期刊文献+

海洋蓝细菌抗肿瘤活性肽类的研究 被引量:1

Antineoplastic lipopeptides from marine cyanobacteria
下载PDF
导出
摘要 海洋蓝细菌种类多分布广,其次生代谢产物具有特殊的化学结构和广泛的生物活性。脂肽类是一类结构新颖的化合物,具有抗菌、抗肿瘤、抗炎等生物活性,近年来受到人们的广泛关注。其中,抗肿瘤化合物的研究及开发显现出十分诱人的前景。以海洋蓝细菌为探讨对象,综述了海洋蓝细菌产生的抗肿瘤活性肽类成分的研究进展,最后对海洋蓝细菌的发展前景进行了展望。 Marine cyanobacteria are a rich source of complex bioactive secondary metabolites which derive from mixed biosynthetic pathways. lipopeptides were characteristic with novel structures and more attentions were paid in the recent years. Lipopeptides showed various bioactivities including antibacterial, anti-tumor, anti-inflammatory, etc. The research and development of antineoplas-tic compounds showed attractive foreground. This paper reviewed antineoplastic lipopeptides of marine cyanobacteria. In addition, the prospects of the development of marine cyanobacteria were also reviewed.
出处 《生物学杂志》 CAS CSCD 2015年第4期77-82,共6页 Journal of Biology
基金 国家自然科学基金(41306134) 高等学校博士点基金(20133305120007)
关键词 海洋蓝细菌 抗肿瘤 肽类成分 生物活性 代谢产物 marine cyanobacteria antineoplastic lipopeptides biological activity metabolites
  • 相关文献

参考文献39

  • 1Bhatnagar I, Kim S K. Immense essence of excellence: marine mi- crobial bioactive compounds [J]. Mar Drugs, 2010, 8: 2673-2701.
  • 2Duffy R, Wade C, Chang R, et al. Discovery of anticancer drugs from antimalarial natural products: a MEDLINE literature review [J]. Drug Discov Today, 2012, 17: 942-953.
  • 3Nunnery J K, Mevers E, Gerwick W H. Biologically active second- ary metabolites from marine cyanobacteria [J]. Curr Opin Bio- tech, 2010, 21: 787-793.
  • 4Isabelle B, Marac R, Salmon J M, et al. Total structure and inhibi- tion of tumor cell porliferation of laxaphycins E J]. J Ivied Chem, 2007, 50: 1266-1279.
  • 5Luesch H, Yoshida W Y, Moore R E, et al. Total structure determi- nation of apratoxin A, a potent novel cytotoxin from the marine cy- anobacterium L.vngbya majuscula [J]. Am Chem Soc, 2001, 123: 5418-5423.
  • 6Luesch H, Chanda S K, Orth P A, et al. A functional genomics ap- proach to the mode of action of apratoxin A [J]. NCB, 2006, 2: 158-167.
  • 7Ma D W, Zou B, Cai G R, et al. Total synthesis of the cyclodepsip- eptide apratoxin A and its analogues and assessment of their bio- logical activities [J]. Chem Eur, 2006, 12: 7615-7626.
  • 8Shen S S, Zhang P T, Lovchik M A, et al. Cyclodepsipeptide toxin promotes the degradation of Hsp90 client proteins through chaper- one mediated autophagy[J]. J Cell Biol, 2009, 185: 629-639.
  • 9Suyama T L, Engene N, Matainaho T, et al. A potent cytotoxic cy- clodepsipeptide from papua new guinea collections of the marine cyanobacteria lyngbya majuscule and lyngbya sordida [ Jl. J Nat Prod, 2008, 71:1099-1103.
  • 10Eugene N, Media J, Doi T, et al. Evolved diversification of a mod- ular natural product pathway: apratoxins F and G, two cytotoxic cyclic depsipeptides from a palmyra collection of lyngbya bouil- lonii [ J ]. Chem Bio Chem, 2010, 11: 1458-1466.

同被引文献8

引证文献1

二级引证文献1

  • 1赵心清.导读[J].生物工程学报,2024,40(6).

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