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Literature summary for 4.2.3.10 extracted from

  • Croteau, R.; Miyazaki, J.H.; Wheeler, C.J.
    Monoterpene biosynthesis: mechanistic evaluation of the geranyl pyrophosphate:(-)-endo-fenchol cyclase from fennel (Foeniculum vulgare) (1989), Arch. Biochem. Biophys., 269, 507-516.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2,3-cyclopropylgeranyl diphosphate competitive inhibitor Anethum foeniculum
2-Fluorogeranyl diphosphate effective competitive inhibitor Anethum foeniculum
2-fluorolinalyl diphosphate effective competitive inhibitor Anethum foeniculum
6,7-dihydrogeranyl diphosphate competitive inhibitor Anethum foeniculum
additional information synergistic effect of sulfonium analog inorganic diphosphate combinations in the inhibition of fenchol cyclase Anethum foeniculum

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.006
-
geranyl diphosphate
-
Anethum foeniculum
0.02
-
2,3-cyclopropylgeranyl diphosphate pH 6.5, 30°C Anethum foeniculum
0.025
-
6,7-dihydrogeranyl diphosphate pH 6.5, 30°C Anethum foeniculum

Metals/Ions

Metals/Ions Comment Organism Structure
Mn2+ Mn2+-dependent formation of ether-soluble products from 6,7-dihydrogeranyl diphosphate Anethum foeniculum

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
geranyl diphosphate Anethum foeniculum
-
(-)-endo-fenchol + diphosphate
-
?

Organism

Organism UniProt Comment Textmining
Anethum foeniculum
-
M. var. vulgare
-

Reaction

Reaction Comment Organism Reaction ID
geranyl diphosphate + H2O = (-)-endo-fenchol + diphosphate reaction mechanism Anethum foeniculum
geranyl diphosphate + H2O = (-)-endo-fenchol + diphosphate (3R)-linalyl diphosphate is an intermediate in the reaction Anethum foeniculum

Source Tissue

Source Tissue Comment Organism Textmining
leaf young emerging leaves from 30-day-old plants Anethum foeniculum
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2,3-cyclopropylgeranyl diphosphate at 53% of the rate of conversion of geranyl diphosphate, formation of ether-soluble products Anethum foeniculum ?
-
?
6,7-dihydrogeranyl diphosphate at 35% of the rate of conversion of geranyl diphosphate, formation of ether-soluble products Anethum foeniculum ?
-
?
dimethylallyl diphosphate at the same rate as the cyclization of geranyl diphosphate Anethum foeniculum dimethylallyl alcohol + diphosphate
-
?
farnesyl diphosphate at 25% of the rate of conversion of geranyl diphosphate, formation of ether-soluble products Anethum foeniculum ?
-
?
geranyl diphosphate
-
Anethum foeniculum (-)-endo-fenchol + diphosphate
-
?
geranyl diphosphate mechanism of the isomerization-cyclization reaction Anethum foeniculum (-)-endo-fenchol + diphosphate
-
?
geranyl diphosphate (3R)-linalyl diphosphate is an intermediate in the reaction Anethum foeniculum (-)-endo-fenchol + diphosphate
-
?

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
30
-
assay at Anethum foeniculum

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
6.5
-
assay at Anethum foeniculum

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
additional information
-
additional information
-
Anethum foeniculum
0.01
-
2-Fluorogeranyl diphosphate pH 6.5, 30°C Anethum foeniculum
0.013
-
2-fluorolinalyl diphosphate pH 6.5, 30°C Anethum foeniculum
0.035
-
2,3-cyclopropylgeranyl diphosphate pH 6.5, 30°C Anethum foeniculum
0.04
-
6,7-dihydrogeranyl diphosphate pH 6.5, 30°C Anethum foeniculum