Metabolic profiling and biological potential of the marine sponge associated Nocardiopsis sp. UR67 along with docking studies

  • Alyaa Hatem Ibrahim
  • , Eman Zekry Attia
  • , Heba A. Hofny
  • , Faisal Alsenani
  • , Ahmed Zayed
  • , Mostafa E. Rateb
  • , Usama Ramadan Abdelmohsen*
  • , Samar Yehia Desoukey
  • , Mostafa Ahmed Fouad
  • , Mohamed Salah Kamel
  • *Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

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    Abstract

    This work was performed to dig into the phytochemical composition and bioactivities of Nocardiopsis sp. UR67 associated with the marine sponge Callyspongia sp. It was fermented in suspension and immobilised in calcium alginate bead cultures. The ethyl acetate extracts, afforded from the broth in each case named EG-49 and J-48g, respectively, revealed 16 chemical principles mostly belonging to polyketides, macrolides, and peptides. EG-49 and J-48g displayed anti-Candida albicans activity with IC50 values of 8.1 and 8.3 µg/mL, and a substantial cytotoxic effect against lung adenocarcinoma H1650 at IC50 12.6 and 13.7 µg/mL, respectively. However, only EG-49 exhibited a noteworthy anti-trypanosomal activity at 7.5 µg/mL. Molecular docking of the characterised compounds against Trypanosoma brucei trypanothione reductase demonstrated the highest binding models of griseochelin-methyl ester (9) and filipin-II (11), which drew considerable significance of the metabolites derived from Nocardiopsis sp. UR67 developing potential T. brucei trypanothione reductase inhibitors.
    Original languageEnglish
    Pages (from-to)3531-3537
    Number of pages7
    JournalNatural Product Research
    Volume37
    Issue number20
    Early online date6 Jun 2022
    DOIs
    Publication statusPublished - 2023

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 14 - Life Below Water
      SDG 14 Life Below Water

    Keywords

    • Nocardiopsis
    • marine sponges
    • metabolomics
    • anti-infective
    • cytotoxicity

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