Literature summary extracted from

E.A. Barnsley
Naphthalene metabolism by pseudomonads: The oxidation of 1,2-dihydroxynaphthalene to 2-hydroxychromene-2-carboxylic acid and the formation of 2'-hydroxybenzalpyruvate (1976), Biochem. Biophys. Res. Commun., 72, 1116-1121.

Natural Substrates/ Products (Substrates)

EC Number	Natural Substrates	Organism	Comment (Nat. Sub.)	Natural Products	Comment (Nat. Pro.)	Rev.	Reac.
4.1.2.45	(E)-2'-hydroxybenzylidenepyruvate + O2	Pseudomonas sp.	naphthalene metabolism	salicylaldehyde + pyruvate	-	?

Organism

EC Number	Organism	UniProt	Comment	Textmining
4.1.2.45	Pseudomonas sp.	-	-	-

Purification (Commentary)

EC Number	Purification (Comment)	Organism
4.1.2.45	partial	Pseudomonas sp.

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
4.1.2.45	(E)-2'-hydroxybenzylidenepyruvate + O2	-	Pseudomonas sp.	salicylaldehyde + pyruvate	-	?
4.1.2.45	(E)-2'-hydroxybenzylidenepyruvate + O2	naphthalene metabolism	Pseudomonas sp.	salicylaldehyde + pyruvate	-	?

Synonyms

EC Number	Synonyms	Comment	Organism
4.1.2.45	2'-hydroxybenzalpyruvate aldolase	-	Pseudomonas sp.

pH Range

EC Number	pH Minimum	pH Maximum	Comment	Organism
4.1.2.45	5	8	the activity is independent of pH between pH 5.5 and 8.0, but above pH 8.0 activity declines rapidly	Pseudomonas sp.

pH Stability

EC Number	pH Stability	pH Stability Maximum	Comment	Organism
4.1.2.45	7	-	the enzyme was very stable in buffer at pH 7, stored either at 0°C or frozen	Pseudomonas sp.

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)