Substrate binding to fluorescent labeled wild type, Lys213Arg, and His233Gln Saccharomyces cerevisiae phosphoenolpyruvate carboxykinases

Claudia Bueno, Fernando D. González-Nilo, María Victoria Encinas, Emilio Cardemil

Resultado de la investigación: Contribución a una revistaArtículo

5 Citas (Scopus)

Resumen

Saccharomyces cerevisiae phosphoenolpyruvate (PEP) carboxykinase is a key enzyme of the gluconeogenic pathway and catalyzes the decarboxylation of oxaloacetate and transfer of the γ-phosphoryl group of ATP to yield PEP, ADP, and CO2 in the presence of a divalent metal ion. Previous experiments have shown that mutation of amino acid residues at metal site 1 decrease the steady-state affinity of the enzyme for PEP, suggesting interaction of PEP with the metal ion [Biochemistry 41 (2002) 12763]. To more completely understand this enzyme interactions with substrate ligands, we have prepared the phosphopyridoxyl (P-pyridoxyl)-derivatives of wild type, Lys213Arg, and His233Gln S. cerevisiae PEP carboxykinase and used the changes in the fluorescence probe to determine the dissociation equilibrium constants of PEP, ATPMn2-, and ADPMn1- from the corresponding derivatized enzyme-Mn2+ complexes. Homology modeling of P-pyridoxyl-PEP carboxykinase and P-pyridoxyl-PEP carboxykinase-substrate complexes agree with experimental evidence indicating that the P-pyridoxyl group does not interfere with substrate binding. ATPMn2- binding is 0.8kcalmol-1 more favorable than ADPMn1- binding to wild type P-pyridoxyl-enzyme. The thermodynamic data obtained in this work indicate that PEP binding is 2.3kcalmol-1 and 3.2kcalmol-1 less favorable for the Lys213Arg and His233Gln mutant P-pyridoxyl-PEP carboxykinases than for the wild type P-pyridoxyl-enzyme, respectively. The possible relevance of N and O ligands for Mn2+ in relation to PEP binding and catalysis is discussed.

Idioma originalInglés
Páginas (desde-hasta)861-869
Número de páginas9
PublicaciónInternational Journal of Biochemistry and Cell Biology
Volumen36
N.º5
DOI
EstadoPublicada - 1 may 2004

Áreas temáticas de ASJC Scopus

  • Bioquímica
  • Biología celular

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