、硅胶柱层析、凝胶柱层析等方法对真菌Eurotiumsp.SCSIO F452的发酵产物进行化学分离,通过NMR、MS等波谱学技术并参阅文献进行化合物结构鉴定,采用SRB法评价化合物的细胞毒活性。结果从菌株SCSIO F452中分离鉴定6个单体化合物,分别为:isodihydroauroglaucin(1)、flavoglaucin(2)、tetrahydroauro-glaucin(3)、2-(1,1-dimethyl-2-propen-1-yl)-1H-indole-3-carboxaldehyde(4)、neoechinulin A(5)和methyl lino-leate(6)。化合物1-5对4种肿瘤细胞系表现出不同强度的细胞毒活性。结论苯甲醛衍生物1-3是真菌SC-SIO F452的优势代谢产物,细胞毒活性较强,具有潜在的研究价值。 Objective To isolate and identify the secondary metabolites of Eurotium sp. SCSIO F452 isola ted from the South China Sea sediment. Methods The fermentation products were purified by solvent extraction and column chromatography (silica gel and sephadex LH-20). The isolated compounds were identified by spectroscopic analysis (NMR and MS) as well as comparison with literatures. Their cyto toxicities were evaluated by SRB method. Results Six compounds were isolated from the acetic ether ex tracts of strain SCSIO F452, and their structures were determined as isodihydroauroglaucin(1), fla voglaucin(2), tetrahydroauroglaucin (3), 2-(1,1-dimethyl 2-propen-l-yl)-lH indole-3-carboxaldehyde (4), neoechinulin A(5), and methyl linoleate(6). Compounds 1-5 showed varied cytotoxic activities a gainst four cancer cell lines. Conclusion Benzaldehyde derivatives 1 3 were dominant metabolites of strain SCSIO F452 and exhibited moderate cytotoxicities. These compounds showed strong potentials for further research.
出处 《中国海洋药物》 CAS CSCD 北大核心 2013年第1期7-12,共6页 Chinese Journal of Marine Drugs
基金 国家重点基础研究发展计划项目(2010CB833800) 国家高技术研究发展计划(2012AA092104) 国家自然科学青年基金(40906076 40906075)资助
关键词 海洋真菌 散囊菌 次生代谢产物 细胞毒活性 沉积物 marine fungi F, urotium sp. secondary metabolites cytotoxicityl sediment
  • 相关文献

参考文献4

二级参考文献29

  • 1[2]Tan RX,Zou WX.Endophytes:a rich source of functional metabolites[J].Nat Prod Rep,2001,18:448-459.
  • 2[3]Feling RH,Buchanan GO,Mincer TJ,et al.Salinosporamide A:a highly cytotoxic proteasome inhibitor from a novel microbial source,a marine bacterium of the new genus Salinospora[J].Angew Chem (Int Ed),2003,42:355-357.
  • 3[4]Reddy LR,Saravanan P,Corey EJ.A simple stereocontrolled synthesis of salinosporamide A[J].J Am Chem Soc,2004,126:6230-6231.
  • 4[5]Macherla VR,Mitchell SS,Manam RR,et al.Structure-activity relationship studies of salinosporamide A (NPI-0052),a novel marine derived proteasome inhibitor[J].J Med Chem,2005,48:3684-3687.
  • 5[6]Chauhan D,Catley L,Li GL,et al.A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib[J].Cancer Cell,2005,8:407-419.
  • 6Tittensor D P, Mora C, Jetz W et al. Global patterns and predictors of marine biodiversity across taxa. Nature,2010,466(7 310): 1 098-1 101.
  • 7Parkes R J, Cragg B A, Bale S Jet al. Deep bacterial biosphere in Pacific Ocean sediments. Nature, 1994,371:410-413.
  • 8Venter J C, Remington K, Heidelberg J F et al. Environmental genome shotgun sequencing of the Sargasso sea. Science, 2004, 304: 66-74.
  • 9Kelecom A. Secondary metabolites from marine microorganisms. An Acad BrasCienc, 2002, 74 (1) 151-170.
  • 10Goodfellow M, Fiedler H P. A guide to successful bioprospecting: informed by actinobacterial systematics. Antonie van Leeuwenhoek, 2010,98 (2): 119-142.

共引文献67

同被引文献23

引证文献4

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部