您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

山东大学学报 (医学版) ›› 2026, Vol. 64 ›› Issue (5): 1-9.doi: 10.6040/j.issn.1671-7554.0.2025.0990

• 重点专题——活性天然产物研究 •    

黄河三角洲来源鹅绒藤内生真菌Aspergillus iizukae RD16次级代谢产物研究

任思齐1,2,张晓琦2,3,吕文元1,2,方舟1,2,齐世洲2,苗双2,宫凯凯2   

  1. 1.滨州医学院附属医院肿瘤科;2.滨州医学院附属医院医学研究中心;3.滨州医学院药学院, 山东 滨州 256603
  • 发布日期:2026-05-13
  • 通讯作者: 苗双. E-mail:keaimiaoshuang@126.com宫凯凯. E-mail:gongkaikai1005@bzmc.edu.cn
  • 基金资助:
    国家自然科学基金(81903537);山东省医药卫生发展计划(202313050516);山东省中医药科技发展计划(Z20244106);滨州市“揭榜挂帅”技术攻关计划(2025JBGS007)

Secondary metabolites of the endophytic fungus Aspergillus iizukae RD16 isolated from Cynanchum chinene in the Yellow River Delta

REN Siqi1,2, ZHANG Xiaoqi2,3, LYU Wenyuan1,2, FANG Zhou1,2, QI Shizhou2, MIAO Shuang2, GONG Kaikai2   

  1. 1. Department of Oncology, Binzhou Medical University Hospital;
    2. Medical Research Center, Binzhou Medical University Hospital;
    3. College of Phamacy, Binzhou Medical University, Binzhou 256603, Shandong, China
  • Published:2026-05-13

摘要: 目的 探讨黄河三角洲来源鹅绒藤内生真菌Aspergillus iizukae RD16的次级代谢产物及细胞毒性。 方法 利用硅胶柱色谱、凝胶柱色谱和半制备高效液相等方法和技术对Aspergillus iizukae RD16大米发酵产物进行分离、纯化。使用NMR及质谱数据分析鉴定化合物的结构;采用CCK-8法评价化合物的细胞毒活性。 结果 从采自黄河三角洲的植物鹅绒藤中分离获得一株内生真菌RD16,鉴定为Aspergillus iizukae RD16;从其大米发酵产物中分离鉴定了7个单体化合物;分别为cytochalasin Z17(1)、cytochalasin Z16(2)、flavichalasine I(3)、aspochalasin J(4)、isorhodoptiometrin(5)、questin(6)、sulochrin(7)。其中化合物(1~4)为细胞松弛素类化合物,化合物(5和6)为蒽醌类化合物,化合物(7)为二苯甲酮类化合物。采用CCK-8法测试所有化合物对五株肿瘤细胞的毒性,其中化合物1对非小细胞肺癌A549细胞有显著的抑制活性,IC50值为2.6 μmol/L;化合物2对A549细胞以及人结直肠腺癌RKO细胞均具有较强的抑制活性,IC50值分别为3.0 μmol/L和2.8 μmol/L;化合物4对RKO细胞的IC50值为5.6 μmol/L,对A549细胞有中等强度的细胞毒活性,其IC50值为11.3 μmol/L。化合物5对SW480细胞有较强的抑制活性,IC50值为5.8 μmol/L,对A549细胞有中等细胞毒活性,IC50值为13.4 μmol/L。化合物6对A375以及A549细胞的IC50值分别为8.5 μmol/L和3.9 μmol/L。 结论 黄河三角洲盐碱地来源植物内生真菌A.iizukae RD16可以产生结构多样的次级代谢产物。细胞松弛素类和蒽醌类化合物,在抗肿瘤先导化合物发掘方面具有一定应用潜力。

关键词: 黄河三角洲, 次级代谢产物, 内生真菌, Aspergillus iizukae RD16, 细胞毒活性

Abstract: Objective To investigate the secondary metabolites and cytotoxic properties of the endophytic fungus Aspergillus iizukae RD16, which was isolated from the plant Cynanchum chinense in the Yellow River Delta. Methods The fermentation products of the Aspergillus iizukae RD16 strain were isolated and purified using silica gel column chromatography, gel filtration chromatography and semi-preparative high performance liquid chromatography. The structures of the compounds were identified using NMR and mass spectrometry data analysis. The CCK-8 assay was used to evaluate the cytotoxic activity of the compounds. Results An endophytic fungus from Cynanchum chinene collected in the Yellow River Delta was identified as A.iizukae RD16. Seven monomeric compounds were isolated and identified in its rice fermentation products: cytochalasin Z17(1), cytochalasin Z16(2), flavichalasine I(3), aspochalasin J(4), isorhodoptiometrin(5), questin(6), and sulochrin(7). Compounds 1-4 belong to the cytochalasins, compounds 5 and 6 are anthraquinones, and compounds 7 is a benzophenone. The cytotoxic effects of all the compounds were tested against five human tumor cell lines using the CCK-8 assay. The results showed that compound 1 exhibited significant inhibitory activity against A549 non-small cell lung cancer cells, with an IC50 value of 2.6 μmol/L. Compound 2 demonstrated potent inhibitory activity against both A549 cells and RKO human colorectal adenocarcinoma cells, with IC50 values of 3.0 μmol/L and 2.8 μmol/L, respectively. Compound 4 exhibited moderate activity against A549 cells, with an IC50 value of 11.3 μmol/L, and an IC50 value of 5.6 μmol/L against RKO cells. Compound 5 displayed strong activity against SW480 cells(IC50 value of 5.8 μmol/L)and moderate activity against A549 cells(IC50 value of 13.4 μmol/L). Compound 6 exhibited IC50 values of 8.5 μmol/L and 3.9 μmol/L against A375 cells and A549 cells, respectively. Conclusion The endophytic fungus Aspergillus iizukae RD16 which is found in the Yellow River Delta produces a variety of secondary metabolites. Among them, Cytochalasins and anthraquinones show potential for the discovery of lead compounds due to their cytotoxic activities.

Key words: Yellow River Delta, Secondary metabolites, Endophytic fungi, Aspergillus iizukae RD16, Cytotoxic activity

中图分类号: 

  • R93
[1] Izzo AA, Stefanska B. Natural products and cancer: from drug discovery to prevention and therapy[J]. Br J Pharmacol, 2025, 182(10): 2069-2074.
[2] Prakash S, Kumari H, Sinha M, et al. Regulation and induction of fungal secondary metabolites: a comprehensive review[J]. Arch Microbiol, 2025, 207(8): 189. doi:10.1007/s00203-025-04386-0
[3] Sun ZL, Wu MY, Zhong BY, et al. Target discovery of dhilirane-type meroterpenoids by biosynthesis guidance and tailoring enzyme catalysis[J]. J Am Chem Soc, 2024, 146(44): 30242-30251.
[4] Liu HB, Edrada-Ebel R, Ebel R, et al. Drimane sesquiterpenoids from the fungus Aspergillus ustus isolated from the marine sponge Suberites domuncula[J]. J Nat Prod, 2009, 72(9): 1585-1588.
[5] Feng T, Deng XL, Xu ZY, et al. Diaporlabanoids A-C, immunosuppressive dinorlabdane diterpene alkaloids with an unprecedented carbon skeleton from mangrove endophytic fungus Diaporthe phaseolorum H3-2[J]. Org Lett, 2025, 27(27): 7267-7272.
[6] Saetang P, Rukachaisirikul V, Phongpaichit S, et al. Antibacterial and antifungal polyketides from the fungus Aspergillus unguis PSU-MF16[J]. J Nat Prod, 2021, 84(5): 1498-1506.
[7] Chen CM, Cai J, Yang C, et al. Striasteroids A-C, three hybrid steroids with neuraminidase inhibitory activities from a marine-derived Striaticonidium cinctum[J]. Org Lett, 2025, 27(14): 3737-3741.
[8] Prajapati J, Goswami D, Rawal RM. Endophytic fungi: a treasure trove of novel anticancer compounds[J]. Curr Res Pharmacol Drug Discov, 2021, 2: 100050. doi:10.1016/j.crphar.2021.100050
[9] Wellensiek BP, Ramakrishnan R, Bashyal BP, et al. Inhibition of HIV-1 replication by secondary metabolites from endophytic fungi of desert plants[J]. Open Virol J, 2013, 7: 72-80. doi:10.2174/1874357920130624002
[10] Skanda S, Vijayakumar BS. Antioxidant and anti-inflammatory metabolites of a soil-derived fungus Aspergillus arcoverdensis SSSIHL-01[J]. Curr Microbiol, 2021, 78(4): 1317-1323.
[11] Saad MMG, Abdelgaleil SAM, Shiono Y. Antibacterial and herbicidal properties of secondary metabolites from fungi[J]. Nat Prod Res, 2021, 35(23): 5446-5451.
[12] 王琦, 杨晓绒, 郑霞, 等. 药用植物内生真菌及其代谢产物研究进展[J]. 中国麻业科学, 2024, 46(6): 344-353. WANG Qi, YANG Xiaorong, ZHENG Xia, et al. Research progress on endophytic fungal diversity and metabolites of medicinal plants[J]. Plant Fiber Sciencesin China, 2024, 46(6): 344-353.
[13] Spanheimer R, Müller V. The molecular basis of salt adaptation in Methanosarcina mazei Gö1[J]. Arch Microbiol, 2008, 190(3): 271-279.
[14] 管博, 于君宝, 陆兆华, 等. 黄河三角洲滨海湿地水盐胁迫对盐地碱蓬幼苗生长和抗氧化酶活性的影响[J]. 环境科学, 2011, 32(8): 2422-2429. GUAN Bo, YU Junbao, LU Zhaohua, et al. Effects of water-salt stresses on seedling growth and activities of antioxidative enzyme of Suaeda salsa in coastal wetlands of the Yellow River Delta[J]. Environmental Science, 2011, 32(8): 2422-2429.
[15] 许言超, 刘培培, 王乂, 等. 黄河三角洲植物真菌的分离、活性菌株筛选及活性产物鉴定[J]. 中国海洋药物, 2014, 33(4): 15-20. XU Yanchao, LIU Peipei, WANG Yi, et al. Isolation and antibiotic screening of fungi associated with plants from Yellow River Delta and identification of the active metabolites[J]. Chinese Journal of Marine Drugs, 2014,33(4): 15-20.
[16] Wang MX, Carver JJ, Phelan VV, et al. Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking[J]. Nat Biotechnol, 2016, 34(8): 828-837.
[17] Lin ZJ, Zhang GJ, Zhu TJ, et al. Bioactive cytochalasins from Aspergillus flavipes, an endophytic fungus associated with the mangrove plant Acanthus ilicifolius[J]. Helv Chim Acta, 2009, 92(8): 1538-1544.
[18] Zhang H-W, Zhang J, Hu S, et al. Ardeemins and cytochalasins from Aspergillusterreus Residing in Artemisia annua[J]. Planta Med, 2010, 76(14): 1616-1621.
[19] Wei GZ, Tan DD, Chen CM, et al. Flavichalasines A-M, cytochalasan alkaloids from Aspergillus flavipes[J]. Sci Rep, 2017, 7: 42434. doi:10.1038/srep42434
[20] Zhou GX, KithsiriWijeratne EM, Bigelow D, et al. Aspochalasins I, J, and K: three new cytotoxic cytochalasans of Aspergillus flavipes from the rhizosphere of Ericameria laricifolia of the Sonoran Desert[J]. J Nat Prod, 2004, 67(3): 328-332.
[21] 周立晓, 黄薇, 张雅婷, 等. 苞叶大黄的化学成分研究[J]. 云南民族大学学报(自然科学版), 2022, 31(1): 1-7. ZHOU Lixiao, HUANG Wei, ZHANG Yating, et al. Chemical constituents of Rheum alexandrae[J]. Journal of Yunnan University of Nationalities(Natural Sciences Edition), 2022, 31(1): 1-7.
[22] Fujimoto H, Fujimaki T, Okuyama E, et al. Immunomodulatory constituents from an ascomycete, Microascus tardifaciens[J]. Chem Pharm Bull, 1999, 47(10): 1426-1432.
[23] Shimada A, Shiokawa C, Kusano M, et al. Hydroxysulochrin, a tea pollen growth inhibitor from the fungus Aureobasidium sp[J]. BiosciBiotechnolBiochem, 2003, 67(2): 442-444.
[24] 吴宇圳, 张慧敏, 安芳芳, 等. 不同生境来源杂色曲霉次级代谢产物研究进展[J]. 天然产物研究与开发, 2023, 35(2): 342-352. WU Yuzhen, ZHANG Huimin, AN Fangfang, et al. Research progress on secondary metabolites of Aspergillus versicolor from different habitats[J]. Natural Product Research and Development, 2023, 35(2): 342-352.
[25] Hwang J, Yi M, Zhang X, et al. Cytochalasin B induces apoptosis through the mitochondrial apoptotic pathway in HeLa human cervical carcinoma cells[J]. Oncol Rep, 2013, 30(4): 1929-1935.
[26] Gomzikova MO, Aimaletdinov AM, Bondar OV, et al. Immunosuppressive properties of cytochalasin B-induced membrane vesicles of mesenchymal stem cells: comparing with extracellular vesicles derived from mesenchymal stem cells[J]. Sci Rep, 2020, 10(1): 10740. doi:10.1038/s41598-020-67563-9
[27] Farias KJS, Machado PRL, de AlmeidaJúnior RF, et al. Brefeldin A and Cytochalasin B reduce dengue virus replication in cell cultures but do not protect mice against viral challenge[J]. Access Microbiol, 2019, 1(6): e000041. doi:10.1099/acmi.0.000041
[28] Trendowski M. Using cytochalasins to improve current chemotherapeutic approaches[J]. Anticancer Agents Med Chem, 2015, 15(3): 327-335
[29] Marinello J, Delcuratolo M, Capranico G. Anthracyclines as topoisomerase II poisons: from early studies to new perspectives[J]. Int J Mol Sci, 2018, 19(11): 3480. doi:10.3390/ijms19113480
[30] da Silva Lamartine-Hanemann S, Ferreira-Silva GÁ, de Oliveira Horvath R, et al. A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines[J]. Toxicol In Vitro, 2020, 68: 104927. doi:10.1016/j.tiv.2020.104927
[1] 张臻,苗双,齐世洲,武艳,蔡国伟,宫凯凯. 黄河三角洲盐碱土壤来源真菌Penicillium terrigenumRD 4-3次级代谢产物及其抗炎抗肿瘤活性[J]. 山东大学学报 (医学版), 2024, 62(3): 28-38.
[2] 张鹏亮,张龙腾,李爱玲,沈涛,娄红祥,王小宁. 植物内生真菌Leptosphaeria sp.中两个新氧杂蒽酮类化合物leptosphaerins H和I的分离及抗炎活性[J]. 山东大学学报(医学版), 2017, 55(11): 27-31.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!