| ULS00383 |
2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UPA00808 |
dibenzofuran degradation~Degradation of dibenzofuran. Dibenzofuran is created as by-products during industrial processes such as incineration, paper bleaching, and chemical synthesis. It has also been used as an insecticide, and is formed from the photolysis of chlorinated biphenyl ethers. Several species of bacteria capable degrading dibenzofuran have been identified, including Pseudomonas, Xanthomonas, Terrabacter, Microbacterium, and Rhodococcus. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00778 |
2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran: step 3/3~1 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-cis,cis-hexa-2,4-dienoic acid + 1 H(2)O => 1 2-hydroxy-2,4-pentadienoate + 1 salicylate. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00776 |
2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran: step 1/3~1 H(+) + 1 NADH + 1 O(2) + 1 dibenzofuran => 1 NAD(+) + 1 biphenyl-2,2',3-triol. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR05411 |
O(2) + biphenyl-2,2',3-triol = 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-cis,cis-hexa-2,4-dienoic acid |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR05434 |
H(+) + NADH + O(2) + dibenzofuran = NAD(+) + biphenyl-2,2',3-triol |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UER00777 |
2-hydroxy-2,4-pentadienoate and salicylate from dibenzofuran: step 2/3~1 O(2) + 1 biphenyl-2,2',3-triol => 1 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-cis,cis-hexa-2,4-dienoic acid. |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|
| UCR05360 |
2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-cis,cis-hexa-2,4-dienoic acid + H(2)O = 2-hydroxy-2,4-pentadienoate + salicylate |
None - {{∅}} |
None - {{∅}} |
Unexplained |
|