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Biosynthesis of a defensive insect alkaloid: epilachnene from oleic acid and serine.

The biosynthesis of the azamacrolide epilachnene by the coccinellid beetle Epilachna varivestis has been studied with 2H-labeled oleic acid, 2H-labeled L-serine, and 13C,15N-labeled L-serine. The incorporation of these precursors into epilachnene defines the origin of the alkaloid's entire carb...

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Autors principals: Attygalle, A B, Blankespoor, C L, Eisner, T, Meinwald, J
Format: Artigo
Idioma:Inglês
Publicat: 1994
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC45525/
https://ncbi.nlm.nih.gov/pubmed/7809122
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