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山东大学学报 (医学版) ›› 2024, Vol. 62 ›› Issue (3): 28-38.doi: 10.6040/j.issn.1671-7554.0.2023.1125

• 基础医学 • 上一篇    下一篇

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

张臻1,苗双1,齐世洲1,武艳1,蔡国伟2,宫凯凯1   

  1. 1.滨州医学院附属医院医学研究中心, 山东 滨州 256603;2.滨州医学院附属医院国家临床药物试验机构, 山东 滨州 256603
  • 发布日期:2024-05-06
  • 通讯作者: 宫凯凯. E-mail:gongkaikai1005@163.com蔡国伟. E-mail:byfycgw@126.com
  • 基金资助:
    国家自然科学基金(81903537)

Secondary metabolites and their activities of Penicillium terrigenum RD 4-3 isolated from saline-alkali soil in the Yellow River Delta

ZHANG Zhen1, MIAO Shuang1, QI Shizhou1, WU Yan1, CAI Guowei2, GONG Kaikai1   

  1. 1. Medical Research Center, Binzhou Medical University Hospital, Binzhou 256603, Shandong, China;
    2. CFDA Certified Clinical Trials Institution, Binzhou Medical University Hospital, Binzhou 256603, Shandong, China
  • Published:2024-05-06

摘要: 目的 研究黄河三角洲盐碱土壤中真菌Penicillium terrigenum RD 4-3的次级代谢产物及其生物活性。 方法 采用多种色谱分离技术对真菌液态发酵次级代谢产物进行分离纯化,并根据化合物的理化性质及波谱数据进行结构鉴定,同时进行细胞毒活性和NO检测,探究其抗肿瘤与抗炎活性。 结果 最终从Penicillium terrigenum RD 4-3发酵产物中分离鉴定14个单体化合物,分别为倍半萜类14-hydroxypetasol(1)、6-dehydropetasol(2)、isopetasol(3)、acremeremophilane G(4)、phomenone(6)、7-hydroxypetasol(7)、sporogen-AO1(9)、petasol(10)、JBIR-28(11)、JBIR-27(12)、3-acetyl-13-deoxyphome(13)、penicilleremophilane A(14),以及苯的衍生物3-chloro-4-hydroxypheylacetamide(5)、phenols(8),其中化合物1(14-hydroxypetasol)为新化合物。活性结果显示,化合物6(phomenone)和9(sporogen-AO1)对非小细胞肺癌细胞A549和H1299均具有显著的抗肿瘤活性,IC50值均在10 μmol/L以下。在浓度为50 μmol/L时,化合物6(phomenone)、10(petasol)、11(JBIR-28)在LPS诱导的炎症模型中表现出一定的抗炎活性。初步的构效关系研究发现,6,7位的氧环结构可以显著提高化合物的抗肿瘤及抗炎活性。 结论 真菌Penicillium terrigenum RD 4-3的次级代谢产物中的倍半萜类在抗肿瘤抗炎先导化合物发现方面具有巨大研发潜力。

关键词: 黄河三角洲, 真菌, Penicillium terrigenum RD 4-3, 次级代谢产物, 抗肿瘤活性, 抗炎活性

Abstract: Objective To study the secondary metabolites and biological activities of fungus Penicillium terrigenum RD 4-3 isolated from saline-alkali soil in the Yellow River Delta. Methods The secondary metabolites were isolated and purified using various chromatographic methods from culture broth, and the structures of the pure compounds were identified based on their physicochemical properties and spectral data. Cytotoxic activity and NO detection were performed to explore antineoplastic activity and anti-inflammatory activity. Results Fourteen pure compounds were isolated and identified from the extracts of Penicillium terrigenum RD 4-3, including sesquiterpenes 14-hydroxypetasol(1), 6-dehydropetasol(2), isopetasol(3), acremeremophilane G(4), phomenone(6), 7-hydroxypetasol(7), sporogen-AO1(9), petasol(10), JBIR-28(11), JBIR-27(12), 3-acetyl-13-deoxyphome(13)and penicilleremophilane A(14), and benzene derivatives 3-chloro-4-hydroxypheylacetamide(5)and phenols(8), among which 14-hydroxypetasol was a new compound. The activity results showed that phomenone(6)and sporogen-AO1(9)exhibited significant antitumor activities against non-small cell lung cancer cells A549 and H1299, with IC50 values below 10 μmol/L. At a concentration of 50 μmol/L, phomenone, petasol and JBIR-28 exhibited anti-inflammatory activity in the LPS-induced inflammation model. Preliminary structure-activity relationship revealed that the 6,7-epoxyl structure could significantly increase the antitumor and anti-inflammatory activities of the compounds. Conclusion The sesquiterpenes of the secondary metabolitesfrom fungus Penicillium terrigenum RD 4-3 from the Yellow River Delta exhibit great potential in the discovery of antitumor and anti-inflammatory lead compounds.

Key words: Yellow River Delta, Fungi, Penicillium terrigenum RD 4-3, Secondary metabolites, Antitumor activity, Anti-inflammatory activity

中图分类号: 

  • R574
[1] Fleming A. On the antibacterial action of cultures of a penicillium, with special reference to their use in the isolation of B influenzæ[J]. Br J Exp Pathol, 1929, 10(3): 226-236.
[2] Schueffler A, Anke T. Fungal natural products in research and development[J]. Nat Prod Rep, 2014, 31(10): 1425-1448.
[3] 刘玉斌,韩美,刘延荣,等.黄河三角洲土壤盐分养分空间分异规律研究[J].人民黄河, 2018, 40(2): 76-80. LIU Yubin, HAN Mei, LIU Yanrong, et al. Spatial distribution of soil salinity and nutrients in the Yellow River Delta[J]. Yellow River, 2018, 40(2): 76-80.
[4] 谭小丽,王岩宏,韩卫东.黄河三角洲湿地土壤剖面理化特征分析[J].资源节约与环保, 2018, 5(12): 9247-9250. TAN Xiaoli, WANG Yanhong, HAN Weidong. Analysis of physical and chemical characteristics of wetland soil profile in Yellow River Delta[J]. Resources Economization & Environment Protection, 2018, 5(12): 9247-9250.
[5] 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 of plant fungi, screening of active strains and identification of active products in the Yellow River Delta[J]. Chinese Journal of Maeine Medicine, 2014, 33(4): 15-20.
[6] 陈正乾,刘培培,王乂,等.黄河三角洲土曲霉Aspergillus terreus OUCMDZ-1925中具抗菌活性的聚酮类天然产物[J].菌物学报, 2013, 32(2): 277-285. CHEN Zhengqian, LIU Peipei, WANG Yi, et al. Polyketide natural products with antimicrobial activity in Aspergillus terreus OUCMDZ-1925 in the Yellow River Delta[J]. Mycosystema, 2013, 32(2): 277-285.
[7] 曲鹏,刘培培,付鹏,等.黄河三角洲耐盐真菌Penicillium chrysogenum HK14-01的次生代谢产物[J].微生物学报, 2012, 52(9): 1103-1112. QU peng, LIU Peipei, FU Peng, et al. Secondary metabolites of salt-tolerant fungus Penicillium chrysogenum HK14-01 in the Yellow River Delta[J]. Acta Microbiologica Sinica, 2012, 52(9): 1103-1112.
[8] 王聪,刘培培,王乂,等. 海洋来源放线菌Streptomyces parvulus OUCMDZ-2554产放线菌素D的发酵条件优化[J]. 中国海洋药物, 2014, 33(3): 34-42. WANG Cong, LIU Peipei, WANG Yi, et al. Optimization of fermentation conditions for actinomycin D production by Streptomyces parvulus OUCMDZ-2554 from marine actinomyces[J]. Chinese Journal of Marine Medicine, 2014, 33(3): 34-42.
[9] Fu P, Liu P, Qu H, et al. Alpha-pyrones and diketopiperazine derivatives from the marine-derived actinomycete Nocardiopsis dassonvillei HR10-5[J]. J Nat Prod, 2011,74(10):2219-2223.
[10] Xu Y, Wang C, Liu H, et al. Meroterpenoids and isocoumarinoids from a Myrothecium fungus associated with Apocynum venetum[J]. Mar Drugs, 2018, 10(1): 1-13.
[11] Wang C, Li J, Yang R, et al. Petasins from the rhizomes of Ligularia fischeri and its derivatives[J]. Records of Natural Products, 2014, 8(2): 156-164.
[12] Li S, Qin C, Cui S, et al. Discovery of a natural-product-derived preclinical candidate for once-weekly treatment of type 2 diabetes[J]. J Med Chem, 2019, 62(5): 2348-2361.
[13] Sugama K, Hayashi K, Nakagawa T, et al. Sesquiterpenoids from Petasites fragrans[J]. Phytochemistry, 1983, 22(7): 1619-1622.
[14] Sugawara F, Hallock YF, Bunkers GD, et al. Phytoactive eremophilanes produced by the weed pathogen Drechslera gigantea[J]. Biosci Biotech Bioch, 1993, 57(2): 236-239.
[15] Cheng ZB, Zhao JJ, Liu D, et al. Eremophilane-type sesquiterpenoids from an Acremonium sp. Fungus isolated from deep-sea sediments[J]. J Nat Prod, 2016, 79(4): 1035-1047.
[16] Davis RA, Watters D, Healy PC. The isolation and synthesis of 3-chloro-4-hydroxyphenylacetamide produced by a plant-associated microfungus of the genus Xylaria[J]. Tetrahedron Lett, 2005, 46(6): 919-921.
[17] Motohashi K, Hashimoto J, Inaba S, et al. New sesquiterpenes, JBIR-27 and -28, isolated from a tunicate-derived fungus, Penicillium sp. SS080624SCf1[J]. J Antibiot, 2009, 62(5): 247-250.
[18] Davis RA, Innocenti A, Poulsen SA, et al. Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library[J]. Bioorgan Med Chem, 2010, 18(1): 14-18.
[19] 高忠杰,曲莉,孙振青,等.烟草内生真菌土曲霉中一个新的苯乙酸类化合物[J].中国药物化学杂志, 2021, 31(8): 597-604. GAO Zhongjie, QU Li, SUN Zhenqing, et al. A new hydroxyphenylacetic acid derivative isolated from the endophyte Aspergillus terreus of Nicotiana tabacum L[J]. Chinese Journal of Medicinal Chemistry, 2021, 31(8): 597-604.
[20] 蔡由生,刘海利,龚景旭,等.中国湛江木榄(Bruguiera gymnorrhiza)的化学成分研究[J]. 中国海洋药物, 2011, 30(1): 15-18. CAI Yousheng, LIU Haili, GONG Jingxu, et al. Chemical constituents of mangrove plant Bruguiera gymnorrhiza[J]. Chinese Journal of Marine Drugs, 2011, 30(1): 15-18.
[21] Huang YF, Qiao L, Lv AL, et al. Eremophilane sesquiterenes from the marine fungus Penicillium sp. BL27-2[J]. Chinese Chem Lett, 2008, 19(5): 562-564.
[22] Daengrot C, Rukachaisirikul V, Tansakul C, et al. Eremophilane sesquiterpenes and diphenyl thioethers from the soil fungus Penicillium copticola PSU-RSPG138[J]. J Nat Prod, 2015, 78(4): 615-622.
[23] 刘德胜.黄河三角洲盐碱地真菌多样性及活性次级代谢产物的初步研究[D]. 青岛:中国海洋大学, 2014.
[24] Fraga BM. Natural sesquiterpenoids[J]. Nat Prod Rep, 2013, 30(9): 1226-1264.
[25] Dickschat JS. Bacterial terpene cyclases[J]. Nat Prod Rep, 2016, 33(1): 87-110.
[26] Mai F, Glomb MA. Structural and sensory characterization of novel sesquiterpene lactones from Iceberg lettuce[J]. J Agric Food Chem, 2016, 64(1): 295-301.
[27] Raupp FM, Spring O. New sesquiterpene lactones from Sunflower root exudate as germination stimulants for Orobanche cumana[J]. J Agric Food Chem, 2013, 61(44): 10481-10487.
[28] Chen R, Feng T, Li M, et al. Characterization of tremulane sesquiterpene synthase from the basidiomycete Irpex lacteus[J]. Org Lett, 2022, 24(31): 5669-5673.
[29] Cheong CB, Peh G, Wei Y, et al. A spirobicyclo[3.1.0] terpene from the investigation of sesquiterpene synthases from Lactarius deliciosus[J]. ACS Chem Bio, 2023, 18(1): 134-140.
[30] Scavo A, Rial C, Varela RM, et al. Influence of genotype and harvest time on the Cynara cardunculus L. sesquiterpene lactone profile[J]. J Agric Food Chem, 2019, 67(23): 6487-6496.
[31] Abraham W. Bioactive sesquiterpenes produced by fungi are they useful for humans as well[J]. Curr Med Chem, 2001, 8(6): 583-606.
[32] Dambolena JS, Zunino MP, Herrera JM, et al. Terpenes: natural products for controlling insects of importance to human health-a structure-activity relationship study[J]. Psyche-J Entomol, 2016: 1-17. doi:10.1155/2016/4595823.
[33] Quintana J, Estevez F. Recent advances on cytotoxic sesquiterpene lactones[J]. Curr Pharm Design, 2018, 24(36): 4355-4361.
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