EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
1.14.12.25 | indole-2-carboxylate + NADH + H+ + O2 |
product rearranges spontaneously forming indigo, indirubin, and isatin |
Pseudomonas putida |
2,3-dihydroxy-2,3-dihydro-1H-indole-2-carboxylic acid + NAD+ |
- |
? |
1.14.12.25 | indole-3-carboxylate + NADH + H+ + O2 |
- |
Pseudomonas putida |
2,3-dihydroxy-2,3-dihydro-1H-indole-3-carboxylic acid + NAD+ |
- |
? |
1.14.12.25 | m-toluate + NADH + H+ + O2 |
- |
Pseudomonas putida |
1,6-dihydroxy-5-methylcyclohexa-2,4-diene-1-carboxylic acid + NAD+ |
- |
? |
1.14.12.25 | p-cumate + NADH + H+ + O2 |
- |
Pseudomonas putida |
2,3-dihydroxy-2,3-dihydro-p-cumate + NAD+ |
- |
? |
1.14.12.25 | p-cumate + NADH + H+ + O2 |
- |
Pseudomonas putida |
2,3-dihydroxy-2,3-dihydro-p-cumate + NAD+ |
the substrate for the ring cleavage of 2,3-dihydroxy-p-cumate is formed from p-cumate in two reactions via a dihydrodiol intermediate (2,3-dihydroxy-4-isopropylcyclohexa-4,6-dienoate). Both hydroxyl atoms of the dihydrodiol are derived from the same molecule of 02 |
? |
1.14.12.25 | p-cumate + NADH + H+ + O2 |
- |
Paraburkholderia xenovorans |
(2R,3S)-2,3-dihydroxy-2,3-dihydro-p-cumate + NAD+ |
- |
? |