EVALUATION OF MICROBIAL QUALITY IN PROCESSED AND PRESERVED PAP

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ABSTRACT


Evaluation of microbial quality in processed and preserved pap was carried out in this study. Two samples of maize (white and yellow) were purchased from Ndoru and Orieugba market in Umuahia Abia State. The microbial load and quality of microorganisms present were determined using pour plate method. Highest heterotrophic bacterial counts occurred at 72 hours in Ndioru market  (8.01x104cfu/ml)) for yellow maize, Highest coliform count at Ndioru market (8.9x102cfu/ml), and Highest fungal count at Ndioru market (4.7x102cfu/ml). The lowest heterotrophic count occurred in 0 hour at Ndioru market for yellow maize (4.0x104cfu/ml), lowest coliform count for White maize 2.0x102cfu/ml) in 0 hour at Orieugba market, (2.9x102cfu/ml) in 0 hour at Ndioru market and 24 hours (2.7x102cfu/ml) for Ndioru market for yellow maize and No growth were recorded for 0 hour in fungal plate count for yellow and white maize. The higher counts were seen in 0 hour for white pap 2.8x104cfu/ml) at Orieugba market and lowest count observed at 72 hours (1.4x104cfu/ml) for yellow pap  at Ndioru market. The coliform plate count had fluctuating count range. Lowest count were observed at 72 hours (0.9x102cfu/ml) in Orieugba market for white pap. The yeast plate count had highest occurrence of (3.7x102cfu/ml) and (1.104cfu/ml) for Ndioru market and Orieugba market for yellow and white pap respectively. Nine (9) microorganism were isolated from this study, they includes Escherichia coliShigella sp., Salmonella sp., Klebsiella sp., Staphylococcus aureusBacillus sp., Saccharomyces cerevisaeLactobacillus sp and Micrococcus sp.  They were identified according to microbiolPapcal guidelines. One (1) fungi, Aspergillus niger was isolated from this study. The highest percentage occurrence of bacteria occurred in Escherichia coli (100%), Salmonella sp. (100%), Bacillus sp. (100%) and Aspergillus sp (100%).  Other bacterial Staphylococcus aureus (50%), Klebsiella sp (50%) and Shigella (50%) have low occurrences for microbial and fungal isolated from steeping of maize varieties. Lactobacillus sp (100%), Saccharomyces cerevisae (100%) and Escherichia coli (100%) had highest occurrence while Micrococcus sp (50%) had lowest occurrences for microbial and yeast isolates from stored pap. The change of pH value and temperature during the steeping of maize for pap production was presented in table 4.1.  The pH values of the white and the yellow maize increased as the steeping hours increases from 0 hr – 72 hrs, while the temperature of the yellow maize and white maize increased tremendously from lower reading 31oC and 31oC to 32oC and 33oC respectively for the maize. . The pH of the pap for 0 hour – 72 hours increased from 4.9 – 5.9 while the temperature increased from 310C - 330C while the TTA increased from 0.13 – 0.27. The water samples were the major sources of microbial contamination of products at all the production stages. The bacteria, yeast and fungi can be linked to the unhygienic practices during production stages. Its recommended that good and personal hygiene practices should be maintained at every stage of production to avoid increase rate in contamination




TABLE OF CONTENTS

Certification                                                                                                                            i

Dedication                                                                                                                              ii

Acknowledgements                                                                                                                iii

Table of Contents                                                                                                                   iv

List of Tables                                                                                                                          v

List of figures                                                                                                                         vi

Abstract                                                                                                                                  vii

CHAPTER ONE

1.0       Introduction                                                                                                                1

1.1       Background of the study                                                                                            1

1.2       Statement of the problem                                                                                           2

1.3       Objectives of the study                                                                                               3

1.4       Significant of the study                                                                                              3

1.5       Scope of the study                                                                                                      4

CHAPTER TWO

2.0       Literature review                                                                                                         5

2.1.1        Types of maize grain                                                                                                   6

2.1.2    Uses of maize grain                                                                                                     7

2.2       Properties of Pap                                                                                                         7

2.2.1        Physical properties of Pap                                                                                           7

2.2.2        Nutritional and chemical properties of Pap                                                                8

2.2.3        Microbial properties of Pap                                                                                         8

2.3          Health hazards of Pap                                                                                                

2.4          Benefits of fermentation                                                                                             9

2.5              Food fermentation in Africa                                                                                       10

2.6              Importance of lactic acid fermentation in Africa                                                       11

2.7        Starter culture in fermented food                                                                               12

2.7.1    Moulds                                                                                                                        12

2.7.2    Yeasts                                                                                                                         12

2.7.3    Bacteria                                                                                                                       12

2.8       Lactic acid bacteria in cereal foods                                                                            13

2.9       Future of fermented foods                                                                                        14

CHAPTER THREE

3.0       Materials and methods                                                                                                17

            3.1       Media used                                                                                                                 17

3.2       Collection of samples                                                                                                  17

3.3       Sample processing                                                                                                       19

3.4       Colony counts of isolated microorganisms                                                                 19

3.5       Characterization and identification of bacteria isolated                                             19

3.5.1    Colony features                                                                                                           20

            3.6       Microscopic features                                                                                                   20

3.7       Gram staining                                                                                                              20

3.7       Biochemical tests                                                                                                        21

3.7.1    Catalase test                                                                                                                21

3.7. 2   Coagulase test                                                                                                             21

3.7.3        Oxidase test                                                                                                                21

3.7.4        Citrate test                                                                                                                  21

3.7.5        Indole test                                                                                                                   22

3.7.6        Motility test                                                                                                                22

3.7.7        Sugar fermentation                                                                                                     22

3.8       Identification of fungi isolates                                                                                   23

            3.9       Physicochemical analysis                                                                                            23

3.9.1    pH determination of the Pap sample                                                                          23

3.9.2    Temperature determination of Pap

CHAPTER FOUR

4.0       Results                                                                                                                        24

CHAPTER FIVE

5.0       Discussion and conclusion                                                                                          37

5.1       Discussion                                                                                                                   37

5.2       Conclusion                                                                                                                  39

5.3       Recommendations                                                                                                      40        References

 

 

 

 

 

 

LIST OF TABLES

Table                                                              Title                                                                Page

 

4.1: Change of pH value and temperature during the steeping of maize for pap production     26

4.4: Morphologiccal and biochemical characterization of bacteria isolated from processed and

       preserved pap                                                                                                                       33                                                                                                         

 4.6: Percentage occurrence of microbial and fungal isolated from steeping of maize varieties 35

 4.7: Percentage occurrence of microbial and yeast isolates from stored pap                               36

 

 

 

 

 

 

 

LIST OF FIGURES

Figure                                                             Title                                                                Page

4.2a: Microbial counts (heterotrophic) during the steeping of maize varieties (102cfu/ml) 27

4.2b: Microbial counts (coliform) during the steeping of maize varieties (102cfu/ml)            28

4.2c: Microbial counts (fungal) during the steeping of maize varieties (102cfu/ml)   29

4.3a: Microbial count (heterotrophic) of stored white and yellow pap                                  30

4.3b: Microbial count (coliform) of stored white and yellow pap                                          31

4.3c: Microbial count (fungal) of stored white and yellow pap                                             32

4.5: Physicochemical parameter of stored pap                                                                        34

 


 

 

 

 

CHAPTER ONE


   1.0          INTRODUCTION

   1.1          BACKGROUND OF THE STUDY

Pap (akamu) is a product of fermented maize (Zea mays) widely eaten in Africa (Amakoromo, 2011). Similar maize preparations in Ghana are referred to as “Akana” or “Kenkey”. Pap is often marketed as a wet cake formerly wrapped in leaves but presently in transparent polythene bags. Gelatinized Pap (a porridge) called “pap” is mainly used as a breakfast meal for adults and weaning food by low income earners who cannot afford the more expensive imported weaning foods (Amakoromo, 2011).

In Nigeria maize is used in the production of Ogi (Yoruba) or Akamu (Igbo). Maize is an important source of carbohydrate, protein, Vitamins B and Minerals. Maize is deficient in two amino acids, lysine and tryptophan making it a poor proteinous food (Jay, 2005). The maize porridge (Pap) has become part of the staple diets for young adults, nursing mothers and weaning ration for infants between the ages of 1-2 yrs (Adebolu, et al., 2007). Pap is a choice meal for patients that are in need of soft and easily digestible foods. Pap is a fermented non-alcoholic starch food that has sour taste. It turns into a semi-solid porridge when cooked. Pap can be consumed with varieties of other food products like bread, fried bean cake (Akara), Moi-moi, fried yam, cooked beans and fried plantain. Pap can also be consumed with milk, tea, sugar and honey to improve its taste and nutrients (Osungbara, 2009).

In most parts of Africa especially in Nigeria, children are fed with mashed adult foods. These foods are bulky and this therefore reduces food intake by a child, often resulting in malnutrition. The development of nutritionally balanced calorie dense, low bulk and easily digestible weaning food becomes mandatory. This involves the use of simple but time consuming traditional technology called fermentation. The traditional fermentation method employed in Pap production is a wild process and microorganisms are not controlled. Microbiological analyses have shown the presence of several genera of bacteria, moulds and yeasts in the fermented maize product- Pap (Amakoromo, 2011)

Pap is fairly acidic (pH 4.8), which tends to inhibit the growth of some bacteria. Its spoilage however, is enhanced by some extrinsic factors amongst which is storage temperature. Extension of the shelf life of Pap is carried out using various techniques, which include refrigeration, freezing and drying (dehydration) to reduce the microbial load and consequently spoilage(Amakoromo, 2011)

Fermentation of Pap is by microorganisms from the environment and quality control is absent in the traditional method of preparation. A lot of nutrient losses occur during processing of cereals for Pap manufacture hence, several attempts have been made to improve the nutritional status of Pap by fortifying it with protein rich substrates. However, nutritional improvements of these fermented cereal gruels with proteineous foods lowered their pasting viscosities and sometimes affected their sensory attributes adversely. These factors are likely to influence consumer acceptability (Osungbaro, 2009).

The microorganisms in Pap have been isolated and identified (Ohenhen, 2002), molds associated with the surface microflora of fermenting corn are Cephalosporium sp, Rhizopus sp, O’ospora sp, Cercospora sp, Fusarium sp and Aspergillus sp, including A. niger and Penicillium sp, Cephalosporium sp predominates. All are eliminated within 6h of steeping. The bacteria are Corynebacterium sp, Clostridium sp, Enterobacter cloacae and Lactobacillus plantarum, Lactobacillus brevis and Acetobacter sp. Yeast isolated were Saccharomyces cerevisiae, Rhodotorula sp and Candida mycoderma. The above microorganisms are not all found in all fermentations (Ohenhen, 2002).


   1.2          STATEMENT OF THE PROBLEM

As a result of the extent in which to which pap is consumed, it is imperative to know how its preparation process is carried out, the step by step approach. Pap is prepared mainly locally, it becomes imperative to know the conditions, sanitary environment, whether it’s exposed to contamination during\ the process of preparation and preservation. The processing and preservation of pap serves as a means of providing a major source of nourishment for large rural populations and contributes significantly to food security by increasing the range of raw material which can be used in the production of edible products (Gabriel, and Akharaiyi, 2007). The use of biological and natural means in the improvement of nutritive value of food products have greater advantages over the use of chemical because biotechnological synthesized products are less toxic and environmentally friendly (Motarjemi, 2002). This study therefore examines the microbial quality of processed and preserved liquid pap.

 

1.3          OBJECTIVES OF THE STUDY

·   The broad objective of the study is to evaluate the microbial quality of processed and preserved pap. The specific objectives of the study are to;

·   To isolate and characterize bacteria involved in the maize fermentation,

·   To analyze the physicochemical parameters during fermentation,

·   To isolate, characterize bacteria in preserved pap.  

 

1.4          SIGNIFICANT OF THE STUDY

One major locally fermented food produced in Nigeria is Pap. Pap is an essential weaning food for infants as well as a dietary staple for adults in West Africa (Bolaji, et al., 2014), prepared from cereals like maize, sorghum and millet (Bolaji, et al., 2014). Omemu (2011) further reported that pap, an acid-fermented cereal gruel is a staple food in several parts of Nigeria. Pap is used as a generic name, but in most states of Nigeria it refers to maize Pap (Ijabadeniyi, 2007). Though Sorghum pap and millet pap which are known as pap baba and papgero respectively also exist and also called furah in some parts of Northern Nigeria (Ijabadeniyi, 2007). Hence this work is aimed at evaluating the microbial quality in processed and preserved pap.

 

1.5          SCOPE OF THE STUDY

Evaluation of microbial quality is the main coverage of this work, with emphasis on the processing and preservation of pap.

 

 

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