Application of stable isotope labelling methodology to the biosynthesis of the mycotoxin, terretonin, by aspergillus terreus: incorporation of 13C-labelled acetates and methionine, 2H- and 13C, 18O-labelled ethyl 3,5-dimethylorsellinate and oxygen-18 gas

Tetrahedron

Volumn 45, Issue 8, 1989, Pages 2307-2321

  McIntyre, C Rupert ^a   Scott, Fiona E ^a   Simpson, Thomas J ^a   Trimble, Laird A ^b   Vederas, John C ^b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

RADIOISOTOPE;

ASPERGILLUS TERREUS; BIOSYNTHESIS; FUNGUS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; TERRETONIN;

EID: 0024522823     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)83433-5     Document Type: Article

References (26)

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5. Structure of ED-1 isolated from Emericella dentata.
6. Biosynthesis of andibenin, a novel polyketide-terpenoid metabolite of Aspergillus variecolor
7. Biosynthesis of the meroterpenoid metabolites, austin and terretonin: incorporation of 3,5-dimethylorsellinate
8. Synthesis and regiospecific deoxygenation of ?-resorcylic ester derivatives to 4-hydroxybenzoates
9. Magnitudes of18O isotope shifts in13C nuclear magnetic resonance spectra of ketones and alcohols
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13. Biosynthesis of the meroterpenoid austin, by Aspergillus ustus: synthesis and incorporation of 13C,18O-labelled ethyl 3,5-dimethylorsellinate