Microcalorimetric determination of the reaction enthalpy changes associated with the carboxylase and oxygenase reactions catalysed by ribulose 1,5-bisphosphate carboxylase/oxygenase (RUBISCO)

The total reaction enthalpy change ΔrH associated with the carboxylation and oxygenation of D-ribulose 1,5-bisphosphate (RuBP) catalysed by RUBISCO from spinach and Rhodospirillum rubrum was measured for the first time with sensitive microcalorimetry. The enthalpy changes Δr,cH and Δr,oH associated with the carboxylase and oxygenase reactions were determined separately using the known ratio of these reactions. Δr,cH and Δr,oH corrected for the heat of neutralisation due to proton release during the overall carboxylation or oxygenation processes. For the corrected enthalpy change Δr,cH′ of the carboxylase reaction catalysed by RUBISCO of spinach a value of −21.34±0.4 kJ mol−1 was determined. In the case of the oxygenase reaction for RUBISCO of spinach a reaction enthalpy change Δr,oH′ of −319.1±9.6 kJ mol−1 which is typical for energy rich reactions, was found. This value is comparable with Δr,oH′=−291.4±5.8 kJ mol−1 associated with the oxygenase reaction catalysed by Co2+-activated RUBISCO from R. rubrum.

[1]  B. McFadden,et al.  Chemiluminescence of the Mn2(+)-activated ribulose-1,5-bisphosphate oxygenase reaction: evidence for singlet oxygen production. , 1990, Biochemistry.

[2]  I. Andersson,et al.  Crystallographic analysis of ribulose 1,5-bisphosphate carboxylase from spinach at 2.4 A resolution. Subunit interactions and active site. , 1990, Journal of molecular biology.

[3]  J F Brandts,et al.  Rapid measurement of binding constants and heats of binding using a new titration calorimeter. , 1989, Analytical biochemistry.

[4]  R. Chollet,et al.  Structural characterization and the determination of negative cooperativity in the tight binding of 2-carboxyarabinitol bisphosphate to higher plant ribulose bisphosphate carboxylase. , 1985, The Journal of biological chemistry.

[5]  D. Jordan,et al.  Species variation in kinetic properties of ribulose 1,5-bisphosphate carboxylase/oxygenase. , 1983, Archives of biochemistry and biophysics.

[6]  A. Keys,et al.  The enzymatic determination of bicarbonate and CO2 in reagents and buffer solutions. , 1983, Analytical biochemistry.

[7]  D. Jordan,et al.  Species variation in the specificity of ribulose biphosphate carboxylase/oxygenase , 1981, Nature.

[8]  G. Lorimer,et al.  The Carboxylation and Oxygenation of Ribulose 1,5-Bisphosphate: The Primary Events in Photosynthesis and Photorespiration , 1981 .

[9]  J. Christeller The effects of bivalent cations on ribulose bisphosphate carboxylase/oxygenase. , 1981, Biochemical Journal.

[10]  Tabita Fr,et al.  Differential effects of metal ions on Rhodospirillum rubrum ribulosebisphosphate carboxylase/oxygenase and stoichiometric incorporation of HCO3- into a cobalt(III)--enzyme complex. , 1979 .

[11]  J. Vater,et al.  Identification of two binding sites of the D-ribulose 1,5-bisphosphate carboxylase/oxygenase from spinach for D-ribulose 1,5-bisphosphate and effectors of the carboxylation reaction. , 1979, Archives of biochemistry and biophysics.

[12]  F. Tabita,et al.  D-ribulose 1,5-diphosphate carboxylase from Rhodospirillum rubrum. II. Quaternary structure, composition, catalytic, and immunological properties. , 1974, The Journal of biological chemistry.

[13]  F. Tabita,et al.  D-ribulose 1,5-diphosphate carboxylase from Rhodospirillum rubrum. I. Levels, purification, and effects of metallic ions. , 1974, The Journal of biological chemistry.

[14]  J. Frank,et al.  Thermodynamics and kinetics of sugar phosphate binding to D-ribulose 1,5-bisphosphate carboxylase/oxygenase (RUBISCO) , 1998 .

[15]  G. Lorimer,et al.  Ribulose-1,5-bisphosphate carboxylase-oxygenase. , 1983, Annual review of biochemistry.

[16]  G. Lorimer,et al.  The activation of ribulose-1,5-bisphosphate carboxylase by carbon dioxide and magnesium ions. Equilibria, kinetics, a suggested mechanism, and physiological implications. , 1976, Biochemistry.