MICROBIAL ANALYSIS OF LOCALLY PREPARED READY TO EAT OKPA

  • 0 Review(s)

Product Category: Projects

Product Code: 00009038

No of Pages: 46

No of Chapters: 1-5

File Format: Microsoft Word

Price :

₦3000

  • $

ABSTRACT


This study was aimed at evaluating the microbiological quality of ready to eat okpa sold in Umuahia metropolis. A total of ten (10) sampled of okpa were collected from two different sales point comprising of five nylon wrapped okpa and five leaf wrapped okpa. The samples were processed aseptically in sterile peptone water and diluted serially in the 10-fold serial dilution. Appropriate diluents were inoculated into nutrient agar for total bacteria count. The samples were also inoculated into MacConkey agar for total coliforn count and potato dextrose agar for fungal counts. The bacterial isolates identified based on their morphological and biochemical characteristics were Bacillus species, E. coli, S. aureus, Mucor species and penicillium species. From the present study the microbial count of okpa revealed that the samples had the total Heterotrophic bacteria counts which ranged from1.0 x 106cfu/g to 7.0 x 106cfu/g, total fungal count range from 1.1 x 104 to 2.9 x 104 and the total coliform count is 1.3 x103. It was observed in this study that S. aureus is the most frequently occurring isolates with a high percentage occurrence of 70% and the least bacteria specie E. coli with a percentage occurrence of 40%. Among the fungal species, Mucor specie is the most predominant and occurring at 40% and penicillium species at 30%. Conclusively, this study revealed facts about okpa showing it's poor shelf life associated with uncontrolled fermentation and packaging on the products and also underscores the need to maintain improved hygiene.







TABLE OF CONTENTS

 

Title page                                                                                                                                                        ii

Certification                                                                                                                                                   iii

Dedication                                                                                                                                                      iv

Acknowledgements                                                                                                                                        v

Table of contents                                                                                                                                            vi

List of tables                                                                                                                                                   viii

Abstract                                                                                                                                                          ix

 

CHAPTER ONE   INTRODUCTION

1.1       Introduction                                                                                                                1

1.2       Objectives                                                                                                                   3

 

CHAPTER TWO   LITERATURE REVIEW

2.1       Origin of Bambara groundnut                                                                                     4

2.2       Varieties and cultivars of Bambara groundnut                                                           5

2.3       Nutritional composition of Bambara groundnut                                                        6

2.4       Anti-nutritional components of Bambara groundnut                                                 6

2.5       Processing and utilization of Bambara groundnut                                                     7

2.6       Pest and disease of Bambara groundnut                                                                     10

2.7       Food spoilage                                                                                                              10

2.7.1    Removal of microorganisms                                                                                      11

2.7.2    Low temperature                                                                                                        11

2.7.3    High temperature                                                                                                        11

2.7.4    Water availability                                                                                                       11

2.7.5    Chemical based preservation                                                                                      12

2.7.6    Microbial product based inhibition                                                                            12

2.8       Microbiological safety                                                                                                12

2.9       Food package                                                                                                              13

2.10     Food control system                                                                                                   14

 

CHAPTER THREE: MATERIALS AND METHODS

3.1       Area of the Study                                                                                                        15

3.2       Sample Collection                                                                                                      15

3.3       Media Preparation                                                                                                      15

3.4       Sample Preparation                                                                                                     16

3.5       Viable count                                                                                                                16

3.6       Identification of isolates                                                                                             16

3.7       Gram staining                                                                                                             16

3.8       Biochemical test                                                                                                         17

3.8.1    Catalase test                                                                                                                17

3.8.2    Coagulase                                                                                                                   17

3.8.3    Indole test                                                                                                                   17

3.8.4    Citrate utilization test                                                                                                 18

3.8.5    Urease test                                                                                                                  18

3.8.6    Hydrogen sulphide production test                                                                             18

 

CHAPTER FOUR: RESULT

4.1       Introduction                                                                                                                20

4.2       Discussion                                                                                                                   25

 

CHAPTER FIVE:  CONCLUSION AND RECOMMENDATIONS

5.1       Conclusion                                                                                                                  28

5.2       Recommendation                                                                                                       28

References                                                                                                                  29

 

 

 

 


LIST OF TABLES

1: Total heterotrophic bacterial and fungal counts of hawked Oklahoma samples                       21

2:  Morphological and biochemical characteristics of the isolation                                       22

3:  Macroscopic and microscopic features of isolated fungi                                                  23

4: Frequency of occurrence of isolates                                                                                   24


 


 

 

 

CHAPTER 1

1.1       INTRODUCTION

Ready to eat foods are defined as foods easily purchased from the food vendors such as restaurants or food hunt. These kinds of foodsare consumed at the point of sale without any further treatment such as heating. In the western part of Nigeria such Abia, Imo Enugu and Anambra foods such as okpa, abacha, fufu, eba and rice aremostly purchased at food vendors. Despite theexcessive patronage of these food vendors/handlers; it is very essential to ensure the safetylevel of these foods from contaminants andmicroorganisms. In some of the Eastern states of Nigeria “Okpa” is considered as second to bread. The bambara seeds are also known to have different names among the different ethnic groups in Nigeria and its regarded as an important legume following its socioeconomic and utilization value (Akpaluet al., 2013). The Igbo call it “Okpa”, the Hausa call it “Fuijiya while the Yoruba’s call it “Erivour”. As a legume crop. It is divided into group namely, the pulse and oil seed.The food legume has a major role to play in the fight against malnutrition and therefore is necessary that their level of consumption, which is already too low in a number of developing countries, should be increased. Over the years Food borne disease outbreak linked with Ready-To-Eat foods have been associated with various foodborne pathogens (Gilbrethet al., 2005; Gibbons et al., 2006). Foodborne diseases are a major global problem causing considerable morbidity and mortality annually (Hanson et al., 2012). Bacteria such a Salmonella species, Escherichia coli and Staphylococcus aureuscan cause food poisoning and other food-borne diseases such a tuberculosis, typhoid fever and cholera (Foskettet al, 2003). Some symptoms of food borne illness among others include stomach pain, diarrhea, vomiting, nausea and headache.

 

The global incidence of foodborne diseases is difficult to estimate but it hasbeen reported that in 2000 alone, 2.1 million people died from diarrheal diseases. A greatproportion of these cases can be attributed tocontamination of food and drinking water (Geneva, 2000). Many studies have shown that the most commonbacteria associated with RTE food areSalmonella spp., Listeria monocytogenes,Campylobacter jejuni, Staphylococcus aureus,Bacillus cereus and Clostridium perfringens. Anumber of observational studies have shown thatthese foods are sometimes held at impropertemperatures, excessively handled by foodvendors and sold at very dirty surroundings (Muinde and Kuria, 2005; Gosh et al 2007).

In addition, the vendors practice poorpersonal hygiene and reports of food vendorsbeing carriers and therefore could serve as apotential source of transmission of enteric feversare many (Oranusiet al., 2013).Most of the food handlers have no proper formaleducation in food handling which can alsopromote transmission of food borne illness. Themajority of students on Campus do not preparefood themselves or take it along with them to theUniversity. This demand for food givesopportunity to the Cafeterias and sellersto serve as the major vending sites wherestudents purchase food daily.

Foodborne illness can be prevented by good hygiene practices such as the use of Hazard Analysis Critical Control Point (HACCP) application in the chain of food production, processing and storage (Oranusiet al., 2004). Educating the food handlers/food vendors on food safety practices and strict supervision of ready-to-eat foods sold to students and staff in the University should be properly investigated by the relevant authorities to prevent epidemics of food borne illness within the university and environment.


1.2       OBJECTIVES

This study aimed to analyze the microbial quality of ready to eat foods produced by various sellers in Umuahia metropolis.

The specific objective is :

·       To isolate and characterize microorganism from okpa.

·       To compare the microbial quality of okpa collected among different sellers.

 

 

Click “DOWNLOAD NOW” below to get the complete Projects

FOR QUICK HELP CHAT WITH US NOW!

+(234) 0814 780 1594

Buyers has the right to create dispute within seven (7) days of purchase for 100% refund request when you experience issue with the file received. 

Dispute can only be created when you receive a corrupt file, a wrong file or irregularities in the table of contents and content of the file you received. 

ProjectShelve.com shall either provide the appropriate file within 48hrs or send refund excluding your bank transaction charges. Term and Conditions are applied.

Buyers are expected to confirm that the material you are paying for is available on our website ProjectShelve.com and you have selected the right material, you have also gone through the preliminary pages and it interests you before payment. DO NOT MAKE BANK PAYMENT IF YOUR TOPIC IS NOT ON THE WEBSITE.

In case of payment for a material not available on ProjectShelve.com, the management of ProjectShelve.com has the right to keep your money until you send a topic that is available on our website within 48 hours.

You cannot change topic after receiving material of the topic you ordered and paid for.

Ratings & Reviews

0.0

No Review Found.


To Review


To Comment