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Svalbamides A and B,Pyrrolidinone-Bearing Lipodipeptides from Arctic Paenibacillus sp.
Authors: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
Institution:1.Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 08826, Korea; (Y.E.D.); (E.S.B.); (J.S.); (S.K.L.);2.Department of Biological Sciences, Inha University, Incheon 22212, Korea; (Y.L.); (J.-C.C.);3.Department of Chemistry and Nanoscience, Ewha Womans University, Seoul 03760, Korea;4.Korea Polar Research Institute, Incheon 21990, Korea;
Abstract: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.
Keywords:Paenibacillus  Arctic  Svalbard  Marfey’  s method  DP4 calculation  quinone reductase  lipopeptide  3-amino-2-pyrrolidinone
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