- Open Access
Dietary fiber, organic acids and minerals in selected wild edible fruits of Mozambique
SpringerPlus volume 2, Article number: 88 (2013)
The harvesting, utilization and marketing of indigenous fruits and nuts have been central to the livelihoods of the majority of rural communities in African countries. In this study we report on the content of dietary fiber, minerals and selected organic acids in the pulps and kernels of the wild fruits most commonly consumed in southern Mozambique. The content of soluble fiber in the pulps ranged from 4.3 to 65.6 g/100 g and insoluble fiber from 2.6 to 45.8 g/100 g. In the kernels the content of soluble fiber ranged from 8.4 to 42.6 g/100 g and insoluble fiber from 14.7 to 20.9 g/100 g. Citric acid was found in all fruits up to 25.7 g/kg. The kernels of Adansonia digitata and Sclerocarya birrea were shown to be rich in calcium, iron, magnesium and zinc. The data may be useful in selecting wild fruit species appropriate for incorporation into diets.
Fruits are generally recognized as essential for health optimisation, with human health depending to a large extent on factors such as high fruit and vegetable consumption (Ibrahim 2011). Deficiencies of essential micronutrients found in fruits can increase the risk of illness or death from infectious diseases by reducing immune and non-immune defenses and by compromising normal physiology and development (Black 2003). Such nutrient deficiencies are highly prevalent in low and middle income countries.
Recent research has shown that a wide range of indigenous fruit trees have the potential to provide rural households with a means to meet their nutritional and medicinal needs (Ekesa et al. 2009). In the past decades several reports have been published on the nutritional composition of wild fruits and vegetables growing in different areas in various African countries and on the effect they could have on combating malnutrition and poverty in the continent (FAO 2011). In June 2008, the European Commission authorised the placing on the market of dried pulp of one wild fruit, Baobab (Adansonia digitata), as a novel food ingredient (Commission Decision 2008). Three components are of special importance for determining whether such ingredients are health-enhancing: the kind and amount of minerals, organic acids and dietary fiber.
Minerals are of great importance in the diet, although they comprise only 4–6% of human bodyweight. Some minerals or macro elements required in amounts greater than 100 mg per day represent 1% or less of bodyweight (Insel et al. 2011; Imelouane et al. 2011). The essential macro elements include calcium, phosphors, magnesium, potassium, sodium, sulfur and chloride. Essential trace elements such as zinc, iron, copper, manganese, selenium, iodine and molybdenum are normally required in amounts of less than 100 mg per day, making up less than 0.01% of the bodyweight (Imelouane et al. 2011).
Dietary fiber is increasingly viewed as an essential aspect of good nutrition. Intake of dietary fiber alters the water content, viscosity, and microbial mass of the intestinal contents, resulting in changes in the rate and ease of passage through the intestine (Elleuch et al. 2011). High intake of dietary fiber plays a significant role in weight control and the prevention of several diseases. For example, dietary fiber improves glucose tolerance, by delaying the transport of carbohydrates into the small intestine, reducing the risk of heart diseases and reduces constipation (Anderson et al. 1994; Rodríguez et al. 2006). Organic acids are involved in human growth, maturation and senescence (Al-Farsi et al. 2005). The organic acids influence organoleptic properties such as flavor, color and aroma and are responsible for many characteristic fruity tastes. They increase shelf life, stability and microbiologic safety (Hasib et al. 2002; Loredana et al. 2006; Nour et al. 2010).
In a previous study we reported on the proximate composition of five wild fruits of Mozambique. Adansonia digitata, Landolphia kirkii, Salacia kraussii, Sclerocarya birrea and Vangueria infausta were evaluated for pH and titratable acidity and their content of dry matter, fat, protein, ash, soluble solids and sugar content (Magaia et al. submitted). The present study was carried out to further analyze the nutritional potential of these fruits. The dietary fiber, organic acids and mineral content of the five wild fruits and selected seeds were determined with the plan to highlight their potential as an effective means to combat macro and micronutrient deficiencies, especially in children.
The contents of insoluble and soluble dietary fiber in the fruits are presented in Table 1. All pulps and kernels contained dietary fiber, but with large variations in concentration among the different fruits. In S. kraussii and in V. infausta, the content of insoluble dietary fiber ranged from 2.6 g/100 g to 45.8 g/100 g in the pulps, and from 14.7 to 20.9 g/100 g in the kernels, respectively. The content of insoluble dietary fiber in A. digitata pulp was significantly higher than that in L. kirkii and S. kraussii. The soluble dietary fiber in the pulps ranged from 4.3 g/100 g in L. kirkii up to 65.6 g/100 g in A. digitata. The content of soluble dietary fiber in A. digitata pulp was significantly higher than in the other fruit pulps.
A chromatogram from the analysis of organic acids in S. kraussii is shown in Figure 1. The peaks corresponding to the different acids are indicated by numbers. The calibration curve was linear within the concentration ranges used for the analysis.
The results of the determination of organic acid content based on wet weight are shown in Table 2. Fruits collected in Manhiça, 2009 were used for this analysis. Citric acid was found in all fruits, with the highest contents in A. digitata (25.7 g/kg) and L. kirkii (21.5 g/kg). Malic acid was detected at concentrations between 0.4 g/kg and 2.1 g/kg. Succinic acid was found at concentrations of 0.1 g/kg or below. Tartaric acid was detected at trace levels only in S. birrea.
The mineral contents in the fruit pulps, kernels and seeds, expressed as mg/100 g dry matter, are presented in Table 3. The relative standard deviation of the mean values was generally below 5%. The content in different fruit samples varied considerably, from undetectable levels of selenium up to 2753 mg/100 g for potassium (S. birrea pulp). The richest source of calcium was A. digitata both for pulp (308 to 366 mg/100 g) and for kernels (293 to 347 mg/100 g.) The iron content in the pulps and kernels generally ranged from 1.0 - 4.0 mg/100 g, while S. kraussii pulp contained 9.0 mg/100 g, and the whole seeds of A. digitata contained 29 mg /100 g. The highest content of magnesium was found in the kernels of A. digitata (626 to 706 mg/100 g) and S. birrea (396 – 436 mg/100 g). Selenium was not analyzed in all fruits, but was detected in V. infausta (1.5 mg/100 g). The richest source of zinc was the kernels of A. digitata (5.2 – 5.7 mg/100 g) and S. birrea (4.5 mg/100 g).
The literature provides little data on dietary fiber in the fruits investigated and we have found no data on soluble or insoluble dietary fiber. Our data thus contributes substantially to knowledge about dietary fiber content in wild fruits. The analyses conducted showed that all fruits selected for the study contained both soluble and insoluble dietary fiber, and the total amount of dietary fiber in the pulps ranged from around 10 to 80 g/100 g dry matter (Table 1), thus indicating their potential for improving nutritional content in the local diet.
The largest amount of dietary fiber was found in A. digitata pulp. The amount 80.3 g/100 g was much higher than in previous studies, which ranged from 5.4 g/100 g in fresh weight to 45 g/100 g in dry weight (Saka and Msonthi 1994; Lockett et al. 2000; Murray et al. 2001; Osman 2004). The high content of dietary fiber in the present study, of which 80% was soluble dietary fiber, could thus provide a substantial contribution to total dietary intake. For example, the consumption of 20 g A. digitata pulp can supply 42 – 52% of the recommended daily intake (RDI) for children from 4 to 13 years of age and also for pregnant women (National Research Council 2005). The high content of soluble dietary fiber could also help to control serum cholesterol levels, reduce other risk factors for cardiovascular disease (Van Duyn and Pivonka 2000), and reduce appetite and caloric intake (Anderson et al. 1994).
V. infausta pulp also contained large amounts of total dietary fiber (on average 62 g/100 g), of which more than half was insoluble dietary fiber. Several studies have shown that intake of fruits rich in insoluble dietary fiber benefits weight control and health of the large intestine; the insoluble fiber decreases intestinal transit time and increases fecal bulk (Al-Farsi et al. 2005; Hamilton et al. 1992). Consumption of 100 g V. infausta pulp can supply up to 40% of RDI for children and pregnant women (National Research Council 2005). In a report on dietary fiber in V. infausta, the content of acid detergent lignin was reported to be 35.5% (fresh weight), acid detergent fiber 39.5% and neutral detergent fiber 39.4% (Amarteifio and Mosase 2006). The discrepancies between our findings and previous research may be due to the difficulty in comparing data on dietary fiber when it isn’t clear whether figures refer to dry or fresh weight. Furthermore, different analytical methods may have been used in different studies, including different types of dietary fiber.
Our data on the amounts of dietary fiber in S. birrea pulp were about half of that found in another study determining dietary fiber after extraction of fat by a gravimetric method, 37.7 g/100 g (Murray et al. 2001). In a report where AOAC method was used, the amount of acid detergent lignin was 13.7% (fresh weight), acid detergent fiber 16.3% and neutral detergent fiber 16.1% (Amarteifio and Mosase 2006).
The total amount of dietary fiber in L. kirkii pulp was low (10 g/100 g) compared with that of the other fruits in this study, but very similar to that of L. oweriensis, of the same family (Effiong and Udo 2010). The amount of dietary fiber in S. kraussii pulp was similar to L. kirkii. The amounts of dietary fiber in S. krausii, and L. kirkii pulps are in the same range as in for example avocado, 6.7 g/100 g, and guava, 12.7 g/100 g (Li et al. 2002).
The whole seeds of A. digitata contained large amounts of insoluble dietary fiber. These seeds are often crushed into a powder in rural cooking and mixed with other ingredients to make a sauce. Increased use of this local custom may thus help to increase the intake of dietary fiber.
In the kernels of A. digitata the total content of dietary fiber was on average 42.2 g/100 g, which is higher than that found in other studies (Murray et al. 2001). The kernels of S. birrea contained similar amounts of insoluble dietary fiber as A. digitata kernels, but the amount of soluble dietary fiber was lower. There is no report in the literature about dietary fiber of S. birrea kernels. However, in cashew nuts and peanuts, which are commonly consumed Mozambique, the total dietary fiber content was 3.9 g/100 g for cashew nuts and 5.2 g/100 g for peanuts in fresh weight (de Oliveira Sousa et al. 2011).
The effects of dietary fiber cannot, however, be considered in isolation. Although dietary fiber provides many health benefits, it may affect mineral absorption negatively due to the capacity of the fibers to bind cations (López and Martos 2004). The ability of dietary fiber to interfere with iron absorption is especially negative for human nutrition (Reinhold et al. 1981). However, citric and malic acids in fruits promote iron absorption (Gillooly et al. 1983), and improve iron solubilization (López and Martos 2004).
Fortunately, citric and malic acid were found in all fruits in this study (Table 2). Citric acid ranged from 0.9 g/kg of wet weight basis in S. Kraussii to more than 20 g/kg in A. digitata and L. kirkii. For malic acid the results were lower and ranged from 0.4 g/kg to 2.1 g/kg. Succinic acid was found in low amounts in all fruits, around 0.1 g/kg, and tartaric acid was detected in trace levels in S. birrea. No data in the literature are available on organic acids in the selected wild fruits; however, one type of wild fruit called medlar (Mespilus germanica L.) was reported to contain around 4 g/kg fresh weight of citric acid and malic acid (Glew et al. 2003). For comparison, the citric acid concentrations in some traditional fruits are: pineapple (2.2 g/kg), orange (4.5 g/kg), grapes (13.1 g/kg) and lime (41.2 g/kg) (Falade et al. 2003).
Although there were large variations in the mineral content in the different fruits (Table 3), we did not observe any pronounced difference between growth place or harvest year, and the small differences found may be explained by soil, climate and weather conditions.
The highest amounts of calcium from the fruits selected in the present study were found in A. digitata pulp and kernel, around 300 mg/100 g dry matter. The amounts are at the same levels as in other reports (Osman 2004; Glew et al. 1997) but higher than in some studies (Saka and Msonthi 1994; Lockett et al. 2000; Amarteifio and Mosase 2006; Eromosele et al. 1991; Sena et al. 1998). S. birrea pulp contained 201 mg/100 g, which is about half the amount reported in the literature (Glew et al. 1997), but higher than that in other reports (Amarteifio and Mosase 2006; Eromosele et al. 1991). Calcium is an important factor in bone health, and a high intake is recommended particularly during pregnancy and infancy (Insel et al. 2011) calcium together with phosphor, magnesium and potassium is important for growth and maintenance of bone, teeth and muscle (Insel et al. 2011) and bone metabolism (Ilich et al. 2003; New 2003; Bonjour et al. 2009).
High amounts of phosphor were found in the kernels: A. digitata kernels contained up to 1500 mg/100 g, which is four times higher than that in another study (Nnam and Obiakor 2003). Regarding the pulp, there are reports showing higher phosphor content than in our study, for example 452 mg/100 g in A. digitata (Sena et al. 1998) and 264 mg/100 g in S. birrea (Glew et al. 1997).
High content of potassium, more than 2000 mg/100 g, was found in pulps from A. digitata, S. kraussii and S. birrea. For A. digitata, this is in agreement with results from other studies (Saka and Msonthi 1994; Amarteifio and Mosase 2006), while some reports show lower values. For S. birrea, our data agree with other results (Amarteifio and Mosase 2006). The content of potassium in V. infausta pulp was on the same level as in one report (Amarteifio and Mosase 2006) but almost 7 times greater than in another report (Saka and Msonthi 1994). The potassium content in kernels of S. birrea was somewhat higher than that in another report (Glew et al. 2004). In the whole seeds of A. digitata, potassium is higher than in other reports (Osman 2004; Nkafamiya et al. 2007). Potassium, together with sodium, regulates muscle contraction and nerve impulse transmission, and a high potassium/sodium ratio may assist the excretion of excessive salt and water (Arthey et al. 2001). All fruits in our study had low amounts of sodium and thus the potassium/sodium ratio was high in the fruits.
The whole seeds of A. digitata had extremely high iron content, 29 mg/100 g, while data in the literature range from 1.83 to 6.36 mg /100 g (Lockett et al. 2000; Osman 2004; Glew et al. 1997; Nkafamiya et al. 2007). S. kraussii had the highest iron content of the pulp, 9 mg/100 g. In the other pulps it was 2 to 4 mg/100 g. In the literature, the amounts of iron in A. digitata ranged from 0.1 to 9.3 mg/100 g (Saka and Msonthi 1994; Lockett et al. 2000; Amarteifio and Mosase 2006; Glew et al. 1997; Eromosele et al. 1991; Sena et al. 1998; Glew et al. 2004) and in S. birrea from 0.07 to 2.49 mg/100 g (Amarteifio and Mosase 2006; Glew et al. 1997; Eromosele et al. 1991). For V. infausta there is one report showing 0.09 mg /100 g (Amarteifio and Mosase 2006) and one showing 28.3 mg/100 g (Saka and Msonthi 1994). Very high iron content, 129 mg/100 g dry matter, was reported in L. oweriensis, which is a fruit in the same family as L. kirkii (Effiong and Udo 2010). Iron is necessary for the transport of oxygen in the blood to the cells and for supplying the body with energy, for immune function and nerve health and in addition, it is a cofactor in numerous reactions (Insel et al. 2011).
The kernels of A. digitata had the highest magnesium content, around 600 – 700 mg/100 g. This is higher than the magnesium content in other kernels or seeds. For example dried pumpkin seeds contain 540 mg/100 g, linseed 392 mg/100 g and sunflower seeds 355 mg/100 g (National Food Agency 2012). Our data on whole seeds are at the same level as in other reports for A. digitata (Lockett et al. 2000; Osman 2004; Glew et al. 1997) and for S. birrea (Glew et al. 2004). Magnesium is of great importance for cardiac and nerve function, is involved in more than 300 biochemical reactions in the body and is involved in energy metabolism and protein synthesis (Insel et al. 2011).
The zinc content in the kernels of A. digitata and S. birrea was around 5 mg/100 g, which is in agreement with literature for S. birrea (Glew et al. 2004) and higher than previous data for A. digitata (Nnam and Obiakor 2003). Zinc increases the affinity of hemoglobin for oxygen, participates in taste perception and interacts with a number of hormones. In addition, the body needs zinc to grow and develop properly during pregnancy, infancy, and childhood (Brown et al. 1999; Insel et al. 2011).
The results of the mineral analysis can be compared with the RDI for children 4–13 years of age and pregnant women 19–30 years of age (National Research Council 2005). For example, 100 g of fresh A. digitata pulp can contribute on average 23% of the iron and 30% of the calcium RDI for children (4–13 years) and almost 29% of the calcium for pregnant women. Furthermore, 100 g S. birrea pulp can contribute 13% of the magnesium RDI for children (4–13 years) and 33% for pregnant women, and almost 41% of zinc requirements. Consumption of 60 g A. digitata kernels can supply around 30% of iron, almost 50% of zinc and more than 100% of magnesium RDI for children.
New data on dietary fiber, organic acids and mineral content have been obtained for five wild fruits and selected seeds. The highest content of dietary fiber was found in A. digitata pulp. It was also found that fresh A. digitata pulp can contribute a large amount of the iron and calcium RDI for children and that kernel of A. digitata and S. birrea can contribute significantly to the magnesium and zinc requirements for pregnant women. Thus some of the fruits and kernels studied show large potential to reduce mineral deficiencies in local diet especially in children. The research results highlight the significance of wild edible fruits as a cheap source of nutrients and the benefits of increasing the use these species as dietary supplements. Initiatives should be put in place to promote consumption and domestication of edible indigenous fruit: to improve the nutritional and health status of women and children, contributing to income generation and stimulating rural economic development.
Materials and methods
Five fruits were used for the analysis: Adansonia digitata (A. digitata) (Fam. Bombaceae, local name n‘buvu or malambe), Landolphia kirkii (L.kirkii) (Fam. Apocynaceae, local name wungwa), Salacia kraussii (S. kraussii) (Fam. Celastraceae, local name phinsha), Sclerocarya birrea (S. birrea) (Fam. Anacardeaceae, local name canhi) and Vangueria infausta (V. infausta) (Fam. Rubiaceae, local name pfilwa). Approximately 5 kg of each fruits were collected in January to July in 2008 and 2009 in four districts of Mozambique, with the exception of the fruits from Sclerocarya birrea, which were collected only in 2009. Unblemished fruits were selected and washed, the skin and seeds were removed and the remaining parts (pulp) were homogenized in a blender to obtain 100 g pulp of each type of fruit. Different numbers of fruit were used, depending on size and mass of pulp. Seeds from Adansonia digitata and Sclerocarya birrea were crushed and the kernels were removed, milled and sieved. The dry matter content in the pulps was determined immediately. Fruit pulps and kernels for analysis of dietary fibre, organic acids and minerals were vacuum packed in plastic bags and stored at −18°C.
Chemicals and solvents were of analytical grade. Sulphuric acid, nitric acid, hydrochloric acid, sodium di-hydrogen phosphate, di-sodium hydrogen phosphate; sodium hydroxide, ethanol and acetone were from Fluka (Sigma-Aldrich, Steinheim, Germany). Pepsin (2000FIP U/g) obtained from Merck (Darmstadt, Germany), pancreatin from Fluka (Sigma-Aldrich, Steinheim, Germany), and celite were used for the analysis of dietary fibre. Lithium chloride, organic acid standards (citric, malic, tartaric and succinic) were from Merck (Darmstadt, Germany).
To determine the dry matter content, 2 g samples were dried in an oven at 105°C until constant weight (AOAC 2000 method 920.151). The samples were weighed before and after drying and the contents of dry matter were calculated. All determinations were performed in triplicate.
The content of total dietary fiber was first analyzed using an enzymatic gravimetric method, and then divided into fractions of either soluble dietary fiber (SDF) or insoluble dietary fiber (IDF) (Asp et al. 1983). All experiments were performed in triplicate. The sample (0.5-1.0 g) was suspended in a phosphate buffer and hydrochloric acid was added to adjust the pH to 1.5. The sample was digested by pepsin for 60 min at +4°C and then the pH was adjusted to 6.8. Pancreatin was added and the sample was incubated for 60 minutes at 40°C and the pH was adjusted to 4.5. The solution was filtered and the insoluble residue was washed with distilled water, 95% and 99% of ethanol and then dried overnight at 105°C, cooled and weighed (IDF). The filtrate was precipitated with hot 95% ethanol and filtered, washed with ethanol (78%, 95% and 99%), dried, cooled and weighed (SDF). The results were corrected for protein and ash contents.
Citric, malic, succinic and tartaric acids were analysed using ion exchange chromatography (Metrohm International, CH-9101, Herisau, Switzerland) with inverse suppression and conductivity detection. Reference samples of the organic acids (Merck, Darmstadt, Germany) were injected via a 20 μl loop onto a column (250 mm × 7.8 mm, 9 μm, polystyrene/divinylbenzene copolymer, Metrosep 6.1005.200, Switzerland) and eluted isocratically at a flow rate of 0.5 mL min-1 and a pressure 3.8 MPa. The suppressor system was regenerated by pumping a solution of 10 mM LiCl, together with Millipore water, through the system. Different ratios of the mobile phase (0.5 mM sulphuric acid and acetone) were tested, as well as different column temperatures (30, 40 and 50°C). The optimal conditions for separation of the organic acids were 0.5 mM sulphuric acid and acetone (85:15, v/v) and 30°C. Stock standard solutions (1 mg/mL) of the organic acids were prepared and kept at +4°C. Different dilutions of the stock solutions were used for the calibration curves. Fruits collected in 2009 in Manhiça were used for this analysis. About 500 mg fruit pulps were mixed with 5 ml sulphuric acid (Ultra Turrax TP18/10) for 2 minutes and then centrifuged at 2000 rpm for 15 minutes. The supernatants were filtered through 0.45 μm membrane filters and diluted with Millipore water to appropriate concentrations. The retention time and peak areas were compared with reference samples run under the same conditions and used to calculate the concentration of the organic acids in the fruit samples. All experiments were performed at least in triplicates.
Selected samples of the pulps, seeds and kernels were prepared for determination of mineral content. The samples were digested in a microwave oven with concentrated nitric acid and then analysed by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES, Perkin Elmer, OPTIMA 3000 DV). The experiments were performed in duplicate.
The results of the dietary fibre were subjected to analysis of variance. Differences between means were tested at 5% probability by Turkey’s test, using SPSS program (version 13).
Al-Farsi M, Alasalvar C, Morris A, Baron M, Shahidi F: Compositional and sensory characteristics of three native Sun-dried date (phoenix dactylifera L.) varieties grown in Oman. J Agr Food Chem 2005, 53(19):7586-7591. 10.1021/jf050578y
Amarteifio JO, Mosase MO: The chemical composition of selected indigenous fruits of Botswana. J Appl Sci Environ Manag 2006, 10(2):43-47.
Anderson JM, Smith BM, Gustafson NJ: Health benefits and practical aspects of high-fiber diets. Am J Clin Nutr 1994, 59(suppl):1242S-1247S.
AOAC: Official methods of analysis of AOAC International. 17th edition. Edited by: Horwitz W. Association of Analytical Communities, AOAC International, Md, USA; 2000.
Arthey D, Ashurst PR: Fruit Processing: nutrition, products and quality management. 2nd edition. Aspen Publishers, USA; 2001.
Asp N-G, Johansson C-G, Hallmer H, Siljeström M: Rapid enzymatic assay of insoluble and soluble dietary fiber. J Agric Food Chem 1983, 31: 476-482. 10.1021/jf00117a003
Black R: Micronutrient deficiency—an underlying cause of morbidity and mortality. Bull World Health Organ 2003, 81(2):79. Published online March 25, 2003
Bonjour JP, Gueguen L, Palacios C, Shearer MJ, Weaver CM: Minerals and vitamins in bone health: the potential value of dietary enhancement. Brit J Nutri 2009, 101(11):1581-1596. 10.1017/S0007114509311721
Brown L, Rosner B, Willett WW, Sacks FM: Cholesterol-lowering effects of dietary fiber: a meta-analysis1, 2. Am J Clin Nutri 1999, 69: 30-42.
Commission Decision: Authorising the placing on the market of Baobab dried fruit pulp as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council. 2008. Accessed at 05/06/2012 http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2008:183:0038:0039:EN:PDF
de Oliveira Sousa AG, Fernandes DC, Alves AM, de Freitas JB, Naves MMV: Nutritional quality and protein value of exotic almonds and nut from the Brazilian Savanna compared to peanut. Food Research Inter 2011, 44(7):2319-2325. 10.1016/j.foodres.2011.02.013
Effiong GS, Udo IF: Nutritive Values of four Indigenous wild fruits in Souteastern Nigeria. Elect J Env, Agric Food Chem 2010, 9(7):1168-1176.
Ekesa BN, Walingo M, Abukutsa-Onyango MO: Accessibility to and composition of indigenous vegetables and fruits by rural households in mutungu division, western Kenya. Afr Food, Agric, Nutri Dev 2009, 9(8):1725-1738.
Elleuch M, Bedigian D, Roiseux O, Besbes S, Blecker C, Attia H: Dietary fibre and fibre-rich by-products of food processing: Characterisation, technological functionality and commercial applications: A review. Food Chem 2011, 124(2):411-421. 10.1016/j.foodchem.2010.06.077
Eromosele IC, Eromosele O, Kuzhkuzha DM: Evaluation of mineral elements and ascorbic acid contents in fruits of some wild plants. Plant Food Hum Nutri 1991, 41: 151-154. 10.1007/BF02194083
Falade OS, Olusoga RS, Oladipo A, Tubosun A, Adewusi SRA: The level of organic acids in some Nigerian fruits and their effect on mineral availability in composite diets. Pak J Nutr 2003, 2(2):82-88.
FAO: Nutrition Country Profile Republic of Mozambique. Food and Agriculture Organization of the United Nations, Rome; 2011. 54 pp
Gillooly M, Bothwell TH, Torrance JD, MacPhail AP, Derman DP, Bezwoda WR, Mills W, Charlton RW, Mayet F: The effects of organic acids, phytates and polyphenols on the absorption of iron from vegetables. Brit J Nutri 1983, 49: 331-342. 10.1079/BJN19830042
Glew RH, Ayaz FA, Sanz C, VanderJagt DJ, Huang HS, Chuang LT, Strnad M: Changes in sugars, organic acids and amino acids in medlar (Mespilus germanica L.) during fruit development and maturation. Food Chem 2003, 83(3):363-369. 10.1016/S0308-8146(03)00097-9
Glew RH, VanderJagt DJ, Lockett C, Grivetti LE, Smith GC, Pastuszyn A, Millson M: Amino acid, fatty acid, and mineral composition of 24 indigenous plants of Burkina Faso1. J Food Comp Anal 1997, 10: 205-217. 10.1006/jfca.1997.0539
Glew RS, VanderJagt DJ, Huang YS, Chuang LT, Bosse R, Glew RH: Nutritional analysis of the edible pit of Sclerocarya birrea in the Republic of Niger (daniya, Hausa). J Food Comp Anal 2004, 17(1):99-111. 10.1016/S0889-1575(03)00101-7
Hamilton CC, Geil PB, Anderson JW: Management of obesity in diabetes mellitus. Diabetes Educ 1992, 18(5):407-410. 10.1177/014572179201800507
Hasib A, Jaouad A, Mahrouz M, Khouili M: HPLC determination of organic acids in Moroccan apricot. Cienc Tecnol Aliment 2002, 3(4):207-211. 10.1080/11358120209487729
Ibrahim F: Fruity response efficacy and fruit consumption among a group of civil servants of Oyo State, Nigeria. A J Clin Nutri 2011, 1(1):44-48.
Ilich JZ, Brownbill RA, Tamborini L: Bone and nutrition in elderly women: protein, energy, and calcium as main determinants of bone mineral density. Europ J Clin Nutr 2003, 57(4):554-565. 10.1038/sj.ejcn.1601577
Imelouane B, Tahri M, Elbastrioui M, Aouinti F, Elbachiri A: Mineral contents of some medicinal and aromatic plants growing in eastern morocco. J Mater Environ Sci 2011, 2(2):104-111.
Insel P, Ross D, McMahon K, Bernstein M: Nutrition, Sudbury Massachusetts. 4th edition. Jones and Bartlett Publishers, USA; 2011.
Li BW, Andrews KW, Pehrsson PR: Individual sugars, soluble, and insoluble dietary fiber contents of 70 high consumption foods. J Food Compos Anal 2002, 15(6):715-723. 10.1006/jfca.2002.1096
Lockett CT, Calvert CC, Grivetti LE: Energy and micronutrient composition of dietary and medicinal wild plants consumed during drought. Study of rural Fulani, Northeastern Nigeria. Inter J Food Sci Nutri 2000, 51(3):195-208. 10.1080/09637480050029700
López MAA, Martos FC: Iron availability: An updated review. Inter J food Sci Nutri 2004, 55(8):597-606. 10.1080/09637480500085820
Loredana L, Diehl H, Socaciu C: HPLC Fingerprint of organic acids in fruit juices. Buletin USAMV-CN 2006, 62: 288-292.
Murray SS, Schoeninger MJ, Bunn HT, Pickering TR, Marlett JA: Nutritional composition of some wild plant foods and honey used by hadza foragers of Tanzania. J Food Compos Anal 2001, 14(1):3-13. 10.1006/jfca.2000.0960
National Food Agency: The National Food Administration’s food database. SLV, Sweden; 2012. Accessed at 30/05/2012 http://www.slv.se/en-gb/
National Research Council: Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients). The National Academies Press, Washington; 2005. Accessed 05/06/2012 http://www.nap.edu/books/0309085373/html/
New SA: Intake of fruit and vegetables: implications for bone health. Proceed Nutr Soci 2003, 62: 889-899.
Nkafamiya II, Osemeahon SA, Dahiru D, Umaru HA: Studies on the chemical composition and physicochemical properties of the seeds of baobab (Adasonia digitata). African J Biotech 2007, 6(6):756-759.
Nnam NM, Obiakor PN: Effect of fermentation on the nutrient and antinutrient composition of baobab (adansonia digitata) seeds and rice (oryza sativa) grains. Ecol of Food and Nutri 2003, 42(4–5):265-277.
Nour V, Trandafir I, Ionica ME: HPLC organic acid analysis in different citrus juices under reversed phase conditions. Not Bot Horti Agrobot Cluj-Napoca 2010, 38(1):44-48.
Osman MA: Chemical and nutrient analysis of baobab (adansonia digitata) fruit and seed protein solubility. Plant Food Hum Nutri 2004, 59: 29-33. 10.1007/s11130-004-0034-1
Reinhold JG, Garcia LJS, Garzon PMD: Binding of iron by fiber of wheat and maize. Am J Clin Nutri 1981, 34: 1384-1391.
Rodríguez R, Jiménez A, Fernández-Bolaños J, Guillén R, Heredia A: Dietary fibre from vegetable products as source of functional ingredients. Trends Food Sci Technol 2006, 17(1):3-15. 10.1016/j.tifs.2005.10.002
Saka JDK, Msonthi JD: Nutritional value of edible fruits of indigenous wild trees in Malawi. Forest Ecol Manag 1994, 64(2–3):245-248.
Sena LP, VanderJagt DJ, Rivera C, Tsin ATC, Muhamadu I, Mahamadou O, Millson M, Pastuszyn A, Glew RH: Analysis of nutritional components of eight famine foods of the Republic of Niger. Plant Food Hum Nutri 1998, 52(1):17-30. 10.1023/A:1008010009170
Van Duyn MAS, Pivonka E: Overview of the health benefits of fruit and vegetable consumption for the dietetics professional: Selected literature. J Am Dietetic Assoc 2000, 100(12):1511-1521. 10.1016/S0002-8223(00)00420-X
This study was supported financially by the Swedish International Development Agency Project “Technology Processing of Natural Resources for Sustainable Development” at Eduardo Mondlane University, Maputo, Mozambique. We thank Dr Ulf Nilsson, Mr Christer Fahlgren and Mr Luqman Masood for their excellent technical assistance.
The authors declare that they have no competing interests.
TM performed most of the experimental work, (apart from the mineral analysis), took part in the evaluation of the results and wrote the manuscript. All authors participated in the design of the study, supervised the field work and data collection and took part in the evaluation of the results. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.