The Mechanism of Kynurenine Hydrolysis Catalyzed by Kynureninase
- 1 November 1979
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Biochemistry
- Vol. 86 (5), 1199-1209
- https://doi.org/10.1093/oxfordjournals.jbchem.a132635
Abstract
Several kynurenine analogs have been prepared and examined for their susceptibility to hydro-lytic cleavage by bacterial kynureninase. In addition to L-kynurenine, 4-fluoro- and 5-fluoro-L-kynurenines were hydrolyzed rapidly. 3-Hydroxy-, 5-hydroxy-, 5-methyl-, and N'-formyl-L-kynurenines, and β-benzoyl-DL-alanine were hydrolyzed slowly, whereas D-kynurenine, S-benzyl-L-cysteine, and L-asparagine were not hydrolyzed. Kinetic parameters for these kynurenine analogs indicate that a substituent on the benzene ring of kynurenine does not greatly affect the affinity of the enzyme for the substrate but does markedly affect the rate of hydrolysis. Γ-(o-Aminophenyl)-L-homoserine was converted into L-alanine and o-amino-benzaldehyde, suggesting that the a-bond electrons between the β- and Γ-carbon atoms of this kynurenine analog remain in the alanyl moiety during the enzyme reaction. Aromatic compounds such as o-aminobenzaldehyde and o-aminoacetophenone strongly inhibited the kynurenine hydrolysis. It was shown that kynurenic acid is not produced by kynureninase by the use of isotopically labeled substrate. A small amount of pyruvate was definitely formed in the kynureninase reaction. On the basis of these results, a reaction mechanism is proposed for the enzymatic kynurenine cleavage, involving hydrolysis of the a.f-diketone intermediate to give anthranilic acid and the pyruvate-pyridoxamine 5’-phosphate Schiff base, which is further converted into the alanine-pyridoxal 5‘-phosphate Schiff base, or directly hydrolyzed to give pyruvate and the pyridoxamine 5’-phosphate form of the enzyme.Keywords
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