EC Number   |
Natural Substrates |
|---|
  1.14.14.58 | (3S)-(E,E)-geranyllinalool + [reduced NADPH-hemoprotein reductase] + O2 |
- |
| 1.14.14.58 | (3S)-(E,E)-geranyllinalool + [reduced NADPH-hemoprotein reductase] + O2 |
biosynthesis of the volatile organic compound (E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene |
| 1.14.14.58 | (3S,6E)-nerolidol + [reduced NADPH-hemoprotein reductase] + O2 |
- |
| 1.14.14.58 | (3S,6E)-nerolidol + [reduced NADPH-hemoprotein reductase] + O2 |
in vitro activity is 5.3fold higher than with (E,E)-geranyllinalool. (3E)-4,8-dimethylnona-1,3,7-triene is not emitted from Arabidopsis leaves (or only in negligible amounts according to our analysis) because of the absence of a prominent (E)-nerolidol synthase activity in this tissue |
| 1.14.14.58 | (E)-nerolidol + [reduced NADPH-hemoprotein reductase] + O2 |
- |
| 1.14.14.58 | (E,E)-geranyllinalool + [reduced NADPH-hemoprotein reductase] + O2 |
- |
| 1.14.14.58 | arabidiol + [reduced NADPH-hemoprotein reductase] + O2 |
- |
| 1.14.14.58 | more |
linalool, (Z)-nerolidol, the primary terpene alcohols (E,E,E)-geranylgeraniol, (E,E)-farnesol, and (E)-geraniol, or fully saturated analogs of (E)-nerolidol and (E,E)-geranyllinalool (3,7,11-trimethyl-3-dodecanol, isophytol) are no functional substrates of the CYP82G1 enzyme |
| 1.14.14.58 | more |
CYP705A1 cleaves the prenyl side chain of arabidiol to produce (E)-4,8-dimethyl-1,3,7-nonatriene, DMNT, and a nonvolatile C19-ketone derivative |
