ABSTRACT
The Anatomy of this project
write-up encompasses the ordinary look of enzymes as organic molecules, rather
it sheds more light into the comprehensive view and determination of the
catalytic and specific activity enzymes particularly- DIASTASE, MALTASE and
ZYMASE can exploit in industrial application, also critically important is the
selective ways of providing fundamental data which allows the society-particularly
small-scale brewers to understand and exploit the chemistry of fermentation by
enzymes. The method employed in this project involves three processes namely.
1.
The
preparation of the enzymes by fermentation
2.
The
preparation of the starch substrate from maize
3.
The
overall process development involving both the products of the 1st and 2nd
processes.
The results of the method
and procedures employed in this project are. That enzyme activities in
biochemical processes involves catalysis- through binding of the enzyme
molecule and the substrates. Finally, all enzymes in fermentation of starch
whose catalytic properties rely on their molecular structure and arrangement
are stabilized by interactions between their constituents. This is conclusively
evident in the chemistry of the fermentation process in starch which is later
discussed and highlighted in this write-up.
TABLE OF CONTENTS
Title page
Certification
Dedication
Acknowledgement
Abstract
CHAPTER ONE
INTRODUCTION
1.1 Background
Information
1.2 Aims
of the Study
1.3
Objectives of the Study
1.4
Limitation of the Study
1.5
Significance of the Study
1.6
Statement of Problem
CHAPTER TWO
LITERATURE REVIEW
2.1 Chemistry
of Fermentation
2.2
The Role of the Enzymes
CHAPTER THREE
MATERIALS AND METHODOLOGY
3.1
Materials and Equipment
3.2
Methodology and Procedures
3.3 The
Process Development
3.4 Preparation
of the Enzymes by Fermentation
3.5
Preparation of the Starch
Substrate from Maize
CHAPTER FOUR
ANALYSIS OF ENZYMES
PRODUCED BY FERMENTATION
4.1 Enzymes
produced by fermentation
4.1.1 α-Amylase
4.1.2 Lactase
4.1.3 Protease
4.1.4
Pectinase
4.1.5 Lipase
4.1.6 Laccase
4.1.7 Xylose (Glucose) Isomerase
4.1.8 Cyclodextrin Glycosyl Transferase
4.1.9 Catalase
4.1.10 Glucose Oxidase
4.1.11 Acetolactate Decarboxylase
4.1.12 Transglutaminase
4.2 Application
of Enzymes in Food Processing
4.2.1 Dairy Industry
4.2.2 Fruit, Vegetable and Oilseed Industries
4.2.3 Bakery Industry
4.2.4 Meat and Fish Industries
4.5 Starch Industries
CHAPTER FIVE
CONCLUSION
5.1
Conclusion
5.2
Recommendations
REFERENCES
CHAPTER
ONE
1.0
INTRODUCTION
1.1 BACKGROUND
INFORMATION
The primary aim of this
project is center on the determination of the catalytic and specific activities
of enzymes in fermentation of starch from maize.
These enzymes are DIATASE,
MALTASE and ZYMASE.
This determination study is
made possible through certain unique properties which these collection of
enzymes possess.
Speaking in concrete terms,
ENZYMES serve as bio-catalysts, speeding up chemical reactions, like those
involved with fermentation of starch. Enzyme molecules accelerate the rate of
reactions, often by many orders of magnitude, thereby allowing the substance
involved undergo a chemical breakdown.
Enzymes in fermentation of starch go about their work in an
ASSEMBLY-LINE fashion; each enzyme performing a specific task at a particular
stage of the fermentation process. For instance, the enzyme-MALTASE, breaks
down MALTASE into two isomeric fermentable sugars namely Glucose and Fructose;
thereby preparing another stage for another enzyme to act during the fermentation
process. Enzymes in fermentation process especially in starch; perform their
work at blinding speed.
A single molecule of enzyme can catalyze thousand of
chemical reactions per second. This is because enzymes in fermentation reaction
particularly in starch; have a marked ability to accelerate the reaction and
also to promote the specific processes involved under the chemically mild
conditions which prevails in the fermentation process.
In all ways, these enzymes readily make essentials
physiochemical contributions to the fermentation process by virtue of their
organized and involved three dimensional structure which reveals certain
regions on the enzyme surface where small solute molecules or ions can bind
reversibly. Such solutes are called LIGANDS; a farm borrowed from ORGANOMETALIC
CHEMISTRY.
There may be many ligard binding sites on the surface of an
enzyme, but each site usually possesses the power to bind only a limited range
of ligards, by virtue of the character of the site. The term “CHARACTER” is
there used to cover not only the three-dimensional shape of the site but also
its charge characteristics and to what degree if is hydrophobic or hydrophilic.
The character of a binding site is clearly a function of
the amino acid side chains that are brought together there by the folding of
the polypeptide chain. Enzymes are distinguished from other protein molecules
by having ACTIVE SITES. The substrate binds at the active site of its enzyme in
much the same way as other ligards might do, but once bound there, a chemical
reaction ensues because of the special nature of the enzyme active site in
respect to their catalysis and specificity in fermentation bioprocess.
1.2
AIMS OF THE STUDY
The aim of this project is
to determine the catalytic and specific activities of enzymes in fermentation
of starch-from maize.
1.3
OBJECTIVVES OF THE STUDY
To prepare the enzymes
through the microbial fermentation of malt/sermination barley extracts in a
culture media and a seed fomenter.
To show the chemistry of fermentation process in starch by
enzymic conversion.
To show the relevance and
usefulness of enzymes in industrial fermentation.
1.4
LIMITATION OF THE STUDY
The scope of this project
work is limited to the determination of the catalytic and specific activities of
enzymes in fermentation bioprocess of starch from maize.
1.5
SIGNIFICANCE OF THE STUDY
The importance of the work
is centered on the catalytic and specific activities of enzymes in fermentation
of starch for industrial usage.
1.6
STATEMENT OF PROBLEM
The cost of the enzymes and
the inability of small scale brewers to understand and exploit the chemistry of
fermentation by enzymic action.
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