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Literature summary for 4.1.2.45 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.
    View publication on PubMed

Natural Substrates/ Products (Substrates)

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

Organism

Organism UniProt Comment Textmining
Pseudomonas sp.
-
-
-

Purification (Commentary)

Purification (Comment) Organism
partial Pseudomonas sp.

Substrates and Products (Substrate)

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

Synonyms

Synonyms Comment Organism
2'-hydroxybenzalpyruvate aldolase
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Pseudomonas sp.

pH Range

pH Minimum pH Maximum Comment Organism
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

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