<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">FNS</journal-id><journal-title-group><journal-title>Food and Nutrition Sciences</journal-title></journal-title-group><issn pub-type="epub">2157-944X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fns.2015.615145</article-id><article-id pub-id-type="publisher-id">FNS-61333</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Nutritional and Anti-Nutrient Composition of Three Kola Nuts (&lt;i&gt; Cola nitida, Cola acuminata &lt;/i&gt; and &lt;i&gt; Garcinia kola &lt;/i&gt;) Produced in Benin
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>urand</surname><given-names>Dah-Nouvlessounon</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adolphe</surname><given-names>Adjanohoun</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Haziz</surname><given-names>Sina</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pacôme</surname><given-names>A. Noumavo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nafan</surname><given-names>Diarrasouba</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Charles</surname><given-names>Parkouda</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yann</surname><given-names>E. Madodé</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mamoudou</surname><given-names>H. Dicko</given-names></name><xref ref-type="aff" rid="aff6"><sup>6</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lamine</surname><given-names>Baba-Moussa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff4"><addr-line>Département de Technologie Alimentaire, IRSAT/CNRST, DTA, Ouagadougou, Burkina Faso</addr-line></aff><aff id="aff5"><addr-line>Département de Nutrition et Sciences Alimentaires, FSA, Université d’Abomey-Calavi, Cotonou, Bénin</addr-line></aff><aff id="aff2"><addr-line>Centre de Recherches Agricoles Sud, Institut National des Recherches Agricoles du Bénin, Attogon, Bénin</addr-line></aff><aff id="aff1"><addr-line>Laboratoire de Biologie et de Typage Moléculaire en Microbiologie, FAST, Université d’Abomey-Calavi, 
Cotonou, Bénin</addr-line></aff><aff id="aff3"><addr-line>UFR des Sciences Biologiques, Université Péléforo Gon Coulibaly, Korhogo, C?te d’Ivoire </addr-line></aff><aff id="aff6"><addr-line>Laboratoire de Biochimie Alimentaire, Enzymologie, Biotechnologie Industrielle et Bioinformatique, Université de Ouagadougou, Ouagadougou, Burkina Faso</addr-line></aff><pub-date pub-type="epub"><day>10</day><month>11</month><year>2015</year></pub-date><volume>06</volume><issue>15</issue><fpage>1395</fpage><lpage>1407</lpage><history><date date-type="received"><day>16</day>	<month>October</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>17</month>	<year>November</year>	</date><date date-type="accepted"><day>20</day>	<month>November</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Kola nuts were regularly chewed by West Africans and Beninese in particularly. The aim of this study was to investigate nutritional and anti-nutrient content of three Benin’s kola nuts (
  <em>Cola nitida, Cola acuminata</em> and 
  <em>Garcinia kola</em>). Proximate composition of the three species of kola nuts was assessed using standard analytical AOAC methods. Phenolics and flavonoids contents were determined by Folin-Ciocalteu and aluminum trichloride methods, respectively. Mineral composition was determined by Atomic Absorption Spectrometry method. Free and total amino acids were separated and quantified by HPLC. Protein content of the three kola nuts ranges from 4.95% (
  <em>G. kola</em>) to 10.64% (
  <em>C. acuminata</em>) whereas fat content ranges from 0.2 &#177; 0.00 (
  <em>C. nitida</em>) to 2.5 &#177; 0.42 (
  <em>G. kola</em>). Total phenolics abounded (2444.96 &#177; 81.56 μg Eq AG/100g) in 
  <em>C. acuminata</em>, while flavonoids predominated (561.69 &#177; 22.10 μgEqQ/100g) in 
  <em>G. kola</em>. The three species are a good source of magnesium and a copper provider was lowest in C. nitida (0.59 &#177; 0.08 mg/g) and in
  <em> C. acuminata</em> (0.65 &#177; 0.02 mg/g). The dominant total essential amino acids were threonine (
  <em>C. acuminata</em>) and methionine (
  <em>C. acuminata</em> and
  <em> G. kola</em>), while the predominant non-essential total amino acids according to species were arginine (
  <em>C. nitida </em>and 
  <em>G. kola</em>), proline (
  <em>C. acuminata</em>) and cysteine (
  <em>G. kola</em>). For the anti-nutrients factors, saponins were in great proportion (8.33% &#177; 0.25%), while the oxalates were in small proportion (0.44% &#177; 0.04%). The three species have an interesting nutritional composition, but these seeds have the relatively lowest amino acids content.
 
</p></abstract><kwd-group><kwd>Kola Nuts</kwd><kwd> Polyphenolic Compound</kwd><kwd> Micronutrient</kwd><kwd> Benin</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Plants are important in human being everyday existence. They provide our foods, produce the oxygen that we breathe, and use as raw materials for many industrial products such as clothes, foot wears and so many others. Plants also provide raw materials for our buildings and in the manufacture of dyes, perfumes, pesticides and drugs [<xref ref-type="bibr" rid="scirp.61333-ref1">1</xref>] . These plants contain the wild fruits currently used for their fruits, seeds, kernels, flowers, sap and other edible products. Indeed, these elements are important in diets food and could powerfully help to solve or minimize the problems of food insecurity [<xref ref-type="bibr" rid="scirp.61333-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.61333-ref3">3</xref>] . Wild fruits are an important (quality and quantity) part of the diet, especially for children [<xref ref-type="bibr" rid="scirp.61333-ref4">4</xref>] . Some wild fruits also can be kept for 4 - 5 months during the dry season [<xref ref-type="bibr" rid="scirp.61333-ref5">5</xref>] . It is generally accepted that the concentration of vitamin C in the indigenous wild fruits is higher than that in exotic fruits [<xref ref-type="bibr" rid="scirp.61333-ref6">6</xref>] . The protein content of seeds and kernels of native species is high. The wild fruits are also good sources of carbohydrate, calcium, magnesium and potassium [<xref ref-type="bibr" rid="scirp.61333-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.61333-ref8">8</xref>] .</p><p>Kola nut (Cola spp.) belongs to the Steruliacea plant family with over 20 species native to the Africa tropical rain forest [<xref ref-type="bibr" rid="scirp.61333-ref9">9</xref>] . Cola nitida and Cola acuminata are the most common Cola species used. These species are sources of caffeine in processing and pharmaceutical industries and often chewed by some ethnic’s group settings as stimulants [<xref ref-type="bibr" rid="scirp.61333-ref10">10</xref>] . The presence of other chemicals in kola nuts such as kolanin and theobromine also makes them suitable for use in drug preparation [<xref ref-type="bibr" rid="scirp.61333-ref11">11</xref>] . In addition, research has shown some potential uses of kola nut in the production of wine, chocolate and many non-alcoholic beverages [<xref ref-type="bibr" rid="scirp.61333-ref12">12</xref>] . Apart of those two species cited above, there is Garcinia kola (angiospermae) belonging to the Clusiaceae family [<xref ref-type="bibr" rid="scirp.61333-ref13">13</xref>] . The seeds of G. kola are currently used in traditional medicine in many herbal formulations and have potential therapeutic benefits due largely to the activity of their flavonoids and other bioactive compounds [<xref ref-type="bibr" rid="scirp.61333-ref14">14</xref>] - [<xref ref-type="bibr" rid="scirp.61333-ref16">16</xref>] .</p><p>In Benin the nuts of these three species are regularly chewed and have varied socio-cultural importance. Unfortunately, in the country, very few scientific studies have been carried out on those species [<xref ref-type="bibr" rid="scirp.61333-ref17">17</xref>] . Apart of the biochemical characterization and the nutritional properties of seeds, it is important to investigate the anti-nu- trienal factors [<xref ref-type="bibr" rid="scirp.61333-ref18">18</xref>] . Indeed, the anti-nutritional factors have been described as substances that block or inhibit important metabolic pathways, especially digestion [<xref ref-type="bibr" rid="scirp.61333-ref19">19</xref>] . These substances are known to reduce the bioavailability of many nutrients such as proteins, vitamins and minerals. For example, minerals and trace elements are inefficiently and variably absorbed from diet due to many factors including anti-nutrients such as phytates, oxalates, tannins, and cyanides in foods [<xref ref-type="bibr" rid="scirp.61333-ref20">20</xref>] . Against this background the following questions are raised: 1) what is the composition of nutritional compounds of studying Benin’s kola nuts? 2) What is the anti-nutritional profile of these three species nuts? In this direction, the essence of this research is to examine the proximate, nutritional and anti-nutrient composition of three species of kola nut collected in Benin.</p></sec><sec id="s2"><title>2. Material and Methods</title><sec id="s2_1"><title>2.1. Collection and Sample Preparation</title><p>Fresh nuts of three plants (C. nitida, C. acuminata and G. kola) were collected in the village of Adjarra (6˚24'0&quot;N, 2˚12'0&quot;E), Oueme region, Benin. The red variety of C. nitida and C. acuminata, were collected. After collection, the nuts were identified at Benin National Herbarium, University of Abomey-Calavi. Smooth kola powder (nuts dried 25˚C &#177; 2˚C for 12 days and milled) as well as fresh nut were stored in airtight glassware and kept in darkness at −20˚C until use.</p></sec><sec id="s2_2"><title>2.2. Nutritional Analysis</title><sec id="s2_2_1"><title>2.2.1. Proximate Analysis</title><p>Standard methods of the Association of Official Analytical Chemists AOAC [<xref ref-type="bibr" rid="scirp.61333-ref21">21</xref>] were used to determine the moisture, crude fat, crude protein, crude fiber, total ash contents of the nuts. Moisture content was determined by desiccation of 5 g of sample to a constant weight at 105˚C for 3 hours. Crude protein content was determined by Kjeldahl method using 6.25 as conversion constant. Crude fat content was assessed though Soxhlet method using petroleum ether as organic solvent. The total sugars were measured by spectrometry method [<xref ref-type="bibr" rid="scirp.61333-ref22">22</xref>] at 492 nm using D-glucose as standard. Reducing sugars were also measured by spectrometry method described by Miller [<xref ref-type="bibr" rid="scirp.61333-ref23">23</xref>] with a reagent 3.5 dinitrosalicylic acid (DNS) at 546 nm using maltose as standard.</p></sec><sec id="s2_2_2"><title>2.2.2. Determination of Total Phenolic Compound</title><p>Total phenolics were quantified in extracts made from 1/15 sample (w:v) fresh nuts of each species once ground with mixer grinder using Folin-Ciocalteu’s method described by Singleton [<xref ref-type="bibr" rid="scirp.61333-ref24">24</xref>] and adapted to 96 well-plate. At first it was revealed the extraction capacity of six solvents (water, water-HCl 1%; ethanol; ethanol-HCl 1%; methanol and methanol-HCl 1%) with C. nitida. Twenty five microlitre of Folin-Ciocalteu’s reagent (50% v/v) was added to 10 &#181;l of 1 mg/ml (w/v) of the nuts extract dissolved in solvents. After incubation (5 mn) at room temperature, 25 &#181;l of 20% (w/v) sodium carbonate (Na<sub>2</sub>CO<sub>3</sub>) and water were added to a final volume of 200 &#181;l per well. Blanks were prepared by replacing the reagent by water to correct for interfering compounds. After incubation (30 min), the absorbence was read at 760 nm using a multiwell plate reader. All the assays were carried out at least in triplicate. Gallic acid (0 - 500 &#181;g/ml) was used as standard and results were expressed as microgram gallic acid equivalent per 100 gram of extract. The solvent that extracts the number of compound was used to determine the total phenolic content of C. acuminata and G. kola following the same method described above.</p></sec><sec id="s2_2_3"><title>2.2.3. Determination of Total Flavono&#239;ds Compound</title><p>The total flavonoids of each sample were quantified by aluminum trichloride method described by Yi et al. [<xref ref-type="bibr" rid="scirp.61333-ref25">25</xref>] and adapted to 96 well-plates. Hundred microlitre of methanolic AlCl<sub>3</sub> (2%) were mixed with 100 &#181;l of appropriate dilution of extracts solution. After incubation (15 min), the absorbence were read at 415 nm with a software “Gen5” using a multi plate Epoch spectrophotometer Biotech connected to a computer against a blank (mixture of 100 &#181;l methanolic extract solution and 100 &#181;l methanol) and compared to a quercetin (0 - 50 &#181;g/ml) calibration curve (R<sup>2</sup> = 0.99). The flavonoid content was expressed as microgram of quercetin equivalents per 100 g of extract.</p></sec><sec id="s2_2_4"><title>2.2.4. Determination of Micro-Nutriments</title><p>The mineral contents (Zn, Mg, Ca, Cu and Fe) of each sample were determined by Atomic Absorption spectrometry after dry ashing of the samples according to method describe by Pinta et al. [<xref ref-type="bibr" rid="scirp.61333-ref26">26</xref>] . Vitamin C was determined by colorimetrie method with 2,6-dichloroph&#233;nolindoph&#233;nol (DIP). For Amino acid profile, separation and quantification of free and total amino acids was accomplished by High Performance Liquid Chromatography (HPLC) with PICO∙TAG method described by Bildlingmeyer et al. [<xref ref-type="bibr" rid="scirp.61333-ref27">27</xref>] . After drying, redrying, hydrolysis and derivatization, 100 &#181;l syringes is used to inject 40 &#181;l samples into the HPLC injector equipped of waters in + line-degaser AF 600 controller and dual l absorbance detector waters 2487 id.nr.13300261. Four microlitre of injection volume is analyzed.</p></sec></sec><sec id="s2_3"><title>2.3. Anti-Nutritional Factors Analysis</title><p>Tannin content was determined by spectrometry method as described by Sombi&#233; et al. [<xref ref-type="bibr" rid="scirp.61333-ref28">28</xref>] . The results were expressed as milligramme of tannic acid equivalents (TAE) per 100 mg of extract (mg TAE/100mg extracts). The content of saponins was determined according to Sathya et al. [<xref ref-type="bibr" rid="scirp.61333-ref29">29</xref>] method. The gravimetric method previously described by Mir et al. [<xref ref-type="bibr" rid="scirp.61333-ref30">30</xref>] was used in the determination of kola nuts total alkaloid contents. Phytic acid was determined according with Lucas and Markakas [<xref ref-type="bibr" rid="scirp.61333-ref31">31</xref>] procedure.</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Proximate Analysis</title><p>The proximate composition of the three species of kola nut is shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Proximate composition of different species of kola nut</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameter (% DM)</th><th align="center" valign="middle"  colspan="3"  >Content (Mean &#177; SD)</th></tr></thead><tr><td align="center" valign="middle" >C. nitida</td><td align="center" valign="middle" >C. acuminata</td><td align="center" valign="middle" >G. kola</td></tr><tr><td align="center" valign="middle" >Moisture</td><td align="center" valign="middle" >12.46 &#177; 0.80</td><td align="center" valign="middle" >10.20 &#177; 0.80</td><td align="center" valign="middle" >8.46 &#177; 0.83</td></tr><tr><td align="center" valign="middle" >Dry matter (DM) %</td><td align="center" valign="middle" >87.53 &#177; 0.80</td><td align="center" valign="middle" >89.80 &#177; 0.80</td><td align="center" valign="middle" >91.53 &#177; 0.83</td></tr><tr><td align="center" valign="middle" >Total ash</td><td align="center" valign="middle" >3.00 &#177; 0.50</td><td align="center" valign="middle" >3.50 &#177; 0.86</td><td align="center" valign="middle" >2.00 &#177; 0.50</td></tr><tr><td align="center" valign="middle" >Fat</td><td align="center" valign="middle" >0.20 &#177; 0.00</td><td align="center" valign="middle" >1.20 &#177; 0.28</td><td align="center" valign="middle" >2.50 &#177; 0.42</td></tr><tr><td align="center" valign="middle" >Protein</td><td align="center" valign="middle" >10.06 &#177; 0.75</td><td align="center" valign="middle" >10.64 &#177; 0.50</td><td align="center" valign="middle" >4.95 &#177; 0.25</td></tr><tr><td align="center" valign="middle" >Total sugars (TS)</td><td align="center" valign="middle" >5.18 &#177; 0.56</td><td align="center" valign="middle" >5.57 &#177; 0.12</td><td align="center" valign="middle" >6.27 &#177; 0.61</td></tr><tr><td align="center" valign="middle" >Reducing sugars (% TS)</td><td align="center" valign="middle" >8.30 &#177; 0.78</td><td align="center" valign="middle" >15.22 &#177; 0.34</td><td align="center" valign="middle" >6.48 &#177; 0.36</td></tr><tr><td align="center" valign="middle" >Energizing value (Kcal∙g<sup>−1</sup>)</td><td align="center" valign="middle" >85.58 &#177; 0.12</td><td align="center" valign="middle" >98.98 &#177; 0.57</td><td align="center" valign="middle" >93.49 &#177; 0.17</td></tr><tr><td align="center" valign="middle" >Crude fibre</td><td align="center" valign="middle" >4.31 &#177; 1.02</td><td align="center" valign="middle" >7.35 &#177; 1.45</td><td align="center" valign="middle" >1.35 &#177; 0.12</td></tr></tbody></table></table-wrap><p>Moisture</p><p>The moisture content of the three species ranged between 8.46 - 12.46, with C. nitida having the highest (12.46 &#177; 0.80) moisture content and G. kola the least (8.46 &#177; 0.83). The values obtained are on the one hand below those found by Ajai et al. [<xref ref-type="bibr" rid="scirp.61333-ref32">32</xref>] , which are between 20.62 - 22.50 for the three species, as well as those found by Odebumi et al. [<xref ref-type="bibr" rid="scirp.61333-ref33">33</xref>] for C. nitida (66.40 &#177; 0.08) and G. kola (60.48 &#177; 0.06). On the over hand, these values are above those obtained by Dewole et al. [<xref ref-type="bibr" rid="scirp.61333-ref18">18</xref>] which obtained 9.73 &#177; 0.02 for C. acuminata and 9.81 &#177; 0.01 for C. nitida and 7.2 &#177; 0.08 for G. kola [<xref ref-type="bibr" rid="scirp.61333-ref1">1</xref>] . This variation of moisture content in the different studies would be related to drying time of the samples before analysis because Lowor et al. [<xref ref-type="bibr" rid="scirp.61333-ref34">34</xref>] showed in their study that the moisture content of a sample varies by drying time of the latter. The high moisture content is an index of spoilage. Too much of moisture in any food sample can make the sample viable for microorganisms growth. This accounts for most of the biochemical and physiological reactions in the plant [<xref ref-type="bibr" rid="scirp.61333-ref35">35</xref>] . Indeed, the low moisture content of the three species of kola nuts is good for their long preservation as it will prevent early spoilage of the nuts. It is like this beneficial to the buyers of three species of kola as most sellers sell by volume and not by weight [<xref ref-type="bibr" rid="scirp.61333-ref36">36</xref>] .</p><p>Protein</p><p>Protein content of the three species ranges from, 4.95 (G. kola) to 10.64% (C. acuminata) but the content of C. nitida (10.06% &#177; 0.75%) is near of those obtains with C. acuminata. Other researches were also showed the proximity between C. nitida and C. acuminata protein content. For the both species, our results were on the one hand higher of those obtained by Arogba [<xref ref-type="bibr" rid="scirp.61333-ref37">37</xref>] with C. nitida (3.5%) and Ajai et al. [<xref ref-type="bibr" rid="scirp.61333-ref32">32</xref>] in Niger which obtained 8.68% for C. nitida and 8.65 for C. acuminata. On the other hand, the results of this study were lower than those obtain Adeyeye et al. [<xref ref-type="bibr" rid="scirp.61333-ref36">36</xref>] concerning C. acuminata (11.95%) and also those obtained by Dewole et al. [<xref ref-type="bibr" rid="scirp.61333-ref18">18</xref>] in Nigeria which obtained 15.24% &#177; 0.58% with C. nitida and 19.14% &#177; 0.25% with C. acuminata. The difference between these studies may be due to pedology and ecological conditions because the water deficit influences the nitrogen supply in the plant [<xref ref-type="bibr" rid="scirp.61333-ref38">38</xref>] . Moreover physiological characteristics of a plant which confers a greater resistance to the nitrogen supply to water deficit are also genetically variable [<xref ref-type="bibr" rid="scirp.61333-ref39">39</xref>] . The protein content relatively high could complement the body’s need of these essential nutrients for growth and development because proteins, another class of food often times referred to as the “Nitrogen-containing natural product”, has been proved to be essential for the survival of human beings and animals [<xref ref-type="bibr" rid="scirp.61333-ref40">40</xref>] . Likewise concerning G. kola, we note that our data were higher than those of Adesuyi et al. [<xref ref-type="bibr" rid="scirp.61333-ref1">1</xref>] which obtained 1.85% &#177; 0.15%. On the contrary Ajai et al. [<xref ref-type="bibr" rid="scirp.61333-ref32">32</xref>] were obtained in their study the content twice higher than ours.</p><p>Fat and Ash</p><p>G. kola presents the higher content (2.5% &#177; 0.42%) in fat while C. nitida have the lowest (0.2% &#177; 0.00%). For C. nitida, this result can be comparable to 0.87% obtains by [<xref ref-type="bibr" rid="scirp.61333-ref32">32</xref>] Ajai et al. (2012). Contrary to our study, Odebunmi et al. [<xref ref-type="bibr" rid="scirp.61333-ref33">33</xref>] have showed that the fat content of G. kola seeds (4.51% &#177; 0.56%) was low to those obtained with C. nitida (5.71% &#177; 0.74%). The low lipid content of these nuts is predictable because these seeds are not oleaginous. For the three species, the ash content is higher than which obtained by Dewole et al. [<xref ref-type="bibr" rid="scirp.61333-ref18">18</xref>] , but the comparable results were obtained by Ajai et al. [<xref ref-type="bibr" rid="scirp.61333-ref32">32</xref>] , Agbeniyi and Ayodele [<xref ref-type="bibr" rid="scirp.61333-ref41">41</xref>] and Adeyeye and Ayejuyo [<xref ref-type="bibr" rid="scirp.61333-ref36">36</xref>] for C. acuminata.</p><p>Carbohydrates and Energy Content</p><p>Among the three species, G. kola has high content of total sugar (6.27% &#177; 0.61%) and also has the lowest content of reducing sugar (6.48% &#177; 0.36%). C. nitida and C. acuminata have similar total sugar content while C. acuminata has highest content of reducing sugar (15.22% &#177; 0.34%). Agbeniyi and Ayodele [<xref ref-type="bibr" rid="scirp.61333-ref41">41</xref>] reported in their study high content of carbohydrate. Furthermore, the results show that G. kola has the highest energy value (93.49 &#177; 0.17 Kcal/g) while C. nitida has the lowest (85.58 &#177; 0.12 Kcal/g).</p><p>The varying composition reported by different authors may imply that the proximate composition of these nuts varies with season, environment and/or condition or time of evaluation.</p></sec><sec id="s3_2"><title>3.2. Polyphenolic and Flavono&#239;ds Content</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> presents the solvent ability to total phenolic compound extraction.</p><p>The best phenolics compound extraction solvent is mixture methanol 1% chlorydric acid. From the starting three solvents (water, ethanol and methanol), the extraction of the phenolic compounds is important when the dipole moment of the solvent is low. The extraction was done therefore according to the polarity of involved solvents. Furthermore, chlorhydric acid addition seems not define the same extraction pattern, but rather revealed a beneficial synergistic effect of extraction ability of each solvent with chlorhydric acid. This effect will vary depending on the solvent and is more beneficial to methanol. Similar results were obtained by Dicko et al. [<xref ref-type="bibr" rid="scirp.61333-ref42">42</xref>] on Sorghum bicolor.</p><p><xref ref-type="table" rid="table2">Table 2</xref> shows the kola nuts total polyphenolic content determined with methanol chlorydric acid (1%) and flavonoids content of three species.</p><p>The three species have a high content of total phenolic compound but which varies according to the plant species. C. acuminata has a high concentration while C. nitida presents a low concentration. Since the three species are regularly chewed, these results are interesting because phenolics can play an important role in adsorbing and neutralizing free radicals, quenching oxygen, or decomposing peroxides. It has been suggested to exert beneficial pharmacological effects on neurological disorders on the basis of in vitro observations [<xref ref-type="bibr" rid="scirp.61333-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.61333-ref44">44</xref>] . Polyphe-</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Variation of C. nitida total phenolics compound according to different solvents. H<sub>2</sub>O: Water; HCl: Chlorydric acid; EtOH: Ethnol; MeOH: Methanol</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/7-2701735x7.png"/></fig><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Polyphenolic and flavono&#239;ds content of three species of kola nut</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Plant species</th><th align="center" valign="middle"  colspan="2"  >Parameters</th></tr></thead><tr><td align="center" valign="middle" >Total phenolic (&#181;gEqAG/100g)</td><td align="center" valign="middle" >Total flavono&#239;ds (&#181;gEqQ/100g)</td></tr><tr><td align="center" valign="middle" >C. nitida</td><td align="center" valign="middle" >679.87 &#177; 5.22</td><td align="center" valign="middle" >374.60 &#177; 80.75</td></tr><tr><td align="center" valign="middle" >C. acuminata</td><td align="center" valign="middle" >2444.96 &#177; 81.56</td><td align="center" valign="middle" >537.38 &#177; 92.99</td></tr><tr><td align="center" valign="middle" >G. kola</td><td align="center" valign="middle" >1970.99 &#177; 35.85</td><td align="center" valign="middle" >561.69 &#177; 22.10</td></tr></tbody></table></table-wrap><p>nolic compounds in plant, exert anti carcinogenic, anti mutagenic and cardio protective effects linked to their free radical scavenging [<xref ref-type="bibr" rid="scirp.61333-ref44">44</xref>] [<xref ref-type="bibr" rid="scirp.61333-ref45">45</xref>] . It has been reported that to be chemopreventive agents by lowering cholesterol and roughly limit cell damage [<xref ref-type="bibr" rid="scirp.61333-ref46">46</xref>] . G. kola has the highest total flavonoids content (561.69 &#177; 22.10 &#181;gEqQ/ 100g). These results show that the total flavonoids represent a large portion in G. kola total phenolics composition. Terashima et al. [<xref ref-type="bibr" rid="scirp.61333-ref47">47</xref>] and Adesuyi et al. [<xref ref-type="bibr" rid="scirp.61333-ref1">1</xref>] reported also that G. kola can be a good dietary source of flavonoids. Indeed, among the three kola nuts, the consumption of G. kola nut would be more advantageous than those of C. nitida and C. acuminata because, flavonoids which are generally found in a variety of foods, such as oranges, tangerines, berries, apples and onions have protective effects including anti inflammatory, anti-oxidant, antiviral, and anti carcinogenic properties [<xref ref-type="bibr" rid="scirp.61333-ref48">48</xref>] .</p></sec><sec id="s3_3"><title>3.3. Micronutrient Content</title><p>The mineral and vitamin C composition of kola nut is shown in <xref ref-type="table" rid="table3">Table 3</xref>.</p><p>The mineral content in the three species of kola nut varied according to species. Calcium (Ca) value ranged between 1.33 - 4.3 mg/g and C. nitida had the highest concentration. C. acuminata and G. kola had the similarly value. However calcium content have not inconsiderable because the level is relatively high compared to the level reported for African Adansonia digitata kernel (0.43 - 3.76 mg/100g) by Ajayi et al. [<xref ref-type="bibr" rid="scirp.61333-ref49">49</xref>] and Nnam and Obiakor [<xref ref-type="bibr" rid="scirp.61333-ref8">8</xref>] . These elements support human biochemical processes by serving structural and functional roles as electrolytes [<xref ref-type="bibr" rid="scirp.61333-ref50">50</xref>] .</p><p>The zinc (Zn) content is relatively low for the three species, but C. acuminata present the highest concentration (1.36 &#177; 0.27 mg/g). Despite the relatively lowest concentration of Zinc, his presence in these nuts is important because zinc has been associated with enzyme systems, particularly oxidation processes [<xref ref-type="bibr" rid="scirp.61333-ref36">36</xref>] . It has a structural and functional role in a large number of macromolecules and is required for over 300 enzymic reactions. Zinc ions (Zn<sup>2+</sup>) participate in all aspects of intermediary metabolism, transmission, and regulation of the expression of genetic information, storage, synthesis, and action of peptide hormones and structural maintenance of chromatin and biomembranes [<xref ref-type="bibr" rid="scirp.61333-ref51">51</xref>] . It is estimated that up to 1% of the human genome codes for zinc finger proteins. In the central nervous system, zinc has an additional role as a neurosecretory product or cofactor [<xref ref-type="bibr" rid="scirp.61333-ref52">52</xref>] .</p><p>Among the three species, the results shown that C. nitida present the highest concentration of iron (4.37 &#177; 0.53 mg/g) while G. kola displayed the lowest (1.37 &#177; 0.17 mg/g). These values differ from earlier reports in other works [<xref ref-type="bibr" rid="scirp.61333-ref53">53</xref>] [<xref ref-type="bibr" rid="scirp.61333-ref41">41</xref>] . The presence in these nuts of this element is good because iron plays an important role for human health [<xref ref-type="bibr" rid="scirp.61333-ref54">54</xref>] . The body requires iron for the synthesis of oxygen transport proteins, in particular hemoglobin and myoglobin, and for the formation of enzymes involved in electron transfer [<xref ref-type="bibr" rid="scirp.61333-ref55">55</xref>] .</p><p>Magnesium is the most abundant mineral element in the three kola nuts. The similarly trend was observed by Agbeniyi and Ayodele [<xref ref-type="bibr" rid="scirp.61333-ref41">41</xref>] and Odebunmi et al. [<xref ref-type="bibr" rid="scirp.61333-ref33">33</xref>] in relation to the studied mineral elements. The magnesium values ranged from 10 &#177; 0.23 mg/g (C. acuminata) to 11.48 &#177; 0.05 mg/g (C. nitida). This account observed in the kola nuts is interesting because, Magnesium is used now, as adjunct to tocolytic therapy, or alone, to prevent premature uterine contractions and preterm births [<xref ref-type="bibr" rid="scirp.61333-ref56">56</xref>] . In addition, magnesium is essential, especially within cells, being the second most common intracellular cation after potassium, with both these elements being vital for numerous physiological functions [<xref ref-type="bibr" rid="scirp.61333-ref57">57</xref>] .</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Micronutrient composition of three species of kola nut</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Elements</th><th align="center" valign="middle"  colspan="3"  >Sample value mg/g (Mean &#177; SD)</th></tr></thead><tr><td align="center" valign="middle" >C. nitida</td><td align="center" valign="middle" >C. acuminata</td><td align="center" valign="middle" >G. kola</td></tr><tr><td align="center" valign="middle" >Ca</td><td align="center" valign="middle" >4.33 &#177; 1.41</td><td align="center" valign="middle" >1.66 &#177; 0.47</td><td align="center" valign="middle" >1.33 &#177; 0.00</td></tr><tr><td align="center" valign="middle" >Zn</td><td align="center" valign="middle" >0.69 &#177; 0.19</td><td align="center" valign="middle" >1.36 &#177; 0.27</td><td align="center" valign="middle" >0.39 &#177; 0.15</td></tr><tr><td align="center" valign="middle" >Fe</td><td align="center" valign="middle" >4.37 &#177; 0.53</td><td align="center" valign="middle" >2.75 &#177; 0.35</td><td align="center" valign="middle" >1.37 &#177; 0.17</td></tr><tr><td align="center" valign="middle" >Mg</td><td align="center" valign="middle" >11.48 &#177; 0.05</td><td align="center" valign="middle" >10.00 &#177; 0.23</td><td align="center" valign="middle" >10.73 &#177; 0.66</td></tr><tr><td align="center" valign="middle" >Cu</td><td align="center" valign="middle" >0.59 &#177; 0.08</td><td align="center" valign="middle" >0.65 &#177; 0.02</td><td align="center" valign="middle" >1.47 &#177; 0.35</td></tr><tr><td align="center" valign="middle" >Vit C (mg/100ml)</td><td align="center" valign="middle" >6.26 &#177; 0.46</td><td align="center" valign="middle" >0.53 &#177; 0.61</td><td align="center" valign="middle" >1.20 &#177; 0.61</td></tr></tbody></table></table-wrap><p>The cooper content in the three kola nuts decreases as follows G. kola &gt; C. acuminata &gt; C. nitida. Whereas C. nitida present the highest value of Vit C (6.26 &#177; 0.46 mg/100 ml) what is not negligible. The vitamin C protects organism against the free radicals because it is the most effective antioxydant. It takes part in several metabolic processes, like the biosynthesis of collagen in conjunctive, and as neurotransmettor. Vit C increases the absorption of calcium and the biodisponibility of iron and is link to the prevention of many degenerative diseases [<xref ref-type="bibr" rid="scirp.61333-ref58">58</xref>] .</p></sec><sec id="s3_4"><title>3.4. Amino Acids Content</title><p><xref ref-type="fig" rid="fig2">Figure 2</xref> shows the auto-scaled chromatogram profile of standard, total and free amino acids while <xref ref-type="table" rid="table4">Table 4</xref> shows their amount.</p><p>The results show that 52.94% (9/17) of amino acids search was obtained in the kola nuts. The total amino acids were more measure than free. In addition, 66.66% of these free amino acids measured were non-essential. For total amino acids, the dominant essential amino acids are threonine (C. acuminata) and methionine (C. acuminata and G. kola), while the predominant non-essential amino acids according to species are arginine (C. nitida and G. kola), and proline (C. acuminata). Beside threonine and lysine are the free essential amino acids measured, therefore the amino acids content varied according to the species. Indeed, 100% of total amino acids measured are present in C. nitida against 90% in C. acuminata and 77.77% in G. kola. Whereas proline is the free amino acids more concentred in the three Cola species but the highest concentration (0.69 &#177; 0.06 w/w % dry weight) is obtained with C. nitida while C. acuminata and G. kola displays the lowest (0.61 &#177; 0.01 w/w % dry weight). However the three species have not great amino acids content, Eleyinmi et al. [<xref ref-type="bibr" rid="scirp.61333-ref59">59</xref>] were reports the relatively low concentrations of amino acids while Adeyeye et al. [<xref ref-type="bibr" rid="scirp.61333-ref60">60</xref>] report the high concentration of amino acids. The difference of results could be explained by the nuts pretreatment before analysis.</p></sec><sec id="s3_5"><title>3.5. Quantitative Anti-Nutrient Screening of Kola Nut</title><p>The <xref ref-type="table" rid="table5">Table 5</xref> shows the anti-nutrient content of three kola nuts. The result shows that C. acuminata has high value (8.33% &#177; 0.25%) of these nuts anti-nutrient (saponin) content while C. nitida has the lowest (0.44% &#177; 0.04%) with the oxalates.</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Total and free amino acids concentration of three species of kola nut w/w% (dry weight)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Amino acids</th><th align="center" valign="middle"  colspan="2"  >C. nitida</th><th align="center" valign="middle"  colspan="2"  >C. acuminata</th><th align="center" valign="middle"  colspan="2"  >G. kola</th></tr></thead><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >Free</td><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >Free</td><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >Free</td></tr><tr><td align="center" valign="middle" >Aspartic acid</td><td align="center" valign="middle" >0.53 &#177; 0.28</td><td align="center" valign="middle" >0.53 &#177; 0.28</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Arginine</td><td align="center" valign="middle" >1.06 &#177; 0.06</td><td align="center" valign="middle" >0.69 &#177; 0.06</td><td align="center" valign="middle" >0.86 &#177; 0.01</td><td align="center" valign="middle" >0.61 &#177; 0.01</td><td align="center" valign="middle" >0.61 &#177; 0.02</td><td align="center" valign="middle" >0.61 &#177; 0.02</td></tr><tr><td align="center" valign="middle" >Threonine<sup>*</sup></td><td align="center" valign="middle" >0.39 &#177; 0.01</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.33 &#177; 0.04</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Alanine</td><td align="center" valign="middle" >0.50 &#177; 0.01</td><td align="center" valign="middle" >0.20 &#177; 0.01</td><td align="center" valign="middle" >0.42 &#177; 0.09</td><td align="center" valign="middle" >0.23 &#177; 0.07</td><td align="center" valign="middle" >0.28 &#177; 0.12</td><td align="center" valign="middle" >0.19 &#177; 0.00</td></tr><tr><td align="center" valign="middle" >Proline</td><td align="center" valign="middle" >0.83 &#177; 0.04</td><td align="center" valign="middle" >0.53 &#177; 0.04</td><td align="center" valign="middle" >1.83 &#177; 0.23</td><td align="center" valign="middle" >1.37 &#177; 0.23</td><td align="center" valign="middle" >0.10 &#177; 0.13</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Valine<sup>*</sup></td><td align="center" valign="middle" >0.35 &#177; 0.01</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.30 &#177; 0.02</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.33 &#177; 0.08</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Methionine<sup>*</sup></td><td align="center" valign="middle" >0.22 &#177; 0.00</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.48 &#177; 0.03</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.43 &#177; 0.26</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Cysteine</td><td align="center" valign="middle" >0.27 &#177; 0.00</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.34 &#177; 0.01</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.19 &#177; 0.27</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Lysine<sup>*</sup></td><td align="center" valign="middle" >0.30 &#177; 0.02</td><td align="center" valign="middle" >0.16 &#177; 0.02</td><td align="center" valign="middle" >0.30 &#177; 0.01</td><td align="center" valign="middle" >0.16 &#177; 0.00</td><td align="center" valign="middle" >0.31 &#177; 0.01</td><td align="center" valign="middle" >0.18 &#177; 0.13</td></tr></tbody></table></table-wrap><p>With<sup>*</sup>: Essential amino acids; Without<sup>*</sup>: Non essential amino acids.</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Anti-nutrient composition of different species of kola nut</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameters</th><th align="center" valign="middle"  colspan="3"  >Kola nuts content (Mean &#177; SD)</th></tr></thead><tr><td align="center" valign="middle" >C. nitida</td><td align="center" valign="middle" >C. acuminata</td><td align="center" valign="middle" >G. kola</td></tr><tr><td align="center" valign="middle" >Alkaloids (%)</td><td align="center" valign="middle" >2.06 &#177; 1.50</td><td align="center" valign="middle" >1.80 &#177; 0.52</td><td align="center" valign="middle" >4.66 &#177; 1.15</td></tr><tr><td align="center" valign="middle" >Saponin (%)</td><td align="center" valign="middle" >4.66 &#177; 0.03</td><td align="center" valign="middle" >8.33 &#177; 0.25</td><td align="center" valign="middle" >5.83 &#177; 0.01</td></tr><tr><td align="center" valign="middle" >Oxalates (%)</td><td align="center" valign="middle" >0.44 &#177; 0.04</td><td align="center" valign="middle" >0.71 &#177; 0.03</td><td align="center" valign="middle" >0.74 &#177; 0.02</td></tr><tr><td align="center" valign="middle" >Phytic acid (%)</td><td align="center" valign="middle" >0.87 &#177; 0.07</td><td align="center" valign="middle" >0.60 &#177; 0.01</td><td align="center" valign="middle" >1.09 &#177; 0.10</td></tr><tr><td align="center" valign="middle" >Tanin (mg TAE/100mg)</td><td align="center" valign="middle" >5.66 &#177; 1.02</td><td align="center" valign="middle" >7.08 &#177; 0.11</td><td align="center" valign="middle" >3.54 &#177; 0.21</td></tr></tbody></table></table-wrap><fig-group id="fig2"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Total, free and standard amino acids auto-scaled chromatogram profile. (a) C. nitida free amino acids; (b) C. nitida total amino acids; (c) C. acuminata free amino acids; (d) C. acuminata total amino acids; (e) G. kola free amino acids; (f) G. kola total amino acids; (g) Pierce H Standard.</title></caption><fig id ="fig2_1"><label>(g)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/7-2701735x8.png"/></fig><fig id ="fig2_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/7-2701735x9.png"/></fig><fig id ="fig2_3"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/7-2701735x10.png"/></fig></fig-group><p>The high value of saponin was foreseeable with the three species because these compounds are glycosides containing a polycyclic aglycone moiety either C<sub>27</sub> steroid or C<sub>30</sub> triterrpenoid attached to carbohydrate and are characterised by a bitter taste and foaming properties [<xref ref-type="bibr" rid="scirp.61333-ref61">61</xref>] . The anti-nutritional effects of saponins have been mainly studied using alfalfa saponins [<xref ref-type="bibr" rid="scirp.61333-ref62">62</xref>] . They also cause haemolysis of red blood cells [<xref ref-type="bibr" rid="scirp.61333-ref63">63</xref>] , and have been demonstrated to have anti-spermal effects on human spermatozoa [<xref ref-type="bibr" rid="scirp.61333-ref64">64</xref>] . Specifically G. kola has the high content of alkaloids (4.66% &#177; 1.15%) and phytic acid (1.09% &#177; 0.10%) than those of the two other species. Similarly, among the three kola nuts, C. acuminata shows the highest value of tannin (7.08 &#177; 0.11 mg TAE/100mg). Tannins are water soluble phenolic compounds with reported antinutritional effects and may be by their ability to form complex with proteins. Indeed, tannins may form a less digestible complex with dietary proteins and may bind and inhibit the endogenous protein, such as digestive enzymes [<xref ref-type="bibr" rid="scirp.61333-ref65">65</xref>] . Besides, in ruminants, dietary condensed tannins (2% - 3%) have been shown to impart beneficial effects because they reduce the wasteful protein degradation in the rumen by the formation of a protein-tannin complex [<xref ref-type="bibr" rid="scirp.61333-ref66">66</xref>] . The low value of oxalates and phytic acid in the three species was good because oxalates and phytates bind minerals like calcium and magnesium and interfere with their metabolism to cause muscular weakness and paralysis [<xref ref-type="bibr" rid="scirp.61333-ref67">67</xref>] .</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>At the end of this study, it appears that the three selected species of kola nuts present an interesting nutritional composition but it varied according to species. The lipid content of the three kola nuts is very low while the protein content is relatively high for C. nitida and C. acuminata. They also have a high energy value. Similarly, the mineral composition of the three species is useful with a high vitamin C content of C. nitida nut in comparison to the two other species (G. kola and C. acuminata). Besides, these three kola nuts contain small quantities of total and free amino acids. In the same way, anti-nutrients factors in these nuts were in low proportion. Thus the nuts of those three kola species can be a good alternative to increase the food security in low income countries.</p></sec><sec id="s5"><title>Acknowledgements</title><p>The authors thank UEMOA for the financial support through the project LBTMM-PAES-UEMOA-2012.</p></sec><sec id="s6"><title>Cite this paper</title><p>DurandDah-Nouvlessounon,AdolpheAdjanohoun,HazizSina,Pac&#244;me A.Noumavo,NafanDiarrasouba,CharlesParkouda,Yann E.Madod&#233;,Mamoudou H.Dicko,LamineBaba-Moussa, (2015) Nutritional and Anti-Nutrient Composition of Three Kola Nuts ( Cola nitida, Cola acuminata and Garcinia kola ) Produced in Benin. Food and Nutrition Sciences,06,1395-1407. doi: 10.4236/fns.2015.615145</p></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.61333-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Adesuyi, A.O., Elumm, I.K., Adaramola, F.B. and Nwokocha, A.G.M. 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