Association of heat-induced conformational change with activity loss of Rubisco.

Circular dichroism (CD), fluorescence, and differential scanning calorimetry (DSC) were used to investigate the thermal conformational change associated with the activity loss of spinach Rubisco. CD and intrinsic fluorescence demonstrated a three stage thermal unfolding of Rubisco. At 25-45 degrees C, the secondary structure did not change but the tertiary and/or quaternary structure changed obviously with increased temperature. In 45-60 degrees C, the secondary structure showed much change with increased temperature and the tertiary and/or quaternary structure changed much faster. Over 60 degrees C, whole conformation changed abruptly with increased temperature and finally unfolded completely. DSC, CD and activity assays after annealing showed that the conformational change and the activity loss of Rubisco were completely reversible if the heating temperature was below 45 degrees C, partly reversible between 45 and 60 degrees C, and irreversible beyond 60 degrees C.

[1]  R. Douillard,et al.  Thermal denaturation and gelation of rubisco: effects of pH and ions. , 1996, International journal of biological macromolecules.

[2]  M. Salvucci,et al.  Rubisco activase constrains the photosynthetic potential of leaves at high temperature and CO2. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[3]  F. C. Hartman,et al.  Mechanism of Rubisco: The Carbamate as General Base. , 1998, Chemical reviews.

[4]  E. Martínez‐Barajas,et al.  Rubisco activase, a possible new member of the molecular chaperone family. , 1995, Biochemistry.

[5]  T. Shikanai,et al.  A Rapid and Sensitive Method for Determination of Relative Specificity of RuBisCO from Various Species by Anion-Exchange Chromatography , 1996 .

[6]  S. Crafts-Brandner,et al.  Effect of heat stress on the inhibition and recovery of the ribulose-1,5-bisphosphate carboxylase/oxygenase activation state , 2000, Planta.

[7]  R. J. Spreitzer,et al.  Complementing Substitutions at the Bottom of the Barrel Influence Catalysis and Stability of Ribulose-bisphosphate Carboxylase/Oxygenase* , 1997, The Journal of Biological Chemistry.

[8]  Y. Tomimatsu Macromolecular properties and subunit interactions of ribulose-1,5-bisphosphate carboxylase from alfalfa. , 1980, Biochimica et biophysica acta.

[9]  N. C. Price,et al.  The application of circular dichroism to studies of protein folding and unfolding. , 1997, Biochimica et biophysica acta.

[10]  E. Freire,et al.  Thermal denaturation methods in the study of protein folding. , 1995, Methods in enzymology.

[11]  M. Chattopadhyay,et al.  Thermal stress induces differential degradation of Rubisco in heat‐sensitive and heat‐tolerant rice , 1999 .

[12]  N. Pon,et al.  Direct spectrophotometric observation of ribulose-11, 5-bisphosphate carboxylase activity. , 1978, Analytical Biochemistry.

[13]  R. J. Spreitzer Questions about the complexity of chloroplast ribulose-1,5-bisphosphate carboxylase/oxygenase , 1999, Photosynthesis Research.

[14]  A. Gatenby,et al.  Rubisco Synthesis, Assembly, Mechanism, and Regulation. , 1995, The Plant cell.

[15]  R. J. Spreitzer,et al.  C172S Substitution in the Chloroplast-encoded Large Subunit Affects Stability and Stress-induced Turnover of Ribulose-1,5-bisphosphate Carboxylase/Oxygenase* , 1999, The Journal of Biological Chemistry.

[16]  H. Bizot,et al.  Differential scanning calorimetric studies of the effects of ions and pH on ribulose 1,5-bisphosphate carboxylase/oxygenase. , 1993, International journal of biological macromolecules.

[17]  Y. Du,et al.  RbcS suppressor mutations improve the thermal stability and CO2/O2 specificity of rbcL- mutant ribulose-1,5-bisphosphate carboxylase/oxygenase. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[18]  F. C. Hartman,et al.  Structure, Function, Regulation, and Assembly of D-Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase , 1994 .

[19]  K. K. Turoverov,et al.  Ultra‐violet fluorescence of actin. Determination of native actin content in actin preparations , 1976, FEBS letters.

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

[21]  A. Yokota,et al.  Modeling of continuously and directly analyzed biphasic reaction courses of ribulose 1,5-bisphosphate carboxylase/oxygenase. , 1996, Journal of biochemistry.

[22]  S. Crafts-Brandner,et al.  Inhibition and acclimation of photosynthesis to heat stress is closely correlated with activation of ribulose-1,5-bisphosphate Carboxylase/Oxygenase , 1999, Plant physiology.

[23]  M. Lane,et al.  Spinach ribulose diphosphate carboxylase. I. Purification and properties of the enzyme. , 1966, Biochemistry.

[24]  N. Greenfield Applications of circular dichroism in protein and peptide analysis , 1999 .

[25]  J. Donovan,et al.  Effect of pH, Mg, CO(2) and Mercurials on the Circular Dichroism, Thermal Stability and Light Scattering of Ribulose 1,5-Bisphosphate Carboxylases from Alfalfa, Spinach and Tobacco. , 1981, Plant physiology.

[26]  R. J. Spreitzer,et al.  Suppressor Mutations in the Chloroplast-encoded Large Subunit Improve the Thermal Stability of Wild-type Ribulose-1,5-bisphosphate Carboxylase/Oxygenase* , 2000, The Journal of Biological Chemistry.

[27]  N. Eckardt,et al.  Heat Denaturation Profiles of Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase (Rubisco) and Rubisco Activase and the Inability of Rubisco Activase to Restore Activity of Heat-Denatured Rubisco , 1997, Plant physiology.

[28]  C. V. van Mierlo,et al.  Protein folding and stability investigated by fluorescence, circular dichroism (CD), and nuclear magnetic resonance (NMR) spectroscopy: the flavodoxin story. , 2000, Journal of biotechnology.