期刊文献+

植物内生链霉菌KIB-271抗植物病原真菌活性成分研究 被引量:3

Secondary Metabolites from an Endophytic Streptomyces sp.KIB-271 and Their Anti-fungus Activity
下载PDF
导出
摘要 利用硅胶柱层析和制备型高效液相色谱等方法从来自杜鹃花科植物的一株内生链霉菌Streptomyces sp.KIB-271的发酵液中分离得到4种戊二酰亚胺类化合物,通过分析其理化性质和波谱数据,分别鉴定为cycloheximide(1)、iso-cycloheximide(2)、2,6-二酮-4-[(E)-2'-((3″S,5″S)-3″,5″-二甲基-2″-酮-环亚己基)]-乙基-哌啶(3)和2,6-二酮-4-[(E)-2'-((3″R,5″S)-3″,5″-二甲基-2″-酮-环亚己基)]-乙基-哌啶(4),其中,4为首次从天然产物中分离得到。抗菌试验研究表明化合物1对多株植物病原真菌具有明显的抗菌活性,可能是Streptomyces sp.KIB-271代谢产物的主要活性物质之一。 Four heterecyclic glntarimide antibiotics, namely eycloheximide ( 1 )iso-eycloheximide ( 2 ), 4- [ 2'- ( 3" (S), 5"(S) -3",5"-dimethyl-2"-oxocyclohexylidene) ethyl] piperidine-2,6-dione (3), and 4-[ 2'-(3"(R) ,5"(S) -3",5"-dime- thyl-2"-oxocyclohexylidene) ethyl] piperidine-2,6-dione (4) ,were isolated from the endophytic actinomycete Streptomy- ees sp. KIB-271. Their structures were identified through mass spectrometry and NMR experiments. Among them, com- pound 4 was reported for the first time as a natural product. In the antimicrobial experiments, 1 exhibited obvious antifun- gal activity in vitro against most of the tested fungus, and was considered as one of the main antimierobial constituent from Streptomyees sp. KIB-271.
出处 《天然产物研究与开发》 CAS CSCD 北大核心 2016年第3期331-334,共4页 Natural Product Research and Development
基金 国家自然科学基金(21262021) 中央高校基本科研业务费专项资金(QN2013039)
关键词 植物内生菌 次级代谢产物 波谱数据 抗菌活性 endophyte secondary metabolites spectrometry antimicrobial
  • 相关文献

参考文献2

二级参考文献12

  • 1Siegel MR, Sisler HD. Inhibition of protein synthesis in vitro by cycloheximide [J]. Nature, 1963, 200: 675-676.
  • 2Croons V, Martinet W, Herman AG, et al. Differential effect of the protein synthesis inhibitors puromycin and cycloheximide on vascular smooth muscle cell viability [J]. J Pharmacol Exp Ther, 2008, 325: 824-832.
  • 3Kit S, Kurimura T, De Tortes RA, et al. Simian virus 40 deoxyribonucleic acid replication. I. Effect of cycloheximide on the replication of SV40 deoxyribonucleic acid in monkey kidney cells and in heterokaryons of SV40-transformed and susceptible cells [J]. J Virol, 1969, 3: 25-32.
  • 4Mark GE, Taylor JM, Broni B, et al. Nuclear accumulation of influenza viral RNA transcripts and the effects of cycloheximide, actinomycin D, and alpha-amanitin [J]. J Virol, 1979, 29: 744-752.
  • 5Crance JM, Biziagos E, Passagot J, et al. Inhibition of hepatitis A virus replication in vitro by antiviral compounds [J]. J Med Virol, 1990, 31: 155-160.
  • 6Irvine JH, Horsfield JA, McKinney CZ, et al. A novel strategy to interfere with human immunodeficiency virus type 1 propagation [J]. N Z Med J, 1998, 111 : 222-224.
  • 7Choudhary SK, Walker RM, Powell DM, et al. CXCR4 tropic human immunodeficiency virus type 1 induces an apoptotic cascade in immature infected thymocytes that resembles thymocyte negative selection [J]. Virology, 2006, 352: 268-284.
  • 8Guo HF, Li YH, Yi H, et al. Synthesis, structures and anti-HBV activities of derivatives of the glutarimide antibiotic cycloheximide [J]. J Antibiot (Tokyo), 2009, 62: 639-642.
  • 9Gensler WJ, Johnson F, Sloan ADB. Compounds related to podophyllotoxin. XII. Podophyllone and dehydropodophyllotoxin [J]. J Am Chem Soc, 1960, 82: 6074-6081.
  • 10崔承彬,王浩,韩冰,宋幼新.假轮枝链霉菌Streptomyces pseudoverticillus生产的Elaiophylin类新细胞周期抑制剂及细胞凋亡诱导剂Ⅲ .化学结构及NMR研究(英文)[J].中国药物化学杂志,2001,11(1):25-31. 被引量:5

共引文献7

同被引文献21

引证文献3

二级引证文献25

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