Jejupeptins A and B, Polyketide–Cyclic Peptide Hybrids with Anti-Corticosterone Activity from <i>Streptomyces</i> sp. KCB15JA151

Two new lipopeptides jejupeptins A (<b>1</b>) and B (<b>2</b>), together with a known compound eurystatin B (<b>3</b>), were isolated from a culture of <i>Streptomyces</i> sp. KCB15JA151. The chemical structures of the compounds were elucidated by using a combination of 1D and 2D NMR spectroscopy analyses. Comprehensive spectroscopic analysis revealed that compounds <b>1</b> and <b>2</b> possess a 1-aminoethyl-2-hydroxy-4-oxopentanoic acid moiety. A plausible biosynthetic pathway for these compounds was proposed. Biological evaluation demonstrated that compounds <b>1</b> and <b>2</b> exhibit protective effects against corticosterone-induced apoptosis and cellular oxidative stress without any associated cytotoxicity.

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Publication Details

Journal
ACS Omega
Published
2025-09-25
DOI
https://doi.org/10.1021/acsomega.5c03784
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39
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article

Jejupeptins A and B, Polyketide–Cyclic Peptide Hybrids with Anti-Corticosterone Activity from Streptomyces sp. KCB15JA151

Hyeok‐Won Lee, Sung‐Kyun Ko, Shunji Takahashi, Gil Soo Kim et al.
1 citations
ACS Omega
Microbial Natural Products and Biosynthesis
1.39
article

Jejupeptins A and B, Polyketide–Cyclic Peptide Hybrids with Anti-Corticosterone Activity from Streptomyces sp. KCB15JA151

Hyeok‐Won Lee, Sung‐Kyun Ko, Shunji Takahashi, Gil Soo Kim, Jihun Park, Jun‐Pil Jang, Jae‐Hyuk Jang, Young‐Soo Hong, Jongtae Roh, Beomcheol Park, Gwi Ja Hwang
article en
1 citations

Abstract

Two new lipopeptides jejupeptins A (<b>1</b>) and B (<b>2</b>), together with a known compound eurystatin B (<b>3</b>), were isolated from a culture of <i>Streptomyces</i> sp. KCB15JA151. The chemical structures of the compounds were elucidated by using a combination of 1D and 2D NMR spectroscopy analyses. Comprehensive spectroscopic analysis revealed that compounds <b>1</b> and <b>2</b> possess a 1-aminoethyl-2-hydroxy-4-oxopentanoic acid moiety. A plausible biosynthetic pathway for these compounds was proposed. Biological evaluation demonstrated that compounds <b>1</b> and <b>2</b> exhibit protective effects against corticosterone-induced apoptosis and cellular oxidative stress without any associated cytotoxicity.

ACS OmegaVol. 10(39)
University of Science and Technology (YE), Biotechnology Research Center (IR), RIKEN Center for Sustainable Resource Science (JP), Central Research Institute (IN), Hanpoong Pharm (South Korea) (KR), Korea Research Institute of Bioscience and Biotechnology (KR), Korea University of Science and Technology (KR)
Openalex Percentile: Top 16%
Microbial Natural Products and Biosynthesis
1.39
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Jejupeptins A and B, Polyketide–Cyclic Peptide Hybrids with Anti-Corticosterone Activity from <i>Streptomyces</i> sp. KCB15JA151 — Hyeok‐Won Lee, Sung‐Kyun Ko, et al. · ACS Omega (2025) | TGRS Research Map | TGRS