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Literature summary for 1.13.11.38 extracted from

  • Adachi, K.; Iwabuchi, T.; Sano, H.; Harayama, S.
    Structure of the ring cleavage product of 1-hydroxy-2-naphthoate, an intermediate of the phenanthrene-degradative pathway of Nocardioides sp. strain KP7 (1999), J. Bacteriol., 181, 757-763.
    View publication on PubMedView publication on EuropePMC
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Organism

Organism UniProt Comment Textmining
Nocardioides sp.
-
 recombinant
-
Nocardioides sp. KP7
-
 recombinant
-

Purification (Commentary)

Purification (Comment) Organism
-
 Nocardioides sp.

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
1567
-
-
 Nocardioides sp.

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1-hydroxy-2-naphthoate + O2
-
 Nocardioides sp. (3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate i.e. trans-2'-carboxybenzalpyruvate. The structure of the ring cleavage product is determined upon separation by high-performance liquid chromatography at pH 2.5 by using nuclear magnetic resonance and mass spectroscopic techniques ?
1-hydroxy-2-naphthoate + O2
-
 Nocardioides sp. KP7 (3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate i.e. trans-2'-carboxybenzalpyruvate. The structure of the ring cleavage product is determined upon separation by high-performance liquid chromatography at pH 2.5 by using nuclear magnetic resonance and mass spectroscopic techniques ?