天然产物研究与开发 ›› 2018, Vol. 30 ›› Issue (11): 1928-1932.doi: 10.16333/j.1001-6880.2018.11.013

• 研究简报 • 上一篇    下一篇

藏药穹代尔中内生真菌的分离及其次级代谢物的生物活性研究

周格格,杨中铎*,孙景云   

  1. 兰州理工大学生命科学与工程学院,兰州 730050
  • 出版日期:2018-12-03 发布日期:2018-12-03
  • 基金资助:

    国家自然科学基金(21762027);甘肃省科技支撑计划(1604FKCA084)

Isolation of Endophytic Fungi from Uncaria scandens and the Biological Activity of Their Secondary Metabolites

ZHOU Ge-ge, YANG Zhong-duo*, SUN Jing-yun   

  1. Lanzhou University of Technology, Lanzhou 730050, China
  • Online:2018-12-03 Published:2018-12-03

摘要: 从藏药穹代尔(攀茎钩藤,Uncaria scandens)的内生真菌中筛选对单胺氧化酶及乙酰胆碱酯酶具有抑制活性的提取物,并对高活性提取物进行化学成分的鉴定。采用组织切块法分离内生菌,发酵、萃取、甲醇回流提取法得到待测提取物,酶标法测定酶活性,波谱解析法鉴定结构。从穹代尔组织中共分离到 9 株内生真菌,检测发现 3 株内生真菌发酵提取物具有一定乙酰胆碱酯酶抑制活性,其抑制率在50%以上。通过分子生物学方法及形态学分析对活性菌株QDE-6进行了菌种鉴定,鉴定为黑曲霉属(Aspergillus sp.)真菌。从内生真菌QDE-6的次级代谢产物中分离鉴定了5个化合物,分别是Aspergiketone(1)、Gliotoxin(2)、Pseurotin A2(3)、Brevianamide F(4)、Pseurotin A1(5)。相比其他化合物,化合物3抑制率为51.67%,具有较高的抗单胺氧化酶活性,化合物4抑制率为42.76%,具有较高的抗乙酰胆碱酯酶活性。可作为进一步研究藏药穹代尔中内生真菌及开发药物的基础。

关键词: 攀茎钩藤, 内生真菌, 次级代谢产物, 单胺氧化酶抑制剂, 乙酰胆碱酯酶抑制剂

Abstract: To isolate endophytic fungus from Uncaria scandens and test monoamine oxidase (MAO) inhibitory and acetylcholinesterase (AChE) inhibitory activity of extracts form endophytic fungus.And the chemical constituents of compounds with high inhibitory activity were identified.Entophytic fungus were isolated by issue-culture method.The extracts were obtained by fermentation,extraction,methanol refluxing etc.The MAO inhibitory and the AChE inhibitory activity of extracts were tested by colorimetric method in 96-well microplates.The structures of compounds were identified by various chromatography methods.9 strains of endophytic fungus were isolated from Uncaria scandens.Three extracts showed anti-AChE activity with inhibitory rate more than 50%.The active strain QDE-6 was identified through molecular biological characterization and morphological methods,it is Aspergillus sp..5 compounds were isolated from endothytic fungi QDE-6 and identified as Aspergiketone(1)、Gliotoxin(2)、Pseurotin A2(3)、Brevianamide F(4)、Pseurotin A1(5).The inhibitory rate of compound 3 was 51.67%,which showed higher anti-MAO activity than other compounds.The AChE activity with inhibitory rate of compound 4 was 42.76%,it is higher other compounds,these can be used as basis for further study on endophytic fungus in Uncaria scandens and the development of drugs.

Key words: Uncaria scandens endophytic fungi, secondary metabolites, monoamine oxidase inhibitors, acetylcholinesterase inhibitors

中图分类号: 

R284.1 Q931.6