Mutants of 4-oxalocrotonate tautomerase catalyze the decarboxylation of oxaloacetate through an imine mechanism

Chembiochem. 2002 Sep 2;3(9):845-51. doi: 10.1002/1439-7633(20020902)3:9<845::AID-CBIC845>3.0.CO;2-2.

Abstract

A designed single amino acid substitution can alter the catalytic activity and mechanism of 4-oxalocrotonate tautomerase (4-OT). While the wild-type enzyme catalyzes only the tautomerization of oxalocrotonate, the Pro1Ala mutant (P1A) catalyzes two reactions--the original tautomerization reaction and the decarboxylation of oxaloacetate. Although the N-terminal amine group of P1A is involved in both reactions, our results support a nucleophilic mechanism for the decarboxylase activity, in contrast to the general acid/base mechanism that has been previously established for the tautomerase activity. These findings demonstrate that a single catalytic group in a 4-OT mutant can catalyze two reactions by two different mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Substitution
  • Catalysis
  • Decarboxylation
  • Imines / chemistry
  • Isomerases / genetics*
  • Isomerases / metabolism
  • Kinetics
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Mutation
  • Oxaloacetic Acid / metabolism*
  • Protein Engineering*
  • Pseudomonas putida / enzymology

Substances

  • Imines
  • Oxaloacetic Acid
  • 4-oxalocrotonate tautomerase
  • Isomerases