Graminoides A-D, antibacterial cyclic octaketides from the desert-derived Streptomyces

Four previously unreported cyclic octaketides, designated as graminotides A-D ( 1 – 4 ), along with the known compound GTRI-02 ( 5 ), were isolated from the desert soil-derived actinomycete Streptomyces graminisoli SD11. The planar structures of 1 – 4 were elucidated through comprehensive spectroscopic analysis including 1D, 2D NMR techniques coupled with HR ESI MS measurements. The absolute configurations were established through combination of NOE and coupling constants analysis, and comparison the experimental and calculated ECD spectra. Notably, the biological evaluation revealed that 1 and 2 showed moderate antibacterial activity against Staphylococcus aureus ATCC25923 with MIC of 64 and 32 μg/mL, while 3 displayed activity against Proteus vulgaris CPCC160013 with MIC of 64 μg/mL, respectively. None of the isolated compounds showed antiproliferative effects against HepG2 and MDA-MB-231cells at a tested concentration of 30 μM.

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Publication Details

Journal
Pharmaceutical Science Advances
Published
2025-11-21
DOI
https://doi.org/10.1016/j.pscia.2025.100106
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00
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article

Graminoides A-D, antibacterial cyclic octaketides from the desert-derived Streptomyces

Wentao Yan, Jie Huang, Shuhong Zhao, Qian Zhang et al.
Pharmaceutical Science Advances
Microbial Natural Products and Biosynthesis
article

Graminoides A-D, antibacterial cyclic octaketides from the desert-derived Streptomyces

Wentao Yan, Jie Huang, Shuhong Zhao, Qian Zhang, Chunhua Lu, Wen‐Jun Li, Lei Hua Dong, Xianggang Hu
article en

Abstract

Four previously unreported cyclic octaketides, designated as graminotides A-D ( 1 – 4 ), along with the known compound GTRI-02 ( 5 ), were isolated from the desert soil-derived actinomycete Streptomyces graminisoli SD11. The planar structures of 1 – 4 were elucidated through comprehensive spectroscopic analysis including 1D, 2D NMR techniques coupled with HR ESI MS measurements. The absolute configurations were established through combination of NOE and coupling constants analysis, and comparison the experimental and calculated ECD spectra. Notably, the biological evaluation revealed that 1 and 2 showed moderate antibacterial activity against Staphylococcus aureus ATCC25923 with MIC of 64 and 32 μg/mL, while 3 displayed activity against Proteus vulgaris CPCC160013 with MIC of 64 μg/mL, respectively. None of the isolated compounds showed antiproliferative effects against HepG2 and MDA-MB-231cells at a tested concentration of 30 μM.

Pharmaceutical Science AdvancesVol. 4
Shandong University of Traditional Chinese Medicine (CN), Shandong University (CN), Sun Yat-sen University (CN)
Openalex Percentile: Top 61%
Microbial Natural Products and Biosynthesis
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