Study on Secondary Metabolites of Endophytic Fungus Ogataea sp. RW-S10 from the Pogostemon cablin
Author:
Fund Project:

Key Research and Development Plan Projects of Hainan Province (Grant No. ZDYF2021SHFZ075), the Ministry of Finance and the Ministry of Agriculture and Rural Affairs of the National Modern Agricultural Industrial Technology System Special Project (Grant No. CARS-21), the Financial Special Project of the Ministry of Agriculture and Rural Affairs (Grant No. NFZX2021), and the Chinese Academy of Tropical Agricultural Sciences basic Scientific Research Business Expenses Special Project (Grant No. 1630052022030).

  • Article
  • | |
  • Metrics
  • |
  • Reference [19]
  • |
  • Related [20]
  • | | |
  • Comments
    Abstract:

    In order to obtain bioactive metabolites from Pogostemon cablin endophytic fungus, seven secondary metabolites were isolated and purified from the patchouli endophytic fungus Ogataea sp. RW-S10 by various chromatographic column techniques. Based on spectral data, their structures were identified as ogataearin (1), phenylalaninol (2), parahydroxyacet-ophenone (3), bis(dethio)bis(methylsulfanyl)gliotoxin (4), N-phenylethyl acetamide (5), lumichrome (6), and dehydroxypaxilline (7). Compound 1 was a new compound and showed α-glucosidase inhibitory activity with IC50 value of 39.38 μmol/L.

    Reference
    [1] QIAN Z Z, QI P, WANG G R. Main revisions on Chinese pharma-copoeia, Volumn 1(2005)[J]. Drug Stand China, 2005, 6(1):25-30.[钱忠直, 齐平, 王国荣. 《中国药典》2005年版(一部)品种主要增修订情况[J]. 中国药品标准, 2005, 6(1):25-30. doi:10.3969/j. issn. 1009-3656.2005.01.013.]
    [2] WU Y G, GUO Q S, ZHENG H Q. Textual research on history of introdution and herbal medicine of Pogostemon cablin[J]. China J Chin Mat Med, 2007, 32(20):2114-2117, 2181.[吴友根, 郭巧生, 郑焕强. 广藿香本草及引种历史考证的研究[J]. 中国中药杂志, 2007, 32(20):2114-2117, 2181. doi:10.3321/j.issn:1001-5302.2007.20.007.]
    [3] SWAMY M K, SINNIAH U R. Patchouli (Pogostemon cablin Benth.):Botany, agrotechnology and biotechnological aspects[J]. Ind Crops Prod, 2016, 87:161-176. doi:10.1016/j.indcrop.2016.04.032.
    [4] XIAN Y F, LI Y C, IP S P, et al. Anti-inflammatory effect of patchouli alcohol isolated from Pogostemonis HERBA in LPS-stimulated RAW 264.7 macrophages[J]. Exp Ther Med, 2011, 2(3):545-550. doi:10. 3892/etm.2011.233.
    [5] KIYOHARA H, ICHINO C, KAWAMURA Y, et al. Patchouli alcohol:In vitro direct anti-influenza virus sesquiterpene in Pogostemon cablin Benth.[J]. J Nat Med, 2012, 66(1):55-61. doi:10.1007/s11418-011-0550-x.
    [6] FENG X X, YU X T, LI W J, et al. Effects of topical application of patchouli alcohol on the UV-induced skin photoaging in mice[J]. Eur J Pharm Sci, 2014, 63(2014):113-123. doi:10.1016/j.ejps.2014.07.001.
    [7] TAN R X, ZOU W X. Endophytes:A rich source of functional meta-bolites[J]. Nat Prod Rep, 2001, 18(4):448-459. doi:10.1039/b100918o.
    [8] KONG F D, YI T F, MA Q Y, et al. Biphenyl metabolites from the patchouli endophytic fungus Alternaria sp. PfuH1[J]. Fitoterapia, 2020, 146:104708. doi:10.1016/j.fitote.2020.104708.
    [9] LÜCKE D, DALTON T, LEY S V, et al. Synthesis of natural and unnatural cyclooligomeric depsipeptides enabled by flow chemistry[J]. Chem Eur J, 2016, 22(12):4206-4217. doi:10.1002/chem.201504457.
    [10] FUJITA T, IIDA A, UESATO S, et al. Structural elucidation of trichosporin-B-Ia, IIIa, IIId and V from Trichoderma polysporum[J]. J Antibiot, 1988, 41(6):814-818. doi:10.7164/antibiotics.41.814.
    [11] KWON H C, LEE K R. Phytochemical constituents of Artemisia japonica ssp. littoricola[J]. Arch Pharm Res, 2001, 24(3):194-197. doi:10.1007/BF02978255.
    [12] RODRIGUES B, SAHM B D B, JIMENEZ P C, et al. Bioprospection of cytotoxic compounds in fungal strains recovered from sediments of the Brazilian Coast[J]. Chem Biodiv, 2015, 12(3):432-442. doi:10. 1002/cbdv.201400193.
    [13] ZOU X W, LIU S C, ZHENG Z H, et al. Two new imidazolone-containing alkaloids and further metabolites from the Ascomycete fungus Tricladium sp.[J]. Chem Biodivers, 2011, 8(10):1914-1920. doi:10.1002/cbdv.201000372.
    [14] TSUKAMOTO S, KATO H, HIROTA H, et al. Lumichrome:A larval metamorphosis-inducing substance in the ascidian Halocynthia roretzi[J]. Eur J Biochem, 1999, 264(3):785-789. doi:10.1046/j.1432-1327. 1999.00642.x.
    [15] HOSOE T, NOZAWA K, UDAGAWA S I, et al. Structures of new indoloditerpenes, possible biosynthetic precursors of the tremorgenic mycotoxins, penitrems, from Penicillium crustosum[J]. Chem Pharm Bull, 1990, 38(12):3473-3475. doi:10.1248/cpb.38.3473.
    [16] KONG F D, HUANG X L, MA Q Y, et al. Helvolic acid derivatives with antibacterial activities against Streptococcus agalactiae from the marine-derived fungus Aspergillus fumigatus HNMF0047[J]. J Nat Prod, 2018, 81(8):1869-1876. doi:10.1021/acs.jnatprod.8b00382.
    [17] JONG-ANURAKKUN N, BHANDARI M R, KAWABATA J. α-Glucosidase inhibitors from Devil tree (Alstonia scholaris)[J]. Food Chem, 2007, 103(4):1319-1323. doi:10.1016/j.foodchem.2006.10.043.
    [18] BÜCHI G, GOLDMAN I M, MAYO D W. The structures of two alkaloids from patchouli oil[J]. J Am Chem Soc, 1966, 88(13):3109-3113. doi:10.1021/ja00965a040.
    [19] WANG D H, YIN Z Q, ZHANG Q W, et al. Nonvolatile chemical constituents from Pogostemon cablin[J]. China J Chin Mat Med, 2010, 35(20):2704-2707.[王大海, 殷志琦, 张庆文, 等. 广藿香非挥发性化学成分的研究[J]. 中国中药杂志, 2010, 35(20):2704-2707. doi:10.4268/cjcmm20102014.]
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

阮武,郭教岑,马青云,杨理,谢晴宜,吴友根,赵友兴.广藿香内生真菌Ogataea sp. RW-S10次级代谢产物研究[J].热带亚热带植物学报,2023,31(5):741~746

Copy
Share
Article Metrics
  • Abstract:266
  • PDF: 614
  • HTML: 598
  • Cited by: 0
History
  • Received:April 08,2022
  • Revised:July 01,2022
  • Adopted:July 21,2022
  • Online: September 26,2023
  • Published: September 20,2023
Article QR Code