GROWTH PERFORMANCE AND MYCO CHEMICAL CONSTITUENTS OF HYPSIZYGUS ULMARIUS (BULL.:FR.) RED-HEAD FRUIT BODIES CULTIVATED ON SOME AGRO WASTES

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ABSTRACT

 

Mushroom science has gain importance mainly because of the nutritional and medicinal values.  The cultivation of mushroom is seen has a profitable agricultural business. This study investigates the cultivation of Hypsizygus ulmarius using local substrates to evaluate their effect on the yield of fruit-bodies and the mycochemical constituents. The substrates used were coconut fibre (CF), maize straw (MS), sugarcane bagasse (SB), coconut fibre + maize straw (CF+MS), coconut fibre + sugarcane bagasse (CF+SB), maize straw + sugarcane bagasse (MS+SB) and coconut fibre + maize straw + sugarcane bagasse (CF+MS+SB). The result revealed that the mean stipe length ranges from 1.87 - 2.43cm, mean cap size varies from 4.43 - 5.77cm, fresh weight ranges from 2.44 - 5.10g, biological yield ranges from 41.32 - 141.72g and biological efficiency varies from 11.81 - 94.48%. The highest mean stipe length was observed in the substrate CF+MS; while the substrate MS+SB recorded highest mean cap size, fresh weight, biological yield and biological efficiency. The analyses indicated the presence of vitamins in the mushrooms cultivated on different substrates which include vitamin B1 (0.78 - 0.94mg/100g), vitamin B2 (0.29 - 0.50mg/100g), vitamin B3 (1.72 - 2.81mg/100g), vitamin A (5.77 - 8.33mg/100g) and vitamin C (7.57 - 8.64mg/100g). The mushroom harvested from different substrates had a good profile for mineral content to include calcium (198.36 - 290.51mg/100g), magnesium (72.00 - 144.44mg/100g), sodium (6.72 - 9.36mg/100g), potassium (314.41 - 395.63mg/100g) and phosphorus (152.17 - 195.23mg/100g). The fruit-bodies indicated the presence of heavy metal such as zinc (1.13 - 2.40mg/kg), iron (6.28 - 16.98mg/kg), lead (0.17 - 0.25mg/kg), cadmium (0.09 - 0.15mg/kg) and copper (0.12 - 0.21mg/kg). The proximate analyses indicated that the mushroom contained appreciable amount of protein (19.25 - 24.50%), carbohydrate (39.59 - 43.25%), fibre (14.98 - 19.73%), ash ( 7.96 - 10.50%), moisture content (4.33 - 6.28%) and fat (3.80 - 4.20%).The result also shows a varying level of bioactive compounds which include tannin (0.56 - 0.74mg/g), alkaloid (4.80 - 7.90mg/g), phenol (2.82 - 4.55mg/g), flavonoid (3.80 - 4.30mg/g), steroid (0.16 - 0.75mg/g), hydrogen cyanide (0.01 - 0.07mg/g), anthocyanin (0.22 - 0.35mg/g) and saponin (2.60 - 10.00mg/g). The mushroom contained low level of Cadmium and Lead which are considered to be highly toxic, thus making it fit for consumption. Generally, the result revealed that the mushroom is of good quality. It contained nutrients which can help to improve the micronutrients and general well-being of the people.





TABLE OF CONTENTS

Title Page                                                                                                                                i

Declaration                                                                                                                             ii

Certification                                                                                                                            iii

Dedication                                                                                                                                 iv

Acknowledgements                                                                                                                v

Table of Contents                                                                                                                    vi

List of Tables                                                                                                                          ix

List of Figures                                                                                                                         x

List of Plates                                                                                                                           xi

Abstract                                                                                                                                  xii

 

CHAPTER 1: INTRODUCTION

1.1       Background to the Study                                                                                            1

1.2       Statement of the Problem                                                                                           4

1.3       Justification                                                                                                                 5

1.4       Aim and Objectives                                                                                                    5

CHAPTER 2: LITERATURE REVIEW

2.1       Related Work                                                                                                              7

2.2       Elm Oyster (Hypsizygus ulmarius)                                                                             14

2.3       Spawn                                                                                                                         15

2.4       Substrate                                                                                                                     16

2.5       Environment                                                                                                               17

2.6       Mushroom Ecology                                                                                                    19

2.7       Importance of Mushrooms                                                                                         20

2.7.1    Nutritional value                                                                                                         20

2.7.2    Medicinal value                                                                                                          21

2.7.3    Bioremediation                                                                                                           22

 

CHAPTER 3: MATERIALS AND METHODS   

3.1       Description of Study Area                                                                                          23

3.2       Source of Materials                                                                                                    23

3.3       Preparation of the Substrates for Cultivation                                                             23

3.4       Inoculation and Incubation                                                                                         24

3.5       Measurement Parameters                                                                                           24

3.5.1    Stipe length (height)                                                                                                   25

3.5.2    Cap (pileus) diameter                                                                                                 25

3.5.3    Fresh weights                                                                                                              25

3.5.4    Biological yield                                                                                                          25

3.5.5    Biological efficiency                                                                                                  25

3.6       Mycochemical Components                                                                                       25

3.7       Determination of Vitamins                                                                                         25

3.7.1    Determination of vitamin A (retinol)                                                                         25

3.7.2    Determination of vitamin B1 (thiamin)                                                                      26

3.7.3    Determination of vitamin B2 (riboflavin)                                                                   26

3.7.4    Determination of vitamin B3 (niacin)                                                                         27

3.7.5    Determination of vitamin C (ascorbic acid)                                                               27

3.8       Determination of Minerals                                                                                         28

3.9       Determination of Heavy Metals                                                                                 28

3.10     Proximate Analysis                                                                                                     29

3.10.1  Moisture content                                                                                                         29

3.10.2  Determination of protein content                                                                               29

3.10.3  Determination of ash contents                                                                                    30

3.10.4  Determination of carbohydrate                                                                                   30

3.10.5  Determination of fats and oils                                                                                    30

3.10.6  Determination of crude fibre                                                                                      31

3.11     Determination of Bioactive Compounds                                                                    31

3.11.1  Determination of alkaloids                                                                                         31

3.11.2  Determination of saponins                                                                                          32

3.11.3  Determination of phenols                                                                                           32

3.11.4  Determination of flavnoids                                                                                         32

3.11.5  Determination of tannins                                                                                            33

3.11.6  Anthocyanin determination                                                                                        33

3.11.7  Hydrogen cyanide (HCN) determination                                                                   33

3.11.8  Determination of steroid                                                                                             34

3.12     Statistical Analysis                                                                                                     34

CHAPTER 4: RESULTS AND DISCUSSION

 

4.1       Results                                                                                                                        35

4.2       Discussion                                                                                                                   55

CHAPTER 5: CONCLUSION AND RECOMMENDATIONS

5.1       Conclusion                                                                                                                  64

5.2       Recommendations                                                                                                      65

References                                                                                                                              66

Appendix                                                                                                                                80





LIST OF TABLES

4.1:      Effect of substrates on the vitamin composition of

Hypsizygus ulmarius (mg/100g)                                                                     42

 

4.2:      Effect of substrates on the mineral composition of

Hypsizygus ulmarius (mg/100g)                                                                     45

 

4.3       Effect of substrates on the heavy metal composition of

Hypsizygus ulmarius (mg/kg)                                                                         48

 

4.4:      Effect of substrates on the proximate composition of

Hypsizygus ulmarius (%)                                                                                51

 

4.5:      Effect of substrates on the Phytochemical Composition of

Hypsizygus ulmarius (mg/g)                                                                           54

 

 

 


 


 

LIST OF FIGURES

4.1:      Effect of substrates on the stipe length of Hypsizygus  ulmarius                 37

4.2:      Effect of substrates on the cap size of Hypsizygus ulmarius                          38

4.3:      Effect of substrates on the fresh weight of Hypsizygus ulmarius                 39

4.4:      Effect of substrates on the biological yield of Hypsizygus ulmarius                        40

4.5:      Effect of substrates on the biological efficiency of Hypsizygus ulmarius          41

 

 



 

LIST OF PLATES

4.1:      Hypsizygus ulmarius blue pinhead                                                                 57

4.2:      Hypsizygus ulmarius growing on different substrates                                    58

 

 

 

 

 


 

 

CHAPTER 1

INTRODUCTION


1.1 BACKGROUND TO THE STUDY

The quest for food sources by man has been consistent in other to improve his biological functions, health and general well-being. Fungi such as yeast, mushroom, and bracket fungi have been widely utilized as food since the origin of mankind (Rahi et al., 2004). The medicinal as well as nutritional values of edible mushrooms have a long history. Mushrooms contain valuable biological active compounds (Rajewska et al., 2004; Manoharachary et al., 2005; Bernas et al., 2006; Deepalakshmi and Mirunalini, 2014). In many countries, especially Europe and Asia, mushrooms are well known and considered as favourite delicacy. Mushrooms such as the wild species have been long used in traditional Chinese medicine. Mushrooms are usually consumed either in the fresh or processed forms and are considered valuable mainly due to their flavour and palatability. Edible mushrooms have the tendency to contribute greatly to food value by supplying both macro and micro-nutrients in the diet (Stamets, 2000 and Manzi et al., 2001).

 

Mushrooms are large, visible fructification of fungi which can be seen with unaided eyes. They have a well-developed and observable spore-bearing structure called pileus (cap) and stipe (stalk). They are referred to as macro-fungi. A mushroom can also be defined as the spore-bearing, large fleshy fruit body of a fungus and produced on a substrate beneath or above ground (Boa, 2004; Oei and Nieuwenhuijzen, 2005; Stevenson and Lentz, 2007). According to Okwulehie and Odunze (2004b), mushrooms are macro-fungi with distinctive body, which can be hypogenous or epigenous, and large enough to be seen with the naked eye and to be picked by hand. In contrast to the vegetative parts of the mushrooms, that are not easily seen with the unaided eye, the mushroom fruiting bodies are large entities that can be seen with unaided eye (Choi, 2004).  

 

In Nigeria, fungal fruit-bodies naturally appear in forests and farm lands during the early and late raining season (April – June and September – November) in great diversity and quantities (Okwulehie and Ogoke, 2013; Mmaduabuchukwu and Mbadiwe, 2013). In nature, mushrooms grow on different substances such as logs of wood; decomposing agro-wastes, decomposing animal wastes, and soil where they obtain their nutrients through external digestion and absorption by the mycelium (Okwulehie and Ogoke, 2013). Similarly, mushrooms have over the years served as an important source of protein, carbohydrates, minerals and vitamins (Okwulehie et al., 2018). Mushrooms are fungus which has a wide range of species. Mushrooms exhibits one or more of these lifestyles; saprophytism, parasitism and symbiotic parasitism (Kong, 2004; Cheung, 2008 and Gwanama, 2011). They play important roles in the ecosystem due to their ability to degrade substrates and make use of agricultural wastes (Ouzouni et al., 2009 and Lee, 2009).  

 

The cultivation of mushroom has gained importance throughout the world and it is seen as the most versatile and profitable agricultural business all over the world (Ikeji, 2010). However, the production of mushroom is an important tool that can be used for poverty alleviation and tackling lack of adequate nourishment (Imtiaj and Rahman, 2008). The world production of mushroom increased from 4.9metric tons in 1994 to 7 million metric tons valued at $30 billion in 1997. This is an increase from the 350 metric tons produced in 1965 (Ikeji, 2010). In Nigeria, mushrooms are consumed as food and for medicinal purposes. Akpaja et al. (2005) reported that, over 90% of the populace consume mushrooms as food, while 22% use some mushrooms for medicinal purposes in southern Nigeria. It has been documented that mushrooms are commonly cultivated either for food and/or medicinal purposes or for poverty interventions across tropical and temperate zones (Eswaran et al., 2000). Some common mushrooms cultivated include: (Agaricus), Shiitake (Lentinus), Oyster (Pleurotus), Straw mushroom (Volvariella), Lion’s Head (Hericium), Jew ear (Auricularis), Ganoderma (Reishi), Maitake (Grifola frondosa), Winter mushroom (Flammulina), White jelly (Tremella), Nameko (Pholiota), and Shaggy Mane mushrooms (Coprinus). International mushroom markets are dominated by Agaricus bisporus, Lentinula edodes and Pleurotus spp, which represent three quarters of mushrooms cultivated globally (Eswaran et al., 2000; FAO, 2002; Bhatti et al., 2007).

 

A major environmental problem facing the world today is the contamination of soil, air and marine habitats by agricultural wastes, toxic chemicals from plastics and crude oil (Lamar and White, 2007). Synthetic polymers, such as polyethylene, are generally difficult to degrade by microorganisms. Research on the use of biological treatment has focused on bacteria, with fungal bioremediation (mycoremediation) attracting interest just within the past two decades (Lamar and White, 2007). Many researches have documented the use of Pleurotus species in detoxifying the environment in the process known as bioremediation. P. tuber-regium (a white-rot fungus) has been reported to ameliorate crude oil polluted soils (Isikhuemhen et al., 2003; Adenipekun, 2008) and the resulting soil sample supported the germination and seedling of Vigna unguiculata. Again, heavy metal concentrations in mushroom are considerably higher than those in agricultural crop plants, vegetables, and fruit. This suggests that mushrooms possess a very effective mechanism that enables them to readily take up some heavy metals from the ecosystem. Many wild edible Mushroom species have been known to accumulate great concentrations of heavy metals such as lead, cadmium, iron, copper, manganese, zinc, chromium, nickel, aluminum, and mercury (Demirbas, 2000; Svoboda et al., 2000; Kalaˇc and Svoboda 2001; Falandysz et al., 2003; Dursun et al., 2006; Cocchia et al., 2006; Chen et al., 2009).

 

1.2 STATEMENT OF PROBLEM

Mushroom has gained lots of interests mainly because of their taste, unique texture, flavour, nutritional and medicinal potentials, bioremediation and fungicidal properties. The multidimensional nature of mushrooms has led to increase in its demand. Mushrooms occur naturally in great diversity, quantity and in different habitats. Anthropogenic activities such as deforestation and technological advancement which result in construction of new roads and industries are reducing forest cover which threatens mushroom natural habitat. Similarly, the absence of commercial cultivation of this mushroom have resulted in it scarcity. The bulk of mushrooms consumed especially in Nigeria are hunted for in the forest; the practice which is often associated with some degree of negativity and fatality since poisonous ones could be inadvertently picked and eaten. Hence, there is need to cultivate mushroom outside their natural habitat. The major factor in mushroom cultivation is the substrates. Unpredictable yields due to use of unsuitable substrate has discouraged most small-scale farmers who are often, unable to keep on with mushrooms cultivation. In view of this, there are needs to look for the cheapest substrates that would not only give desired qualities in terms of good taste, vigour and increase in the mycochemical contents of the mushroom. It will ensure the existence and continuity of mushrooms while also providing the opportunity for people to eat their desired mushrooms with maximum assurance at season.

 

1.3 JUSTIFICATION

Mushroom constitutes an integral part of the normal human diet especially in the Eastern part of Nigeria and the amounts of consumption have been raised greatly. Mushrooms have been documented to have food and medicinal values (Fillipie and Umek, 2002; Hu et al., 2006;  Ngai et al., 2006; Okwulehie et al., 2008; Okwulehie et al., 2017). They are seasonal, and in short supply; hence, absent or minimal commercial cultivation may escalate its scarcity. In Nigeria, Hypsizygus ulmarius is a new mushroom variety which is attractive in shape, fleshy and with excellent taste (Sumi and Geetha, 2016). Despite these attractive qualities, its production in tropical climate has not yet been fully explored.  This research stems at looking for a way of cultivating this mushroom, through the use of easily obtainable local wastes to find out their efficiency for the better production of H. ulmarius fruit-bodies in great quantities and qualities. The substrates are chosen mainly because they are cheap and readily available for farmers. This study is also design to strengthen mushroom production sector as it could be essential in order to enable the rural economy to keep its vibrancy and development, increasing and diversifying business and employment opportunities in the rural areas, and providing income opportunities of small family farms.

 

1.4 AIM AND OBJECTIVES

The aim of this study is to produce Hypsizygus ulmarius mushroom on three different agro-wastes to determine their suitability for use by both commercial and small-scale farmers in mushroom production with a view to increase the awareness of people about the significance of this food item. The objectives include:

1.     To undertake the cultivation of Hypsizygus ulmarius to produce fruit-body in the tropical condition

2.     To examine the growth and yield performance of Hypsizygus ulmarius fruit-body cultivated on different agro-wastes

3.     To investigate the relationship between various substrates and the vitamins, minerals, heavy metals, proximate and bioactive composition of Hypsizygus ulmarius cultivated on agro-wastes

 

 

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