Professional Documents
Culture Documents
INTRODUCTION
Garden egg also known as eggplants are widely grown in most parts of sub-Saharan Africa,
especially, in the urban and rural areas, and they constitute the most macro and micro nutrients
which can be purchased in affordable price. The name “Egg plant” was derived from the shape
of the fruits of some varieties which are white and shaped like chicken eggs (Osei et al., 2010).
The plant (Solanum spp) is a vegetable with increasing popularity in the world (Sanchez et al.,
2010).), and it originated from Tropical Africa. It is an economic flowering plant belonging to
the family Solanaceae, of which members of about 1,400 species are found in the temperate and
tropical regions of the world. The fruits of the plant come in a wide array of shapes and colours,
some are yellow, green, white, yellow stripes and green stripes fruits are widely grown in most
Nutritionally, the fruits of an eggplant contain water (92.5%), protein (1%), fat (0.3%), and
carbohydrates (6%) (Sabo and Dia, 2009). They contain between 30 and 50% of iron (Fe), fiber,
potassium (K), manganese (Mn), copper (Cu) and vitamins; thiamin (vitamin B1), B6, folate,
magnesium (Mg), sodium (Na) and niacin. Eggplant also contains phyto-nutrients such as
nasunin and chlorogenic acid (Sabo and Dia, 2009). It is a very good source of dietary fiber.
Eggplant are medically processed and used in the preparation of condiments and products used in
treating different diseases and health problems (Burkill, 1985). A meal of eggplants is proven to
be of benefits to patients suffering from raised intraocular pressure (glaucoma) and convergence
insufficiency, as well as in heart diseases and Arteriosccerosis (Harish et al., 2008). The plant
can be regarded as a brain food because it houses the anthocyanin phytonutrient found in its skin,
1
Nasunin, a potent antioxidant and free radical scavenger that has been shown to protect cell
However, the presence of toxic factors or anti-nutritional components in eggplants has been one
major challenge in realising the full benefits of the nutritional value. Although the presence of
these anti nutritional factors is always in small quantities, they have been established to play
significant roles in the nutritional quality of food. The anti-nutritional factors (ANFs) interfere
with metabolic processes and availability of nutrients, which may also cause toxicity during
period of scarcity (Chinedu et al., 2011). The ANFs in this vegetable can be either tannins
phytate, oxalate, saponins, alkaloid and cyanides. Tannins have the ability to precipitate certain
proteins. They combine with digestive enzymes thereby making them unavailable for digestion
Phytic acid (inositol hexa phosphate) is an organic acid found in plant materials. Phytic acid
combines with some essential elements such as iron, calcium, zinc and phosphorus to form
insoluble salts called phytate, which are not absorbed by the body thereby reducing the
availability of these elements. Oxalate binds to calcium to form complexes (calcium oxalate
crystals). These oxalate crystals prevent the absorption and utilization of calcium by the body
causing diseases such as rickets and osteomalacia (Ladeji et al., 2004). The calcium crystal may
also precipitate around the renal tubules thereby causing renal stones. The formation of oxalate
crystal is said to take place in the digestive tract. Alkaloids cause gastrointestinal and
2
CHAPTER TWO
LITERATURE REVIEW
Garden egg or eggplant (Solanum melongena L.) Eggplant aubergine or brinjal (South Asia and
South Africa is a plant species in the nightshade family Solanaceae. Solanum melongena is
grown worldwide for its edible fruit. Most commonly purple, the spongy, absorbent fruit is used
As a member of the genus Solanum, it is related to tomato and potato. Like the tomato, its skin
and seeds can be eaten, but, like the potato, it is usually eaten cooked. Eggplant is nutritionally
low in macronutrient and micronutrient content, but the capability of the fruit to absorb oils and
flavors into its flesh through cooking expands its use in the culinary arts (Singh et al., 2006)
It was originally domesticated from the wild nightshade species thorn or bitter apple, S. incanum
probably with two independent domestications: one in South Asia, and one in East Asia (Singh
et al., 2006).
Eggplants have a strong and well-developed root system. The stem is 0.5–2 m tall and may often
be spiny. Leaves are large (10–20 cm), lanceolate, and coarsely lobulated (Figure 21.1). Most
varieties bloom in three to five flowers bunches. Flowers are large, white, or purple-white and
have a five-lobed corolla and large anthers. Their long style difficult self-pollination, but the
plant is mainly autogamous (Zaro et al., 2014). Some early cultivars having ovoid fruit are
thought to be responsible for the name “egg-plant.” The berries require a period of 25–40 days to
reach harvest maturity. In fully developed fruit, the calyx remains as accessory tissue. In contrast
3
to other fruits in which growth and ripening are clearly delimited, eggplant expansion continues
until advanced ripening stages. Remarkable variability in fruit color (white to green, yellow,
purple, black, or striped), shape (ovoid, rounded, elongate, or pyriform), and size (15–1500 g) is
found among cultivars The seeds are white or yellow and may keep their viability for 4–6 years
(Sekara et al., 2007). The edible portion includes the pulp placental tissue and seeds and in some
Different classifications have used to group eggplant varieties. Bailey’s (1947) identified three
varietal groups: var. esculentum which comprises the commercially common forms with
intermediate size, var. serpentinum including varieties with very long fruit, and var. depressum
grouping genotypes with small fruit. Other attributes used for classification purposes are the
pericarp color, the presence of spines in the calyx, and the fruit length covered by the calyx.
Purple eggplants are more popular in Western markets. From a commercial perspective,
Cantwell and Suslow (2013) subdivided the most common varietal groups marketed in the
United States:
American: Oval or globular in shape, firm, with dark purple skin, and green calyx.
Japanese: Oblong, thin, light or dark purple colored skin and very perishable fruit.
White: Small fruit, oval or globular in shape, with thin and light skin.
Eggplant is a warm-season crop that requires 60–85 days for cycle completion. The plant needs a
10–12 h photoperiod and performs best at relatively high temperatures (the optimum being
4
around 23°C–26°C) (Sekara et al., 2007). Thus, the crop is grown during the summer season.
Eggplants are very sensitive to cool weather and do not perform well when exposed to low
temperature. In cool seasons flowering, fertility, and fruit set are severely affected. At 10°C–
12°C growth is arrested and flowering and fructification are markedly compromised. Well-
drained sandy loam, loam, or clay loam soils having a good supply of organic matter and pH of
6.0–6.5 are best for growing eggplants. Plant spacing varies from 45 to 60 cm between plants,
and 60 to 100 cm between rows depending on the cultivar and cultural practices. Since yields
and fruit quality are reduced in 2 year plants, eggplants are normally managed as a single season
2.1.2 Taxonomy
Garden egg belongs to the family Solanaceae and is known under the botanical name Solanum
melongena L. The family contains 75 genera and over 2000 species, out of which, about 150-200
are tuber bearing and belong to section Tuberarium. The majority of species (about 1800) are
non-tuber bearing. Cytological studies have indicated that basic chromosomal number 2n = 24 is
same in almost all the varieties and species. There are 3 main botanical varieties under the
species melongena (Choudhury, 1976). The common garden egg, to which large, round or egg-
shaped fruited forms belong, are grouped under var. esculentum. The long, slender types are
included under var. serpentinum and the dwarf brinjal plants are put under var. depressum.
Taking into account the competition between the vegetative growth and fruit production, garden
5
2.1.3 Composition
Though the level of bioactive components may depend on the cultivar (Zaro et al., 2014), fruit
proximate composition remains fairly constant across genotypes. Water is by far the most
abundant components with more than 90% of the total fruit weight. Fiber is particularly abundant
(3%) compared to other foods and even to other vegetable sources. Proteins and lipids are
present at very low levels. The major sugars are glucose and fructose which range between 0.8%
and 1.5%. Sucrose and maltose are present but in low concentration. Organic acids found at
relatively low levels (0.1%) and are more abundant in the outer pulp (near to the peel) as
opposed to sugars which are more prevalent in the inner flesh (Zaro et al., 2014). As for other
vegetables, eggplant has low energy density (25 and 19 cal per 100 g of raw and cooked fruit,
respectively). The fruit has moderate levels of most vitamins and minerals but are relatively rich
in potassium. The berries are low in sodium and have no cholesterol (Popova1 and Mihaylova,
2019).
Similarly, to other Solanaceous species, eggplants were at once believed to be poisonous due to
the presence of steroidal glycoalkaloids. Recent studies have indicated that low intakes of some
glycoalkaloids may exert some potentially beneficial effects such as the inhibition of some types
of cancerous cells and the formation of complexes with cholesterol (Sánchez-Mata et al., 2010).
Solasonine and solamargine, the main eggplants alkaloids are normally present at nontoxic
6
In the last years, eggplants have received higher interest due to their high levels of bioactive
eggplants ranked within the top 10. Eggplant extracts inhibited inflammation and radical-
hepatoprotective (Akanitapichat et al., 2010) and hypolipidemic effects also reduced plasma
Eggplant berries are not particularly rich in ascorbic acid or carotenoids (Zaro et al., 2014). The
health-promoting effects have been associated with phenolic compounds which are particularly
abundant (0.5%–1.5% dry weight) both in the peel and flesh. Hydroxycinnamic acid derivatives,
and mainly free chlorogenic acid (ChA, 5-O-caffeoylquinic acid) is the major phenolic in
eggplant ChA, 5-O-caffeoylquinic acid is high at early developmental stages and decreases by
50% at commercial harvest maturity (Zaro et al., 2014). Other forms (3-O-, 4-O-, and 5-O-cis
isomers) of caffeoylquinic acid, 3,5- and 4,5-dicaffeoylquinic acid, amide, and acetyl ester
conjugates have been identified. ChA, 5-O-caffeoylquinic acid shows an uneven distribution
within the fruit, being more abundant in the inner pulp than in the outer flesh (near to the peel)
where is mainly associated with fruit fibers and vasculature (Zaro et al., 2014). Other flavonoids,
Garden egg is considered a native to India where the major domestication of large fruited
cultivars occurred. In “Origin of cultivated plants” published in 1886 De Candolle, stated that the
7
species S. melongena has been known in India from ancient times and regarded it as a native of
Asia. Vavilov (1928) was of the opinion that its centre of origin was in the Indo-Burma region.
Various forms, colours and shapes of garden egg are found throughout South-East Asia,
suggesting that this area is an important centre of variation. A centre of diversity is believed to be
in the region of Bangladesh and Myanmar (Former India-Burma border). Evidence to this was
given by Isshiki et al (1994) based on the isoenzyme and morphological variation noticed in
large germplasm collection from India. According to Zeven and Zhukovsky (1975), it originated
in India but spread eastward and by the 5th century B.C. was in China, which became a secondary
centre of variation. Thus, it has been known for the last 1500 years in China. Arabic traders were
responsible for subsequent movement to Africa and Spain. Garden egg cultivation in the
Mediterranean region is relatively recent. Portuguese colonies took it to Brazil. It is now widely
cultivated for its fruits in the tropical, subtropical and warm temperate zones, especially in
Southern Europe and the Southern United States. It was suggested the African origin of this crop,
but there is no evidence that S. melongena is native there though there are spiny African garden
Garden egg is usually transplanted rather than direct seeded in the field as it provides the best
means of establishing a uniform and complete stand of plants. Garden egg seeds germinate one
to two weeks after sowing. Seedlings grown in containers are ideal because they allow field
planting without disturbing the root system. A main stem with 6-10 leaves develop before the
appearance of first flower. Depending on whether the sowing period corresponds to more or less
8
favourable agro climatic conditions, the first flower appears one and a half to three months after
sowing. At the level of each flower, there is dichotomous branching that grows more or less
regularly, depending on the species and variety. The sympodia generally consist of two leaves
and the axillary bud of the leaf below each flower frequently gives rise to a new branch. Growth
and flowering are continuous throughout the life of the plant (Popova1 and Mihaylova, 2019).
2.2 ANTINUTRIENT
Food is an essential part of people’s lives. Despite the world produces enough food for everyone,
over 800 million people still go to bed hungry. Furthermore, malnutrition and hunger-related
diseases cause over 60% of deaths. Eliminating hunger and malnutrition is one of the most
fundamental challenges facing humanity (Popova1 and Mihaylova, 2019). Moreover, food
sufficiency is not the last aspect of importance; food nutritional quality is of critical demand as
well as the effects of the accepted food portion, in particular. From this point of view,
antinutrients raises essential questions about human health and contributes to the understanding
of what people actually eat and what the possible resulting effects can be. Antinutrients are
natural or synthetic compounds that interfere with the absorption of nutrients (Gemede and Ratia,
2014).
synthetic origin, which interfere with the absorption of nutrients, and act to reduce nutrient
intake, digestion, and utilization and may produce other adverse effects. Antinutrients are
frequently related to plant-based, raw or vegan diets and are naturally synthesized in plants
(Gemede and Ratia, 2014). Some of the common symptoms exhibited by a large number of
9
antinutrients in the body can be nausea, bloating, headaches, rashes, nutritional deficiencies, etc.
(Essack et al., 2017). On the other hand, such chemical compounds can be evidently
advantageous to humankind when consumed wisely. In fact, plants, for their own defense,
Although people’s sensitivity to antinutrients widely differs, adequate food processing is initially
recommended to reduce antinutritional factors. A person cannot eliminate antinutrients once they
have been introduced to the body. Eliminating and reintroducing specific foods that contain
antinutrients can clear the correlation between symptoms and effects on human health. In this
regard, the biochemical effects of the anti-nutritional factors are an object of research interest
(Popova1 and Mihaylova, 2019). Most of the secondary metabolites, acting as anti-nutrients,
elicit very harmful biological responses, while some of them are widely applied in nutrition and
as pharmaco-logically-active agents.
Anti-nutrients are found in their highest concentrations in grains, beans, legumes and nuts, but
can also be found in leaves, roots and fruits of certain varieties of plants. The major antinutrients
found in plant-based foods are phytates, tannins, lectins, oxalates, etc. Antinutrients in
vegetables, whole grains, legumes and nuts are a concern only when a person’s diet is composed
Antinutrients has been found to have some very detrimental effect on the body. Oxalate, for
instance, prevents calcium from being absorbed in the body by binding with it (Savage and
Klunklin, 2018). Raw spinach, kale, broccoli and soybeans usually contain oxalates. When
consuming excessive tannins, which are associated with tea, wine, some fruit, and chocolate,
10
enzymes responsible for protein absorption may be inactivated. Consumption of foods rich in
phytate such as grains, nuts and seeds, while peppers, eggplants, and tomatoes may lead a lower
A classic approach to remove antinutrients is to treat the product thermally, use methods such as
antinutrients include saponins, lectins, exorphins, raffinose oligosaccharides e.t.c. (Popova1 and
Mihaylova, 2019).
2.2.1.1 Phytates
Phytates occur in several vegetable products. Seeds, grains, nuts and legumes store phosphorus
as phytic acid in their husks in the form of phytin or phytate salt. Their presence may affect
carbohydrates (Sakamoto et al., 2014). Phytic acid is most concentrated in the bran of grains. In
legumes, phytic acid is found in the cotyledon layer and can be removed prior to consumption
The digestive enzyme phytase can unlocked the phosphorus stored as phytic acid. In the absence
of phytase, phytic acid can impede the absorption of other minerals like iron, zinc, magnesium
and calcium by binding to them (Masum et al., 2011). This results in highly insoluble salts that
are poorly absorbed by the gastrointestinal tract leading to lower bioavailability of minerals.
Phytates also inhibit digestive enzymes like pepsin, trypsin and amylase (Popova1 and
Mihaylova, 2019).
2.2.1.2 Tannins
11
Tannins are a group of water-soluble polyphenols of intermediate to high molecular weight.
Tannins are highly hydroxylated molecules and can form insoluble complexes with
carbohydrates, proteins and digestive enzymes, thereby reducing food digestibility. They can
also bind cellulose and many mineral elements (Santos-Buelga and Scalbert, 2000).
Tannins are two major types, nonhydrolyzable or condensed (catechins) and hydrolysable
tannins (or tannic acid). Condensed tannins are widely distributed in vegetables, fruits, cocoa and
certain grains (Ref’at et al., 2008). On the other hand, hydrolysable tannins are present only in
trace amounts in commonly consumed foods (Chung et al., 1998b). Tannins are abundant in
many plant parts including the fruit, cortex, leaves, roots and other parts (Santos-Buelga and
Scalbert, 2000). In human diets, tannins are present in plant’s beverages, legumes, some cereals,
fruits and berries, herbs and condiments. Tannin-containing foods such as tea and red wine
remain popular and contribute nutritionally significant amounts of tannins. Condensed tannins
experimental animals usually results in diminished weight gain, lowered efficiency of feed
utilization and increased fecal nitrogen. These effects have been interpreted in terms of inhibition
by tannin of the digestion of dietary protein (Ref’at et al., 2008). Recent studies suggest that
inhibition of digestion is much less significant than inhibition of the utilization of digested and
absorbed nutrients. These recognized nutritional inhibitors were reported to inhibit nonheme iron
absorption and adversely affect protein utilization by decreasing its digestibility (Ref’at et al.,
2008). Tannins from different plant species have variable effects on iron utilization. There are
other possible interactions of tannins with vitamin A and zinc in the body (Santos- Buelga and
12
Scalbert, 2000; Layrisse et al., 2000). It has been found that cooking has the ability to decrease
the negative effects of tannin on proteins. This alleviation of negative effects is partly due to
complexing of the proteins of foods with tannins during cooking (Ref’at et al., 2008).
2.2.1.3 Oxalate
Oxalic acid can form soluble (potassium and sodium) or insoluble (calcium, magnesium, iron)
salts or esters called oxalates that are commonly found in plants i.e. leafy vegetables or
synthesized in the body (Akwaowo et al., 2000). Insoluble salts cannot be processed out of the
urinary tract once processed through the digestive system. Calcium oxalate can have a
deleterious effect on human nutrition and health by accumulating kidney stones (Olawoye and
chard, spinach, parsley, beets, rhubarb, black pepper, chocolate, nuts, berries (blueberries, black-
berries) and beans are some of the foods with high amounts of oxalates. Most people can induct
normal amounts of oxalate rich foods, while people with certain conditions, such as enteric and
primary hyperoxaluria, need to lower their oxalate intake. In sensitive people, even small
amounts of oxalates can result in burning in the eyes, ears, mouth, and throat; large amounts may
cause abdominal pain, muscle weakness, nausea, and diarrhea (Popova1 and Mihaylova, 2019).
2.2.1.4 Alkaloids
Alkaloids are a class of naturally occurring organic compounds that mostly contain basic
nitrogen atoms. This group also includes some related compounds with neutral and even weakly
acidic properties (Luch, 2009). Some synthetic compounds of similar structure may also be
13
termed alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain
oxygen, sulfur and, more rarely, other elements such as chlorine, bromine, and phosphorus.
Alkaloids are produced by a large variety of organisms including bacteria, fungi, plants, and
animals. They can be purified from crude extracts of these organisms by acid-base extraction, or
solvent extractions followed by silica-gel column chromatography. Alkaloids have a wide range
chelerythrine), and antihyperglycemic activities (e.g. piperine). Many have found use in
traditional or modern medicine, or as starting points for drug discovery. Other alkaloids possess
psychotropic (e.g. psilocin) and stimulant activities (e.g. cocaine, caffeine, nicotine,
theobromine), and have been used in entheogenic rituals or as recreational drugs. Alkaloids can
be toxic too (e.g. atropine, tubocurarine). Although alkaloids act on a diversity of metabolic
systems in humans and other animals, they almost uniformly evoke a bitter taste. (Kittakoop et
al., 2014)
edible garden egg ( Solanum macrocarpon L, (purple)) and (Solanum macrocarpon L, (yellow))
14
CHAPTER THREE
3.1 MATERIALS
3.2 METHODS
Matured fruits of the various S. melongena (eggplants) varieties were purchased from local
Markets in Ekpoma, Esan-west Local Government Area of Edo state and transported to the
department of Biochemistry Lab, Ambrose Alli University for processing and further analysis.
15
Matured fruits of the various S. melongena (eggplants) varieties were identified and
authenticated at the Department of Biochemistry Lab, Ambrose Alli University, Ekpoma. The
fruits were then diced, dried, pulverized and stored in two containers labelled sample A and
A part of extract residue was dissolved in 2N HCL and then filtered. 1 ml of this solution
was transferred to separatory funnel and washed with 10 ml chloroform (3 times). The
pH of this solution was adjusted to neutral with 0.1N NaOH. Then 5 ml of BCG solution
and 5 ml of phosphate buffer were added to this solution. The mixture was shaken and
complex extracted with 1, 2, 3 and 4 ml chloroform by vigorous shaking, the extract was
4,000rpm for 10 min. 1 ml of 0.03 M Ferric solution was added to the supernatant and
left to stand for 15 min in order to allow chelation of the iron molecules by the
indigenous plant phytate. At the end of the incubation, it was capped and heated for 20
min, 7.5 ml of distilled water was added to it and vortexed. Thereafter, 0.1 ml of 1.33 M
16
NH4SCN (Ammonium sulphocyanide) solution was added and absorbance read at
465nm. The amount of phytate was extrapolated from a standard calibration curve for
calcium phytate.
The titrimetric method of Day &Underwood (1986) was used in the determination of
oxalate in the two S. melongena varieties. 150 ml of 15N H 2SO4 was added to 5 g of the
pulverized Solanum sample and the solution was carefully stirred intermittently with a
magnetic stirrer for 30 minutes and filtered using 1 filter paper, after which 25 ml of the
filtrate was collected and titrated against 0.1 N KMnO4 solution until a faint pink color
Spectrophotometric method of Trease & Evans (1989) was used in the determination of
tannin in the two varieties of S. melongena. 5g of the powdery form of Solanum samples
were extracted with 20ml of warm water and filtered. 0.5ml of the filtrate was added to
0.5 ml of 0.5M ferric solution in an alkaline medium and allowed to stand for 30 minutes
for color development. The absorbance was read at 760 nm and the amount of tannin was
17
3.5 STATISTICAL ANALYSIS
Statistical analysis was carried out using IBM SPSS statistical package version 26. The data were
subjected to an independent t-test with the means considered to be significantly different when (P
<0.05)
CHAPTER FOUR
RESULT
Table 4.1. Comparative levels of some antinutritional component in two varieties of edible
garden.
Parameter
Solanum melongena L. Solanum melongena L.
(Purple) (yellow)
Oxalate 4.03 ± 0.025 2.80 ± 0.095
Phytate 4.13 ± 0.176 4.12 ± 0.116
Alkaloids 2.83 ± 0.050 3.02 ± 0.017
Tannins 1.1 0.003 ND
Result are presented as mean ± standard error of the mean (SEM) of the triplicate. Means
with different superscripts within the same row are significantly different (P>0.05).
18
CHAPTER FIVE
DISCUSSION AND CONCLUSION
5.1 DISCUSSION
Antinutritional factors are primarily associated with compounds or substances of natural or
synthetic origin, which interfere with the absorption of nutrients, and act to reduce nutrient
intake, digestion, and utilization and may produce other adverse effects. Antinutrients are
frequently related to plant-based, raw or vegan diets and are naturally synthesized in plants.
Some foods have been found to contain this antinutrients more than the others. Research has
shown that the consumption foods with high antinutrients content impedes the digestion of other
nutrients in the food and its accumulation may lead to very fatal complication.
This study was carried out to investigate some antinutrients components of edible garden egg and
From the observed result of this study recorded in Table 4.1, there was a significant different in
the composition of oxalate between sample A (Solanum melongena L. Purple) and sample B
(Solanum melongena L. Yellow) Sample A was found have a higher content of oxalate and
sample B with values of (4.03 ± 0.025 and 2.80 ± 0.095) respectively. Although there was
19
significant difference between the oxalate content of the two varieties of edible garden egg, their
In this study no significant difference was observed between in the pyhtate content of the two
samples, as both samples phytate content were similar at p<0.05 with values of (4.13 ± 0.176 and
4.12 ± 0.116) respectively. The daily recommended intate of phytate is 2100-2500mg hence we
can say that this varieties of edible garden are within the recommended amount.
From the observed result of this study as recorded in table 4.1., there was also no significant
difference observed in the Alkaloids content of the two samples. In this research study, tannin
was undetected for sample B and a very minute amount was detected which can easily be
In comparison with other studies the antinutrients content of the two varieties studies seem to be
low when compared with other varieties. Tannin was reported to be slightly present in other
varieties Solanum aethiopicum L. and Solanum macrocarpon L. (Chinedu et al., 2011). Also the
oxalate, phytate and alkaloids contents of this two varieties were also low when compared to the
those of other varieties such as Solanum aethiopicum L. and Solanum macrocarpon L. (Chinedu
Ossamulu et al reported close values to that of this study when it examined nutrient and
macrocarpon L (round), Solanum gilo, and Solanum macrocarpon L, (oval) but his values were
still slight higher that of this studies. This difference can easily be accounted for as a result of
20
different methods used or precision of his equipment being that an automated equipment was
5.2 CONCLUSION
From our observation it can be concluded that these varieties of edible garden egg are very save
for consumption as the antinutrients content falls with the recommended range by the world
health organization.
REFERENCES
Akanitapichat, P., Phraibung, K., Nuchklang, K., Prompitakkul, S. (2010). Antioxidant and
hepatoprotective activities of five eggplant varieties. Food Chemistry and Toxicology.
48(10): 3017–3021.
Akwaowo, E.U., Ndon, B.A. and Etuk, E.U. (2007). Minerals and antinutrients in fluted
pumpkin (Telfairia occidentalis Hook f.). Food Chemistry. 70(2):235-40.
Bailey, L. (1947). The Standard Cyclopedia of Horticulture. Macmillan, New York. pp. 234-323.
Chinedu, S.N., Olasumbo, A.C., Eboji, O.K., Emiloju, O.C., Arinola, O.K. and Dania, D.I.
(2011). Proximate and Phytochemical Analyses of Solanum aethiopicum L. and Solanum
macrocarpon L. Fruits. Research Journal of Chemical Sciences. 1(3): 234-263.
Choudhary, B (1976) Vegetables (4th edn.), National Book Trust, New Delhi, pp.50-58
Emem, E.U.and Adedayo, B.C. (2017). In-vitro characterization and biological properties of
polyphenols extract of ripe garden egg (Solanum gilo). Journal of Experimental Biology
and Agricultural Sciences. 5(1).061.069
21
Essack, H., Odhav, B. and Mellem, J.J. (2017). Screening of traditional South African leafy
vegetables for selected anti-nutrient factors before and after processing. Food Science
and Technology. 3: 462-1.
Gemede, H.F. and Ratia, N. (2014). Antinutritional factors in plant foods: potential health
benefits and adverse effects. International Journal of Nutrition and Food Science.
3(4):284-289.
Harish, B.N., Babu, P.A., Mahesh, T. and Venkatesh, Y.P. (2008). A cross–Sectional Study
on the Prevalence of Food Allergy to Eggplant. Clinical and Experimental Allergy. 1:22-
34.
Isshiki, S., Okubo, H. and Fujieda, K. (1994). Genetic control of isozymes in eggplant and its
wild species. Euphytica. 80: 145-150
Layrisse, M., Garcia-Casal, M.N., Solano, M.A., Arguello, F., Liovera, D., Ramirez, J.,
Leets, I. and Tropper, E. (2000). New property of vitamin A and beta-carotene on
human iron absorption: effect on phytate and polyphenols as inhibitors of iron absorption.
Arch. Latinoam. Nutr. 50: 243-248
Luch, A. (2009). Molecular, clinical and environmental toxicology. Springer. New York. p. 20
Masum, A., Crawford H, Berthold J, Talukder ZI, Hossain K. (2011). Minerals (Zn, Fe, Ca
and Mg) and antinutrients (Phytic acid) constituents in common bean. American Journal
of Food Technology. 6(3): 235-43.
22
Olawoye, B.T. and Gbadamosi, S.O. (2017). Effect of different treatments on in vitro protein
digestibility, annutrients, anoxidant properties and mineral composition of
Amaranthus viridis seed. Cogent Food Agric. 3: 1.
Osei M.K., Banful1 B., Osei C K. and Oluoch M. O. (2014). Characterization of African
Eggplant for Morphological Characteristics. Journal of Agriculture Science and
Technology. 4(3):33-37.
Ossamulu, I.F., Akanya, H.O., Jigam, A.A. and Egwim, E.C. :(2014). Evaluation of nutrient
and phytochemical constituents of four eggplant cultivars. Elixir Food Science.
73:26424-26428
Ref’at A. A., Hamed R.T.and Heba A (2008). Tannin Contents of Selected Plants Used in
Jordan. Jordan Journal of Agricultural Sciences. 4(3):265
Sakamoto Y, Suzuki Y, Iizuka I, (2014). S46 peptidases are the first exopeptidases to be
members of clan PA. Science Report. 4: 4977.
Sanchez-Mata M-C., Yokoyama W. E., Hong YJ. and Prohens J. (2010).Solasonine and
Solamargine Contents of Gboma (Solanum macrocarpon L.) and Scarlet (Solanum
aethiopicum L.) Eggplants, Journal of Agriculture and Food Chemistry. 58 (9):5502–
5508
23
Sánchez-Mata, M., Yokoyama, W., Hong, Y. and Prohens, J. (2010). Solasonine and
solamargine contents of gboma (Solanum macrocarpon L.) and scarlet (Solanum
aethiopicum L.) eggplants. Jornal of Agriculture and Food Chemistry. 58(9): 5502–5508.
Savage, G. and Klunklin, W. (2018). Oxalates are found in many different european and asian
foods - effects of cooking and processing. Journal of Food Research. 7(3):342-345.
Singh, A.K. Singh, M., Singh, R., Kumar, S and Kallo, G. (2006). Genetic diversity within
the genus Solanum (Solanaceae) as revealed by RAPD markers. Current Science
90(5):23.
Vavilov, N.I. (1928). Geographical centers of our cultivated plants Proc. 5 International
Congress of Genetics, New York, pp. 342-69
Zaro, M.J., Ariel, R., Vicente, C.M., Ortiz, A. Chaves, R. and Concellón, A. (2010).
Eggplant In: Handbook of Vegetable Preservation and Processing. Springer.New York,
pp. 342-69
Zeven, A.C. and Zhukovsky, P.M. (1975) Dictionary of Cultivated Plants and their Centres of
Diversity,Wageningen, Netherlands, p.219
24