Marine Drugs (Apr 2021)

Svalbamides A and B, Pyrrolidinone-Bearing Lipodipeptides from Arctic <i>Paenibacillus</i> sp.

  • Young Eun Du,
  • Eun Seo Bae,
  • Yeonjung Lim,
  • Jang-Cheon Cho,
  • Sang-Jip Nam,
  • Jongheon Shin,
  • Sang Kook Lee,
  • Seung-Il Nam,
  • Dong-Chan Oh

DOI
https://doi.org/10.3390/md19040229
Journal volume & issue
Vol. 19, no. 4
p. 229

Abstract

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Two new secondary metabolites, svalbamides A (1) and B (2), were isolated from a culture extract of Paenibacillus sp. SVB7 that was isolated from surface sediment from a core (HH17-1085) taken in the Svalbard archipelago in the Arctic Ocean. The combinational analysis of HR-MS and NMR spectroscopic data revealed the structures of 1 and 2 as being lipopeptides bearing 3-amino-2-pyrrolidinone, d-valine, and 3-hydroxy-8-methyldecanoic acid. The absolute configurations of the amino acid residues in svalbamides A and B were determined using the advanced Marfey’s method, in which the hydrolysates of 1 and 2 were derivatized with l- and d- forms of 1-fluoro-2,4-dinitrophenyl-5-alanine amide (FDAA). The absolute configurations of 1 and 2 were completely assigned by deducing the stereochemistry of 3-hydroxy-8-methyldecanoic acid based on DP4 calculations. Svalbamides A and B induced quinone reductase activity in Hepa1c1c7 murine hepatoma cells, indicating that they represent chemotypes with a potential for functioning as chemopreventive agents.

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