FERMENTATIVE PRODUCTION AND MICROBIOLOGICAL ANALYSES OF CASSAVA (MANIHOT ESCULENTA) FLOUR

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Product Code: 00008601

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ABSTRACTS

The fermentative production of cassava (Manihot esculenta crantz) flour was done in two different methods, which were the fixed and unfixed fermentation method. The cassava tubers were harvested from the N.R.C.R.I, Umudike, peeled, washed, sliced into big bits of about 5 to 8cm in length and allowed to ferment. The microbial load, succession, pH and cyanide content of the cassava were determined during retting and after production. The results showed the presence of E.coli and Lactobacillus spp, Bacillus spp, Staphylococcus spp, Aspergillus spp, Penicillum spp, yeast, and Geotichum spp  after the first day of fermentation. The dominant organisms after fermentation were Lactobacillus spp and Yeast. The Bacteria load was 1.59x105 to 0.61x105 cfu/g,  fungi load of 1.10x103 to 0.40x 103 cfu/g for fixed fermented cassava flour. The unfixed had the Bacteria load of 1.64 to 0.61x 105 cfu/g and fungi load of 1.10x103 and 0.45x103 cfu/g. On the other hand, the Hydrogen cyanide content and pH decreases as the fermentation period increases in both flour. It is therefore recommended that cassava tubers should be fermented at a minimum of 48 hours as its cyanide content decreases with increase fermentation period.   






TABLE OF CONTENTS

Title page                                                                                                                                i

Certification                                                                                                                           ii

Dedication                                                                                                                              iii

Acknowledgement                                                                                                                  iv

Table of Contents                                                                                                                   v

List of Figures                                                                                                                         vii

List of Tables                                                                                                                          viii

Abstract                                                                                                                                  x

CHAPTER ONE

INTRODUCTION                                                                                                                1

1.1       Background of Study                                                                                                  1

1.2       Aims and Objectives                                                                                                  2

CHAPTER TWO

LITERATURE REVIEW                                                                                                    3

2.1       Description of Cassava                                                                                               3

2.2       Habitat                                                                                                                        3

2.3       History of Cassava                                                                                                      3

2.4       Physiology and Morphology of Cassava Plant                                                           5

2.4.1    Toxicity                                                                                                                      5

2.4.2    Varieties                                                                                                                     8

2.5       Cassava Processing and Utilization                                                                            8

2.6       Nutritional Composition of Cassava                                                                          13

2.7       Fermentation Technology                                                                                          15

2.7.1    Methods of Fermenting Cassava to Flour                                                                  16

2.8       Health and Benefits                                                                                                    18

2.9       Acute and Chronic Effects of Cyanide                                                                       19

 

CHAPTER THREE

MATERIALS AND METHOD                                                                                           21

3.1       Cassava Roots Used                                                                                                   21

3.2       Sample and Media Preparation                                                                                  21

3.2.1    Fixed Fermentation Method                                                                                       21

3.2.2    Unfixed Fermentation Method                                                                                   22

3.3       Media Preparation                                                                                                      24

3.4       Microbial Analysis                                                                                                     24

3.4.1    Determination of Microbial Load                                                                               24

3.4.2    Determination of Microbial Flora                                                                              25

3.4.3    Determination of Hydrogen Cyanide                                                                         26

3.4.4    Determination of pH                                                                                                   26

3.4.5    Characterization of Bacteria Isolates                                                                          27

3.5       Cultural Examination                                                                                                 27

3.5.1    Gram Reaction                                                                                                           27

3.5.2    Microscopic Features                                                                                                 27

3.6       Characterization of Fungi Isolates                                                                              28

3.6.1    Viable Counting of the Fungi Growth                                                                        28

3.6.2    Identification of Fungi                                                                                                28

3.6.3    Colony Features of Fungi Isolates                                                                              28

3.6.4    Microscopic Features                                                                                                 28

3.6.5    Identification of Isolates                                                                                             29

3.7       Biochemical Tests                                                                                                      29

3.7.1    Oxidase Test                                                                                                               29

3.7.2    Coagulase Test                                                                                                           29

3.7.3    Citrate Test                                                                                                                 29

3.7.4    Indole                                                                                                                          30

3.7.5    Test for Carbohydrate                                                                                                 30

 

CHAPTER FOUR

RESULTS                                                                                                                              31

HCN

CHAPTER FIVE

DISCUSSION, CONCLUSION AND RECOMMEMDATON                                        38

5.1       Discussion                                                                                                                   38

5.2       Conclusion                                                                                                                  39

5.3       Recommendation                                                                                                       39

References                                                                                                                  40








LIST OF FIGURES

 

Figure      Title                                                                            Page

2.1:      Metabolic pathway of Linamarin and Lotaustralin                                                    7

2.2:      General sequence of unit for processing cassava roots into various products          12

3.1:      Diagram for the production of Cassava Flour                                                                        23

 

 

 

 

 

 

 

LIST OF TABLES

 

Table        Title                                                                           Page

2.1:                  Microorganism associated with some local Fermented Foods              17

4.1:                  Cultural Identification and Biochemical Characteristics of the Isolates      33

4.2:                  Determination of Microbial Load                                                                   34

4.3:                  Percentage occurrence of Bacteria                                                                 35

4.4:                  percentage occurrence of Fungi Isolates                                                        36

4.5:                  Determination of pH and Hydrogen Cyanide content                                    37

 

 

 


 

 

CHAPTER ONE

INTRODUCTION


1.1       BACKGROUND OF STUDY

Cassava (Manihot esculenta cranzt) is a food crop of great importance for the nutrition of over 500 million people in the tropic. Cassava roots are potentially toxic due to presence of cyanogenic glycoside especially linamarin (Butler, 1965). Microbial deterioration occurs in cassava roots after harvest accompanied by physiological deterioration. The fermentation of cassava prevents the root from rapid spoilage after harvest. Cassava roots are more perishable than other tuber crops, such as yam and sweet potato (Poulter et al., 1995). The fermentation of cassava roots called retting allows the reduction of potentially toxic endogenous cyanogens, which are present in variable concentrations (300-500ppm) and improves their palatability for further processing.

Microorganism plays a number of roles in cassava processing either positive or negative. The pH effects are generally regarded as part of fermentation process namely, product preservation, flavor development, cyanide elimination etc. while the negative effect include spoilage of cassava product and contamination by pathogenic microorganism.

Retting of cassava involves steeping roots in water for 3 to 4 days, during the consequent fermentation; roots are softened (Okafor et al., 1984). In Africa, the retted roots are mainly processed into foo-foo (cassava flour). These products provide almost 50% of the caloric intake of the population.

To make cassava suitable for human consumption, it is usually subjected to different processing method, which varies from location to location. Such method generally aims at reducing the toxicity, improving palatability and converting the perishable fresh roots into stable product. The fermentation process is initiated as a result of chance inoculation by microorganisms from the environment. The presence of unspecified microorganisms complicates the control of the fermentation process and lead to the production of objectionable odours.

Despite the economic importance of these processed products, most of the published work of cassava retting as focused on the detoxification of the cyanogenic glycosides during fermentation (Ampe, et al., 1995). Utilization of cassava for food has been greatly affected by the presence of cyanogenic glycosides (Linamarin). Cyanide is very poisonous because it binds to an enzyme cytochrome oxidase and stops its action in respiration, which is a key energy conversion process in the body. Therefore to provide a basis for understanding the microbiology of this fermentation is needed to improve the quality of this staple food, determine the microbial load of the flour and to monitor the hydrogen cyanide content of the processed flour.


1.2       AIMS AND OBJECTIVES.

The specific aims of this research work include:

1.     To produce cassava flour by fermentation

2.     To determine the microbial succession and load of cassava during fermentation and after production.

3.     To reduce the toxicity of the hydrogen cyanide content in cassava through fermentation.


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