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JM47, a cyclic tetrapeptide HC-toxin analogue from a marine Fusarium species

  • Zhong Jiang
  • , Marc Olivier Barret
  • , Kenneth G. Boyd
  • , David R. Adams
  • , Alan S.F. Boyd
  • , J. Grant Burgess

Resultado de pesquisa: Articlerevisão de pares

41 Citações (Scopus)

Resumo

The known metabolite, enniatin B, and a cyclic tetrapeptide, JM47, which is a new natural product, were extracted from brown rice cultures of a marine fungus, identified as a Fusarium species, isolated from the marine alga Codium fragile. NMR studies, including 15N HMQC and 15N HMBC, established the structure of JM47 as cyclo(Ala-Ala-Aoh-Pro), where Aoh is the amino acid, (2S,9S)-2-amino-8-oxo-9-hydroxydecanoic acid. The absolute stereochemistry of the Aoh side chain carbinol centre was determined using Mosher ester methodology. Analysis of NOESY data assisted by molecular modelling revealed an alternating L-, D-, L-, D-configuration for the tetrapeptide core. The absolute stereochemistry of the core was determined by acidic hydrolysis and chiral TLC analysis of the proline residue. JM47 belongs to the HC-toxin family of cyclic tetrapeptides which possess a 2-amino-8-oxo-9, 10-epoxydecanoic acid residue in place of the Aoh unit. This is the first report of an analogue of HC-toxin from a marine Fusarium species.

Idioma originalEnglish
Páginas (de-até)33-38
Número de páginas6
RevistaPhytochemistry
Volume60
Número de emissão1
DOIs
Estado da publicaçãoPublished - 10 mai. 2002

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