Identification of Xylaria cubensis Isolated from Moringa oleifera Leaves and Its Antibacterial Potentials

The escalating threat of antimicrobial resistance underscores the need for novel natural therapeutic agents. Endophytic fungi are recognised as prolific producers of bioactive metabolites with antimicrobial potential. In this study, an endophytic fungus isolated from mature leaves of Moringa oleifera was molecularly identified as closely related to Xylaria cubensis. Its ethyl acetate extract exhibited notable antibacterial activity against Bacillus subtilis, with a minimum inhibitory concentration (MIC) of 25 mg/mL and a minimum bactericidal concentration (MBC) of 100 mg/mL. Scanning electron microscopy revealed pronounced morphological alterations in treated B. subtilis cells, including shrinkage and lysis, consistent with membrane disruption. Gas chromatography–mass spectrometry (GC–MS) analysis identified four major compounds: 2,4‑di‑tert‑butylphenol, pyrrolo[1,2‑a]pyrazine‑1,4‑dione (hexahydro‑3‑(1‑methylethyl)), 3‑furanacetic acid (4‑hexyl‑2,5‑dihydro‑2,5‑dioxo‑) and 1,3,5‑xylenol. These findings highlight the antibacterial potential of endophytic X. cubensis from M. oleifera, particularly against B. subtilis, and support the role of endophytic fungi as promising sources of natural antimicrobial compounds for future therapeutic development.

Authors

Publication Details

Journal
Tropical Life Sciences Research
Published
2026-10-28
DOI
https://doi.org/10.21315/tlsr2026.37.3.9
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Identification of Xylaria cubensis Isolated from Moringa oleifera Leaves and Its Antibacterial Potentials

Latiffah Zakaria, Syarifah Ab Rashid, Nurul Farizah Azuddin, Siti Aisyah Daud et al.
1 links
Tropical Life Sciences Research
Microbial Natural Products and Biosynthesis
article

Identification of Xylaria cubensis Isolated from Moringa oleifera Leaves and Its Antibacterial Potentials

Latiffah Zakaria, Syarifah Ab Rashid, Nurul Farizah Azuddin, Siti Aisyah Daud, Wong Chaim Tung, Tan Wen Nee, Nurhaida, Yee Simone
article en

Abstract

The escalating threat of antimicrobial resistance underscores the need for novel natural therapeutic agents. Endophytic fungi are recognised as prolific producers of bioactive metabolites with antimicrobial potential. In this study, an endophytic fungus isolated from mature leaves of Moringa oleifera was molecularly identified as closely related to Xylaria cubensis. Its ethyl acetate extract exhibited notable antibacterial activity against Bacillus subtilis, with a minimum inhibitory concentration (MIC) of 25 mg/mL and a minimum bactericidal concentration (MBC) of 100 mg/mL. Scanning electron microscopy revealed pronounced morphological alterations in treated B. subtilis cells, including shrinkage and lysis, consistent with membrane disruption. Gas chromatography–mass spectrometry (GC–MS) analysis identified four major compounds: 2,4‑di‑tert‑butylphenol, pyrrolo[1,2‑a]pyrazine‑1,4‑dione (hexahydro‑3‑(1‑methylethyl)), 3‑furanacetic acid (4‑hexyl‑2,5‑dihydro‑2,5‑dioxo‑) and 1,3,5‑xylenol. These findings highlight the antibacterial potential of endophytic X. cubensis from M. oleifera, particularly against B. subtilis, and support the role of endophytic fungi as promising sources of natural antimicrobial compounds for future therapeutic development.

Tropical Life Sciences ResearchVol. 37(3)
Good health and well-being
Openalex Percentile: Top 13%
Microbial Natural Products and Biosynthesis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon