Ph and thermal stabilities of peroxidase isolated from ripening tomato fruits (sonalum lycopersicon)
Table Of Contents
Chapter ONE
INTRODUCTION
- 1.1Introduction
- 1.2Background of Study
- 1.3Problem Statement
- 1.4Objective of Study
- 1.5Limitation of Study
- 1.6Scope of Study
- 1.7Significance of Study
- 1.8Structure of the Research
- 1.9Definition of Terms
Chapter TWO
LITERATURE REVIEW
- 2.1Overview of Peroxidase Enzyme
- 2.2Sources of Peroxidase Enzyme
- 2.3Structure and Function of Peroxidase Enzyme
- 2.4Factors Affecting Peroxidase Activity
- 2.5Role of Peroxidase in Ripening Fruits
- 2.6Methods of Peroxidase Isolation
- 2.7Studies on Peroxidase from Tomato Fruits
- 2.8Applications of Peroxidase Enzyme
- 2.9Current Research Trends in Peroxidase Studies
- 2.10Gaps in Existing Literature
Chapter THREE
RESEARCH METHODOLOGY
- 3.1Research Design
- 3.2Sampling Techniques
- 3.3Data Collection Methods
- 3.4Experimental Procedures
- 3.5Data Analysis Techniques
- 3.6Quality Control Measures
- 3.7Ethical Considerations
- 3.8Limitations of the Methodology
Chapter FOUR
DATA PRESENTATION AND ANALYSIS
- 4.1Analysis of Experimental Results
- 4.2Comparison of Peroxidase Activity in Ripening Tomato Fruits
- 4.3Effect of pH on Peroxidase Stability
- 4.4Effect of Temperature on Peroxidase Stability
- 4.5Interpretation of Findings
- 4.6Discussion on the Significance of Results
- 4.7Comparison with Previous Studies
- 4.8Suggestions for Further Research
Chapter FIVE
SUMMARY, CONCLUSION AND RECOMMENDATIONS
- 5.1Summary of Findings
- 5.2Conclusions Drawn from the Study
- 5.3Implications of the Research
- 5.4Recommendations for Future Research
- 5.5Practical Applications of the Study
Project Abstract
<p> Peroxidase (EC 1.11.1.7) extracted from Sonalum lycopersicon was purified, on a two-step purification process of ammonium sulphate precipitation and gel filtration. The specific activity of the crude enzyme was 55.45μ/mg. The crude enzyme was purified to the level of gel filtration using Sephadex-G100 via ammonium sulphate precipitation. After ammonium sulphate precipitation and gel filtration, the enzyme was purified 3.3 fold and the specific activities were 35.93μ/mg and 119.61μ/mg respectively when o-dianisidine was used as substrate. The optimum pH and temperature was found to be 6.0 and 50°C respectively. Kinetics of peroxidase inactivation was studied over temperature range of 40-80°C. The enzyme obeyed Michealis-Menten kinetics and the Km and Vmax values were calculated and found to be 5.44mg/ml and 12.57μmol/min respectively. Biphasic inactivation curves were observed for the enzyme, where the initial heat inactivation is rapid followed by much slower inactivation periods. The inactivation kinetics followed a first-order model with k values between 3.5×10-2 – 8.14×10-2 min-1 and z value of 25.5°C. The decreasing trend of k values with increasing temperature indicates a faster inactivation of peroxidase at higher temperature. The study has shown that peroxidase from Sonalum lycopersicon is stable at temperature of 40 and 50°C as activity was maintained above 50% for 2 hours and less stable at a high temperature of about 60oC and stability dropped drastically at 70 and 80oC within 10min of heat treatment suggesting that high temperature short time treatment could easily inactivate the enzyme. The activation energy (Ea) of 127.34KJMol-1K- was calculated from the slope of Arrhenius plot. Thermodynamic parameters (^H, G ^, ^S) for inactivation of peroxidase at different temperatures (40-80°C) were studied. The Peroxidase activity was found to be pH-dependent and was stable at pH range of 6—8 …………. result from this research has shown that peroxidase from Sonalum lycopersicon has high pH and thermal stabilities and hence, could be a good source of peroxidase for industries where high temperature and pH stabilities are required for production processess. <br></p>
Project Overview