应用化学 ›› 2018, Vol. 35 ›› Issue (6): 708-713.DOI: 10.11944/j.issn.1000-0518.2018.06.170281

• 研究论文 • 上一篇    下一篇

来源湛江红树内生真菌的二氢异香豆素及其抑菌活性

凌惠平a,陈晓晴a,谢胜男a,陈月间a,佘志刚b,林永成b,陶移文a*()   

  1. a广州医科大学药学院 广州 511436
    b中山大学化学与化学工程学院 广州 510275
  • 收稿日期:2017-08-10 接受日期:2017-11-29 出版日期:2018-06-01 发布日期:2018-05-28
  • 通讯作者: 陶移文
  • 基金资助:
    广东省自然科学基金 (2016A030313588)广州市教育局项目(1201610155)2017年海洋和渔业发展专项资金(科技攻关与研发)(A201701C07)和2018年度广州医科大学大学生实验室开放项目资助

Dihydroisocoumarin Compounds from Endophytic Fungi of Rhizophora apiculata and Its Antibacterial Activity

LING Huipinga,CHEN Xiaoqinga,XIE Shengnana,CHEN Yuejiana,SHE Zhigangb,LIN Yongchengb,TAO Yiwena*()   

  1. aSchool of Pharmaceutical Sciences,Guangzhou Medical University,Guangzhou 511436,China
    bSchool of Chemistry and Chemical Engineering,Sun Yat-sen University,Guangzhou 510275,China
  • Received:2017-08-10 Accepted:2017-11-29 Published:2018-06-01 Online:2018-05-28
  • Contact: TAO Yiwen
  • Supported by:
    Supported by the Natural Science Program of Guangdong Province(No.2016A030313588), the Education Bureau Project of Guangzhou City(No.1201610155), the Projects of Guangdong Oceanic and Fishery Administration in 2017(No.A201701C07), the Open-Laboratory Project of Guangzhou Medical University in 2018

摘要:

为了研究湛江红树(Rhizophora apiculata)植物内生真菌Fusarium sp.F67和B42的二氢异香豆素类次级代谢产物及其抑菌活性,采用色谱技术对菌株F67和B42的代谢产物进行分离纯化,确认所得化合物的结构为:3,6,8-三羟基-3,4,5,7-四甲基-3,4-二氢异香豆素(sclerotinin A)(1),二氢橘霉素(2)、5-甲基蜂蜜曲菌素(3)、5-羧基蜂蜜曲菌素(4)、4-羟基蜂蜜曲菌素(5)和蜂蜜曲菌素(6),并利用滤纸片琼脂扩散法检测化合物对7种常见致病菌的抑菌活性。 在1.0 g/L质量浓度下化合物1~4对受试菌株的抑菌圈范围为5.1~11.0 mm,其中化合物4的抑菌活性相对较强,抑菌谱相对较广,可为挖掘新型抗菌药物的研究提供补充。

关键词: 红树林, 内生真菌, 异香豆素, 抑菌活性

Abstract:

In order to study the secondary metabolites of dihydroisocoumarin compounds from mangrove endophytic fungi Fusarium sp. F67 and B42, the metabolites of strains F67 and B42 were isolated and purified by chromatographic techniques, and their structures were determined as follows: 3,6,8-trihydroxy-3,4,5,7-tetramethyl-3,4-dihydroisocoumarin(sclerotinin A)(1), dihydrocitrinone(2), 5-methylmellein(3), 5-carboxymellein(4), 4-hydroxymellein(5) and mellein(6). Antibacterial activities of compounds 1~4 in 1.0 g/L show that the inhibitory zone against the tested strains ranges from 5.1 to 11.0 mm. Among them, compound 4 has the strongest antibacterial activities and the broadest bacteriostatic spectra. These results provide supplement to the research and development of new antibacterial drug.

Key words: Rhizophora apiculata, endophytic fungi, dihydroisocoumarins, antibacterial activity