Antimicrobial Macrolide Levantilide D from Rare Marine Micromonospora sp.

Introduction: One new levantilide D (2) with a 20-membered macrolide, along with one known levantilide C (1), was isolated from a rare marine actinomycetes Micromonospora sp. (FIMYZ52). Methods: The structural elucidation of the compounds was based on integrated analyses involving 1D and 2D NMR spectroscopy and HR-ESI-MS. Results: The relative and absolute configurations of compounds 1 and 2 were ascertained by integrating multispectral ROESY and NOESY information from analogs in conjunction with theoretical TDDFT-ECD calculations. Levantilide D (2) exhibited antibacterial activity against Staphylococcus aureus. Conclusion: A plausible biosynthetic pathway of the macrolide compounds (1-2) was proposed.

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Publication Details

Journal
The Natural Products Journal
Published
2024-10-11
DOI
https://doi.org/10.2174/0122103155325417241001112138
Citations
2
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.50
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article

Antimicrobial Macrolide Levantilide D from Rare Marine Micromonospora sp.

Meilu Zhao, Honglei Jiang, Yichao Ge, Wei Zhao et al.
2 citations
The Natural Products Journal
Chemical Synthesis and Reactions
0.50
article

Antimicrobial Macrolide Levantilide D from Rare Marine Micromonospora sp.

Meilu Zhao, Honglei Jiang, Yichao Ge, Wei Zhao, Jian Zhou, Hong Jiang, Bin Wu, Jingming Zhou, Ru Lin
article en
2 citations

Abstract

Introduction: One new levantilide D (2) with a 20-membered macrolide, along with one known levantilide C (1), was isolated from a rare marine actinomycetes Micromonospora sp. (FIMYZ52). Methods: The structural elucidation of the compounds was based on integrated analyses involving 1D and 2D NMR spectroscopy and HR-ESI-MS. Results: The relative and absolute configurations of compounds 1 and 2 were ascertained by integrating multispectral ROESY and NOESY information from analogs in conjunction with theoretical TDDFT-ECD calculations. Levantilide D (2) exhibited antibacterial activity against Staphylococcus aureus. Conclusion: A plausible biosynthetic pathway of the macrolide compounds (1-2) was proposed.

The Natural Products JournalVol. 16(4)
Zhejiang Ocean University (CN), Fujian Institute of Microbiology (CN), Zhejiang University (CN)
Life below water
Openalex Percentile: Top 39%
Chemical Synthesis and Reactions
0.50
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