Two new polyketides from the mangrove endophytic fungus <i>Penicillium</i> sp. FDZ-018-102

Two new polyketides polyketiliums A and B (1 and 2), together with ten known polyketides (3–12) were isolated from the mangrove endophytic fungus Penicillium sp. FDZ-018-102. Their chemical structures were elucidated by spectroscopic methods. The absolute configurations of polyketilium B (2) was determined by electronic circular dichroism (ECD) calculations. All compounds were evaluated for their antifungal and antibacterial activities. The antifungal activity of compound 11 against Fusarium oxysporum f. sp. cubense was notable, with an EC50 value of 18.12 µg/mL, surpassing the efficacy of captan (EC50: 49.16 µg/mL) by more than twofold. Compound 11 showed equal MIC values of 32 μg/mL against both Staphylococcus epidermidis and Bacillus cereus, while compound 12 exhibited MIC values of 16 and 32 μg/mL, respectively.

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Publication Details

Journal
Natural Product Research
Published
2026-06-25
DOI
https://doi.org/10.1080/14786419.2026.2691379
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Two new polyketides from the mangrove endophytic fungus Penicillium sp. FDZ-018-102

Mei‐Zhu Wu, Guang‐Ying Chen, Hong-Jie Chen, Xin-Ming Song et al.
Natural Product Research
Microbial Natural Products and Biosynthesis
article

Two new polyketides from the mangrove endophytic fungus Penicillium sp. FDZ-018-102

Mei‐Zhu Wu, Guang‐Ying Chen, Hong-Jie Chen, Xin-Ming Song, Xue-Ming Zhou, Hong-Ling Cheng, Enkhchimeg Chuluunbaatar
article en

Abstract

Two new polyketides polyketiliums A and B (1 and 2), together with ten known polyketides (3–12) were isolated from the mangrove endophytic fungus Penicillium sp. FDZ-018-102. Their chemical structures were elucidated by spectroscopic methods. The absolute configurations of polyketilium B (2) was determined by electronic circular dichroism (ECD) calculations. All compounds were evaluated for their antifungal and antibacterial activities. The antifungal activity of compound 11 against Fusarium oxysporum f. sp. cubense was notable, with an EC50 value of 18.12 µg/mL, surpassing the efficacy of captan (EC50: 49.16 µg/mL) by more than twofold. Compound 11 showed equal MIC values of 32 μg/mL against both Staphylococcus epidermidis and Bacillus cereus, while compound 12 exhibited MIC values of 16 and 32 μg/mL, respectively.

Natural Product Research
Hainan Normal University (CN)
National Natural Science Foundation of China
Life below water
Openalex Percentile: Top 9%
Microbial Natural Products and Biosynthesis
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