Anti‐Proliferative and Antioxidant Potential of Podophyllotoxin From the Endophytic Fungus <i>Dactylonectria torresensis</i>

The study investigated Dactylonectria torresensis as a sustainable source of podophyllotoxin (PTOX), a key precursor for anticancer drugs such as etoposide and teniposide. The fungus was identified through morphological analysis and ITS rDNA sequencing. PTOX from the fungal extract was isolated and characterized using high-performance liquid chromatography, high-resolution mass spectrometry, and nuclear magnetic resonance spectroscopy. Antioxidant activity was evaluated via 2,2-diphenyl-1-picrylhydrazyl (DPPH) and reducing power assays, showing comparable 50% inhibition (IC<sub>50</sub>) values for standard and fungal PTOX - 297.4 versus 309.8 µg/mL (DPPH) and 306.6 versus 316.3 µg/mL (reducing power). Cytotoxicity against MCF-7 breast cancer cells also revealed similar IC<sub>50</sub> values: 3.083 µM for standard and 3.188 µM for fungal PTOX. PTOX production was optimized through a two-phase statistical approach: Plackett-Burman Design followed by Face-Centered Central Composite Design. Initially, D. torresensis produced 78.46 µg/g dry weight (DW) of PTOX, which increased 6.35-fold to 498.76 µg/g DW after optimization.

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Journal
Chemistry & Biodiversity
Published
2026-02-01
DOI
https://doi.org/10.1002/cbdv.202503761
Primary Topic
Plant-derived Lignans Synthesis and Bioactivity
Type
article
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article

Anti‐Proliferative and Antioxidant Potential of Podophyllotoxin From the Endophytic Fungus Dactylonectria torresensis

Anviksha Anviksha, M. Sudhakara Reddy
Chemistry & Biodiversity
Plant-derived Lignans Synthesis and Bioactivity
article

Anti‐Proliferative and Antioxidant Potential of Podophyllotoxin From the Endophytic Fungus Dactylonectria torresensis

Anviksha Anviksha, M. Sudhakara Reddy
article en

Abstract

The study investigated Dactylonectria torresensis as a sustainable source of podophyllotoxin (PTOX), a key precursor for anticancer drugs such as etoposide and teniposide. The fungus was identified through morphological analysis and ITS rDNA sequencing. PTOX from the fungal extract was isolated and characterized using high-performance liquid chromatography, high-resolution mass spectrometry, and nuclear magnetic resonance spectroscopy. Antioxidant activity was evaluated via 2,2-diphenyl-1-picrylhydrazyl (DPPH) and reducing power assays, showing comparable 50% inhibition (IC<sub>50</sub>) values for standard and fungal PTOX - 297.4 versus 309.8 µg/mL (DPPH) and 306.6 versus 316.3 µg/mL (reducing power). Cytotoxicity against MCF-7 breast cancer cells also revealed similar IC<sub>50</sub> values: 3.083 µM for standard and 3.188 µM for fungal PTOX. PTOX production was optimized through a two-phase statistical approach: Plackett-Burman Design followed by Face-Centered Central Composite Design. Initially, D. torresensis produced 78.46 µg/g dry weight (DW) of PTOX, which increased 6.35-fold to 498.76 µg/g DW after optimization.

Chemistry & BiodiversityVol. 23(2)
Thapar Institute of Engineering & Technology (IN)
Openalex Percentile: Top 65%
Plant-derived Lignans Synthesis and Bioactivity
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