有机化学 ›› 2026, Vol. 46 ›› Issue (6): 2482-2486.DOI: 10.6023/cjoc202511024 上一篇    下一篇

研究简报

天山假狼毒根部来源曲霉Aspergillus sp. L06的次级代谢产物及抗菌活性研究

董莉萍a,, 杨金花a,, 方容a, 张兴a, 朱小强a, 毕晓宾b,*(), 雷亮a,*()   

  1. a 武汉市第四医院 武汉 430033
    b 华中科技大学药学院 武汉 430030
  • 收稿日期:2026-02-03 修回日期:2026-03-02 发布日期:2026-04-02
  • 通讯作者: 毕晓宾, 雷亮
  • 作者简介:

    共同第一作者.

  • 基金资助:
    武汉市卫生健康委员会科研项目(WZ22Q21); 武汉市卫生健康委员会科研项目(WZ24B14); 国家自然科学基金(32000282); 国家自然科学基金(823041523)

Study on the Secondary Metabolites and Antibacterial Activity of a Fungus Aspergillus sp. L06 from the Roots of Stelleropsis tianschanica (Pobed)

Liping Donga, Jinhua Yanga, Rong Fanga, Xing Zhanga, Xiaoqiang Zhua, Xiaobin Bib,*(), Liang Leia,*()   

  1. a Wuhan Fourth Hospital, Wuhan 430033
    b School of Pharmacy, Huazhong University of Science and Technology, Wuhan 430030
  • Received:2026-02-03 Revised:2026-03-02 Published:2026-04-02
  • Contact: Xiaobin Bi, Liang Lei
  • About author:

    The authors contributed equally to this work.

  • Supported by:
    Wuhan Municipal Health Commission(WZ22Q21); Wuhan Municipal Health Commission(WZ24B14); National Natural Science Foundation of China(32000282); National Natural Science Foundation of China(823041523)

采用正相硅胶、反相硅胶、凝胶柱色谱以及高效液相色谱等方法, 对1株天山假狼毒根部来源真菌Aspergillus sp. L06的大米发酵产物进行分离纯化, 得到4个化合物. 通过理化性质和波谱方法分别鉴定为aspeverchromone A (1)、杂色曲霉素(2)、nidurufin (3)、versicolorin B (4), 其中化合物1为新化合物. 体外抗菌活性结果表明, 化合物1对多重耐药铜绿假单胞菌有较强抑制作用, 最小抑菌浓度(MIC)为4.0 μg/mL, 优于阳性对照庆大霉素(MIC为8.0 μg/mL).

关键词: 天山假狼毒, Aspergillus sp. L06, 次级代谢产物, 结构鉴定, 体外抗菌活性

This study aims to find monomer compounds with antimicrobial activity from the secondary metabolites of a soil-derived fungus Aspergillus sp. L06 isolated from the roots of Stelleropsis tianschanica (Pobed) in Xinjiang pastoral areas. Four compounds were obtained from the ethyl acetate layer of the fermentation of Aspergillus sp. L06 by silica gels, Sephadex LH-20, octadecylsilyl (ODS) column chromatography, and HPLC methods. Their structures were identified as aspever- chromone A (1), sterigmatocystin (2), nidurufin (3), and versicolorin B (4) by NMR, MS and other spectroscopic techniques. Among them, compound 1 is a new compound. The results of in vitro antibacterial activity indicated that compound 1 exhibited a strong inhibitory effect on multidrug-resistant Pseudomonas aeruginosa, with a minimum inhibitory concentration (MIC) of 4.0 μg/mL, which was superior to the positive control gentamicin (8.0 μg/mL).

Key words: Stelleropsis tianschanica (Pobed), Aspergillus sp. L06, secondary metabolites, structural identification, in vitro antibacterial activity