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Literature summary for 4.1.2.47 extracted from

  • Lou, W.Y.; Xu, R.; Zong, M.H.
    Hydroxynitrile lyase catalysis in ionic liquid-containing systems (2005), Biotechnol. Lett., 27, 1387-1390.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
additional information cleavage of mandelonitrile proceeds more rapidly in monophasic aqueous media containing 1-propyl-3-methylimidazolium tetrahydroborate than in media containing acetonitrile or tetrahydrofuran Manihot esculenta

Inhibitors

Inhibitors Comment Organism Structure
1-butyl-3-methylimidazolium tetrahydroborate 2-6% v/v, inactivates Manihot esculenta
1-hexyl-3-methylimidazolium tetrahydroborate 2-6% v/v, inactivates Manihot esculenta
1-pentyl-3-methylimidazolium tetrahydroborate 2-6% v/v, inactivates Manihot esculenta
1-propyl-3-methylimidazolium tetrahydroborate 2-6% v/v, inactivates Manihot esculenta

Organism

Organism UniProt Comment Textmining
Manihot esculenta
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(S)-mandelonitrile
-
Manihot esculenta HCN + benzaldehyde
-
?

Synonyms

Synonyms Comment Organism
MeHNL
-
Manihot esculenta

Temperature Stability [°C]

Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
additional information
-
the enzyme is much more thermostable in 1-propyl-3-methylimidazolium tetrahydroborate than in acetonitrile or tetrahydrofuran Manihot esculenta