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EC 1.14.14.39 Details
EC number
1.14.14.39
Accepted name
isoleucine N-monooxygenase
Reaction
L-isoleucine + 2 [reduced NADPH—hemoprotein reductase] + 2 O2 = (1E,2S)-2-methylbutanal oxime + 2 [oxidized NADPH—hemoprotein reductase] + CO2 + 3 H2O (overall reaction);;(1a) L-isoleucine + [reduced NADPH—hemoprotein reductase] + O2 = N-hydroxy-L-isoleucine + [oxidized NADPH—hemoprotein reductase] + H2O;;(1b) N-hydroxy-L-isoleucine + [reduced NADPH—hemoprotein reductase] + O2 = N,N-dihydroxy-L-isoleucine + [oxidized NADPH—hemoprotein reductase] + H2O;;(1c) N,N-dihydroxy-L-isoleucine = (1E,2S)-2-methylbutanal oxime + CO2 + H2O (spontaneous)
Other name(s)
CYP79D3 (gene name), CYP79D4 (gene name)
Systematic name
L-isoleucine,[reduced NADPH—hemoprotein reductase]:oxygen oxidoreductase (N-hydroxylating)
Comment
This cytochrome P-450 (heme-thiolate) enzyme, found in plants, catalyses two successive N-hydroxylations of L-isoleucine, the committed step in the biosynthesis of the cyanogenic glucoside lotaustralin. The product of the two hydroxylations, N,N-dihydroxy-L-isoleucine, is labile and undergoes dehydration followed by decarboxylation, producing the oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. The enzyme can also accept L-valine, but with a lower activity. cf. EC 1.14.14.38, valine N-monooxygenase.
History
created 2010 as EC 1.14.13.117, transferred 2017 to EC 1.14.14.39
EC Tree
1.14.14.2 created 1972, deleted 1976
1.14.14.4 created 2000, deleted 2002