BACTERIOLOGICAL QUALITY OF TAPIOCA SOLD IN UMUAHIA

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Product Code: 00008640

No of Pages: 37

No of Chapters: 1-5

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ABSTRACT

The bacteriological quality of tapioca were analyzed for bacterial contamination. Samples were collected from 10 different vendors in 10 different markets (Ahieke, Ariam, Amawom, Ndioro, Ubani, Ahia gate, Orie Ugba, Ahia Umuariaga, Ahia Penno annex market) in Umuahia, Abia state and were transported to the laboratory. These samples were bacteriologically analyzed using a standard method. The samples from Ahiaeke and Ndioro market had the highest total viable count out of 10 samples. Ahia gate and Ahia Ukwu market had the least viable count. During the study the entire samples were contaminated with bacteria. The predominant bacteria isolates from tapioca were E-coli, micrococcus, streptococcus, Klebsella. This study suggested that most of the tapioca sold in the selected markets in Umuahia might be  a source of food poisoning and can cause public health hazards and is also based on the hygiene level of the food vendors and handlers.






TABLE OF  CONTENTS

Title page                                                                                                                                i

Certification                                                                                                                           ii

Dedication                                                                                                                              iii

Acknowledgement                                                                                                                  iv

Table of contents                                                                                                                    v

Lists of Tables                                                                                                                        vii

List of figure                                                                                                                           viii

Abstract                                                                                                                                  ix

 

CHAPTER 1

1.0    Introduction                                                                                                              1

1.1       Aims of the study                                                                                                        2

1.2       Objectives of the study                                                                                               2

1.3       Statement of the problem                                                                                           2

1.4       Significance of study                                                                                                  3

1.5       Scope of study                                                                                                            3

 

CHAPTER 2

LITERATURE REVIEW

2.1 Tapioca                                                                                                                             4

2.2 Classification and processing methods of Tapioca                                                          5

2.2.1 Production Environment:                                                                      7


2.2.2 Microbiology of Processing Tapioca                                              7


2.2.3 Microbial Contamination of Tapioca                                                 7


2.3       Nutritional value of Tapioca                                                                                      8

2.4       Indicator organisms                                                                                                    9

2.4.1    Enterobacteriaceae                                                                                                     9

2.4.2    Escherichia coli                                                                                                          9

2.4.3    Streptococcus species                                                                                                 9

2.4.4    Micrococcus spp                                                                                                         9

2.4.5    Klebsiella spp                                                                                                             10

2.5       Routes of contamination                                                                                            10

 

CHAPTER THREE

3.0       MATERIALS AND METHODS

3.1       Collection of Samples                                                                                                11

3.2       Sites of Collection                                                                                                      11

3.3       Sterilization of Glasswares and Media                                                                       11

3.4       Sample Preparation for Culture                                                                                  11

3.5       Serial Dilution                                                                                                            11

3.6       Plating of Samples (Inoculation)                                                                                12

3.6.1    Incubation                                                                                                                   12

3.7       Colony Counting                                                                                                        12

3.8       Isolation of pure culture (sub culture)                                                                        12

3.9       Identification of bacteria Isolates                                                                               13

3.9.1    Macroscopic examination                                                                                           13

3.9.2    Microscopic Examination                                                                                          13

3.9.3    Gram Staining                                                                                                             13

3.10     Biochemical Test                                                                                                        13

3.10.1  Triple sugar ion test                                                                                                    13

3.10.2  Coagulase Test                                                                                                           14

3.10.3  Catalase Test                                                                                                               14

3.10.4  Indole                                                                                                                          14

3.10.5  Oxidase Test                                                                                                               15

3.10.6  Citrate Utilization Test                                                                                               15

 

CHAPTER FOUR

4.1       RESULT                                                                                                                    16

 

CHAPTER FIVE

DISCUSSION, CONCLUSION AND RECOMMENDATION

5.1       Discussion                                                                                                                   22

5.2       Conclusion                                                                                                                  23

5.3       Recommendation                                                                                                       23

 

REFERENCES

 

 

 

 

 

 

LIST OF TABLES


Table 1:           Distribution of isolates from different sources                                               17

Table 2:           Bacteria isolates obtained from different samples and percentage Occurance                                                                     18

Table 3:           Total Microbial viable counts of the samples                                                19

Table 4:           Antibiotic susceptibility patterns of isolates from samples                                    20

Table 5;           Morphological and biochemical characteristics of isolates                                    21

 

 


 

 

LIST OF FIGURE


Figure1.  Flow chart of Tapioca preparation                                           6

 

 

 

 


 

CHAPTER 1


1.0    INTRODUCTION

Cassava (maniliot utilisima) is a root crop cultivated and consumed as staple  food in many regions of the developing countries. The importance of cassava is attributed to its ability to produce reasonable yields on poor agricultural land (De Bruijn and fresco, 1989). Cassava is well known for its ability to tolerate drought and yet maintain reasonable yields it can be harvested at any time from 7months to 3 years after planting (CIAT, 1993). The root and leaves are consumed and stems are used for propagation. The roots are a good source of carbohydrate and are commonly processed to remove naturally occurring toxins and provide storable products that can be consumed or used in the production of secondary products (Lancaster et al., 1982). Cassava is consumed by more than 500 million people (Cock , 1982) and is a typical crop in developing countries. Cassava root are potentially toxic to the due to the presence of cyanogeinc glucosides especially linamarin (Butler,1965).physiological  deterioration occurs in cassava roots 2-5 days after harvesting followed by microbial deterioration 3-5days later (Rickard and Coursey, 1981).

Cassava farming populations have empirically developed several processing methods for stabilizing cassava and reducing its toxicity(Lancaster et al., 1982).

The fermentation process is initiated as a result of chance inoculation by micro-organisms from the environment. Although, convenient there are concerns about its reliability the  control of which is the basis of all technological measures that are used  to obtain product at a defined quality.

The presence of unspecified microorganisms complicates the control of the fermentation  process and  lead to the production of object ionable odors. Such problems have led to the development of several other processing techniques  suitable for odour less fufu (Okpokiri et al., 1984, Ezeronye, 2003). Okolie et al.(1992)

Tapioca is processed by harvesting cassava tubers, after which they are peeled, washed and cooked. These are then shredded into fine thin slice, and soaked over night for fermentation so as to thoroughly the starch and hydrogen cyanide from the cassava.

It has been established that the nutrient rich crops in Nigeria which are fomented and used as foods. The Nigeria indigenous fermented foods NLFF constitute a group of foods that are produced in homes, village, and small scale cottage industries. They are sold to the rural populace who buy them for food and social ceremonies.


1.1       AIMS OF THE STUDY

To compare the microbial load of tapioca sample from different selected vendors in different markets in Umuahia.


1.2       OBJECTIVES OF THE STUDY

1.     To determine the bacteriological quality of tapioca that is sold in Umuahia

2.     To isolate and identify organism that contaminates tapioca.

3.     To determine the prevalence of pathogenic microganisms present in tapioca.


1.3       STATEMENT OF THE PROBLEM

Water, poor environmental and personal hygiene of handlers and food vendors can serve as the source of contamination.

 

1.4       SIGNIFICANCE OF STUDY

Hazard analysis critical control point (HACCP) application and good manufacturing practices (GMP) implementation is employed to avoid contamination by food vendors or handlers.


1.5       SCOPE OF STUDY

The scope of the study is to identify and isolate the bacteria contamination found in tapioca in Umuahia metropolis.

 

 

 

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