4.7 Article

Kahalalides V-Y isolated from a Hawaiian collection of the sacoglossan mollusk Elysia rufescens

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 71, Issue 5, Pages 772-778

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/np070508g

Keywords

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Funding

  1. NCRR NIH HHS [5 P20 RR 021919, C06 RR 14503-01, P20 RR021929, R21 RR021919, C06 RR014503] Funding Source: Medline
  2. NIAID NIH HHS [5 K02 AI 01502, R01 AI036596, R01 AI 036596] Funding Source: Medline

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Four new kahalalides, V (1), W (2), X (3), and Y (4), as well as six previously characterized kahalalides have been isolated from a two-year collection of the sacoglossan mollusk Elysia rufescens. Curiously, kahalalide B, previously isolated in high yield from E. rufescens, was found to be essentially absent from these collections despite identical collection sites and times with previous collections. In addition, kahalalide K, which to date has only been reported from Bryopsis sp., was found in this collection of E. rufescens, suggesting that the production of these metabolites could potentially be from a microbial association with the mollusk and algae, and this relationship is continuously evolving in response to changes in the environment and predation. The structures of new peptides have been established on the basis of extensive 1D and 2D NMR spectroscopic data analysis. Kahalalide V (1) was ascertained to be an acyclic derivative of kahalalide D (5), while kahalalide W (2) was determined to have a 4-hydroxy-L-proline residue instead of the proline in 5. The arginine residue of kahalalide X (3), an acyclic derivative of kahalalide C, was determined to have an L configuration. Kahalalide Y (4) was found to have an L-proline residue instead of the hydroxyproline in kahalalide K. It is clear from this collection of E. rufescens that the discovery of new kahalalide-related metabolites is still highly feasible.

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