EC Number   |
Substrates |
Organism |
Products |
Reversibility |
|---|
  1.1.9.1 | iso-amyl alcohol + ferricyanide |
ADH IIB, 100% of the activity with 1-butanol. ADH IIG, 93% of the activity with 1,2-propanediol |
Pseudomonas putida |
3-methylbutanol + ferrocyanide |
- |
? |
| 1.1.9.1 | more |
no substrate: D-glucose, D-galactose, D-fructose, Alpha-D-methylglucoside, mannitol |
Comamonas testosteroni |
? |
- |
? |
| 1.1.9.1 | more |
The affinity of the enzyme for aliphatic alcohols increases with the chain length of the substrate. The same property is observed for secondary alcohols in the series 2-propanol to 2-octanol |
Comamonas testosteroni |
? |
- |
? |
| 1.1.9.1 | n-butanol + ferricyanide |
- |
Comamonas testosteroni |
butanal + ferrocyanide |
- |
? |
| 1.1.9.1 | octanal + reduced N,N,N',N'-tetramethyl-p-phenylenediamine |
- |
Comamonas testosteroni |
1-octanol + N,N,N',N'-tetramethyl-p-phenylenediamine |
- |
r |
| 1.1.9.1 | propanal + ferrocyanide |
ADH IIB, 125% of the activity with 1-butanol. ADH IIG, 58% of the activity with 1,2-propanediol |
Pseudomonas putida |
1-propanol + ferricyanide |
- |
? |
| 1.1.9.1 | rac-2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane + ferricyanide |
i.e. solketal. Enantiomeric ratio is 30 for solketal and 6 for rac-2,2-dimethyl-4-[1,1-2H]hydroxymethyl-1,3-[5,5,4-2H]dioxolane, d5-solketal. Isotopic substitution affects the relative kinetic weights of the initial hydron/deuteron transfer from substrate to cofactor and the subsequent proton/deuteron shift in the cofactor-product complex |
Comamonas testosteroni |
? + ferrocyanide |
- |
? |
