Premium
Biosynthesis of the Spiroacetal Suite in Bactrocera tryoni
Author(s) -
Booth Yvonne K.,
Kitching William,
De Voss James J.
Publication year - 2011
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.201000481
Subject(s) - biosynthesis , cytochrome p450 , biochemistry , chemistry , stereochemistry , metabolic pathway , biology , botany , metabolism , gene
In pursuit of a more environmentally benign method of controlling the highly pestiferous Queensland fruit fly, Bactrocera tryoni , the biosynthesis of the minor components in the suite of spiroacetals released by females has been investigated. This follows on the biosynthetic definition of the pathway to the major component, ( E , E )‐ 1 . The origins of the C 12 and C 13 spiroacetals ( E , E )‐ 2 and ( E , E )‐ 3 , respectively, have been investigated by the administration of over 30 deuterated potential precursors. Analysis of the relative incorporation levels and identification of some of the exceptionally minor spiroacetals that were biosynthesised established that B. tryoni processes fatty acids to 2,6‐dioxygenated precursors by a modified β‐oxidation pathway, with a suite of putative cytochromes P450 employed in the crucial oxidative steps, prior to cyclisation of the proposed ketodiol.