Production and optimization of glucoamylases from plants and aspergillusniger for starch hydrolysis in a batch bioreactor | Blazingprojects Postgraduate Thesis
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Production and optimization of glucoamylases from plants and aspergillusniger for starch hydrolysis in a batch bioreactor

 

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 Glucoamylases
  • 2.2Sources of Glucoamylases
  • 2.3Properties of Glucoamylases
  • 2.4Enzymatic Mechanism of Glucoamylases
  • 2.5Applications of Glucoamylases
  • 2.6Production of Glucoamylases in Plants
  • 2.7Production of Glucoamylases in Aspergillus niger
  • 2.8Optimization Techniques for Glucoamylase Production
  • 2.9Factors Affecting Glucoamylase Production
  • 2.10Comparative Analysis of Glucoamylases from Plants and Aspergillus niger

Chapter THREE

RESEARCH METHODOLOGY

  • 3.1Research Methodology Overview
  • 3.2Selection of Plant Species for Glucoamylase Production
  • 3.3Cultivation and Harvesting Techniques for Glucoamylase Extraction
  • 3.4Fermentation Process for Glucoamylase Production in Aspergillus niger
  • 3.5Enzyme Purification Methods
  • 3.6Enzyme Assay Techniques
  • 3.7Optimization of Glucoamylase Production Conditions
  • 3.8Statistical Analysis Methods for Experimental Data

Chapter FOUR

DATA PRESENTATION AND ANALYSIS

  • 4.1Analysis of Glucoamylase Production Results
  • 4.2Comparison of Glucoamylase Yield from Plants and Aspergillus niger
  • 4.3Effect of Environmental Factors on Glucoamylase Production
  • 4.4Enzyme Stability Studies
  • 4.5Substrate Specificity of Glucoamylases
  • 4.6Industrial Applications of Plant-derived Glucoamylases
  • 4.7Industrial Applications of Aspergillus niger Glucoamylases
  • 4.8Future Prospects for Glucoamylase Research

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • 5.1Summary of Findings
  • 5.2Conclusion
  • 5.3Recommendations for Future Research
  • 5.4Implications of the Study
  • 5.5Contribution to Scientific Knowledge

Thesis Abstract

Glucoamylases were produced from both plants and microorganisms and were optimized for starch hydrolysis in batch bioreactor. Amylase activity was monitored in germinating guinea corn seeds for seven days. Highest amylase activity was observed on days 3 and 7. A study of the amylopectin content of millet, guinea corn, cassava, corn and tigernut starch showed that tiger nut had the highest amylopectin content while cassava starch had the lowest. Moist amylopectin frommillet, guinea corn, cassava, corn and tiger nut starch were exposed on the shelf to triger microbial growth. Luxurial growths were noticed on amylopectin from guinea corn, tigernut and cassava starch. Pure isolates were obtained by subculturing and identified as Aspergillus niger. A 14 day fermentation study to determine the optimal production time using the organism and amylopectin from guinea corn, tigernut and cassava starch was carried out. The fermentation studies showed a two peak profile for each amylopectin used.The first on day 3 or 4, while the second peak on day 11 and 12, respectively. Large scale production of glucoamylase was carried out on these days of highest enzyme production. Glucoamylase activities from both germinating guinea corn seeds and Aspergillusniger were enhanced by calcium (Ca2+), zinc (Zn2+), cobolt (Co2+), iron (Fe2+) and manganespre (Mn2+) ionbut Lead ion (Pb2+) completely inactivated the enzymes. The Michaelismenten constant (Km) and the maximum velocity (Vmax)obtained from Lineweaver-Burk plot of initial velocity data at different substrate concentrations showed high affinity of the glucomylases for their substrates. The optimal pH and temperature of glucoamylases from both germinating seeds and Aspergillusniger were in the range of 4.5-8.5 and 45-60 ËšC, respectively.The glucoamylases were screened for α and β glucosidase activities and glucoamylase obtained on day 7 from germinating guinea corn seeds (GluGERGC7) and that obtained on days 11 and 12 from Aspergillusniger grown in broth containing amylopectin from cassava and tiger nut starch (GluAgCSV11) and (GluAgTN12), respectively were found to exhibit high α glucosidase activity. The rate of substrate utilization or the efficiency of batch bioreactor at the predetermined optimal conditions was predicted using Kmand Vmaxobtained from a modified form of Michaelis-Menten’s equation and were found within the range of 40- 460mg/ml and 0.811-50 µmol/min, respectively using cassava, guinea corn and tiger nut starch as substrates. The results suggest that the glucoamylases obtained from both germinating guinea corn seeds and Aspergillusniger possess the qualities of biotechnological applications in which the optimal conditions could be predicted.

Thesis Overview

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