Characterization of pentaclethra macrophylla benth through protein electrophoresis

 

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 Protein Electrophoresis
  • 2.2Pentaclethra Macrophylla Benth: An Introduction
  • 2.3Importance of Studying Pentaclethra Macrophylla Benth
  • 2.4Historical Perspective on Protein Electrophoresis
  • 2.5Types of Protein Electrophoresis Techniques
  • 2.6Applications of Protein Electrophoresis in Botanical Studies
  • 2.7Protein Electrophoresis in Plant Taxonomy
  • 2.8Protein Electrophoresis in Plant Genetics
  • 2.9Protein Electrophoresis in Plant Disease Research
  • 2.10Recent Developments in Protein Electrophoresis Technologies

Chapter THREE

RESEARCH METHODOLOGY

  • 3.1Research Methodology Overview
  • 3.2Selection of Pentaclethra Macrophylla Benth Samples
  • 3.3Preparation of Protein Samples
  • 3.4Protein Electrophoresis Protocol
  • 3.5Gel Electrophoresis Techniques
  • 3.6Data Analysis Methods
  • 3.7Statistical Analysis Procedures
  • 3.8Research Ethics and Compliance

Chapter FOUR

DATA PRESENTATION AND ANALYSIS

  • 4.1Analysis of Electrophoresis Results
  • 4.2Identification of Protein Bands
  • 4.3Comparison of Protein Profiles
  • 4.4Interpretation of Electrophoresis Data
  • 4.5Correlation of Protein Patterns with Botanical Traits
  • 4.6Discussion on Protein Variability in Pentaclethra Macrophylla Benth
  • 4.7Implications of Findings in Plant Research
  • 4.8Future Research Directions

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • 5.1Conclusion and Summary
  • 5.2Recap of Research Objectives
  • 5.3Key Findings and Contributions
  • 5.4Limitations of the Study
  • 5.5Recommendations for Future Studies

Project Abstract

<p> Sodium Dodecyl Sulphate – Polyacrylamide Gel Electrophoresis (SDS – PAGE) is a technique commonly used for the separation of proteins according to their molecular weight, based on their differential rates of migration through a sieving matrix (a gel) under the influence of an applied electrical field. SDS – PAGE was used in assessing the genetic diversity among twelve accessions of African oil bean (Pentaclethra macrophylla) germplasms obtained from NACGRAB (Ibadan) and five villages around Nsukka vicinity. Protein banding patterns were scored for presence and absence and analysed for genetic similarities and dissimilarities among the accessions. A total of 11 different bands were found in the accessions from NACGRAB and total of 9 bands were found in accessions from Nsukka zone. The highest number of bands (10) were found in Accessions A1 and A2 (Nac1 and Nac2) while the lowest (5) band was found in Accession A7 (Nac7). The banding pattern revealed that some of the bands present in the accessions from NACGRAB were absent in the accessions from Nsukka zone. A dendrogram constructed on the basis of genetic distance matrix by the Unweighted Pair Group Method with Arithmetic Mean Algorithm (UPGMA), using the NTSYS-pc software resolved the germplasm into three distinct clusters and six groups. Cluster one and two had six and five members respectively while cluster three had only one member. Cluster 1 was made up of three groups (1, 2 and 3), cluster 2 was made up of two groups (4 and 5) while cluster 3 was made up of only one group (group 6). Accessions from NACGRAB except Nac7 formed groups 1, 2 and 3 while accessions from Nsukka zone were found in groups 4 and 5 Group 6 was observed to be entirely different from other groups having only one germplasm (Nac7) with the highest genetic diversity as member and therefore considered as an outgroup. The present study has helped in resolving the genetic relatedness among the twelve accessions of P. macrophylla germplasm. The information will be suitable for future breeding for the improvement of the species. <br></p>

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