Home / Biochemistry / Aestivation induction and evidence of conformational differences between oxy-haemocyanin and deoxy-haemocyaninin aestivating and non-aestivating snails

Aestivation induction and evidence of conformational differences between oxy-haemocyanin and deoxy-haemocyaninin aestivating and non-aestivating snails

 

Table Of Contents


Chapter ONE

1.1 Introduction
1.2 Background of Study
1.3 Problem Statement
1.4 Objective of Study
1.5 Limitation of Study
1.6 Scope of Study
1.7 Significance of Study
1.8 Structure of the Research
1.9 Definition of Terms

Chapter TWO

2.1 Overview of Haemocyanin in Snails
2.2 Aestivation Process in Snails
2.3 Structural Differences in Oxy-Haemocyanin and Deoxy-Haemocyanin
2.4 Previous Studies on Snail Aestivation
2.5 Role of Haemocyanin in Aestivating Snails
2.6 Physiological Changes during Aestivation
2.7 Molecular Adaptations in Aestivating Snails
2.8 Comparative Studies on Haemocyanin Forms
2.9 Evolutionary Significance of Aestivation in Snails
2.10 Future Research Directions

Chapter THREE

3.1 Research Design
3.2 Sampling Methods
3.3 Data Collection Techniques
3.4 Data Analysis Procedures
3.5 Ethical Considerations
3.6 Participant Recruitment
3.7 Instrumentation and Materials
3.8 Variables and Measurements

Chapter FOUR

4.1 Haemocyanin Levels in Aestivating Snails
4.2 Structural Analysis of Oxy-Haemocyanin and Deoxy-Haemocyanin
4.3 Comparative Study of Haemocyanin Conformations
4.4 Physiological Changes in Aestivating Snails
4.5 Molecular Adaptations in Haemocyanin Structure
4.6 Impact of Aestivation on Snail Health
4.7 Environmental Factors Influencing Aestivation
4.8 Discussion on Findings

Chapter FIVE

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

Project Abstract

ABSTRACT

Haemocyanin is a high molecular weight, dioxygen, transport, copper-glycoprotein with a di-copper active site found in the haemolymph of several marine and terrestrial invertebrates belonging to the phyla Mollusca and Arthropoda. Haemocyanin exists in two distinct conformers the T-conformer (Tense) and the R-conformer (Relaxed).Knowledge of the molecular architecture around the copper atoms in the active site of haemocyanin is important in understanding how these proteins reversibly bind oxygen. Induction of aestivation and the evidence of conformational differences between oxy-haemocyanin and deoxy-haemocyanin in aestivating and non-aestivating snails was studied.Aestivation induction was studied by treating five groups of snails (groups A, B, C, D and E) with respective volumes of oxy-haemocyanin from aestivating snails, respective volumes of oxy-haemocyanin from non-aestivating snails and respective volumes of distilled water. Evidence of conformational differences between oxy-haemocyanin and deoxy-haemocyanin was also studied by treating the haemolymph of two snail samples (Snail 1 and Snail 2) with nitrogen gas.After the induction of aestivation, it was observed that the snails in groups A, B and C administered with the respective volumes of haemolymph extracted from aestivating rsnails began to synthesize epiphragm layer on the 4th day after injection, on the 5th day after injection, the epiphragm layer was completely formed. Whereas the snails in groups D and E began to synthesize epiphragm layer on the 5th day, on the 6th day, the epiphragm layer was completely formed. It was also observed that the snails in groups A, B and C that were injected with haemolymph extracted from non-aestivating snails beganto synthesize epiphragm layer on the 4th day, on the 5th day, the epiphragm layer was completely formed. It was also observed that the snails in groups D and E that were injected with different volumes of water, began to synthesize epiphragm layer on the 3rd day, at about 4 days and 8hours after injection, the epiphragm layer was completely formed. Whereas the snails in groups A, B and C began to synthesize epiphragm layer on the 4th day, at about 5 days after injection, the epiphragm layer was completely formed. Results from the UV-Visible scanning showed that oxyhaemocyanin exhibited spectral activity both in the near-UV region and in the mid-UV region, whereas deoxyhaemocyanin only showed spectral activity in the near-UV region.


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