Actinomycetoquinones A–E, Anthraquinone-γ-Pyrones Discovered from Marine-Derived <i>Actinomycetospora</i> sp. Bacterium

Facilitated by LC-MS-PCA metabolomics methods and effective molecular networking for strain prioritization and dereplication, five new anthraquinone-γ-pyrones, actinomycetoquinones A-E (<b>1</b>-<b>5</b>), were isolated from a marine-derived <i>Actinomycetospora</i> sp. bacterium. The structures of <b>1</b>-<b>5</b> were elucidated by analysis of their HRMS and NMR spectroscopic data. The absolute configuration of <b>1</b> was unequivocally determined by single-crystal X-ray diffraction analysis using Cu Kα radiation. Actinomycetoquinone C exhibited antibacterial activity against methicillin-resistant <i>S. aureus</i> (MRSA) and <i>E. coli</i> with MIC values of 1 and 4 μg/mL, respectively.

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Publication Details

Journal
Journal of Natural Products
Published
2025-09-25
DOI
https://doi.org/10.1021/acs.jnatprod.5c00578
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39
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article

Actinomycetoquinones A–E, Anthraquinone-γ-Pyrones Discovered from Marine-Derived Actinomycetospora sp. Bacterium

Zachary Bennett, Gene E. Ananiev, Ilia A. Guzei, Scott R. Rajski et al.
1 citations
Journal of Natural Products
Microbial Natural Products and Biosynthesis
1.39
article

Actinomycetoquinones A–E, Anthraquinone-γ-Pyrones Discovered from Marine-Derived Actinomycetospora sp. Bacterium

Zachary Bennett, Gene E. Ananiev, Ilia A. Guzei, Scott R. Rajski, Tae Hyun Lee, Shaurya Chanana, Song Guo, Tim S. Bugni, Thomas C. Brunold, Fan Zhang, Christopher D. Roberts, Doug R. Braun
article en
1 citations

Abstract

Facilitated by LC-MS-PCA metabolomics methods and effective molecular networking for strain prioritization and dereplication, five new anthraquinone-γ-pyrones, actinomycetoquinones A-E (<b>1</b>-<b>5</b>), were isolated from a marine-derived <i>Actinomycetospora</i> sp. bacterium. The structures of <b>1</b>-<b>5</b> were elucidated by analysis of their HRMS and NMR spectroscopic data. The absolute configuration of <b>1</b> was unequivocally determined by single-crystal X-ray diffraction analysis using Cu Kα radiation. Actinomycetoquinone C exhibited antibacterial activity against methicillin-resistant <i>S. aureus</i> (MRSA) and <i>E. coli</i> with MIC values of 1 and 4 μg/mL, respectively.

Journal of Natural ProductsVol. 88(10)
University of Wisconsin–Madison (US), University of Wisconsin Carbone Cancer Center (US)
Openalex Percentile: Top 16%
Microbial Natural Products and Biosynthesis
1.39
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