Skip to content
2000
Volume 15, Issue 6
  • ISSN: 2210-3155
  • E-ISSN: 2210-3163

Abstract

Background

Secondary metabolites from the mangrove-derived fungi have great potential to produce natural products with novel structures and significant biological activities.

Objective

The objective of this study was to isolate and identify the secondary metabolites from the mangrove-derived fungus sp. WHUF0342, and evaluate their antibacterial activities.

Methods

The compounds were isolated and purified by silica gel column chromatography, Sephadex LH-20 gel chromatography, and semi-preparative high-performance liquid chromatography (HPLC). Their structures were elucidated by comparing the NMR and MS spectroscopic data with those of literature. The antibacterial activity were evaluated by modified broth microdilution assay.

Results

Eight compounds were isolated from the fermented extracts of the fungus sp. WHUF0342 and identified as chaxine B (), nafuredin (), dichlorodiaportin (), ferulaic acid (), bis(2-ethylhexyl) benzene-1,2-dicarboxylate (), methyl 4-hydroxyphenylacetate (), 4-hydroxyphenyl acetate (), and 4-hydroxyphenylethyl acetate (). Chaxine B () showed antibacterial activity against the phytopathogenic bacterium with a minimum inhibitory concentration (MIC) value of 16 μg/mL. The antibacterial activity against plant pathogen of compound was reported for the first time in this study.

Conclusion

This study not only enriched the secondary metabolites of mangrove-derived fungi but also provided a valuable resource for the prevention of agricultural pathogen infections.

Loading

Article metrics loading...

/content/journals/npj/10.2174/0122103155311374240517062929
2024-05-27
2025-12-13
Loading full text...

Full text loading...

References

  1. CarrollA.R. CoppB.R. DavisR.A. KeyzersR.A. PrinsepM.R. Marine natural products.Nat. Prod. Rep.202340227532510.1039/D2NP00083K 36786022
    [Google Scholar]
  2. WangH.N. SunS.S. LiuM.Z. YanM.C. LiuY.F. ZhuZ. ZhangZ. Natural bioactive compounds from marine fungi (2017-2020).J. Asian Nat. Prod. Res.202224320323010.1080/10286020.2021.1947254 34253101
    [Google Scholar]
  3. AtanasovA.G. ZotchevS.B. DirschV.M. SupuranC.T. Natural products in drug discovery: Advances and opportunities.Nat. Rev. Drug Discov.202120320021610.1038/s41573‑020‑00114‑z 33510482
    [Google Scholar]
  4. NewmanD.J. CraggG.M. Natural products as sources of new drugs over the nearly four decades from 01/1981 to 09/2019.J. Nat. Prod.202083377080310.1021/acs.jnatprod.9b01285 32162523
    [Google Scholar]
  5. BaharudinM.M.A. NgalimatM.S. ShariffM.F. YusofB.Z.N. KarimM. BaharumS.N. SabriS. Antimicrobial activities of Bacillus velezensis strains isolated from stingless bee products against methicillin-resistant Staphylococcus aureus.PLoS One2021165e025151410.1371/journal.pone.0251514 33974665
    [Google Scholar]
  6. UpadhayayA. LingJ. PalD. XieY. PingF.F. KumarA. Resistance-proof antimicrobial drug discovery to combat global antimicrobial resistance threat.Drug Resist. Updat.20236610089010.1016/j.drup.2022.100890 36455341
    [Google Scholar]
  7. LeeS.Y. Mangrove macrobenthos: Assemblages, services, and linkages.J. Sea Res.2008591-2162910.1016/j.seares.2007.05.002
    [Google Scholar]
  8. LiK. ChenS. PangX. CaiJ. ZhangX. LiuY. ZhuY. ZhouX. Natural products from mangrove sediments-derived microbes: Structural diversity, bioactivities, biosynthesis, and total synthesis.Eur. J. Med. Chem.202223011411710.1016/j.ejmech.2022.114117 35063731
    [Google Scholar]
  9. ChenS. CaiR. LiuZ. CuiH. SheZ. Secondary metabolites from mangrove-associated fungi: Source, chemistry and bioactivities.Nat. Prod. Rep.202239356059510.1039/D1NP00041A 34623363
    [Google Scholar]
  10. XuJ. Bioactive natural products derived from mangrove-associated microbes.RSC Advances20155284189210.1039/C4RA11756E
    [Google Scholar]
  11. GuoX. JiaS. ZengF. YuQ. ChenY. XieJ. Sterol compounds from Ganoderma atrum: Isolation, antimicrobial activity and protective effect on Caco-2 cell oxidation damage.Food Chem. Adv.2022110011710.1016/j.focha.2022.100117
    [Google Scholar]
  12. NaM.W. LeeE. KangD.M. JeongS.Y. RyooR. KimC.Y. AhnM.J. KangK.B. KimK.H. Identification of antibacterial sterols from Korean wild mushroom Daedaleopsis confragosavia bioactivity- and LC-MS/MS profile-guided fractionation.Molecules2022276186510.3390/molecules27061865 35335230
    [Google Scholar]
  13. ZhuX.C. HuangG.L. MeiR.Q. WangB. SunX.P. LuoY.P. XuJ. ZhengC.J. One new α, β -unsaturated 7-ketone sterol from the mangrove-derived fungus Phomopsis sp.MGF222.Nat. Prod. Res.202135213970397610.1080/14786419.2020.1752210 32290694
    [Google Scholar]
  14. LiW. XiongP. ZhengW. ZhuX. SheZ. DingW. LiC. Identification and antifungal activity of compounds from the mangrove endophytic fungus Aspergillus clavatus R7.Mar. Drugs201715825926910.3390/md15080259 28825634
    [Google Scholar]
  15. YangX. YuH. RenJ. CaiL. XuL. LiuL. Sulfoxide-containing bisabolane sesquiterpenoids with antimicrobial and nematicidal activities from the marine-derived fungus Aspergillus sydowii LW09.J. Fungi20239334710.3390/jof9030347 36983515
    [Google Scholar]
  16. ZhangJ. ZhangB. CaiL. LiuL. New dibenzo-α-pyrone derivatives with α-glucosidase inhibitory activities from the marine-derived fungus Alternaria alternata.Mar. Drugs2022201277810.3390/md20120778 36547925
    [Google Scholar]
  17. DuanC. WangS. HuoR. LiE. WangM. RenJ. PanY. LiuL. LiuG. Sorbicillinoid derivatives with the radical scavenging activities from the marine-derived fungus Acremonium chrysogenum C10.J. Fungi20228553010.3390/jof8050530 35628785
    [Google Scholar]
  18. ChoiJ.H. OgawaA. AbeN. MasudaK. KoyamaT. YazawaK. KawagishiH. ChaxinesB.C. D, and E from the edible mushroom Agrocybe chaxingu.Tetrahedron200965479850985310.1016/j.tet.2009.09.064
    [Google Scholar]
  19. UiH. ShiomiK. YamaguchiY. MasumaR. NagamitsuT. TakanoD. SunazukaT. NamikoshiM. OmuraS. Nafuredin, a novel inhibitor of NADH-fumarate reductase, produced by Aspergillus niger FT-0554.J. Antibiot.200154323423810.7164/antibiotics.54.234 11372780
    [Google Scholar]
  20. LarsenT.O. BreinholtJ. Dichlorodiaportin, diaportinol, and diaportinic acid: Three novel isocoumarins from penicillium nalgiovense.J. Nat. Prod.19996281182118410.1021/np990066b 10479334
    [Google Scholar]
  21. LiangY. ZhangL. LaiC. OuyangZ. ZhangJ. Evaluation of antibacterial activity of compounds isolated from the peel of Newhall navel orange.Nat. Prod. Res.202337122060206410.1080/14786419.2022.2116580 36008769
    [Google Scholar]
  22. KatadeS.R. PawarP.V. TungikarV.B. TambeA.S. KalalK.M. WakharkarR.D. DeshpandeN.R. Larvicidal activity of bis(2-ethylhexyl) benzene-1,2-dicarboxylate from Sterculia guttata seeds against two mosquito species.Chem. Biodivers.200631495310.1002/cbdv.200690006 17193215
    [Google Scholar]
  23. HuK. ZhangM. WuD. XieY. RenJ. A novel synthesis of pimavanserin: A selective serotonin 5-HT2A receptor inverse agonist.Org. Prep. Proced. Int.2020521697610.1080/00304948.2019.1697613
    [Google Scholar]
  24. NawazN.U.A. SaeedM. KhanK.M. AliI. BhattiH.A. Sabi-Ur-Rehman; Shahid, M.; Faizi, S. Isolation of tyrosine derived phenolics and their possible beneficial role in anti-inflammatory and antioxidant potential of Tithonia tubaeformis.Nat. Prod. Res.202135224286429410.1080/14786419.2019.1705813 31872778
    [Google Scholar]
  25. SakakuraA. PauzeM. NamikiA. TagoF.M. TamuraH. HanayaK. HigashibayashiS. SugaiT. Chemoenzymatic synthesis of hydroxytyrosol monoesters and their suppression effect on nitric oxide production stimulated by lipopolysaccharides.Biosci. Biotechnol. Biochem.201983218519110.1080/09168451.2018.1530970 30319060
    [Google Scholar]
  26. HuangY. HangX. JiangX. ZengL. JiaJ. XieY. LiF. BiH. In vitro and in vivo activities of zinc linolenate, a selective antibacterial agent against Helicobacter pylori.Antimicrob. Agents Chemother.2019636e00004e0001910.1128/AAC.00004‑19 30936098
    [Google Scholar]
/content/journals/npj/10.2174/0122103155311374240517062929
Loading
/content/journals/npj/10.2174/0122103155311374240517062929
Loading

Data & Media loading...

Supplements

The NMR spectra of the compounds are available as supplementary material on the publisher's website along with the published article.

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test