Osmolytic Effect of Sucrose on Thermal Denaturation of Pea Seedling Copper Amine Oxidase

• Published in: Protein Journal Vol. 36; no. 2; pp. 147 - 153
• Main Authors: Amani, Mojtaba, Barzegar, Aboozar, Mazani, Mohammad
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.04.2017; Springer; Springer Nature B.V
• Subjects: Amine Oxidase (Copper-Containing) - chemistry; Amine Oxidase (Copper-Containing) - metabolism; Amines; Analysis; Animal Anatomy; Biochemistry; Bioorganic Chemistry; Calorimetry; Calorimetry, Differential Scanning; Chemistry; Chemistry and Materials Science; Circular Dichroism; Denaturation; Differential scanning calorimetry; Enzymatic activity; Enzymes; Fluorescence spectroscopy; Histology; Kinetics; Legumes; Morphology; Organic Chemistry; Oxidases; Pisum sativum - enzymology; Protein Denaturation; Protein folding; Proteins; Proteins - chemistry; Proteins - metabolism; Seedlings; Seedlings - enzymology; Sucrose; Sucrose - chemistry; Temperature; Thermodynamics; Differential scanning calorimetry; Stability; Sucrose; Pea seedlings amine oxidase
• ISSN: 1572-3887; 1875-8355; 1573-4943; 1875-8355
• DOI: 10.1007/s10930-017-9706-1

Protein stability is a subject of interest by many researchers. One of the common methods to increase the protein stability is using the osmolytes. Many studies and theories analyzed and explained osmolytic effect by equilibrium thermodynamic while most proteins undergo an irreversible denaturation. In current study we investigated the effect of sucrose as an osmolyte on the thermal denaturation of pea seedlings amine oxidase by the enzyme activity, fluorescence spectroscopy, circular dichroism, and differential scanning calorimetry. All experiments are in agreement that pea seedlings amine oxidase denaturation is controlled kinetically and its kinetic stability is increased in presence of sucrose. Differential scanning calorimetry experiments at different scanning rates showed that pea seedlings amine oxidase unfolding obeys two-state irreversible model. Fitting the differential scanning calorimetry data to two-state irreversible model showed that unfolding enthalpy and T * , temperature at which rate constant equals unit per minute, are increased while activation energy is not affected by increase in sucrose concentration. We concluded that osmolytes decrease the molecular oscillation of irreversible proteins which leads to decline in unfolding rate constant.