Picolinic Acid Derivatives and Biosynthetic Pathway from <i>Epicoccum sorghinum</i> SDU-F549

Two new picolinic acid derivatives, ethylfusaric acid A (<b>1</b>) and ethylfusaric acid B (<b>2</b>), along with two known picolinic acid derivatives (<b>3</b>-<b>4</b>), were isolated from the culture of <i>Rehmannia glutinosa</i> endophytic fungus <i>Epicoccum sorghinum</i> SDU-F549. The chemical structures of the compounds were elucidated by the combination of 1D and 2D nuclear magnetic resonance spectroscopy and electronic circular dichroism calculations. Compounds <b>1</b>-<b>4</b> exhibited antibacterial activity against a panel of <i>Staphylococcus aureus</i> strains, with MIC values ranging from 16 to 32 <i>μ</i>g/mL. In contrast, they showed no significant cytotoxic activity against a range of human tumor cell lines at 10 <i>μ</i>M. Furthermore, bioinformatic analysis revealed that the <i>bty</i> biosynthetic gene cluster in <i>E. sorghinum</i> SDU-F549 is responsible for assembling the picolinic acid derivatives, enabling us to propose the biosynthetic pathways of compounds <b>1</b>-<b>4</b>.

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Journal
Journal of Natural Products
Published
2026-01-02
DOI
https://doi.org/10.1021/acs.jnatprod.5c01344
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Picolinic Acid Derivatives and Biosynthetic Pathway from Epicoccum sorghinum SDU-F549

Zeping Chen, Jianhua Ju, Runping Fang, Yingying Chen et al.
Journal of Natural Products
Microbial Natural Products and Biosynthesis
article

Picolinic Acid Derivatives and Biosynthetic Pathway from Epicoccum sorghinum SDU-F549

Zeping Chen, Jianhua Ju, Runping Fang, Yingying Chen, Liuhai Chen, Hongjie Zhu, Feng Li, Changfen Li
article en

Abstract

Two new picolinic acid derivatives, ethylfusaric acid A (<b>1</b>) and ethylfusaric acid B (<b>2</b>), along with two known picolinic acid derivatives (<b>3</b>-<b>4</b>), were isolated from the culture of <i>Rehmannia glutinosa</i> endophytic fungus <i>Epicoccum sorghinum</i> SDU-F549. The chemical structures of the compounds were elucidated by the combination of 1D and 2D nuclear magnetic resonance spectroscopy and electronic circular dichroism calculations. Compounds <b>1</b>-<b>4</b> exhibited antibacterial activity against a panel of <i>Staphylococcus aureus</i> strains, with MIC values ranging from 16 to 32 <i>μ</i>g/mL. In contrast, they showed no significant cytotoxic activity against a range of human tumor cell lines at 10 <i>μ</i>M. Furthermore, bioinformatic analysis revealed that the <i>bty</i> biosynthetic gene cluster in <i>E. sorghinum</i> SDU-F549 is responsible for assembling the picolinic acid derivatives, enabling us to propose the biosynthetic pathways of compounds <b>1</b>-<b>4</b>.

Journal of Natural ProductsVol. 89(1)
Shandong University (CN), Institute of Oceanology (CN), South China Sea Institute Of Oceanology (CN)
Openalex Percentile: Top 98%
Microbial Natural Products and Biosynthesis
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Picolinic Acid Derivatives and Biosynthetic Pathway from <i>Epicoccum sorghinum</i> SDU-F549 — Zeping Chen, Jianhua Ju, et al. · Journal of Natural Products (2026) | TGRS Research Map | TGRS