Antibacterial Sterigmatocystin Derivatives From <i>Humicola</i> sp. MN006389.1 Associated With <i>Gardenia Jasminoides</i>

The bioactive metabolites produced by the fungal strain Humicola sp. MN006389.1, isolated from fresh Gardenia jasminoides blossoms, were investigated. This study led to the identification of a novel sterigmatocystin derivative named 4-methoxysterigmatocystin (1), along with two known analogues: sterigmatocystin (2) and acyl-hemiacetal sterigmatocystin (3). Structure elucidation of the isolated compounds was achieved with nuclear magnetic resonance (NMR) spectroscopy, high-resolution electrospray ionization mass spectrometry (HR-ESI-MS), and X-ray crystallographic data. Notably, compound 1 demonstrated significant antibacterial activity against B. subtilis and S. aureus (MIC values of 4 µg/mL), while compound 3 displayed antibacterial activity against E. coli and B. subtilis with MIC values of 4 and 16 µg/mL, respectively.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2026-04-01
DOI
https://doi.org/10.1002/cbdv.202503802
Primary Topic
Aquatic Ecosystems and Phytoplankton Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Antibacterial Sterigmatocystin Derivatives From Humicola sp. MN006389.1 Associated With Gardenia Jasminoides

Lei Li, Jinhua Yu, Z-L Ding, D. Y. Wang et al.
Chemistry & Biodiversity
Aquatic Ecosystems and Phytoplankton Dynamics
article

Antibacterial Sterigmatocystin Derivatives From Humicola sp. MN006389.1 Associated With Gardenia Jasminoides

Lei Li, Jinhua Yu, Z-L Ding, D. Y. Wang, Yan‐Li Zhang, Han‐Wei Ruan, Dong Gan, Jie‐Zhen Shi, Xiao‐Xin Xu, Liang Deng
article en

Abstract

The bioactive metabolites produced by the fungal strain Humicola sp. MN006389.1, isolated from fresh Gardenia jasminoides blossoms, were investigated. This study led to the identification of a novel sterigmatocystin derivative named 4-methoxysterigmatocystin (1), along with two known analogues: sterigmatocystin (2) and acyl-hemiacetal sterigmatocystin (3). Structure elucidation of the isolated compounds was achieved with nuclear magnetic resonance (NMR) spectroscopy, high-resolution electrospray ionization mass spectrometry (HR-ESI-MS), and X-ray crystallographic data. Notably, compound 1 demonstrated significant antibacterial activity against B. subtilis and S. aureus (MIC values of 4 µg/mL), while compound 3 displayed antibacterial activity against E. coli and B. subtilis with MIC values of 4 and 16 µg/mL, respectively.

Chemistry & BiodiversityVol. 23(4)
Yunnan University (CN), Kunming Medical University (CN), Second Affiliated Hospital of Kunming Medical College (CN), Yunnan University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China
Life in Land
Openalex Percentile: Top 17%
Aquatic Ecosystems and Phytoplankton Dynamics
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