Antibacterial phenolic compounds target GMPS from the endophytic Chaetomium grande -JPT2

Plant bacterial diseases threaten global food security and agricultural product quality. This study aimed to explore natural products with anti-phytopathogenic bacterial activity towards the new target guanosine monophosphate synthase (GMPS). Twelve phenolic compounds, including a new one, peniquinone L (1), were isolated using column chromatography and semipreparative HPLC from Chaetomium grande-JPT2. The molecular structures of the isolated compounds were determined by HRESIMS, 1D and 2D NMR spectrometry. High-throughput activity screening revealed that compound 11 could inhibit GMPS, yielding an EC50 value of 58.83 μg/mL. Molecular docking further revealed that the binding interaction between 11 and GMPS was primarily stabilised by two hydrogen bonds formed between the hydroxyl group in 11 and amino acid residues in GMPS. This is the first report on GMPS inhibition by phenolic compounds. Furthermore, compounds 4 and 7 displayed antibacterial activity against Xanthomonas axonopodis by two-fold serial dilution method, with MIC values of 100 μg/mL.

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Publication Details

Journal
Natural Product Research
Published
2026-08-20
DOI
https://doi.org/10.1080/14786419.2026.2709586
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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Antibacterial phenolic compounds target GMPS from the endophytic Chaetomium grande -JPT2

Kangwen Xu, Wen Li, Shuqi Li, Donglin Zhao et al.
Natural Product Research
Microbial Natural Products and Biosynthesis
article

Antibacterial phenolic compounds target GMPS from the endophytic Chaetomium grande -JPT2

Kangwen Xu, Wen Li, Shuqi Li, Donglin Zhao, Peng Zhang, Wenjun Li, Mei Wang
article en

Abstract

Plant bacterial diseases threaten global food security and agricultural product quality. This study aimed to explore natural products with anti-phytopathogenic bacterial activity towards the new target guanosine monophosphate synthase (GMPS). Twelve phenolic compounds, including a new one, peniquinone L (1), were isolated using column chromatography and semipreparative HPLC from Chaetomium grande-JPT2. The molecular structures of the isolated compounds were determined by HRESIMS, 1D and 2D NMR spectrometry. High-throughput activity screening revealed that compound 11 could inhibit GMPS, yielding an EC50 value of 58.83 μg/mL. Molecular docking further revealed that the binding interaction between 11 and GMPS was primarily stabilised by two hydrogen bonds formed between the hydroxyl group in 11 and amino acid residues in GMPS. This is the first report on GMPS inhibition by phenolic compounds. Furthermore, compounds 4 and 7 displayed antibacterial activity against Xanthomonas axonopodis by two-fold serial dilution method, with MIC values of 100 μg/mL.

Natural Product Research
Shandong University of Traditional Chinese Medicine (CN), Qingdao Agricultural University (CN), Tobacco Research Institute (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 11%
Microbial Natural Products and Biosynthesis
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