BIOSYNTHESIS OF CYANOGENIC GLUCOSIDES IN THE LEPIDOPTERA - INCORPORATION OF [U-C-14]-2-METHYLPROPANEALDOXIME, 2S-[U-C-14]-METHYLBUTANEALDOXIME AND D,L-[U-C-14]-N-HYDROXYISOLEUCINE INTO LINAMARIN AND LOTAUSTRALIN BY THE LARVAE OF ZYGAENA-TRIFOLII
G. Holzkamp et A. Nahrstedt, BIOSYNTHESIS OF CYANOGENIC GLUCOSIDES IN THE LEPIDOPTERA - INCORPORATION OF [U-C-14]-2-METHYLPROPANEALDOXIME, 2S-[U-C-14]-METHYLBUTANEALDOXIME AND D,L-[U-C-14]-N-HYDROXYISOLEUCINE INTO LINAMARIN AND LOTAUSTRALIN BY THE LARVAE OF ZYGAENA-TRIFOLII, Insect biochemistry and molecular biology, 24(2), 1994, pp. 161-165
[U-C-14]-2-methylpropanealdoxime was incorporated into the cyanogenic
glucoside linamarin (1-cyano-1-methylethyl-beta-D-glucopyraraoside) an
d D,L-[U-C-14]-N-hydroxyisoleucine and 2S-[U-C-14]-methylbutanealdoxim
e were incorporated into the cyanogenic glucoside lotaustralin (R-1-cy
ano-1-methylpropyl-beta-D-glucopyranoside) after injection into the ha
emocoele of larvae of Zygaena trifolii. The incorporation rates of the
aldoximes were 17-22% and of the N-hydroxyamino acid 4-5%. The result
s indicate that both aldoximes and N-hydroxyamino acids are intermedia
tes in the biosynthesis of linamarin and lotaustralin by the larvae by
Zygaena trifolii.