Erysiopeptides A−D, Lipopeptides from the Marine Bacterium Vibrio sp. AFB22-4MB1

Abstract Four new lipopeptides, erysiopeptides A−D, were isolated from the marine bacterium Vibrio sp. AFB22-4MB1. Their planar structures were elucidated on the basis of comprehensive spectroscopic analyses. A candidate biosynthetic gene cluster (BGC) for their production, encoding a non-ribosomal peptide synthetase, was identified in the genome sequence, and a corresponding biosynthetic proposal was developed. The absolute configurations of the component amino acids were established by advanced Marfey’s analysis and corroborated by bioinformatic predictions from the BGC. The stereochemistry of the β-hydroxyl group in the fatty chain was determined by derivatization of the hydrogenated product. Erysiopeptides exhibited moderate iron chelating as well as antibacterial activity against the Gram-positive bacterium Bacillus subtilis.

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Publication Details

Journal
Journal of Natural Products
Published
2026-11-04
DOI
https://doi.org/10.1021/acs.jnatprod.6c00771
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Erysiopeptides A−D, Lipopeptides from the Marine Bacterium Vibrio sp. AFB22-4MB1

Thao N. Phan, Reiko Ueoka, Eric J. N. Helfrich, Yuhi Kato et al.
Journal of Natural Products
Microbial Natural Products and Biosynthesis
article

Erysiopeptides A−D, Lipopeptides from the Marine Bacterium Vibrio sp. AFB22-4MB1

Thao N. Phan, Reiko Ueoka, Eric J. N. Helfrich, Yuhi Kato, Kota Sato, Taichi Higaki
article en

Abstract

Abstract Four new lipopeptides, erysiopeptides A−D, were isolated from the marine bacterium Vibrio sp. AFB22-4MB1. Their planar structures were elucidated on the basis of comprehensive spectroscopic analyses. A candidate biosynthetic gene cluster (BGC) for their production, encoding a non-ribosomal peptide synthetase, was identified in the genome sequence, and a corresponding biosynthetic proposal was developed. The absolute configurations of the component amino acids were established by advanced Marfey’s analysis and corroborated by bioinformatic predictions from the BGC. The stereochemistry of the β-hydroxyl group in the fatty chain was determined by derivatization of the hydrogenated product. Erysiopeptides exhibited moderate iron chelating as well as antibacterial activity against the Gram-positive bacterium Bacillus subtilis.

Journal of Natural Products
Goethe University Frankfurt (DE), Senckenberg Research Institute and Natural History Museum Frankfurt/M (DE), Kitasato University (JP)
Openalex Percentile: Top 15%
Microbial Natural Products and Biosynthesis
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Erysiopeptides A−D, Lipopeptides from the Marine Bacterium Vibrio sp. AFB22-4MB1 — Thao N. Phan, Reiko Ueoka, et al. · Journal of Natural Products (2026) | TGRS Research Map | TGRS