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International Journal of Food Science logoLink to International Journal of Food Science
. 2022 Jul 28;2022:7722138. doi: 10.1155/2022/7722138

Physicochemical Characterization of Detarium microcarpum Seeds from Northern Benin

Adamou Gani Issa 1, Andriano Jospin Djossou 1, Mouaïmine Mazou 1, Guy Alain Alitonou 1, Fidèle Paul Tchobo 1,
PMCID: PMC9352502  PMID: 35938085

Abstract

The objective of this work is to determine the physicochemical characteristics of the Detarium microcarpum seeds from North Benin, specially the proximate composition, colour, minerals, and antinutritional factors using standard analytical methods. The results show that the contents of moisture, protein, total sugars, lipid, crude fiber, and ash ranged, respectively, from 10.85 to 14.69%, from 13.54 to 17.82%, from 19.69 to 32.04%, from 8.68 to 11.90%, from 19.78 to 34.24%, and from 1.5 to 3.49%. The luminance (l∗), red saturation (a∗), and yellow saturation (b∗) have, respectively, ranged from 60.45 to 67.64, from 5.44 to 8.86, and from 8.24 to 9.28. Seeds contain interesting contents of potassium, calcium, magnesium, manganese, sodium, and iron; they have, respectively, varied from 6141.88 to 12305.16 mg/kg, from 1254.47 to 2168.62 mg/kg, from 1298.87 to 2533.06 mg/kg, from 75.18 to 307.23 mg/kg, from 53.52 to 136.19 mg/kg, and from 28.46 to 181.42 mg/kg. The investigation of antinutritional factors indicates the presence of oxalates, phytates, total phenolic compounds, and saponins with contents that have varied, respectively, from 1.01 to 2.36%, from 0.37 to 0.87%, from 3.13 to 7.61%, and from 1.35 to 4.59%. On average, the physicochemical characteristics of the Sudanian and Sudano-Guinean zones are similar, except for total sugar content.

1. Introduction

In the world, there is an urgent need for new food plants or new sources to meet the nutritional needs of the ever-growing populations. Indeed, according to the Food and Agriculture Organization of the United Nations (FAO), the prevalence rate of undernourishment is 9.9% in the world, 21% in Africa [1], and 7.4% in Benin [2].

Food insecurity persists in most African countries due to the increase in demographic pressure, the insufficiency of basic cereals [3]. The consequences of this situation are mainly hunger, malnutrition, and the increase of food-related diseases despite the availability of certain plant resources [4, 5]. Therefore, utilizing plant resources that produce edible fruits that are not exploited or not used optimally and available locally for food processing in developing countries can be an approach to achieve food security [6]. Indeed, nontimber forest products (NTFPs) for food provide food security, which contribute to household economic development [7, 8]. These are wild or cultivated plants that provide economic and food survival support for local populations [9]. According to the World Health Organization (WHO), wild plants are involved in meeting the health and dietary needs of 80% of people living in developing countries [10]. Detarium microcarpum Guill. & Perr. (Fabaceae-Caesalpinioideae) is one of these plant resources, present in arid regions of West and Central Africa from Senegal and Gambia to Sudan [11], whose fruits are underexploited. The sweet pulp of the fruit is consumed raw at maturity while the seeds are almost unexploited [12, 13]. However, the cooked seeds are sometimes used to thicken soup for human consumption [13]. Observations by [14] in Mali show that farmers sell the fruit at a loss, because they are unaware that the seed can also bring in money. The use of local edible materials requires being informed on the physicochemical characteristics of these materials [15], because their better exploitation in the nutritional field depends on it [6].

Physicochemical characterization has been reported on Detarium microcarpum seeds collected in Nigeria [1621]. However, no studies seem to have been conducted on the physicochemical characteristics in relation to the provenance of Detarium microcarpum seeds. The objective of the present work is to determine the physicochemical characteristics of Detarium microcarpum seeds from North Benin and to study the variation of these characteristics according to the origin of the seeds.

2. Materials and Methods

2.1. Plant Material

The fruits of Detarium microcarpum were collected in twenty-two (22) localities in North Benin (Figure 1). They were transported to the “Research Unit in Enzymatic and Food Engineering (URGEA) of the Laboratory of Study and Research in Applied Chemistry” (LERCA) of the “Ecole Polytechnique d'Abomey-Calavi” (EPAC) of Abomey-Calavi University (UAC) for pretreatment and analysis.

Figure 1.

Figure 1

Map of Benin showing Detarium microcarpum seed harvesting sites.

2.2. Methods

The collected D. microcarpum fruits were manually peeled with a hammer to separate the seeds from the pericarp. The obtained seeds were then crushed and ground using a Moulinex type of electric grinder. The flour was wrapped in aluminium paper before being submitted to various analyses.

2.2.1. Proximate Composition of D. microcarpum Seeds

The content of water and volatile elements, oil, total ash, total sugars (expressed as glucose), protein, and crude fiber were determined, respectively, according to the French standard NF V03-921 of the French Association for Standardization (AFNOR) [22], the Soxhlet method [23] using petroleum ether, AACC 08-01 standard [24], the phenol-sulfuric colorimetric method developed by [25], the Kjeldhal method [26], and the filter bag technique (ANKOM200) [27].

2.2.2. Measurements of the Color of D. microcarpum Seed Meal

The color was determined according to the standards of the “International Lighting Committee” (CIE) using a Konica Minolta Chromameter in the trichromatic system (CIELAB L∗ a∗ b∗) calibrated with a white reference ceramic whose color coordinates are as follows: X = 0.3194, Y = 86.1, and Z = 0.3369. The recorded color parameters are L∗ (luminance index), a∗ (red saturation index), and b∗ (yellow saturation index).

2.2.3. Determination of Mineral and Trace Element Content of D. microcarpum Seeds

The mineral elements were determined by Atomic Absorption Spectrophotometry (AAS) with a VARIANT type flame equipped with a spectra A110 software. A hollow cathode lamp and standard solutions of each mineral element were used.

2.2.4. Composition of Antinutritional Factors in D. microcarpum Seeds

Oxalates, phytates, total phenolics, and saponins (saponosides) were determined. The method described in [28] was used to determine the oxalate content. Phytates were determined by the method of [29], and phenolics were determined by the method of Folin-Ciocalteu [30]. As for the saponin content, it was determined by the method of [31] modified by [32].

2.2.5. Statistical Analysis

All determinations were performed in duplicate, and data were processed using Microsoft Excel 2010 and SPSS 25 software. An analysis of variance followed by the Student-Newman-Keuls (SNK) test was performed to compare the samples. To investigate the influence of phytogeographic zone, means were compared using the independent samples t-test.

3. Results and Discussion

3.1. Proximate Composition of D. microcarpum Seed Samples

The proximate composition of the seeds is presented in Table 1. The results show that the water and volatile element content of the collected samples varied significantly from 10.85 to 14.69%. These values are higher than 5.9% and 7.2%, reported by [16, 20] in Nigeria, respectively, but close to 10.58% and 12.5%, reported by [19, 33], respectively. This variation in moisture content in the different studies is believed to be related to environmental factors and sample drying time before analysis, as [34] showed in their study that the moisture content of a sample varies with the drying time of the sample. Furthermore, the moisture contents of D. microcarpum seeds obtained in different studies are lower than the 15% required as a safety limit for the storage of plant foods [35]. Therefore, D. microcarpum seeds can be stored for a long period of time without developing molds. Indeed, [36] showed that high moisture content decreases storage time and impacts seed quality.

Table 1.

Proximate composition of Detarium microcarpum seeds in North Benin.

Areas Municipalities Water and volatile matter content (%) Protein (% DM) Total sugar content (% DM) Lipid content (% DM) Raw fibers (% DM) Ash content (% DM)
Sudanian Banikoara 13.40 ± 0.20de 15.66 ± 0.25b 24.43 ± 0.65a 10.60 ± 0.12c 30.93 ± 1.75bc 2.52 ± 0.18abc
Kandi 12.40 ± 0.43bc 15.57 ± 0.12b 26.8 ± 3.08a 10.15 ± 0.19bc 28.68 ± 3.07bc 2.18 ± 1.17abc
Malanville 12.24 ± 0.19bc 15.05 ± 0.62ab 22.83 ± 1.23a 11.90 ± 0.74d 31.79 ± 0.87bc 2.08 ± 1.03abc
Karimama 13.01 ± 0.06cd 15.14 ± 0.27ab 21.925 ± 1.59a 9.01 ± 0.08ab 26.49 ± 0.64bc 2.57 ± 0.04abc
Ségbana 10.85 ± 0.04a 15.44 ± 0.10ab 27.73 ± 2.33a 10.33 ± 0.07c 31.29 ± 0.46bc 2.73 ± 0.25abc
Gogounou 12.51 ± 0.14bcd 17.82 ± 0.21b 22.12 ± 1.67a 8.76 ± 0.29a 29.32 ± 2.93bc 1.50 ± 0.01a
Kérou 12.31 ± 0.29bc 15.43 ± 0.52ab 21.62 ± 2.21a 10.24 ± 0.23bc 31.14 ± 0.18bc 2.95 ± 0.08bc
Kouandé 12.65 ± 0.22bcd 14.42 ± 0.02ab 19.69 ± 2.92a 9.79 ± 0.23abc 31.54 ± 4.85bc 2.35 ± 0.07abc
Péhunco 13.46 ± 0.54de 14.03 ± 0.01ab 23.98 ± 2.31a 9.85 ± 0.32abc 27.86 ± 4.65bc 2.35 ± 0.35abc
Tanguiéta 12.03 ± 0.26bc 13.54 ± 0.44a 25.17 ± 1.63a 9.82 ± 0.28abc 31.51 ± 1.61bc 2.57 ± 0.10abc
Boukombé 14.69 ± 0.42f 15.41 ± 0.83ab 26.86 ± 1.05a 8.68 ± 0.02a 19.78 ± 1.13a 2.92 ± 0.04abc
Bembèrèkè 11.78 ± 0.15b 15.29 ± 0.33ab 23.48 ± 4.86a 10.12 ± 0.10bc 31.99 ± 0.98bc 2.27 ± 0.18abc
Sinendé 12.75 ± 0.50bcd 15.72 ± 0.34b 26.65 ± 2.38a 9.65 ± 0.01abc 32.22 ± 1.17bc 2.32 ± 0.18abc
Djougou 13.85 ± 0.14e 14.86 ± 0.92ab 23.82 ± 5.78a 10.40 ± 0.07c 30.04 ± 1.31bc 3.17 ± 0.11bc
Copargo 12.63 ± 0.06bcd 14.42 ± 0.92ab 24.95 ± 0.95a 10.17 ± 0.10bc 28.97 ± 4.58bc 1.76 ± 0.01ab
Sudanese-Guinean N'Dali 12.68 ± 0.19bcd 15.08 ± 0.22ab 30.41 ± 5.59a 10.44 ± 0.21c 30.62 ± 1.22bc 2.33 ± 0.04abc
Parakou 11.83 ± 0.42b 14.87 ± 0.93ab 27.14 ± 2.69a 9.43 ± 0.08abc 27.31 ± 2.42bc 2.35 ± 0.14abc
Pèrèrè 12.31 ± 0.40bc 14.66 ± 0.04ab 27.96 ± 4.16a 10.12 ± 0.41bc 32.71 ± 0.54bc 2.85 ± 0.15abc
Kalalé 12.85 ± 0.16bcd 14.22 ± 0.61ab 25.68 ± 4.55a 10.22 ± 0.78bc 32.59 ± 3.22bc 2.17 ± 0.11abc
Tchaourou 12.80 ± 0.25bcd 15.68 ± 0.04b 32.04 ± 2.96a 9.75 ± 0.30abc 32.03 ± 4.33bc 2.58 ± 0.04abc
Nikki 12.14 ± 0.21bc 15.07 ± 0.59ab 27.41 ± 3.59a 11.63 ± 0.69d 34.24 ± 0.59c 2.32 ± 0.24abc
Bassila 13.83 ± 0.04e 15.63 ± 0.37b 29.32 ± 2.96a 10.15 ± 0.52bc 22.785 ± 2.29ab 3.49 ± 0.08c
Total 12.68 ± 0.84 15.14 ± 0.90 25.54 ± 3.75 10.05 ± 0.79 29.81 ± 3.79 2.47 ± 0.51

Values with different letters in the same column are significantly different at the 5% level.

As for the protein content of D. microcarpum seeds, it varied significantly (P ≤ 0.05) from 13.54 to 17.82% observed in Tanguiéta and Gogounou, respectively. These values are close to those reported in Nigeria by [16, 19, 33, 20, 21] who found 14.8%, 11.11%, 18.6%, 12.54%, and 14.22%, respectively, but lower than 35.94% reported by [18] in Nigeria. The difference between these values could be related to environmental factors, such as the difference in soil nitrogen content [37] and ecological conditions, because water deficit influences the protein content of seeds [38]. Furthermore, the values found in the present study are globally higher than the protein content (14%) of baobab (Adansonia digitata) flour used in Benin as a food supplement [39]. These seeds, having an interesting protein content, can constitute a protein complement in the preparation of soup and could complete the body's need for these nutrients for growth and development. Indeed, protein deficiency leads to stunted growth, muscle wasting, abnormal belly swelling, and fluid accumulation in the body [40].

As for the lipid content of D. microcarpum seeds, it averaged 10.05%. It varied significantly (P ≤ 0.05) from 8.68% to 11.90% obtained, respectively, in the samples from Boukombé and Malanville. The values of lipid content obtained from the seeds in the present study are higher than 7.42%, 7.61%, and 8.43% obtained by [20, 41, 21] in Nigeria, respectively. However, they are lower than 12%, 15%, and 14.2% as reported by [16, 17, 19] in Nigeria, respectively. These variations in seed oil content between countries and spatially could be attributed to the environmental and geological conditions of the regions where the seeds were collected [42]. Furthermore, the lipid content (8.68%–11.90%) of D. microcarpum seeds characterized in the present work is lower than that of industrial oilseeds, for example shea (51.86%) [43]. Thus, D. microcarpum seed cannot be considered an oilseed. However, seeds can be incorporated into food preparations, including the thickening of sauces, without fear of obesity and cardiovascular disease. Indeed, [44] reported that low-fat foods reduce cholesterol levels and obesity.

As for the total sugar content, it averaged 25.54% and ranged from 19.69% to 32.04%. No significant variation (P ≥ 0.05) was observed between the total sugar contents of the D. microcarpum seed samples studied. These values are lower than 42.22%, 54.4%, and 48% obtained by the difference in Nigeria by [16, 18, 19], respectively. Moreover, since these contents are relatively high, D. microcarpum seeds can be an energy source for the body. Indeed, total sugar is the primary energy source used by the body [45]. Furthermore, seeds can be used in the manufacture of commercial products such as glucose.

The crude fiber content of D. microcarpum seed samples ranged from 19.78% to 34.24% observed in Boukombé and Nikki, respectively. The analysis of variance revealed a significant variability (P ≤ 0.05) within the samples. These values reflect a relative richness in crude fiber compared to the crude fiber content of baobab seeds (Adansonia digitata) which is 21.2% DM as reported by [39]. On the other hand, the values in the present study are higher than 10.7%, 3.42%, and 3.5% reported in Nigeria by [16, 18, 19], respectively, but lower than 50% reported by [46]. The variations in crude fiber content observed in the present study, between countries, and in space are certainly due to the environmental conditions undergone by the seeds. Crude fiber is a compound that has the properties of providing a satisfactory dietary balance, facilitating intestinal transit, and softening stools, thus preventing constipation. They also reduce cholesterol levels and the risk of diseases such as coronary heart disease, hypertension, and cancer [47].

The average ash content of the D. microcarpum seeds studied was 2.47% DM. It varied significantly (P ≤ 0.05) from 1.5% to 3.49% observed, respectively, in Gogounou and Bassila. Our data are close to those reported in Nigeria by [16, 18, 19, 33] who found 2.2%, 2.77%, 3.2% and 3.49%, respectively. These data reflect a relative richness in mineral elements compared to those of maize, millet, and sorghum with contents of 1.50%, 1.90%, and 1.60% MS, respectively [48]. The variations in ash content of D. microcarpum seeds are certainly due to environmental conditions, especially the different nature of the soils.

3.2. Color Parameters of D. microcarpum Seed Samples

Table 2 shows the color parameters of Detarium microcarpum seeds. It shows that for an average luminance or brightness of 63.98, the red (a∗) and yellow (b∗) saturation of D. microcarpum seeds averaged 7.23 and 8.89, respectively. These seed color parameters varied significantly (P ≤ 0.05) from 60.45 to 67.64 for luminance; from 5.44 to 8.86 for red saturation; and from 8.24 to 9.28 for yellow saturation. The intensities (quantities) of the yellow hues (b∗) are slightly higher than those of the red hues (a∗), and this is true for all samples analyzed (Table 2).

Table 2.

Color parameters of Detarium microcarpum seeds.

Areas Municipalities l∗ a∗ b∗
Sudanian Banikoara 64.38 ± 0.01h 6.74 ± 0.06c 8.71 ± 0.06bc
Kandi 62.88 ± 0.26d 7.58 ± 0.03f 9.28 ± 0.01f
Malanville 63.43 ± 0.01e 7.52 ± 0.05f 8.82 ± 0.04cd
Karimama 62.54 ± 0.12c 8.25 ± 0.06i 8.89 ± 0.06de
Ségbana 64.31 ± 0.02h 7.55 ± 0.04f 9.00 ± 0.03e
Gogounou 60.45 ± 0.04a 8.86 ± 0.07j 9.15 ± 0.06f
Kérou 62.61 ± 0.01c 7.73 ± 0.05g 9.18 ± 0.07f
Kouandé 61.95 ± 0.00b 7.44 ± 0.03f 8.89 ± 0.03de
Péhunco 62.64 ± 0.01c 7.44 ± 0.08f 8.89 ± 0.01de
Tanguiéta 62.68 ± 0.02c 7.73 ± 0.09g 8.24 ± 0.00a
Boukombé 65.77 ± 0.00k 6.05 ± 0.04b 8.64 ± 0.03b
Bembèrèkè 62.46 ± 0.01c 7.91 ± 0.07h 9.25 ± 0.06f
Sinendé 67.64 ± 0.03m 6.79 ± 0.02c 8.97 ± 0.04e
Djougou 64.02 ± 0.13g 6.67 ± 0.08c 8.29 ± 0.03a
Copargo 65.57 ± 0.04j 6.96 ± 0.02d 8.78 ± 0.03cd
Sudanese-Guinean N'Dali 63.80 ± 0.01f 6.94 ± 0.01d 8.77 ± 0.02cd
Parakou 64.41 ± 0.13h 7.16 ± 0.01e 8.70 ± 0.04bc
Pèrèrè 65.86 ± 0.09k 6.60 ± 0.01c 8.72 ± 0.03bc
Kalalé 64.38 ± 0.04h 7.14 ± 0.01e 8.61 ± 0.03b
Tchaourou 64.53 ± 0.12h 7.58 ± 0.03f 9.28 ± 0.01f
Nikki 64.80 ± 0.00i 7.10 ± 0.06e 9.22 ± 0.06f
Bassila 66.49 ± 0.05l 5.44 ± 0.04a 9.27 ± 0.05f
Total 63.98 ± 1.65 7.23 ± 0.72 8.89 ± 0.30

Values with different letters in the same column are significantly different at the 5% level.

3.3. Mineral Elements of D. microcarpum Seed Samples

The contents of some mineral elements could be determined and are presented in Table 3 below. It was found that potassium was the main mineral element in D. microcarpum seeds with an average content of 8541.85 mg/kg. It varied significantly (P ≤ 0.05) from 6141.88 to 12305.16 mg/kg. The highest value was observed in seeds harvested in Kerou while the lowest was observed in Péhunco. Our data are lower than those reported by [18, 21, 19] who found 23900 mg/kg, 105000 mg/kg and 35000 mg/kg, respectively, in Nigeria; but [49] in Nigeria found 6260 mg/kg which is between the values in the present study. Since D. microcarpum seeds are rich in potassium, then they can be used to reduce the risk of hypertension. Indeed, [50] showed that a diet rich in potassium reduces the risk of hypertension. In addition, [51] reported that potassium in intracellular and extracellular fluid in humans helps maintain electrolyte balance and membrane fluidity.

Table 3.

Contents of some mineral elements in Detarium microcarpum seeds.

Areas Municipalities Sodium (Na), mg/kg Potassium (K), mg/kg Manganese (Mn), mg/kg Calcium (Ca), mg/kg Magnesium (mg), mg/kg Iron (Fe), mg/kg
Sudanian Banikoara 136.19 ± 0.01v 7117.31 ± 0.07e 75.18 ± 0.01b 1590.55 ± 0.01e 1708.35 ± 0.02l 57.54 ± 0.04q
Kandi 64.56 ± 0.01f 8420.44 ± 0.04n 78.94 ± 0.01c 1254.48 ± 0.01a 1577.07 ± 0.01h 48.87 ± 0.04j
Malanville 76.67 ± 0.04l 6913.85 ± 0.06d 82.08 ± 0.02g 2168.62 ± 0.02u 1602.65 ± 0.03j 88.75 ± 0.03u
Karimama 56.94 ± 0.04b 8146.73 ± 0.03l 153.26 ± 0.04s 1274.47 ± 0.05b 1924.62 ± 0.01q 37.17 ± 0.01e
Ségbana 66.94 ± 0.04h 8446.73 ± 0.03p 133.26 ± 0.04n 1254.47 ± 0.05a 1524.62 ± 0.01g 47.17 ± 0.01h
Gogounou 70.42 ± 0.01j 8100.84 ± 0.03k 79.79 ± 0.01d 1890.04 ± 0.03p 1672.48 ± 0.03k 54.51 ± 0.01m
Kérou 66.23 ± 0.01g 12505.46 ± 0.07v 81.64 ± 0.01f 1963.67 ± 0.01q 1745.16 ± 0.01o 36.63 ± 0.01d
Kouandé 61.83 ± 0.01d 12305.16 ± 0.01u 113.85 ± 0.03j 1650.63 ± 0.01j 2533.06 ± 0.05v 55.33 ± 0.04o
Péhunco 83.85 ± 0.05o 6141.88 ± 0.02a 142.57 ± 0.03r 1750.65 ± 0.04l 1444.15 ± 0.06e 88.53 ± 0.01t
Tanguiéta 98.42 ± 0.01s 7193.23 ± 0.04f 100.43 ± 0.01i 1748.56 ± 0.04k 1722.96 ± 0.03m 81.07 ± 0.01s
Boukombé 83.07 ± 0.01n 8408.14 ± 0.04m 195.07 ± 0.04u 1606.83 ± 0.03h 1298.87 ± 0.03a 28.46 ± 0.01a
Bembèrèkè 53.52 ± 0.03a 7214.06 ± 0.04g 94.69 ± 0.01h 1759.06 ± 0.04m 1498.87 ± 0.01f 36.12 ± 0.03c
Sinendé 80.27 ± 0.03m 10110.66 ± 0.02r 131.04 ± 0.01m 1800.17 ± 0.01n 1982.27 ± 0.03r 55.19 ± 0.01n
Djougou 69.52 ± 0.01i 6699.53 ± 0.02c 307.23 ± 0.01v 1983.29 ± 0.01r 1358.64 ± 0.02b 53.23 ± 0.04l
Copargo 62.34 ± 0.03e 7783.16 ± 0.01h 138.74 ± 0.01q 2024.23 ± 0.03s 1365.25 ± 0.01c 181.42 ± 0.01v
Sudanese-Guinean N'Dali 57.12 ± 0.01c 7993.36 ± 0.02i 81.44 ± 0.01e 2099.92 ± 0.03t 1369.28 ± 0.02d 61.44 ± 0.01r
Parakou 84.16 ± 0.05p 10115.96 ± 0.02s 135.54 ± 0.01o 1802.27 ± 0.01o 1987.27 ± 0.03s 50.16 ± 0.04k
Pèrèrè 88.94 ± 0.01r 6408.83 ± 0.01b 161.26 ± 0.02t 1649.82 ± 0.01i 1780.64 ± 0.04p 56.06 ± 0.02p
Kalalé 84.98 ± 0.04q 8443.15 ± 0.06o 137.54 ± 0.01p 1477.60 ± 0.01d 1592.64 ± 0.04h 39.72 ± 0.01f
Tchaourou 117.85 ± 0.01u 11684.26 ± 0.01t 122.24 ± 0.01l 1605.83 ± 0.03g 2030.35 ± 0.01t 40.54 ± 0.03g
Nikki 112.47 ± 0.03t 9768.63 ± 0.03q 64.23 ± 0.04a 1593.46 ± 0.02f 1741.86 ± 0.01n 47.84 ± 0.01i
Bassila 72.75 ± 0.00k 7999.47 ± 0.04j 119.98 ± 0.04k 1354.58 ± 0.01c 2266.51 ± 0.01u 33.64 ± 0.04b
Total 79.50 ± 20.89 8541.85 ± 1800.90 124.09 ± 52.26 1695.60 ± 263.40 1714.89 ± 306.15 58.15 ± 31.66

Values with different letters in the same column are significantly different at the 5% level.

The calcium content of D. microcarpum seeds is 1802.27 mg/kg and ranges from 1254.47 to 2168.62 mg/kg. The analysis of variance shows us a significant difference (P ≤ 0.05) between the calcium contents of the different samples. The highest content was observed in Malanville while the seeds from Segbana presented the lowest content. These values are lower than those reported by [18, 21, 19] who found 2700 mg/kg, 23000 mg/kg, and 11500 mg/kg, respectively, in Nigeria; but they are higher than the 680 mg/kg reported by [49] in Nigeria. Calcium is a mineral necessary for dentition and ossification.

Regarding the magnesium content of D. microcarpum seeds, it varied significantly (P ≤ 0.05) from 1298.87 to 2533.06 mg/kg observed in Boukombé and Kouandé, respectively. These values are higher than those reported by [18, 21, 49] who found 700 mg/kg, 220 mg/kg, and 740 mg/kg, respectively, in Nigeria; but they are lower than 10500 mg/kg reported by [19] in Nigeria. Magnesium is a transmitter of nerve impulses and an activator of coenzymes in carbohydrate and protein metabolism [52].

As for the manganese content of D. microcarpum seeds, it is 135.54 mg/kg on average. The analysis of variance showed a significant variation (P ≤ 0.05) from 75.18 to 307.23 mg/kg obtained, respectively, in Banikoara and Djougou. The value 195 mg/kg reported in Nigeria by [49] is located between the values of the present study. Our values are much higher than those of [21] who found 1.7 mg/kg in Nigeria. Manganese is required for normal bone metabolism, enzymatic reactions, and maintenance of normal nerve, brain, and thyroid functions [53]. In addition, [54] reported that manganese acts as a catalyst and cofactor in many enzymatic processes such as mucopolysaccharide and glycoprotein synthesis, involved in fatty acid and cholesterol synthesis.

The mineral elements investigated in D. microcarpum seeds, sodium, and iron are present in low levels compared to the other elements investigated in the present study. Sodium content varied significantly (P ≤ 0.05) from 53.52 to 136.19 mg/kg as observed in Bembèrèkè and Banikoara, respectively. These values are lower than those reported by [18, 19, 49] who found 2200 mg/kg, 2380 mg/kg, and 450 mg/kg, respectively, in Nigeria, but higher than 28.29 mg/kg reported by [21] in Nigeria. [51] states that sodium in intracellular and extracellular fluid in humans helps to maintain electrolyte balance and membrane fluidity.

For the iron content, it varied significantly (P ≤ 0.05) from 28.46 to 181.42 mg/kg observed in Boukombé and Copargo, respectively. Our values are lower than those reported in Nigeria by [18, 19, 49] who found 810 mg/kg, 3120 mg/kg, and 200 mg/kg, respectively; but they are higher than 6 mg/kg reported by [21] in Nigeria. Iron is an important element for pregnant women, lactating mothers, and infants to prevent anemia [55]. The variations in the contents of the different mineral elements observed in the present study, between countries, and in space could be related to the different nature of the soils.

These values are high compared to those of maize whose calcium, potassium, magnesium, sodium, and iron contents are 145.00, 700.00, 220.00, 175.00, and 27.50 mg/kg DM, respectively [56]. The richness of D. microcarpum seeds in these different minerals gives it a prominent place in human and animal nutrition.

3.4. Antinutritional Factors of D. microcarpum Seed Samples

Table 4 presents the antinutritional factors sought in D. microcarpum oilcake. These substances are known to reduce the bioavailability of nutrients [48], particularly proteins and minerals [57]. From Table 4, it is clear that the cakes contain total phenols, phytates, oxalates, and saponins with average contents of 4.89%, 0.67%, 1.73%, and 3.08%, respectively. Except for oxalate contents, total phenols, phytates, and saponin contents varied significantly (P ≤ 0.05) from 3.13% to 7.61%, from 0.37% to 0.87%, and from 1.35% to 4.59%, respectively.

Table 4.

Antinutritional factors of Detarium microcarpum cake.

Areas Municipalities Oxalate (%) Phytate (%) Total phenols (%) Saponin (%)
Sudanian Banikoara 1.68 ± 0.48a 0.37 ± 0.03a 4.93 ± 0.11bcde 4.59 ± 0.12e
Kandi 1.67 ± 0.47a 0.87 ± 0.06e 6.62 ± 0.09f 2.41 ± 0.13ab
Malanville 1.67 ± 0.47a 0.76 ± 0.13cde 4.70 ± 0.03abcde 1.35 ± 0.21a
Karimama 1.34 ± 0.00a 0.76 ± 0.05cde 5.78 ± 0.66def 3.55 ± 0.83cde
Ségbana 1.01 ± 0.47a 0.51 ± 0.07abc 5.01 ± 0.04cde 4.01 ± 0.08cde
Gogounou 2.03 ± 0.01a 0.60 ± 0.21abcde 7.61 ± 0.54g 3.53 ± 0.04cde
Kérou 1.34 ± 0.95a 0.79 ± 0.04cde 3.43 ± 0.02abc 1.44 ± 0.37a
Kouandé 2.03 ± 0.95a 0.64 ± 0.01bcde 5.04 ± 0.20de 1.81 ± 0.29a
Péhunco 1.69 ± 0.47a 0.83 ± 0.01de 3.38 ± 0.02ab 3.48 ± 0.74cde
Tanguiéta 1.34 ± 0.95a 0.72 ± 0.06bcde 5.77 ± 0.35def 4.11 ± 0.02de
Boukombé 1.69 ± 0.47a 0.57 ± 0.06abcd 3.13 ± 0.11a 2.91 ± 0.06bc
Bembèrèkè 1.68 ± 0.47a 0.53 ± 0.01abc 5.73 ± 0.37def 4.47 ± 0.47e
Sinendé 1.69 ± 0.47a 0.60 ± 1.11abcde 5.00 ± 0.28cde 3.11 ± 0.01bcd
Djougou 2.36 ± 0.47a 0.76 ± 0.05cde 3.33 ± 0.09a 2.40 ± 0.00ab
Copargo 1.69 ± 0.48a 0.70 ± 0.04bcde 4.52 ± 0.17abcde 3.75 ± 0.35cde
Sudanese-Guinean N'Dali 2.02 ± 0.95a 0.73 ± 0.08cde 4.11 ± 0.59abcd 3.70 ± 0.42cde
Parakou 2.01 ± 0.00a 0.72 ± 0.06bcde 4.65 ± 0.49abcde 2.29 ± 0.12ab
Pèrèrè 1.68 ± 0.48a 0.77 ± 0.10cde 4.13 ± 0.11abcd 4.05 ± 0.07de
Kalalé 2.02 ± 0.00a 0.82 ± 0.04de 5.77 ± 0.13def 4.14 ± 0.04de
Tchaourou 1.35 ± 0.95a 0.58 ± 0.04abcd 4.52 ± 1.10abcde 2.40 ± 0.01ab
Nikki 1.68 ± 0.47a 0.78 ± 0.11cde 5.99 ± 0.44ef 2.92 ± 0.07bc
Bassila 2.35 ± 0.48a 0.46 ± 0.00ab 4.52 ± 0.00abcde 1.45 ± 0.36a
Total 1.73 ± 0.49 0.67 ± 0.14 4.89 ± 1.15 3.08 ± 1.03

Values with different letters in the same column are significantly different at the 5% level.

The oxalate (0.16%) and phytate (0.26%) contents reported in Nigeria by [33] are lower than those obtained in the present study. However, our values are lower than 5.57% obtained by [18] in Nigeria. The saponin contents of 0.13% and 0.20% obtained by [18, 33], respectively, as well as the total phenol content 0.073% obtained by [16] are lower than the values in the present study. This difference observed between the different results could be due to the environmental conditions experienced by the seeds.

Phytic acid is an antinutritional factor, known as a major inhibitor of the absorption of iron and calcium, zinc, and other minerals [58]. Phytate levels obtained in D. microcarpum seed meals are not negligible. However, the toxicity levels of these antinutrients have not been established [59]. However, treatments such as soaking or fermentation and cooking before consumption of these seeds would be necessary for the improvement of their quality [48, 60]. On the other hand, phytic acid can be used as an antioxidant in food products by inhibiting iron-catalyzed oxidative reactions [61].

Oxalates have also been reported to inhibit the absorption of minerals, particularly calcium, magnesium, zinc, and mercury [62]. The calcium oxalate precipitates formed are deposited in the kidneys promoting kidney stones [63]. The maximum tolerable limit of oxalate is between 0.2 and 0.5 g/100 g [64].

This implies that above this value, the adverse effects of oxalate in the human body, namely, limited bioavailability of minerals (Ca, Na, and K), kidney stones (calcium oxalate), and severe irritation of the intestinal wall, will be experienced [65]. The values obtained in the present study are much higher than the maximum tolerable limit. Cooking of D. microcarpum seeds before processing or consumption is essential. Indeed, the high content of oxalate in foodstuffs can be reduced if they are precooked before processing or consumption [66].

Phenolic compounds are known for their antioxidant properties [67], and they allow grain storage because they prevent losses due to premature germination and mold damage [68]. However, they are also substances that have a negative effect on the digestibility of nutrients. Indeed, the chelation property of phenolic compounds contributes to their antioxidant activity but, at the same time, to their inhibiting effect on the bioavailability of minerals [65].

High saponin content causes gastroenteritis manifested by diarrhea and dysentery [59]. However, saponins have cholesterol-lowering properties [69] and play a major role in the treatment of inflamed tissues as well as in cancer prevention [70].

Furthermore, the phenolic compound contents of D. microcarpum seeds obtained in the present study are between 0.2 and 10.3% DM reported by [71] on Sorghum grains.

3.5. Influence of Phytogeographic Zones on the Physicochemical Characteristics of Detarium microcarpum Seed Samples

The physicochemical characteristics of D. microcarpum seeds, evaluated in the present study, were all subjected to the independent samples t-test to estimate the influence of phytogeographic zones on the means of the said characteristics. The results obtained are presented in Table 5 below. It is shown that except the total sugar content, there is no significant difference (P ≥ 0.05) between the means of physicochemical characteristics of seeds from the two phytogeographic zones. Thus, on average, the physicochemical characteristics of the Sudanian and Sudano-Guinean zones are close except the total sugar content. In other words, the phytogeographic zone does not influence the physicochemical characteristics of D. microcarpum seeds except total sugars.

Table 5.

Influence of phytogeographical zones on the physicochemical characteristics of Detarium microcarpum seeds.

Sudanian Sudanese-Guinean
Proximate composition Moisture 12.70 ± 0.91a 12.63 ± 0.64a
Protein 15.19 ± 0.97a 15.03 ± 0.52a
Total sugar 21.09 ± 2.01a 24.76 ± 2.01b
Lipid content 9.96 ± 0.79a 10.25 ± 0.69a
Raw fibers 27.80 ± 4.88a 28.96 ± 7.77a
Ash content 2.41 ± 0.44a 2.58 ± 0.46a
Color settings L∗ 63.55 ± 1.78a 64.89 ± 0.94a
a∗ 7.41 ± 0.70a 6.85 ± 0.69a
b∗ 8.86 ± 0.31a 8.94 ± 0.30a
Mineral components Na 75.38 ± 20.51a 88.32 ± 21.21a
K 8367.14 ± 1894.72a 8916.23 ± 1733.54a
Mn 127.18 ± 60.63a 117.46 ± 33.69a
Ca 1714.65 ± 283.73a 1654.78 ± 240.69a
Mg 1663.93 ± 311.53a 1824.08 ± 298.32a
Fe 63.33 ± 37.52a 47.05 ± 9.78a
Antinutrients Oxalate 1.66 ± 0.33a 1.87 ± 0.33a
Phytate 0.67 ± 0.14a 0.69 ± 0.13a
Total phenols 4.93 ± 1.28a 4.81 ± 0.76a
Saponin 3.13 ± 1.05a 2.99 ± 1.02a

Values with different letters in the same line are significantly different at the 5% level.

4. Conclusion

The present study provided scientific data on the proximate composition and antinutritional factors of Detarium microcarpum seeds from Benin. According to the results obtained, Detarium microcarpum seeds can be good sources of total sugars, crude fiber, protein, lipid, and minerals such as potassium, calcium, magnesium, and manganese. The obtained oxalate and phytate contents can reduce the bioavailability of nutrients, especially minerals contained in the seeds. On average, the physicochemical characteristics of the Sudanian and Sudano-Guinean zones are close except the total sugar content.

Acknowledgments

This work received financial support from the Competitive Research Fund Program of the University of Abomey-Calavi (PFCR/UAC, 3rd phase) 2019-2021 and the Olga Triballat Institute through the project “Model of an Endogenous Enhancement of Unconventional Fruit Resources: Case of Detarium spp. (ProDETOF)”, which we sincerely thank.

Data Availability

There is no data to support the findings of this study.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

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Data Availability Statement

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