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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
1.14.12.22
naphthalene + NAD(P)H + H+ + O2
18 h reaction time, 23.6% substrate remaining
Pseudomonas sp.
cis-1,2-dihydroxy-1,2-dihydronaphthalene + NAD(P)+
-
?
1.14.12.22
naphthalene + NADH + H+ + O2
-
Janthinobacterium sp. J3
?
-
?
1.14.12.22
naphthalene + NADH + H+ + O2
-
Neptuniibacter sp. CAR-SF
?
-
?
1.14.12.22
phenanthrene + NAD(P)H + H+ + O2
-
Pseudomonas sp.
? + NAD(P)+
products are three dihydrodiols
?
1.14.12.22
phenanthrene + NAD(P)H + H+ + O2
18 h reaction time, 5.4% substrate remaining
Pseudomonas sp.
? + NAD(P)+
-
?
1.14.12.22
phenanthrene + NAD(P)H + H+ + O2
-
Kordiimonas gwangyangensis
phenanthrene dihydrodiol + monohydroxyphenanthrene + NAD(P)+
70% phenanthrene dihydrodiol and 9% monohydroxyphenanthrene in Escherichia coli expressing terminal oxygenase gene CarAa and ferredoxin component gene CarAc
?
1.14.12.22
phenanthrene + NADH + H+ + O2
-
Pseudomonas sp. GBS.5
?
-
?
1.14.12.22
phenazine + NAD(P)H + H+ + O2
-
Pseudomonas sp.
? + NAD(P)+
-
?
1.14.12.22
phenothiazine + NAD(P)H + H+ + O2
18 h reaction time, 7.6% substrate remaining
Pseudomonas sp.
? + NAD(P)+
-
?
1.14.12.22
phenoxathiin + NAD(P)H + H+ + O2
-
Pseudomonas sp.
2,2',3-trihydroxydiphenyl sulfide + NAD(P)+
angular dioxygenation by CARDO occurs at the angular position adjacent to the oxygen atom to yield hetero ring-cleaved compounds
?
Results
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