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First published online June 20, 2002; 10.1104/pp.001263 Plant Physiol, July 2002, Vol. 129, pp. 1066-1075 Leucine-Derived Cyano Glucosides in Barley1Plant Biochemistry Laboratory, Department of Plant Biology (K.A.N., K.P., B.L.M.), Center for Molecular Plant Physiology (K.A.N., C.E.O., K.P., B.L.M.), and Department of Chemistry (C.E.O.), 40 Thorvaldsensvej, Royal Veterinary and Agricultural University, DK-1871 Frederiksberg C, Copenhagen, Denmark
Barley (Hordeum vulgare) seedlings contain
five cyano glucosides derived from the amino acid L-leucine
(Leu). The chemical structure and the relative abundance of the cyano
glucosides were investigated by liquid chromatography-mass spectrometry
and nuclear magnetic resonance analyses using spring barley cultivars
with high, medium, and low cyanide potential. The barley cultivars showed a 10-fold difference in their cyano glucoside content, but the
relative content of the individual cyano glucosides remained constant.
Epiheterodendrin, the only cyanogenic glucoside present, comprised 12%
to 18% of the total content of cyano glucosides. It is proposed that
the aglycones of all five cyano glucosides are formed by the initial
action of a cytochrome P450 enzyme of the CYP79 family converting
L-Leu into Z-3-methylbutanal oxime and
subsequent action of a less specific CYP71E enzyme converting the oxime
into 3-methylbutyro nitrile and mediating subsequent hydroxylations at
the 1 This work was supported in part by the Danish National Research Foundation. * Corresponding author; e-mail kani{at}kvl.dk; fax 35-28-33-33. © 2002 American Society of Plant Physiologists This article has been cited by other articles:
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