New Curvularin and Norlignanolide Derivatives From Cocultures of Marine Mangrove Endophytic Fungus <i>Penicillium brocae</i> MA‐231 and Phytopathogen <i>Curvularia spicifera</i> QA‐26

A new curvularin derivative, curvulone C (1) and a pair of new norlignanolide diastereomers, aspergilfuranone E (2) and 8-epi-aspergilfuranone E (3), together with six known secondary metabolites (4-9) were isolated and identified from the coculture of the marine mangrove endophytic fungus Penicillium brocae MA-231 and phytopathogen Curvularia spicifera QA-26. Their structures were elucidated on the basis of spectroscopic analysis, and the absolute configurations were assigned on the basis of time-dependent density functional theory-electronic circular dichroism calculations. Compounds 1 and 4 showed inhibitory activities against several human and aquatic pathogens.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-03-26
DOI
https://doi.org/10.1002/cbdv.202500761
Citations
2
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
2.79
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article

New Curvularin and Norlignanolide Derivatives From Cocultures of Marine Mangrove Endophytic Fungus Penicillium brocae MA‐231 and Phytopathogen Curvularia spicifera QA‐26

Xiaoshan Shi, Ling‐Hong Meng, Bin‐Gui Wang, A. M. Zhang
2 citations
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
2.79
article

New Curvularin and Norlignanolide Derivatives From Cocultures of Marine Mangrove Endophytic Fungus Penicillium brocae MA‐231 and Phytopathogen Curvularia spicifera QA‐26

Xiaoshan Shi, Ling‐Hong Meng, Bin‐Gui Wang, A. M. Zhang
article en
2 citations

Abstract

A new curvularin derivative, curvulone C (1) and a pair of new norlignanolide diastereomers, aspergilfuranone E (2) and 8-epi-aspergilfuranone E (3), together with six known secondary metabolites (4-9) were isolated and identified from the coculture of the marine mangrove endophytic fungus Penicillium brocae MA-231 and phytopathogen Curvularia spicifera QA-26. Their structures were elucidated on the basis of spectroscopic analysis, and the absolute configurations were assigned on the basis of time-dependent density functional theory-electronic circular dichroism calculations. Compounds 1 and 4 showed inhibitory activities against several human and aquatic pathogens.

Chemistry & BiodiversityVol. 22(8)
Chinese Academy of Sciences (CN), Institute of Oceanology (CN), Qingdao National Laboratory for Marine Science and Technology (CN), University of Chinese Academy of Sciences (CN)
Life below water
Openalex Percentile: Top 12%
Microbial Natural Products and Biosynthesis
2.79
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