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Journal of Biology, Agriculture and Healthcare www.iiste.org
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.4, No.16, 2014
13
Comparative Studies on Some Anti-Nutritional Factors in Seeds
of Mucuna Pruriens (Velvet Beans) and Sphenostylis Stenocarpa
(African Yam Beans)
Amira, P. Olaniyi; Daramola, A. Success and Oyelade W. Abimbola
Department of Science Technology Federal Polytechnic, Ado-Ekiti, Ekiti State, Nigeria
E-mail: philipamira@yahoo.com
Abstract
The concentrations of some anti-nutritional factors present in seeds of Mucuna pruriens (velvet beans) and those
of Sphenostylis stenocarpa (african yam beans) were determined. The seeds of Mucuna pruriens were found to
contain Saponin: 0.30mg/100g, Phytate: 8.33mg/100g, Oxalate: 28.79mg/100g, Cyanogenic glucoside:
9.80mg/100g, Tannin:0.26mg/100g while the seed of Sphenostylis stenocarpa were found to contain Saponin:
0.17mg/100g, Phytate: 6.63mg/100g, Oxalate: 16.33mg/100g, Cyanogenic glucoside: 17.80mg/100g and Tannin:
1.22mg/100g. Consequently, Mucuna pruriens seeds have lower concentration of Cyanogenic glucoside
(9.80mg/100g) than Sphenostylis stenocarpa (17.80mg/100g) and this may make the seeds of Mucuna pruriens
(velvet beans) more fit for consumption because cyanogenic glucoside appears to be the most toxic of all the
anti-nutrients studied.
Keywords: Sphenostylis stenocarpa, Mucuna pruriens, Saponin, Oxalate, Phytate, Cyanogenic glucoside,
Tannin.
Introduction
Mucuna pruriens is a tropical legume known as velvet beans or cowitch. The plant is an annual,
climbing shrub with long vines that can reach over 15m in length. When the plant is young, it is almost
completely covered with fuzzy hairs, but when older, it is almost completely free of hairs. The leaves are
tripinnate, ovate, reverse ovate, rhombus shaped or widely ovate. The sides of the leaves are often heavily
grooved and the tips pointy. In young Mucuna pruriens plants, both sides of the leaves have hairs. The steps of
the leaflets are two to three millimeters long. Additional adjacent leaves are present and about 5mm long (Yerra
et al, 2005).
In the fruit ripening stage, a 4 to 13cm long, a 1 to 2 cm wide, unwinged leguminous fruit develops.
There is a ridge along the length of the fruit. The husk is very hairy and carries up to seven seeds. The seeds are
flattened uniform ellipsoid, 1 to 1.9cm long, 0.8 to 1.3cm wide and 4 to 6.5cm thick. Mucuna pruriens plants
have white, lavenders, or purple flowers. Its seed pods are about 10cm long and covered in loose orange hairs
that cause a severe itch if they come in contact with skin. The chemical compounds responsible for the itch are a
protein, mucunain and serotonin. It is found in tropical Africa, India and the Carribean (Yerra et al, 2005).
In many parts of the world Mucuna pruriens is used as an important forage, fallow and green manure
crop. Since the plant is in the legume family (pear and beans), it with the help of nitrogen-fixing bacteria, take
nitrogen gas from the air and combines it with other chemical compounds producing fertilizer and improving the
soil. Mucuna pruriens is a wide spread fodder plant in the tropics and to that end, whole plant is fed to animals
as silage, dried hay or dried seeds. Mucuna pruriens silage contains 11-25% crude protein, 35-40% crude fibre
and the dried beans 20-35% crude protein (Katzenschlager et al, 2004).
In history, Mucuna pruriens have been used as an effective aphrodisiac. It is still used to increase
libido in both men and women due to its dopamine inducing properties. Dopamine has a profound influence in
sexual function. A typical dose for a man is 15g of ground seeds mixed with cow’s milk (Yerra et al, 2005).
Mucuna pruriens has also recently become popular among lucid dreaming enthusiasts. When combined with
other supplements that stimulate the cholinergic system, the dopamine presumably produced from the
consumption of Mucuna pruriens confers upon the lucid dreamer greater motivation and confidence (Manyam et
al, 2004). Mucuna pruriens is one of the most important sources of L-dopa, a common component of nootropics
(“smart drugs”), it also contain serotonin 5-HTP, nicotine and some decidedly psychoactive compound
(Ramachandran, 2006). Mucuna pruriens pods hairs are a common ingredient in itching powder.
Mucuna pruriens beans have been wining its popularity over the last few years in the natural products
market mainly because of the sport industry, though it has plenty of health benefits. As Mucuna pruriens seed is
proved to increase testosterone and stimulate growth hormone, it makes it rather desirable for men in sport as it
increases muscle mass. Various products (as powders, tinctures, extracts and decoctions) help to gain weight
loss, improve memory, increase libido and for visual enhancement. The seeds of velvet bean are high in protein
(20-29%), lipids (6-7%), dietary fiber (8-10%), ash (3%), carbohydrates (50-60%) and minerals (Adebowale and
Lawal, 2003).
Journal of Biology, Agriculture and Healthcare www.iiste.org
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.4, No.16, 2014
14
According to studies on men, oral intake of the seeds of Mucuna pruriens promotes fertility and sperm
production and also improves erection, duration of coitus, and post-coital satisfaction after only four weeks of
treatment. For years it has been used in folk medicine for treating diarrhea, impotence, intestinal gas, worms,
rheumatic disorders, tuberculosis, cough, sterility, muscular pain, menstrual disorders, diabetes and even
snakebites. All these issues have been proven by animal studies (Guiliano and Allard, 2001).
Sphenostylis stenocarpa (african yam beans) like other legumes, is grown both for its edible seeds and
tubers. It is a vigorous vine, which twines and climbs to a height of about 3m and requires staking. It flowers
profusely in 100 to 150 days, producing a bright colour flowers which may be pink, purple or greenish white.
The slightly woody pods contain 20 to 30seeds and mature within 170 days. The plant produces underground
tubers that are used as food in some parts of African countries that serve as agent of perennation in the wilds
(Duke et al, 1977).
A major factor limiting the wider food use of many tropical plants (including legumes) or also making
the processing lengthen before fit for eating is the ubiquitous occurrence in them of a diverse range of natural
compounds capable of precipitating deleterious effects in man and animals. Manifestation of toxicity range from
source reduction in food intake and nutrients utilization to profound neurological effects and death. Compound,
which act to reduce nutrient and/or food intake are often referred to as anti-nutritional factors (Osagie, 1998).
The medical implication of plants have been highly researched and it has been proven to result from
active principles such as saponins, glycosides, oxalases, acid phenols, toxins, amino acids etc. These agents
have been implicated to have antimicrobial activities (Sofowora, 1987; Asakawa, 1990).
Although toxic compounds are widely distributed in the plant kingdom, it is generally considered that
tropical legumes contain a more complex array of these substances followed by cassava than other crop species.
The presence of these anti-nutritional factors constitute a major setback, limiting the nutritional and food
qualities of plant because they are known to exert a deleterious effect when ingested by man or animal without
adequate processing (Ogun et al, 1989).
Saponins are steroid or terpenoid glycoside often referred to as ‘natural detergents’. There are a group
that are now classified as subgroup of the glycosides and are characterized by their bitter and astringent taste,
foaming properties and their hemolytic effect on the red blood cells. They are widely distributed in the plant
kingdom being found in over five hundred genera (Mahato and Nand, 1991). Saponin have been shown to
possess both beneficial (cholesterol lowering, inhibition of cancer cells, energy booster, antibiotic) and
deleterious properties (Oakenful and Sidhu, 1989).
Oxalate, a C2 dicarboxylic acid anion is produced and accumulated in many crop plants and pasture
weeds. Oxalate may be present in plants as the soluble salts, potassium, sodium or ammonium oxalic acid or as
insoluble calcium oxalate. They possess inhibitory effect on digestion. Oxalate affect calcium and magnesium
metabolism (Oke, 1968) and react with proteins to form complexes, thus presenting an inhibitory action on
peptic digestion (Oboh and Tenic, 1986).
Phytic acid (phytate), a hexaphosphate derivative of inositol is an important storage form of
phosphorous in plants. It is insoluble and cannot be absorbed in the human intestine. Phytic acid has 12
replaceable hydrogen atoms with which it could form soluble salts with metals such as calcium, iron, zinc and
magnesium. Phytate can also inhibit digestibility by chelating with calcium binding with substrate or proteolytic
enzyme (Osagie, 1998).
Glycosides are a group of compound sometimes referred to as glucoside when the basic organic
component is glucose. Glycosides vary considerably in their chemical composition but have in common the
production of a sugar and other substrate known as genin or a glycone on enzyme or acid hydrolysis. Some
glycosides following enzyme hydrolysis, produce hydrocyanic acid and are known as cyanogenic glycosides.
Cyanogenic glycosides are a group of 0-glycosides formed from decarboxylated amino acids (the group arises
from ∝-carbon atom and the amino group).
Any plant phenolic substance with a molecular weight greater than about 500 can be considered to be a
tannin. The two distinctive groups are the hydrolysable tannin so called because they may be readily hydrolysed
into a mixture of carbohydrate and phenols and condensed tannins which are complex flavonoid polymers.
Tannins may decrease protein quantity by decreasing digestibility and palatability. Other nutritional effects
which have been attributed to tannin include damage to intestinal tract, toxicity of tannin absorbed from the gut
and interference with the absorption of iron, a possible carcinogenic effect (Osagie and Eka, 1998). Tannin
compounds accumulate in considerable amount in tissue such as barks, roots, wood, leaves and fruits and prevent
effective utilization of forages by binding to dietary protein, thereby causing digestive problems for grazing
animals.
In this study, results are presented to show the desirability or otherwise of the fitness of seeds of
Mucuna pruriens (velvet beans) for human and animal consumption when compared with seeds of Sphenostylis
stenocarpa (african yam beans) on the basis of the concentrations of some anti-nutritional factors present in them.
Journal of Biology, Agriculture and Healthcare
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.4, No.16, 2014
Materials and Methods
Dry seeds of Mucuna pruriens
Ado-Ekiti and the identity authenticated at the soil and crops unit of the
Federal Polytechnic, Ado-Ekiti, Ekikti State, Nigeria. Dry seeds of
were purchased from Erinfun Market, Ado
Department of Agricultural Technology, Federal Polytechnic, Ado
Saponin content of the samples was determined using filtration and crystallization methods (Harringer,
1994). Determination of oxalate content was accompl
phytate contents of the samples obtained were determined using filtration and titration method (AOAC, 1984).
The concentration of cyanogenic glucoside in the bean samples was determined by distil
titration (Wang and Filled, 1992). Tannin concentration was determined using colorimetric method (AOAC,
1984).
Results
Table 1 shows the concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin as determined fo
seeds of Mucuna pruriens (velvet bean) and
Table 1: Concentrations of saponin, oxalate, phytate, cyanogenic glucoside and tannin of seeds
of Mucuna pruriens (velvet beans) and
Sample Saponin
Mucuna pruriens
Sphenostylis stenocarpa
030
0.17
Values are Mean+S.D. obtained in triplicates.
Fig. 1: Concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin in seeds of
and Sphenostylis stenocarpa.
Discussion
From the results presented, the concentration of saponin in
than those in Sphenostylis stenocarpa
cholesterol lowering, inhibition of cancer cells and energy boosting (Oakenful and Sidhu, 1989).
The concentration of oxalate in
are
093X (Online)
15
Mucuna pruriens (velvet beans) were obtained from the compound of Federal Polytechnic,
Ekiti and the identity authenticated at the soil and crops unit of the Department of Agricultural Technology,
Ekiti, Ekikti State, Nigeria. Dry seeds of Sphenostylis stenocarpa
were purchased from Erinfun Market, Ado-Ekiti and the identity authenticated at the soil and crops unit
Department of Agricultural Technology, Federal Polytechnic, Ado-Ekiti, Ekiti State, Nigeria.
Saponin content of the samples was determined using filtration and crystallization methods (Harringer,
1994). Determination of oxalate content was accomplished using both filtration and titration methods while the
phytate contents of the samples obtained were determined using filtration and titration method (AOAC, 1984).
The concentration of cyanogenic glucoside in the bean samples was determined by distillation, condensation and
titration (Wang and Filled, 1992). Tannin concentration was determined using colorimetric method (AOAC,
Table 1 shows the concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin as determined fo
(velvet bean) and Sphenostylis stenocarpa (african yam bean).
Concentrations of saponin, oxalate, phytate, cyanogenic glucoside and tannin of seeds
(velvet beans) and Sphenostylis stenocarpa (african yam bean).
Saponin Oxalate Phytate Cyanogenic
glucoside
Concentration in mg/100g
030±0.001
0.17±0.001
28.79±0.02
16.33±0.01
8.33±0.01
6.63±0.005
9.80
17.80
S.D. obtained in triplicates.
Fig. 1: Concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin in seeds of
From the results presented, the concentration of saponin in Mucuna pruriens (velvet beans) is higher
Sphenostylis stenocarpa (african yam beans) and saponin have been shown to be beneficial in
cholesterol lowering, inhibition of cancer cells and energy boosting (Oakenful and Sidhu, 1989).
ration of oxalate in Mucuna pruriens is higher than that in Sphenostylis stenocarpa
www.iiste.org
(velvet beans) were obtained from the compound of Federal Polytechnic,
Department of Agricultural Technology,
Sphenostylis stenocarpa (african yam bean)
Ekiti and the identity authenticated at the soil and crops unit of the
Ekiti, Ekiti State, Nigeria.
Saponin content of the samples was determined using filtration and crystallization methods (Harringer,
ished using both filtration and titration methods while the
phytate contents of the samples obtained were determined using filtration and titration method (AOAC, 1984).
lation, condensation and
titration (Wang and Filled, 1992). Tannin concentration was determined using colorimetric method (AOAC,
Table 1 shows the concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin as determined for
Concentrations of saponin, oxalate, phytate, cyanogenic glucoside and tannin of seeds
am bean).
Cyanogenic
glucoside
Tannin
9.80±0.01
17.80±0.01
0.26±0.001
1.22±0.002
Fig. 1: Concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin in seeds of Mucuna pruriens
(velvet beans) is higher
(african yam beans) and saponin have been shown to be beneficial in
cholesterol lowering, inhibition of cancer cells and energy boosting (Oakenful and Sidhu, 1989).
Sphenostylis stenocarpa and
Journal of Biology, Agriculture and Healthcare www.iiste.org
ISSN 2224-3208 (Paper) ISSN 2225-093X (Online)
Vol.4, No.16, 2014
16
oxalate affect calcium and magnesium metabolism (Oke, 1968) and react with proteins to form complexes, thus
presenting an inhibitory action on peptic digestion (Oboh and Tenic, 1986).
The concentrations of phytate in both Mucuna pruriens seeds and Sphenostylis stenocarpa are about the
same. Phytate can also inhibit digestibility by chelating with calcium binding with substrate or proteolytic
enzyme (Osagie, 1998).
The concentration of cyanogenic glucoside in seeds of Sphenostylis stenocarpa is very much higher
than that in seeds of Mucuna pruriens and this may make the seeds of Mucuna pruriens more fit for consumption
because cyanogenic glucoside appears to be the most toxic of all the anti-nutrients studied.
The concentration of tannin in seeds of Mucuna pruriens (0.26mg/100g) is much lower than that in
seeds of Sphenostylis stenocarpa (1.22mg/100g). Tannin may decrease protein digestibility and palatability.
Other nutritional effects which have been associated with tannin include damage to intestinal tract, toxicity of
tannin absorbed from the gut and interference with the absorption of iron and a possible carcinogenic effect
(Osagie and Eka, 1998).
Conclusion
This study has established the presence of anti-nutritional factors in seeds of both the velvet beans
(Mucuna pruriens) and african yam beans (Sphenostylis stenocarpa). But from the results obtained, seeds of
velvet beans (Mucuna pruriens), if properly processed, may be fit for human consumption as well as those of
african yam beans (Sphenostylis stenocarpa). However because of lower cyanogenic glucoside and tannin levels
in seeds of Mucuna pruriens and its numerous beneficial health effects, it may be recommended that meals that
include seeds of Mucuna pruriens be advocated in our diets.
References
Adebowale, K.O. and Lawal, O.S. (2003): Functional Properties and Retrogradation Behaviour of Native and
Chemically Modified Starch of Mucuna Bean (Mucuna pruriens). Journal of Science of Food and
Agriculture, 83: 1543-1546
A.O.A.C (1984): Official Methods of Analysis, 14th
Edition Association of Official Analytical Chemists,
Washington DC, USA.
Asakawa, Y. (1990): Biologically Active Substances from bryophytes. In: Bryophyte Development: Physiology
and Biochemistry, R.N. Chopra, S.C. Bhata(Eds), 259-287, CRC Press, Boca Raton.
Duke, J.A.; Okigbo, B.B. and Reed, C.F. (1997): (Sphenostylis stenocarpare Hocchist ex A. Rich) Harins. Trop.
Grain Leg-Bull 10:4-6 (Sphere Moslylissteocarpa) Trop. Sci., 30 : 59-63
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Oakenfunl, D. and Sidhu, A.S. (1989): Saponins in “Toxicants of Plants Origin” Vol. II Acad. Press, N.Y. 78-
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Oboh, S.A. and Tenic, O. (1986): Some Aspects of the Biochemistry and Nutritional Value of the Sweet Potato
(Ipomea batatas). Ed. Chem. 31 : 9-12.
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Oke, O.L. (1968): Chemical Changes in some Nigerian Vegetable During Growth. Euplt. Agric. , 345-346.
Osagie, A.U. (1998): Some Anti-nutritional Constituents in ten Staple Food Items Grown in Nigeria. Trop. Sc.
(U.K.) 36: 109-112.
Osagie, A.U. and Eka, F.O. (1998): Some Anti-nutritional Constituents in some Food Items Grown in Nigeria.
Trop. Sc. (U.K.) 36 : 109-115.
Ramachandran, P. (2006): Herbs of Siddha Medicines, Murugan pathippagana , 212-219.
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Edition) John
Wiley and Sons, London; 5-12.
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Agron. Soc. Environ 3 : 303-310.
Yerra, R.A.R; Malaya G. and Upal, K.M. (2005): In vitro Lipid Peroxidation and Antimicrobial Activity of
Mucuna pruriens Seeds, Iran J. Pharmacol. & Therapeutics, 4: 32-35.
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Comparative studies on some anti nutritional factors in seeds of mucuna pruriens (velvet beans) and sphenostylis stenocarpa

  • 1. Journal of Biology, Agriculture and Healthcare www.iiste.org ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.4, No.16, 2014 13 Comparative Studies on Some Anti-Nutritional Factors in Seeds of Mucuna Pruriens (Velvet Beans) and Sphenostylis Stenocarpa (African Yam Beans) Amira, P. Olaniyi; Daramola, A. Success and Oyelade W. Abimbola Department of Science Technology Federal Polytechnic, Ado-Ekiti, Ekiti State, Nigeria E-mail: philipamira@yahoo.com Abstract The concentrations of some anti-nutritional factors present in seeds of Mucuna pruriens (velvet beans) and those of Sphenostylis stenocarpa (african yam beans) were determined. The seeds of Mucuna pruriens were found to contain Saponin: 0.30mg/100g, Phytate: 8.33mg/100g, Oxalate: 28.79mg/100g, Cyanogenic glucoside: 9.80mg/100g, Tannin:0.26mg/100g while the seed of Sphenostylis stenocarpa were found to contain Saponin: 0.17mg/100g, Phytate: 6.63mg/100g, Oxalate: 16.33mg/100g, Cyanogenic glucoside: 17.80mg/100g and Tannin: 1.22mg/100g. Consequently, Mucuna pruriens seeds have lower concentration of Cyanogenic glucoside (9.80mg/100g) than Sphenostylis stenocarpa (17.80mg/100g) and this may make the seeds of Mucuna pruriens (velvet beans) more fit for consumption because cyanogenic glucoside appears to be the most toxic of all the anti-nutrients studied. Keywords: Sphenostylis stenocarpa, Mucuna pruriens, Saponin, Oxalate, Phytate, Cyanogenic glucoside, Tannin. Introduction Mucuna pruriens is a tropical legume known as velvet beans or cowitch. The plant is an annual, climbing shrub with long vines that can reach over 15m in length. When the plant is young, it is almost completely covered with fuzzy hairs, but when older, it is almost completely free of hairs. The leaves are tripinnate, ovate, reverse ovate, rhombus shaped or widely ovate. The sides of the leaves are often heavily grooved and the tips pointy. In young Mucuna pruriens plants, both sides of the leaves have hairs. The steps of the leaflets are two to three millimeters long. Additional adjacent leaves are present and about 5mm long (Yerra et al, 2005). In the fruit ripening stage, a 4 to 13cm long, a 1 to 2 cm wide, unwinged leguminous fruit develops. There is a ridge along the length of the fruit. The husk is very hairy and carries up to seven seeds. The seeds are flattened uniform ellipsoid, 1 to 1.9cm long, 0.8 to 1.3cm wide and 4 to 6.5cm thick. Mucuna pruriens plants have white, lavenders, or purple flowers. Its seed pods are about 10cm long and covered in loose orange hairs that cause a severe itch if they come in contact with skin. The chemical compounds responsible for the itch are a protein, mucunain and serotonin. It is found in tropical Africa, India and the Carribean (Yerra et al, 2005). In many parts of the world Mucuna pruriens is used as an important forage, fallow and green manure crop. Since the plant is in the legume family (pear and beans), it with the help of nitrogen-fixing bacteria, take nitrogen gas from the air and combines it with other chemical compounds producing fertilizer and improving the soil. Mucuna pruriens is a wide spread fodder plant in the tropics and to that end, whole plant is fed to animals as silage, dried hay or dried seeds. Mucuna pruriens silage contains 11-25% crude protein, 35-40% crude fibre and the dried beans 20-35% crude protein (Katzenschlager et al, 2004). In history, Mucuna pruriens have been used as an effective aphrodisiac. It is still used to increase libido in both men and women due to its dopamine inducing properties. Dopamine has a profound influence in sexual function. A typical dose for a man is 15g of ground seeds mixed with cow’s milk (Yerra et al, 2005). Mucuna pruriens has also recently become popular among lucid dreaming enthusiasts. When combined with other supplements that stimulate the cholinergic system, the dopamine presumably produced from the consumption of Mucuna pruriens confers upon the lucid dreamer greater motivation and confidence (Manyam et al, 2004). Mucuna pruriens is one of the most important sources of L-dopa, a common component of nootropics (“smart drugs”), it also contain serotonin 5-HTP, nicotine and some decidedly psychoactive compound (Ramachandran, 2006). Mucuna pruriens pods hairs are a common ingredient in itching powder. Mucuna pruriens beans have been wining its popularity over the last few years in the natural products market mainly because of the sport industry, though it has plenty of health benefits. As Mucuna pruriens seed is proved to increase testosterone and stimulate growth hormone, it makes it rather desirable for men in sport as it increases muscle mass. Various products (as powders, tinctures, extracts and decoctions) help to gain weight loss, improve memory, increase libido and for visual enhancement. The seeds of velvet bean are high in protein (20-29%), lipids (6-7%), dietary fiber (8-10%), ash (3%), carbohydrates (50-60%) and minerals (Adebowale and Lawal, 2003).
  • 2. Journal of Biology, Agriculture and Healthcare www.iiste.org ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.4, No.16, 2014 14 According to studies on men, oral intake of the seeds of Mucuna pruriens promotes fertility and sperm production and also improves erection, duration of coitus, and post-coital satisfaction after only four weeks of treatment. For years it has been used in folk medicine for treating diarrhea, impotence, intestinal gas, worms, rheumatic disorders, tuberculosis, cough, sterility, muscular pain, menstrual disorders, diabetes and even snakebites. All these issues have been proven by animal studies (Guiliano and Allard, 2001). Sphenostylis stenocarpa (african yam beans) like other legumes, is grown both for its edible seeds and tubers. It is a vigorous vine, which twines and climbs to a height of about 3m and requires staking. It flowers profusely in 100 to 150 days, producing a bright colour flowers which may be pink, purple or greenish white. The slightly woody pods contain 20 to 30seeds and mature within 170 days. The plant produces underground tubers that are used as food in some parts of African countries that serve as agent of perennation in the wilds (Duke et al, 1977). A major factor limiting the wider food use of many tropical plants (including legumes) or also making the processing lengthen before fit for eating is the ubiquitous occurrence in them of a diverse range of natural compounds capable of precipitating deleterious effects in man and animals. Manifestation of toxicity range from source reduction in food intake and nutrients utilization to profound neurological effects and death. Compound, which act to reduce nutrient and/or food intake are often referred to as anti-nutritional factors (Osagie, 1998). The medical implication of plants have been highly researched and it has been proven to result from active principles such as saponins, glycosides, oxalases, acid phenols, toxins, amino acids etc. These agents have been implicated to have antimicrobial activities (Sofowora, 1987; Asakawa, 1990). Although toxic compounds are widely distributed in the plant kingdom, it is generally considered that tropical legumes contain a more complex array of these substances followed by cassava than other crop species. The presence of these anti-nutritional factors constitute a major setback, limiting the nutritional and food qualities of plant because they are known to exert a deleterious effect when ingested by man or animal without adequate processing (Ogun et al, 1989). Saponins are steroid or terpenoid glycoside often referred to as ‘natural detergents’. There are a group that are now classified as subgroup of the glycosides and are characterized by their bitter and astringent taste, foaming properties and their hemolytic effect on the red blood cells. They are widely distributed in the plant kingdom being found in over five hundred genera (Mahato and Nand, 1991). Saponin have been shown to possess both beneficial (cholesterol lowering, inhibition of cancer cells, energy booster, antibiotic) and deleterious properties (Oakenful and Sidhu, 1989). Oxalate, a C2 dicarboxylic acid anion is produced and accumulated in many crop plants and pasture weeds. Oxalate may be present in plants as the soluble salts, potassium, sodium or ammonium oxalic acid or as insoluble calcium oxalate. They possess inhibitory effect on digestion. Oxalate affect calcium and magnesium metabolism (Oke, 1968) and react with proteins to form complexes, thus presenting an inhibitory action on peptic digestion (Oboh and Tenic, 1986). Phytic acid (phytate), a hexaphosphate derivative of inositol is an important storage form of phosphorous in plants. It is insoluble and cannot be absorbed in the human intestine. Phytic acid has 12 replaceable hydrogen atoms with which it could form soluble salts with metals such as calcium, iron, zinc and magnesium. Phytate can also inhibit digestibility by chelating with calcium binding with substrate or proteolytic enzyme (Osagie, 1998). Glycosides are a group of compound sometimes referred to as glucoside when the basic organic component is glucose. Glycosides vary considerably in their chemical composition but have in common the production of a sugar and other substrate known as genin or a glycone on enzyme or acid hydrolysis. Some glycosides following enzyme hydrolysis, produce hydrocyanic acid and are known as cyanogenic glycosides. Cyanogenic glycosides are a group of 0-glycosides formed from decarboxylated amino acids (the group arises from ∝-carbon atom and the amino group). Any plant phenolic substance with a molecular weight greater than about 500 can be considered to be a tannin. The two distinctive groups are the hydrolysable tannin so called because they may be readily hydrolysed into a mixture of carbohydrate and phenols and condensed tannins which are complex flavonoid polymers. Tannins may decrease protein quantity by decreasing digestibility and palatability. Other nutritional effects which have been attributed to tannin include damage to intestinal tract, toxicity of tannin absorbed from the gut and interference with the absorption of iron, a possible carcinogenic effect (Osagie and Eka, 1998). Tannin compounds accumulate in considerable amount in tissue such as barks, roots, wood, leaves and fruits and prevent effective utilization of forages by binding to dietary protein, thereby causing digestive problems for grazing animals. In this study, results are presented to show the desirability or otherwise of the fitness of seeds of Mucuna pruriens (velvet beans) for human and animal consumption when compared with seeds of Sphenostylis stenocarpa (african yam beans) on the basis of the concentrations of some anti-nutritional factors present in them.
  • 3. Journal of Biology, Agriculture and Healthcare ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.4, No.16, 2014 Materials and Methods Dry seeds of Mucuna pruriens Ado-Ekiti and the identity authenticated at the soil and crops unit of the Federal Polytechnic, Ado-Ekiti, Ekikti State, Nigeria. Dry seeds of were purchased from Erinfun Market, Ado Department of Agricultural Technology, Federal Polytechnic, Ado Saponin content of the samples was determined using filtration and crystallization methods (Harringer, 1994). Determination of oxalate content was accompl phytate contents of the samples obtained were determined using filtration and titration method (AOAC, 1984). The concentration of cyanogenic glucoside in the bean samples was determined by distil titration (Wang and Filled, 1992). Tannin concentration was determined using colorimetric method (AOAC, 1984). Results Table 1 shows the concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin as determined fo seeds of Mucuna pruriens (velvet bean) and Table 1: Concentrations of saponin, oxalate, phytate, cyanogenic glucoside and tannin of seeds of Mucuna pruriens (velvet beans) and Sample Saponin Mucuna pruriens Sphenostylis stenocarpa 030 0.17 Values are Mean+S.D. obtained in triplicates. Fig. 1: Concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin in seeds of and Sphenostylis stenocarpa. Discussion From the results presented, the concentration of saponin in than those in Sphenostylis stenocarpa cholesterol lowering, inhibition of cancer cells and energy boosting (Oakenful and Sidhu, 1989). The concentration of oxalate in are 093X (Online) 15 Mucuna pruriens (velvet beans) were obtained from the compound of Federal Polytechnic, Ekiti and the identity authenticated at the soil and crops unit of the Department of Agricultural Technology, Ekiti, Ekikti State, Nigeria. Dry seeds of Sphenostylis stenocarpa were purchased from Erinfun Market, Ado-Ekiti and the identity authenticated at the soil and crops unit Department of Agricultural Technology, Federal Polytechnic, Ado-Ekiti, Ekiti State, Nigeria. Saponin content of the samples was determined using filtration and crystallization methods (Harringer, 1994). Determination of oxalate content was accomplished using both filtration and titration methods while the phytate contents of the samples obtained were determined using filtration and titration method (AOAC, 1984). The concentration of cyanogenic glucoside in the bean samples was determined by distillation, condensation and titration (Wang and Filled, 1992). Tannin concentration was determined using colorimetric method (AOAC, Table 1 shows the concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin as determined fo (velvet bean) and Sphenostylis stenocarpa (african yam bean). Concentrations of saponin, oxalate, phytate, cyanogenic glucoside and tannin of seeds (velvet beans) and Sphenostylis stenocarpa (african yam bean). Saponin Oxalate Phytate Cyanogenic glucoside Concentration in mg/100g 030±0.001 0.17±0.001 28.79±0.02 16.33±0.01 8.33±0.01 6.63±0.005 9.80 17.80 S.D. obtained in triplicates. Fig. 1: Concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin in seeds of From the results presented, the concentration of saponin in Mucuna pruriens (velvet beans) is higher Sphenostylis stenocarpa (african yam beans) and saponin have been shown to be beneficial in cholesterol lowering, inhibition of cancer cells and energy boosting (Oakenful and Sidhu, 1989). ration of oxalate in Mucuna pruriens is higher than that in Sphenostylis stenocarpa www.iiste.org (velvet beans) were obtained from the compound of Federal Polytechnic, Department of Agricultural Technology, Sphenostylis stenocarpa (african yam bean) Ekiti and the identity authenticated at the soil and crops unit of the Ekiti, Ekiti State, Nigeria. Saponin content of the samples was determined using filtration and crystallization methods (Harringer, ished using both filtration and titration methods while the phytate contents of the samples obtained were determined using filtration and titration method (AOAC, 1984). lation, condensation and titration (Wang and Filled, 1992). Tannin concentration was determined using colorimetric method (AOAC, Table 1 shows the concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin as determined for Concentrations of saponin, oxalate, phytate, cyanogenic glucoside and tannin of seeds am bean). Cyanogenic glucoside Tannin 9.80±0.01 17.80±0.01 0.26±0.001 1.22±0.002 Fig. 1: Concentration of saponin, oxalate, phytate, cyanogenic glucoside and tannin in seeds of Mucuna pruriens (velvet beans) is higher (african yam beans) and saponin have been shown to be beneficial in cholesterol lowering, inhibition of cancer cells and energy boosting (Oakenful and Sidhu, 1989). Sphenostylis stenocarpa and
  • 4. Journal of Biology, Agriculture and Healthcare www.iiste.org ISSN 2224-3208 (Paper) ISSN 2225-093X (Online) Vol.4, No.16, 2014 16 oxalate affect calcium and magnesium metabolism (Oke, 1968) and react with proteins to form complexes, thus presenting an inhibitory action on peptic digestion (Oboh and Tenic, 1986). The concentrations of phytate in both Mucuna pruriens seeds and Sphenostylis stenocarpa are about the same. Phytate can also inhibit digestibility by chelating with calcium binding with substrate or proteolytic enzyme (Osagie, 1998). The concentration of cyanogenic glucoside in seeds of Sphenostylis stenocarpa is very much higher than that in seeds of Mucuna pruriens and this may make the seeds of Mucuna pruriens more fit for consumption because cyanogenic glucoside appears to be the most toxic of all the anti-nutrients studied. The concentration of tannin in seeds of Mucuna pruriens (0.26mg/100g) is much lower than that in seeds of Sphenostylis stenocarpa (1.22mg/100g). Tannin may decrease protein digestibility and palatability. Other nutritional effects which have been associated with tannin include damage to intestinal tract, toxicity of tannin absorbed from the gut and interference with the absorption of iron and a possible carcinogenic effect (Osagie and Eka, 1998). Conclusion This study has established the presence of anti-nutritional factors in seeds of both the velvet beans (Mucuna pruriens) and african yam beans (Sphenostylis stenocarpa). But from the results obtained, seeds of velvet beans (Mucuna pruriens), if properly processed, may be fit for human consumption as well as those of african yam beans (Sphenostylis stenocarpa). However because of lower cyanogenic glucoside and tannin levels in seeds of Mucuna pruriens and its numerous beneficial health effects, it may be recommended that meals that include seeds of Mucuna pruriens be advocated in our diets. References Adebowale, K.O. and Lawal, O.S. (2003): Functional Properties and Retrogradation Behaviour of Native and Chemically Modified Starch of Mucuna Bean (Mucuna pruriens). Journal of Science of Food and Agriculture, 83: 1543-1546 A.O.A.C (1984): Official Methods of Analysis, 14th Edition Association of Official Analytical Chemists, Washington DC, USA. Asakawa, Y. (1990): Biologically Active Substances from bryophytes. In: Bryophyte Development: Physiology and Biochemistry, R.N. Chopra, S.C. Bhata(Eds), 259-287, CRC Press, Boca Raton. Duke, J.A.; Okigbo, B.B. and Reed, C.F. (1997): (Sphenostylis stenocarpare Hocchist ex A. Rich) Harins. Trop. Grain Leg-Bull 10:4-6 (Sphere Moslylissteocarpa) Trop. Sci., 30 : 59-63 Guiliano F. and Allard, J. (2001): Dopamine and Male sexual Function. Eururol, 40 : 601-608. Harringer, L. (1994): Nutrient and Minerals in Cowpea and Pigeon Pea: A Review, Food Chem. 15 : 2719 Katzenschlager, R; Evans, A. and Manson, A. (2004): Mucuna pruriens in Parkinson’s Disease. A Double Blind Clinical and Pharmacological Study J. Neurol Neurosurg Psychiatry 7 : 1672-1677. Mahato, S.B. and Nand, A.K. (1991): Triterpenoid Saponin Discovered with gossypol, Arch-Biochem. Biophys. 84 : 486-489. Manyam B.V.; Dhanase K.M. and Hare T.A. (2004): Neuroprotective Effects of the Anti-parkinson Drug, Mucuna pruriens, Phytotherapy Research, 18(9): 706-712 Oakenfunl, D. and Sidhu, A.S. (1989): Saponins in “Toxicants of Plants Origin” Vol. II Acad. Press, N.Y. 78- 113. Oboh, S.A. and Tenic, O. (1986): Some Aspects of the Biochemistry and Nutritional Value of the Sweet Potato (Ipomea batatas). Ed. Chem. 31 : 9-12. Ogun, P.O.; Markakis, P. and Weth, W. (1989): Effect of Processing on certain Antinutrients in Cowpea (Vigna unguiculata). J. fd Sc. 54:1084-1085. Oke, O.L. (1968): Chemical Changes in some Nigerian Vegetable During Growth. Euplt. Agric. , 345-346. Osagie, A.U. (1998): Some Anti-nutritional Constituents in ten Staple Food Items Grown in Nigeria. Trop. Sc. (U.K.) 36: 109-112. Osagie, A.U. and Eka, F.O. (1998): Some Anti-nutritional Constituents in some Food Items Grown in Nigeria. Trop. Sc. (U.K.) 36 : 109-115. Ramachandran, P. (2006): Herbs of Siddha Medicines, Murugan pathippagana , 212-219. Sofowora, A. (1987): Medicinal Plants and Traditional Potential Medicine in West African (1st Edition) John Wiley and Sons, London; 5-12. Wang, E. and Filled, M. (1992): Effects of Saponins, Phytate, Oxalate and Tannin in Nutrition Biotechnology. Agron. Soc. Environ 3 : 303-310. Yerra, R.A.R; Malaya G. and Upal, K.M. (2005): In vitro Lipid Peroxidation and Antimicrobial Activity of Mucuna pruriens Seeds, Iran J. Pharmacol. & Therapeutics, 4: 32-35.
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