Acessibilidade / Reportar erro

Physicochemical Characterization, Proximate Composition and Fatty Acid Profile of Fruits from Brazilian Northeast Agrobiodiversity

Abstract

The objective was to evaluate the physicochemical characteristics, nutritional composition and fatty acid profile of eleven exotic fruits in Brazil Northeast. The fruits, except pequi, presented acid pH, high moisture, low protein, low lipid and low energetic contents. Pequi is highlighted by its high protein content (2.79 g.100 g-1), lipid (13.6 g.100 g-1), carbohydrates (28.71 g.100 g-1), titratable acidity (2.75 g citric acid.100 g-1) and pH (2.54-5.19). Unpeeled and peeled jenipapo presented higher ash composition (1.26-1.38g.100 g-1), soluble solids (20.29-21.17 ºBrix) and carbohydrates (22.55-23.66 g.100 g-1) compared to others fruits. Fourteen fatty acids were quantified and classified as saturated fatty acids, monounsaturated fatty acids and polyunsaturated fatty acids. The concentrations of total fatty acids ranged from 1.92 to 1293.21 mg.100 g-1, being palmitic acid and oleic acid more prevalent. The fruits composition data indicated potential for improvement of diets, food industry and gastronomic market.

Keywords:
tropical fruits; biodiversity; nutritional composition; fatty acids; physico-chemical characterization; Brazilian fruits

HIGHLIGHTS

Chemical composition was first performed in Psidium sobralianum Landrum & Proença.

Pequi and Jenipapo are important energy contributors of diets.

Pequi oil has the potential to replace trans fatty acids in food industry.

Chemical compounds used in this study:

Methanol (PubChem CID: 887, Synth®), hydrochloric acid (PubChem CID: 313, Synth®), sulfuric acid (PubChem CID: 1118, Dinâmica®), ethanol (PubChem CID: 702, Dinâmica®), chloroform (PubChem CID: 6212, Vetec®), boric acid (PubChem CID: 7628, Vetec®), sodium hydroxide (PubChem CID: 14798, Vetec®), potassium sulphate (PubChem CID: 24507, Vetec®), copper sulphate (PubChem CID: 24462, Vetec®), sodium sulfate (PubChem CID: 24436, Vetec®), sodium chloride (PubChem CID: 5234, Vetec®), selenium (PubChem CID: 6326970, Vetec®), ammonium chloride (PubChem CID: 25517, Vetec®), hexane (PubChem CID: 8058, Neon®). All chemicals were of analytical grade.

INTRODUCTION

The decline in the use of nutrient-rich foods from the local biodiversity are associated to the increase in the consumption of low-nutrient, energy-rich and less diversified industrial processed foods [11 WHO-World Health Organization. 2015. Healthy diet: Fact sheet No. 394. Available from: http://www.who.int/mediacentre/factsheets/fs394/en/
http://www.who.int/mediacentre/factsheet...
]. It contributes to nutritional deficiencies [22 FAO- Food and Agriculture Organization of the United Nations. 2017. The State of Food Insecurity in the World 2017: Leveraging Food Systems for Inclusive Rural Transformation, Rome. Available from: http://www.fao.org/3/a-I7658e.pdf
http://www.fao.org/3/a-I7658e.pdf...
] and chronic noncommunicable diseases [33 Brazil. 2017. Ministry of Health. Health Surveillance Secretariat. Strategic and Participatory Management Secretariat. Surveillance Department of Diseases and Noncommunicable Diseases and Health Promotion. Vigitel Brasil 2017: Risk factors surveillance and protection for chronic diseases by telephone survey. Brasília: Ministry of Health. 160p.].

In this context, neglected and underutilized plant species rich in nutrients can assist in food security among other benefits such as reducing biodiversity loss and alleviating climate change; as long as science, partnerships, policy, programs, and awareness are better interconnected [44 Hunter D, Borelli T, Beltrame DMO, Oliveira CNS, Coradin L, Wasike VW et al. The potential of neglected and underutilized species for improving diets and nutrition. Planta. 2019 Sep; 250:709-29. Doi: 10.1007/s00425-019-03169-4.
https://doi.org/10.1007/s00425-019-03169...
].

Analysis of the nutritional composition of underutilized food biodiversity, as well as the dissemination of this data, is essential to encourage and increase the consumption and marketing of these fruits [55 Biazotto KR, Mesquita LMS, Neves BV, Braga ARC, Tangerina MMP, Vilegas W, et al. Brazilian Biodiversity Fruits: Discovering Bioactive Compounds from Underexplored Sources. J. Agric. Food Chem. 2019 Feb; 67:1860-76. Doi: 10.1021/acs.jafc.8b05815.
https://doi.org/10.1021/acs.jafc.8b05815...
]. This analysis can foster databases in the area of public health, helping to understand the consumption of these foods and their impact, as well as in the planning of public policy. In the area of research, the analysis of this data provides large-scale epidemiological studies and intervention plans. The food technology sector uses this data to reformulate foods, design nutritional labeling, support nutritional health claims, and develop nutrition-related digital tools. The data also impacts consumers through technological tools that increase awareness and access to nutritional information [66 Traka MH, Plumb J, Berry R, Pinchen H, Finglas PM. Maintaining and updating food composition datasets for multiple users and novel technologies: Current challenges from a UK perspective. Nutr Bull. 2020 Jun;45:230-40. Doi: 10.1111/nbu.12433.
https://doi.org/10.1111/nbu.12433....
].

Regarding the nutritional potential of fruits from the Cerrado in Brazil, researchers have observed high moisture levels varying from 74.30% (marolo) to 89.74% (cagaita); the ash, protein, and lipid contents varied between 0.30% (cagaita) and 1.01% (buriti), 0.42% (araçá), 1.43% (buriti), and 0.48% (yellow hunting) and 7.72% (buriti), respectively. The authors also identified carbohydrate and fiber contents of 4.47% (buriti) to 18.65% (marolo), and 0.61% (cagaita) to 21.62% (marolo), respectively. The energy value of the pulps ranged from 38.62 kcal.100 g-1 (araçá) to 113.65 kcal.100 g-1 (marolo). The marolo reported the highest total phenolic compounds (728.17 mg GAEs.100g-1), and a high antioxidant potential. Buriti contained the highest carotenoid content (2.85 mg. 100 g-1of lycopene e 4.65 mg. 100 g-1 of β-carotene) [77 Schiassi MCEV, Souza VRD, Lago AMT, Campos LG, Queiroz F. Fruits from the Brazilian Cerrado region: Physico-chemical characterization, bioactive compounds, antioxidant activities, and sensory evaluation. Food Chem. 2018 Apr; 245:305-11.].

In the evaluation of unexplored Amazon fruits, high levels of total lipids were found in uxi pulp (20.48 mg.100 g-1), umari varieties (17-18 mg.100 g-1) and piquiá pulp (14 .40 mg.100 g-1). The highest level of oleic acid (18:1n-9) was found in the pulp of Pajurá (775. mg 100 g-1), while the highest levels of linoleic acid (18:2n-6) and α-linolenic acid (18:3n-3) were found in the pulp of Piquiá (305.06 mg.100g-1) and the pulp of uxi (412. 97 mg.100g-1), respectively [88 Berto A, Silva AF, Visentainer JV, Matsushita M, Souza NE. Proximate compositions, mineral contents and fatty acid compositions of native Amazonian fruits. Food Res Int. 2015 Nov; 77:441-9. Doi: 10.1016/j.foodres.2015.08.018.
https://doi.org/10.1016/j.foodres.2015.0...
].

As for the physicochemical characteristics and nutritional value of fruits from Brazilian biodiversity, some data are still limited and, at times, non-existent [99 Pereira MC, Steffens RS, Jablonski A, Hertz PF, Rios AO, Vizzotto M, et al. Characterization and Antioxidant Potential of Brazilian Fruits from the Myrtaceae Family. J. Agric. Food Chem. 2012 Mar; 60:3061-7. Doi: 10.1021/jf205263f.
https://doi.org/10.1021/jf205263f....
]. This is the case for the species Psidium sobralianum, recently identified in Northeast Brazil [1010 Landrum LR, Proença CEB. A new species of Psidium (Myrtaceae) from the Brazilian Northeast. Brittonia. 2015 Oct;67(4):324-7. Doi: 10.1007/s12228-015-9396-y.
https://doi.org/10.1007/s12228-015-9396-...
], which has only a profile of soluble vitamins, carotenoids and minerals [1111 Assis RC, Soares RLG, Siqueira ACSP, Rosso VV, Sousa PHM, Mendes AEP, et al. Determination of water-soluble vitamins and carotenoids in Brazilian tropical fruits by High Performance Liquid Chromatography. Heliyon. 2020 Oct;6(10):e05307. Doi: 10.1016/j.heliyon.2020.e05307.
https://doi.org/10.1016/j.heliyon.2020.e...
-1212 Assis RCD, Siqueira ACP, Oliveira JPDS, Silva FLFD, Matos WO, Gouveia ST, et al. Characterization of Mineral Content in Fruits of Northeast Agrobiodiversity of Brazil. Braz. Arch. Biol. Technol. 2022 Jan; 65:e22200759. Doi: 10.1590/1678-4324-2022200759.
https://doi.org/10.1590/1678-4324-202220...
].

In the Caatinga region, the available food resources have diversity and quality to face the challenges imposed by the region's characteristics and current food systems, defending the recognition of these vegetables as strategies in the development of a food biodiversity research agenda [1313 Jacob MCM, Medeiros MFA, Albuquerque UP. 2020. Biodiverse food plants in the semiarid region of Brazil have unknown potential: A systematic review. Plos One, 15(5): e0230936. Doi: 10.1371/journal.pone.0230936
https://doi.org/10.1371/journal.pone.023...
].

The present study aimed to analyze and evaluate physicochemical parameters, proximate composition and fatty acid profile of underutilized fruits occurring in Brazil Northeast. The fruits were chosen based on the "Plants for the Future" national plan. This study highlights the potential availability of native fruits in Brazil Northeast as a source of nutrients for inclusion in the dietary habits of the local population.

MATERIAL AND METHODS

Sample collection and preparation

Eleven species cultivated and consumed in Brazilian Northeast were selected, as shown in the supplementary material (Table S1). Each fruit species was purchased, according to Greenfield and Southgate [1414 Greenfield H, Southgate DAT. 2003. Food Composition Data: Production, Management and Use. FAO: Rome. Available from: http://www.fao.org/docrep/pdf/008/y4705e/y4705e.pdf
http://www.fao.org/docrep/pdf/008/y4705e...
], in supply centers, fairs, municipal markets or farms, in different cities of the Brazilian Northeast during 2015-2016, according to their harvest availability.

The fruits without damages were selected and sent for edible part separation. The edible parts were manually separated and then processed in a Skymsen® semi-industrial blender, placed in plastic bags and sealed. Moisture (g.100 g-1), soluble solids (TSS, °Brix) and pH were immediately measured, according to methodologies in 2.2.2. The remaining samples were stored at -18 °C until further analyzes.

Methods

Physical properties

Before processing, each fruit lot was weighed in a Balmak® digital scale for yield analysis. Fruit yield was obtained using the formula: Edible fruit part massa (g)/ Total fruit mass (g) x 100.

From each lot, ten fruit units were randomly chosen and used to perform physical analyzes. The individual mass (g) were measured using a Pocket Scale® digital scale. The longitudinal (length) and transverse (width) (mm) fruits diameters were measured with a caliper (Perel Tool®, HMC150, USA).

Physicochemical characterization

The physicochemical analyzes were performed according to AOAC [1515 AOAC-Association of Official Analytical Chemists. 2005. Official Methods of Analysis of the AOAC International. In Horwitz, W., & Latimer, G. W. (Eds.). (18th ed.). Gaithersburg, MD. AOAC International.]. The pH was determined using a digital pH meter (Jenway, model 3505, USA), periodically calibrated with buffered solutions (pH 4.0 and 7.0). Soluble solids (SS) was measured by a digital refractometer (Pal-1 model, Atago, Brazil) and the results were expressed in ºBrix. The titratable acidity (g citric acid.100 g-1) was determined by titration with 0.1 M NaOH solution using phenolphthalein as indicator.

Proximate composition

Moisture, ash and protein analyzes were carried out according to AOAC [1515 AOAC-Association of Official Analytical Chemists. 2005. Official Methods of Analysis of the AOAC International. In Horwitz, W., & Latimer, G. W. (Eds.). (18th ed.). Gaithersburg, MD. AOAC International.] and the results were expressed on a wet basis. Samples crude protein content was estimated by micro-Kjeldahl method, using 6.25 as corrector factor [1515 AOAC-Association of Official Analytical Chemists. 2005. Official Methods of Analysis of the AOAC International. In Horwitz, W., & Latimer, G. W. (Eds.). (18th ed.). Gaithersburg, MD. AOAC International.]. Total lipid content determination was performed as described by Bligh and Dyer [1616 Bligh EG, Dyer WJ. Canadian Journal of Biochemistry and Physiology. Can. J. Biochem. 1959;37(8):911-7.]. Total carbohydrates were estimated by difference. The total energy was calculated by multiplying the protein, lipid and carbohydrate contents in grams by their combustion values (4.0, 9.0 and 4.0 kcal, respectively) [1515 AOAC-Association of Official Analytical Chemists. 2005. Official Methods of Analysis of the AOAC International. In Horwitz, W., & Latimer, G. W. (Eds.). (18th ed.). Gaithersburg, MD. AOAC International.]. The analyzes were performed in triplicate.

Fatty acids profile

Fruit edible parts were subjected to extraction using a soxhlet apparatus. Hexane PA was applied as solvent. The fatty acid methyl esters were prepared by methylation of the lipid fraction [1717 Hartman L. Rapid preparation of fatty acid methyl esters from lipids. Lab.Pract. 1973;22(7):475-6. 18 Adams RP. Identification of essential oil components by gas chromatography/mass spectrometry, 4th Ed. Biochem. Syst. Ecol. 1995;24(6):594.].

The fatty acid methyl esters were separated by gas chromatography coupled with mass spectrometry (GC-MS) in Agilent model (GC-7890B / MSD-5977A - quadrupole) with electron impact at 70 eV, HP-5MS methylpolysiloxane column (30 mx 0.25 mm x 0.25 μm, Agilent). Carrier gas (He) flow rate was 1.0 mL.min1, injector temperature 250°C, detector temperature 150°C, transfer line temperature 280°C. Chromatographic oven programming: initial temperature was 35°C with a heating ramp of 15°C.min-1 till 180°C, then increased to 250°C at a rate of 5°C.min-1 and held for 10 minutes. The identification of the compounds was performed by comparing their mass spectra (MS) and retention indices (RI) with those reported in the literature and in the equipment database (NIST version 2.0 of 2012 - 243.893 compounds).

Statistical analysis

The data were analyzed by analysis of variance (ANOVA) with 5% of significance. Tukey's mean test was applied at the same level of significance. The values ​​were reported as the mean ± standard deviation. Principal Component Analysis (PCA) was applied to physicochemical data and centesimal composition in order to easy results visualization. All analyzes were performed in the Statistical software and data analysis add-in for Excel (XLSTAT 2018, version 1.0) software.

RESULTS

Table 1 shows the physical and physical-chemical parameters of the edible parts of 36 samples of tropical fruits from the Brazilian northeastern agrobiodiversity. The centesimal composition and energy value were presented in Table 2.

Table 1
Physical and physicochemical parameters of the edible parts of 36 samples of tropical fruits from Brazilian Northeast agrobiodiversity. Values expressed as mean ± standard deviation
Table 2
Centesimal composition and energetic value of tropical fruits from Brazilian Northeast agrobiodiversity. Values expressed as mean ± standard deviation.

Table 3 show the content of fatty acid composition of tropical fruits from northeastern agrobiodiversity.

Table 4 shows the sum of fatty acid composition Total fatty acids; TFA: Total fatty acids; SFA: Saturated fatty acids; MFA: Monounsaturated fatty acids; and PUFA: Polyunsaturated fatty acids. n-9: omega-9 fatty acids. n-6: omega-6 fatty acids of tropical fruits from northeastern agrobiodiversity.

Figure 1 present Principal Components Analysis (PCA) of tropical fruits from Brazilian Northeast agrobiodiversity, considering physicochemical and centesimal composition.

Figure 1
Principal Components Analysis (PCA) of tropical fruits from Brazilian Northeast agrobiodiversity. First main component (PC1) versus second main component (PC2) plot. (a) Loading plot of physicochemical and centesimal composition variables; (b) Samples distribution on the chart.

Table 3
Fatty acids composition of tropical fruits from Brazilian Northeast agrobiodiversity, quantified as mg AG/100 g
Table 4
Fatty acids composition of tropical fruits from Brazilian Northeast agrobiodiversity (∑)

DISCUSSION

The majority of fruits analyzed presented yield superior to 60%. Cajuí, araçá, umbu and umbu-cajá presented the highest yields. Pequi (9%) and bacuri (11%) presented the lowest yields. Fruits with higher yields are more desirable for commercialization, once commercial value is associated to the percentage of the fruit edible part [2929 Barbagallo RN, Di Silvestro I, Patanè C. Yield, physicochemical traits, antioxidant pattern, polyphenol oxidase activity and total visual quality of field-grown processing tomato cv. Brigade as affected by water stress in Mediterranean climate. J Sci Food Agric. 2013;93(6):1449-57.].

All species studied, except pequi, are classified as acidic according to the classification proposed by the Food and Drug Administration [3030 FDA - Food and Drug Administration. 2018. Hazard Analysis and Risk-Based Preventive Controls for Human Food: Guidance for Industry. Available from: https://www.fda.gov/downloads/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/UCM517610.pdf/
https://www.fda.gov/downloads/Food/Guida...
]. FDA considers acid fruit if it has natural pH less than or equal to 4.6. All species have pH < 3.7. The low pH restricts pathogenic bacteria development, such as Clostridium botulinum [3131 Alezandro MR, Dubé P, Desjardins Y, Lajolo FM, Genovese MI. Comparative study of chemical and phenolic compositions of two species of jaboticaba: Myrciaria jaboticaba (Vell.) Berg and Myrciaria cauliflora (Mart.) O. Berg. Food Res Int. 2013 Nov;54(1):468-77. Doi: 10.1016/j.foodres.2013.07.018.
https://doi.org/10.1016/j.foodres.2013.0...
]. The studied fruits pH’s are similar to more usual fruits, such as strawberry (3.73), jaboticaba (3.28) and blackberry (2.99) [3232 Souza VRD, Pereira PAP, Silva TLT, Lima LCO, Pio R, Queiroz F. Determination of the bioactive compounds, antioxidant activity and chemical composition of Brazilian blackberry, red raspberry, strawberry, blueberry and sweet cherry fruits. Food Chem. 2014 Aug; 156:362-8. Doi: 10.1016/j.foodchem.2014.01.125.
https://doi.org/10.1016/j.foodchem.2014....
-3333 Abdualrahman MAY, Ma H, Zhou C, Yagoub AEA, Ali AO, Tahir HE, et al. Postharvest physicochemical properties of the pulp and seed oil from Annona squamosa L. (Gishta) fruit grown in Darfur region, Sudan. Arab. J. Chem. 2019 Dec;12(8):4514-21.].

For Schiassiand coauthors [77 Schiassi MCEV, Souza VRD, Lago AMT, Campos LG, Queiroz F. Fruits from the Brazilian Cerrado region: Physico-chemical characterization, bioactive compounds, antioxidant activities, and sensory evaluation. Food Chem. 2018 Apr; 245:305-11.] and Abdualrahmanand coauthors [3333 Abdualrahman MAY, Ma H, Zhou C, Yagoub AEA, Ali AO, Tahir HE, et al. Postharvest physicochemical properties of the pulp and seed oil from Annona squamosa L. (Gishta) fruit grown in Darfur region, Sudan. Arab. J. Chem. 2019 Dec;12(8):4514-21.], fruits with high levels of soluble solids (SS) are more likely to be accepted by consumers and industry, because of their sweetness [3434 Beckles DM. Factors affecting the postharvest soluble solids and sugar content of tomato (Solanumly copersicum L.) fruit. Postharvest Biol Tec. 2012 Jan;63(1):129-40. Doi: 10.1016/j.postharvbio.2011.05.016.
https://doi.org/10.1016/j.postharvbio.20...
]. Peeled and unpeeled jenipapo, pequi and bacuri showed the highest SS content (above 14%) among the species studied.

The SS/AT ratio is the most representative parameter for fruit taste analysis in relation to isolated measures of sugar or acidity analysis. Bacuri, unpeeled and peeled jenipapo presented the highest SS/AT ratio. It is related to a more pleasant flavor due to the balance between sweetness and acidity. It was observed that pitanga (1.22-3.73), umbu (2.76-4.90), murici (1.28-6.06) and umbu-cajá (4.47-5.17) presented the lowest values of SS/AT ratio, which can cause restrictions of fresh consumption. Although, they have good potential to be incorporated into the diets as juices, ice creams, pastes, jams, jellies, pulps, liquors, and smoothies.

It was observed significant differences (p < 0.05) among lots for the same fruit specie. These differences are due to a set of factors. In addition to fruit genetics and physiological maturity at its harvest, environmental factors such as: conditions during plant development, post-harvest practices, cultivation practices, solar radiation, temperature, soil mineral content, fertilization regime, pruning techniques and water availability [3434 Beckles DM. Factors affecting the postharvest soluble solids and sugar content of tomato (Solanumly copersicum L.) fruit. Postharvest Biol Tec. 2012 Jan;63(1):129-40. Doi: 10.1016/j.postharvbio.2011.05.016.
https://doi.org/10.1016/j.postharvbio.20...
-3535 Navarro JM, Botía P, Pérez-Pérez JG. Influence of deficit irrigation timing on the fruit quality of grapefruit (Citrus paradisi Mac.). Food Chem. 2015 Dec; 175:329-36. Doi: 10.1016/j.foodchem.2014.11.152.
https://doi.org/10.1016/j.foodchem.2014....
] can interfere in fruit physicochemical characteristics. Irregularities of rainfall and large periods of water scarcity are very characteristic pictures of Brazil Northeast region. The average amount of precipitation varies between 300 and 2000 mm per year. Rain irregularities depend on several geographic factors, including loss of vegetation [3636 Barbosa HA, Kumar TVL, Paredes F, Elliott S, Ayuga JG. Assessment of Caatinga response to drought using Meteosat-SEVIRI Normalized Difference Vegetation Index (2008-2016). ISPRS J Photogramm. 2019 Feb; 148:235-52. Doi: 10.1016/j.isprsjprs.2018.12.014.
https://doi.org/10.1016/j.isprsjprs.2018...
].

The proximate composition of the 36 fruit samples was analyzed. In most cases, the fruits presented high moisture content, low levels of ash, macronutrients, and energy. High moisture values were observed for several fruits ranging from 54.09 ± 5.37% in pequi to 90.76 ± 0.59% in pitanga. High moisture content favors greater sensory acceptance, however high moisture levels affect texture and flavor, promotes proliferation of microorganisms, undesirable chemical reactions and shorter fruit shelf life [3333 Abdualrahman MAY, Ma H, Zhou C, Yagoub AEA, Ali AO, Tahir HE, et al. Postharvest physicochemical properties of the pulp and seed oil from Annona squamosa L. (Gishta) fruit grown in Darfur region, Sudan. Arab. J. Chem. 2019 Dec;12(8):4514-21.]. It justifies the high perishability of fruits and the need for the development of processing and marketing techniques for better use of them.

In relation to ash content, peeled and unpeeled jenipapo presented higher values 1.38 ± 0.18%, 1.26 ± 0.28%, respectively, and cajuí presented the lowest value 0.40 ± 0.09%.

The ash content may be an indicator of the minerals present in the fruit [3636 Barbosa HA, Kumar TVL, Paredes F, Elliott S, Ayuga JG. Assessment of Caatinga response to drought using Meteosat-SEVIRI Normalized Difference Vegetation Index (2008-2016). ISPRS J Photogramm. 2019 Feb; 148:235-52. Doi: 10.1016/j.isprsjprs.2018.12.014.
https://doi.org/10.1016/j.isprsjprs.2018...
]. Therefore, jenipapo consumption should be stimulated to contribute to the mineral supply. It would improve food security of Brazilian population, which has high prevalence of inadequate minerals intake, such as calcium, phosphorus, iron, zinc, potassium, magnesium and manganese [3737 Sales CH, Fontanelli MDM, Vieira DAS, Marchioni DM, Fisberg RM. Inadequate dietary intake of minerals: Prevalence and association with socio-demographic and lifestyle factors. Brit J Nutr. 2017 Jan;117(2):267-77. Doi: 10.1017/S0007114516004633.
https://doi.org/10.1017/S000711451600463...
-3838 Sena A, Ebi KL, Freitas C, Corvalan C, Barcellos C. Indicators to measure risk of disaster associated with drought: Implications for the health sector. PLoS One. 2017 Jul; 12(7). Doi: 10.1371/journal.pone.0181394.
https://doi.org/10.1371/journal.pone.018...
].

The lipid and protein content for most fruits in this study were less than 1%. This result was expected since fruits, in general, are characterized by higher amounts of water, vitamins, minerals, bioactive compounds and antioxidant capacity [77 Schiassi MCEV, Souza VRD, Lago AMT, Campos LG, Queiroz F. Fruits from the Brazilian Cerrado region: Physico-chemical characterization, bioactive compounds, antioxidant activities, and sensory evaluation. Food Chem. 2018 Apr; 245:305-11.,3939 Hossain A, Begum P, Zannat MS, Rahman MH, Ahsan M, Islam SN. Nutrient composition of strawberry genotypes cultivated in a horticulture farm. Food Chem. 2016 May; 199:648-52. Doi: 10.1016/j.foodchem.2015.12.056.
https://doi.org/10.1016/j.foodchem.2015....
].

It was remarkable that pequi showed the highest protein and lipid values with 2.79 ± 0.16% and 13.61 ± 1.78%, respectively, contributing to the protein and lipid profile of a diet. Pequi consumption, besides enriching the diet with high content of carotenoids, zinc, magnesium, calcium and polyphenols, has an important lipid contribution, unlike other fruits, helping in the energy supply and absorption of fat soluble compounds [4040 Nascimento-Silva NRR, Mendes NSR, Silva FA. Nutritional composition and total phenolic compounds content of pequi pulp (Caryocar brasiliense Cambess.). J. Bioen. Food Sci. 2020; 07:1-10.].

The highest fruits caloric contribution is derived mainly from carbohydrates, once the values of lipids and proteins did not substantially affect the total fruits energetic value. This assumption cannot be considered for pequi, which presented the highest lipid values, contributing to a higher total energy value (TEV) with 248.52 ± 29.10 kcal.100 g-1. The lowest caloric content was found in pitanga with 35.23 ± 1.11 kcal.100g-1.

Pequi, unpeeled and peeled jenipapo showed higher carbohydrate content. The mean values were 28.71 ± 3.92%, 23.66 ± 3.44% and 22.55 ± 3.21%, respectively. Pitanga had the lowest carbohydrate content (7.89 ± 0.17%). Carbohydrate consumption is fundamental for energy metabolism in humans, being the main source of energy for brain cells [4141 Barazzoni R, Deutz NEP, Biolo G, Bischoff S, Boirie Y, Cederholm T, et al. Carbohydrates and insulin resistance in clinical nutrition: Recommendations from the ESPEN expert group. Clin Nutr. 2017 Apr;36(2):355-63. Doi: 10.1016/j.clnu.2016.09.010.
https://doi.org/10.1016/j.clnu.2016.09.0...
].

The IDF and SDF observed in the samples ranged from 1.14% (cashew) to 6.35% (murici and unpeeled jenipapo) and 0.73% (pitanga) to 2.49% (peeled jenipapo), respectively. Regarding the TDF, the values found ranged from 1.14% (cashew) to 7.93% (murici).

Murici (7.93%) and unpeeled jenipapo (7.27%) presented higher TDF values. Murici and peeled jenipapo contained more TDF than the fruits studied by Souza and coauthors [4242 Souza VRD, Pereira PAP, Queiroz F, Borges SV, Carneiro JDS. Determination of bioactive compounds, antioxidant activity and chemical composition of Cerrado Brazilian fruits. Food Chem. 2012 Sept;134(1):381-386. Doi: 10.1016/j.foodchem.2012.02.191.
https://doi.org/10.1016/j.foodchem.2012....
], in Uberlândia, Minas Gerais (Brazil). The authors found 3.08% of TDF for murici and the 1.15% for unpeeled jenipapo. The IDF, SDF and TDF data are scarce in the literature for the fruits under study.

Fourteen fatty acids were detected, quantified and characterized as Saturated Fatty Acids (SFAs), Monounsaturated Fatty Acids (MFAs) and Polyunsaturated Fatty Acids (PUFAs). Chromatograms are presented in the supplementary material Figures S2 to S13. Total fatty acids concentrations (TFA) ranged from 1.92 to 1293.21 mg.100 g-1 fresh matter. The fruits did not present significant amounts of fatty acids, excepted pequi, which showed the highest lipid profile, corroborating with total lipid analysis.

SFA concentrations found in the samples ranged from 0.91 to 4947.33 mg.100g-1.

SFAs are related to the risk of developing cardiometabolic diseases [4242 Souza VRD, Pereira PAP, Queiroz F, Borges SV, Carneiro JDS. Determination of bioactive compounds, antioxidant activity and chemical composition of Cerrado Brazilian fruits. Food Chem. 2012 Sept;134(1):381-386. Doi: 10.1016/j.foodchem.2012.02.191.
https://doi.org/10.1016/j.foodchem.2012....
]. However, vegetable foods have no direct influence on the etiology of these diseases, as they have protective components such as vitamins, minerals and bioactive compounds, providing health benefits [4343 Wu JHY, Micha R, Mozaffarian D. Dietary fats and cardiometabolic disease: mechanisms and effects on risk factors and outcomes. Nat. Rev. Cardiol. 2019 Oct;16(10):581-601. Doi:10.1038/s41569-019-0206-1.
https://doi.org/0.1038/s41569-019-0206-1...
,4444 Mozaffarian D, Wu JHY. Flavonoids, dairy foods, and cardiovascular and metabolic health: a review of emerging biologic pathways. Circ. Res. 2018 Jan;122(2):369-84. Doi: 10.1161/CIRCRESAHA.117.309008.
https://doi.org/10.1161/CIRCRESAHA.117.3...
].

Palmitic acid is the main component of palm oil, popularly known in Brazil as dendê oil. It has been widely used in the production of biofuels and in the food industry. Palm oil can replace trans fatty acids, which promotes dyslipidemia and cardiovascular diseases [4545 Rees A, Dodd GF, Spencer JPE. The effects of flavonoids on cardiovascular health: A review of human intervention trials and implications for cerebrovascular function. Nutrients. 2018 Dec;10(12):1852. Doi: 10.3390/nu10121852.
https://doi.org/10.3390/nu10121852....
]. Pequi presented higher levels of palmitic acid. Nowadays, the main palm oil source is the monoculture of palm trees (Elaeisguineenses Jacq.) in the Brazilian Amazon [4646 May CY, Nesaretnam K. Research advancements in palm oil nutrition. Eur J Lipid Sci Tech. 2014 Oct; 116(10):1301-15. Doi: 10.1002/ejlt.201400076.
https://doi.org/10.1002/ejlt.201400076....
]. It is bringing negative environmental impacts such as forest degradation and loss of biodiversity [4747 Mendes-Oliveira AC, Peres CA, Maués PCRDA, Oliveira GL, Mineiro IGB, Silva de Maria SL, et al. Oil palm monoculture induces drastic erosion of an Amazonian forest mammal fauna. PLoS One. 2017 Nov;12(11):1-19. Doi: 10.1371/journal.pone.0187650.44.
https://doi.org/10.1371/journal.pone.018...
]. Therefore, the extraction of palmitic acid from pequi oil can be useful to diminish Amazon forest exploration.

The studied fruits showed MFAs levels ranging from 0.79 to 6337.09 mg.100 g-1 of fresh matter. The lowest and highest values were found in pitanga and pequi, respectively. In this study, MFAs are mainly composed by oleic acid (18:1, n9), in consonance with fruits studied by Bertoand coauthors [88 Berto A, Silva AF, Visentainer JV, Matsushita M, Souza NE. Proximate compositions, mineral contents and fatty acid compositions of native Amazonian fruits. Food Res Int. 2015 Nov; 77:441-9. Doi: 10.1016/j.foodres.2015.08.018.
https://doi.org/10.1016/j.foodres.2015.0...
] Oleic acid has been associated with beneficial cardiovascular effects, reducing low-density lipoprotein (LDL) levels [4848 Handl J, Meloun M, Muzáková V. Inflammatory markers in dependence on the plasma concentration of 37 fatty acids after the coronary stent implantation. J Pharmaceut Biomed. 2018 Feb;149,96-105. Doi: 10.1016/j.jpba.2017.10.033.
https://doi.org/10.1016/j.jpba.2017.10.0...
] In this way, fruits with high levels of oleic acid can be included in the diet and promote human health benefit.

The 12 tested samples showed low levels of PUFAs. Only linoleic acid (18:2, n6), which varied from 0.22 mg.100 g-1 in pitanga to 230.01 mg.100 g-1 in pequi. Unlike the results found in this study, linoleic and linolenic acids (18:3, n3) are commonly found in fruit pulps [88 Berto A, Silva AF, Visentainer JV, Matsushita M, Souza NE. Proximate compositions, mineral contents and fatty acid compositions of native Amazonian fruits. Food Res Int. 2015 Nov; 77:441-9. Doi: 10.1016/j.foodres.2015.08.018.
https://doi.org/10.1016/j.foodres.2015.0...
]. Linoleic and linolenic acids are considered essential fatty acids. They should be obtained in the diet, to work as precursors of others long-chain PUFAs (LC-PUFAs) by the elongase and desaturase enzymes action [4949 Ganesan B, Brothersen C, McMahon DJ. Fortification of Foods with Omega-3 Polyunsaturated Fatty Acids. Crit Rev Food Sci. 2014;54(1),98-114. Doi: 10.1080/10408398.2011.578221.
https://doi.org/10.1080/10408398.2011.57...
]. The difference observed in fatty acids compositions may be due to different biosynthesis phase of these compounds, as well as their accumulation [5050 Ercisli S. Chemical composition of fruits in some rose (Rosa spp.) species. Food Chem. 2007;104(4):1379-84. Doi: 10.1016/j.foodchem.2007.01.053.
https://doi.org/10.1016/j.foodchem.2007....
].

Considering the diversity of the presented data, it is observed that fruits consumption indication varies. In natura, some of them do not have an important energy or macronutrient contribution. This diversity makes cajuí, murici, pitanga, bacuri, araçá, cajá, umbu and umbu-cajá indicated to compose diets of caloric restriction and pequi and jenipapo (peeled and unpeeled) to compose normal or hypercaloric diets.

The development of new products with these species can meet the domestic market needs, under the perspective of healthy food. It would increase food security and combat chronic noncommunicable diseases such as obesity and diabetes.

The two principal components (PC) of the present study represented 79.15% of the total variance. PC1 and PC2 contributed 61.12% and 18.03%, respectively. Samples exhibiting higher values for a selected variable occupy the same variable quadrant.

Most of the samples were positioned on the bottom left quadrant due to the higher moisture contents. This characteristic, in common with most fruits, confirms that the group of foods studied has moisture as the component with the greatest quantity, as also reported in less popular fruit species, such as fisalis, açai, arumbeva, and passion fruit, with moisture variations of 73-89% [5151 Rockett FC, Schmidt HO, Pagno CH, Fochezatto ES, Oliveira VR, Silva VL, et al. Native fruits from southern Brazil: Physico‐chemical characterization, centesimal composition, and mineral content. J. Food Process. Preserv. 2020 May;44(8):e14582. Doi: 10.1111/jfpp.14582.
https://doi.org/10.1111/jfpp.14582....
], as well as in more popular fruit species, such as banana, pineapple, orange, and guava, with moisture variations of 71-90% [5252 TACO. [Brazilian Food Composition Table]. 1ª ed. Campinas: NEPA - UNICAMP, 2004. 42 p.].

Pequi lots were positioned on the bottom right quadrant because they had higher carbohydrates, proteins, lipids, titratable acidity, pH and total energy values. This total energy value can be explained by the fact that pequi pulp and kernel have a balanced proportion of saturated and unsaturated fatty acids, containing a triacylglycerol of great interest to the food industry [5353 Guedes AMM, Antoniassi R, Faria-Machado AF. Pequi: A Brazilian fruit with potential uses for the fat industry. EDP Sciences, 2017 Sep;24(5):1-4. Doi: 10.1051/ocl/2017040.
https://doi.org/10.1051/ocl/2017040....
]. Furthermore, as it is a food source that contains all macronutrients, it can be used in various culinary preparations such as breads made with pequi pulp and peel [5454 Cunha MC, Cunha MC, Lago RC, Melo RS, Almeida LC, Pereira J, et al. Using Response Surface Methodology to evaluate the effect of pequi flour, and pulp and by-product on sweet bread development. Acta Scientiarum. Technology 2021 Apr;43(1): e51850. Doi:. 10.4025/actascitechnol.v43i1.51850.
https://doi.org/10.4025/actascitechnol.v...
] and cookies made with pequi flour [5555 Sousa EO, Santos AMM, Duarte AMS, Silva MTG. [Use of residual flour from pequi pulp cake (Caryoca rcoriacium Wittm) in the development and characterization of sequilho biscuits]. Rev. Bras. Eng. Biossistemas. 2021 Dec;15(4):632-643. Doi: 10.18011/bioeng2021v15n4p632-643.
https://doi.org/10.18011/bioeng2021v15n4...
]. The profile of this fruit can also demonstrate the feasibility of using pequi pulp as a polymeric matrix, with the extraction of pectin proving to be a suitable raw material for the production of biodegradable films with great antioxidant and antimicrobial action [5656 Alves-Silva GF, Romani VP, Martins GV. Different crosslinking as a strategy to improve films produced from external mesocarp of pequi (Caryocar brasiliense). Food Chem. 2024Jun; 432:137202. Doi: 10.1016/j.foodchem.2023.137202.
https://doi.org/10.1016/j.foodchem.2023....
].

Jenipapo groups (peeled or unpeeled) presented higher values for ash and soluble solids, thus, it is in the top right quadrant. The studies that have shown high carbohydrate content in jenipapo pulp [5757 Ribeiro J, Barros HEA, Viana EBM, Gualberto S, Silva A, Souza C, et al. Composition, Antinutrients and Antioxidant Capacity of Genipap (Genipa americana L.): Activity of Phenolic Constituents on the Thermal Stability of β-carotene. J. Culin. Sci. Technol. 2023 Apr;21(2):215-37. Doi: 10.1080/15428052.2021.1914263.
https://doi.org/10.1080/15428052.2021.19...
-5858 Silva MS. Evaluation of the chemical composition and antioxidant activity of Genipa americana L. (jenipapo) from the brazilian cerrado. Top Acad. J. of Environ. Agric. Sci. 2021 Oct;6(5):27-35.], as well as the high energy content of bars made with jackfruit, jenipapo [5959 Altamirano-Fortoul R, Avdić G, Al-Dmoor HM, Babić J, Balaž D, Balestra F, et al. Flour - Bread '13: Proceedings of the 7th International Congress Flour - Bread '13 and 9th Croatian Congress of Cereal Technologists. In: Hassan CZ, Jamal AF, Kal-kausar MA, Ismail S. UDC 664.782: 28-442-027.568 2014. 119p], and cookie-type cookies [6060 Butke W, Amaral LA, Santos EF, Novello D. [Addition of jenipapo flour in cookie alters physico-chemical composition and sensory acceptability among children]. Multitemas. 2019 Jun;24(56):247-60. Doi: 10.20435/multi.v24i56.2084.
https://doi.org/10.20435/multi.v24i56.20...
]. With regard to the ash content in this quadrant, low quantitative values were observed, which can be evidenced by an extensive study that characterized the mineral content of fruits from the agrobiodiversity of Northeast Brazil, concluding that the fruits studied did not have sufficient content for dietary recommendations for the intake of trace elements [1212 Assis RCD, Siqueira ACP, Oliveira JPDS, Silva FLFD, Matos WO, Gouveia ST, et al. Characterization of Mineral Content in Fruits of Northeast Agrobiodiversity of Brazil. Braz. Arch. Biol. Technol. 2022 Jan; 65:e22200759. Doi: 10.1590/1678-4324-2022200759.
https://doi.org/10.1590/1678-4324-202220...
].

CONCLUSION

In conclusion, the physicochemical and nutritional analyzes of the eleven fruits showed variation among the lots. All fruits but pequi presented acidic profile, high moisture content, low protein, low lipid content, and low total energy.

The pequi presented the highest energy value, macronutrients, titratable acidity, and pH; while jenipapo was highlight by its high ash, soluble solids, and carbohydrates. The fatty acids composition varied with a high prevalence of SFA (palmitic acid) and MFA (oleic acid).

Acknowledgments

The authors wish to thank “Biodiversity for food and nutrition (BFN)” project for research stimuli, maintenance and biodiversity preservation and also the State University of Ceara and Federal University of Ceara.

REFERENCES

  • 1
    WHO-World Health Organization. 2015. Healthy diet: Fact sheet No. 394. Available from: http://www.who.int/mediacentre/factsheets/fs394/en/
    » http://www.who.int/mediacentre/factsheets/fs394/en
  • 2
    FAO- Food and Agriculture Organization of the United Nations. 2017. The State of Food Insecurity in the World 2017: Leveraging Food Systems for Inclusive Rural Transformation, Rome. Available from: http://www.fao.org/3/a-I7658e.pdf
    » http://www.fao.org/3/a-I7658e.pdf
  • 3
    Brazil. 2017. Ministry of Health. Health Surveillance Secretariat. Strategic and Participatory Management Secretariat. Surveillance Department of Diseases and Noncommunicable Diseases and Health Promotion. Vigitel Brasil 2017: Risk factors surveillance and protection for chronic diseases by telephone survey. Brasília: Ministry of Health. 160p.
  • 4
    Hunter D, Borelli T, Beltrame DMO, Oliveira CNS, Coradin L, Wasike VW et al. The potential of neglected and underutilized species for improving diets and nutrition. Planta. 2019 Sep; 250:709-29. Doi: 10.1007/s00425-019-03169-4.
    » https://doi.org/10.1007/s00425-019-03169-4.
  • 5
    Biazotto KR, Mesquita LMS, Neves BV, Braga ARC, Tangerina MMP, Vilegas W, et al. Brazilian Biodiversity Fruits: Discovering Bioactive Compounds from Underexplored Sources. J. Agric. Food Chem. 2019 Feb; 67:1860-76. Doi: 10.1021/acs.jafc.8b05815.
    » https://doi.org/10.1021/acs.jafc.8b05815.
  • 6
    Traka MH, Plumb J, Berry R, Pinchen H, Finglas PM. Maintaining and updating food composition datasets for multiple users and novel technologies: Current challenges from a UK perspective. Nutr Bull. 2020 Jun;45:230-40. Doi: 10.1111/nbu.12433.
    » https://doi.org/10.1111/nbu.12433.
  • 7
    Schiassi MCEV, Souza VRD, Lago AMT, Campos LG, Queiroz F. Fruits from the Brazilian Cerrado region: Physico-chemical characterization, bioactive compounds, antioxidant activities, and sensory evaluation. Food Chem. 2018 Apr; 245:305-11.
  • 8
    Berto A, Silva AF, Visentainer JV, Matsushita M, Souza NE. Proximate compositions, mineral contents and fatty acid compositions of native Amazonian fruits. Food Res Int. 2015 Nov; 77:441-9. Doi: 10.1016/j.foodres.2015.08.018.
    » https://doi.org/10.1016/j.foodres.2015.08.018.
  • 9
    Pereira MC, Steffens RS, Jablonski A, Hertz PF, Rios AO, Vizzotto M, et al. Characterization and Antioxidant Potential of Brazilian Fruits from the Myrtaceae Family. J. Agric. Food Chem. 2012 Mar; 60:3061-7. Doi: 10.1021/jf205263f.
    » https://doi.org/10.1021/jf205263f.
  • 10
    Landrum LR, Proença CEB. A new species of Psidium (Myrtaceae) from the Brazilian Northeast. Brittonia. 2015 Oct;67(4):324-7. Doi: 10.1007/s12228-015-9396-y.
    » https://doi.org/10.1007/s12228-015-9396-y.
  • 11
    Assis RC, Soares RLG, Siqueira ACSP, Rosso VV, Sousa PHM, Mendes AEP, et al. Determination of water-soluble vitamins and carotenoids in Brazilian tropical fruits by High Performance Liquid Chromatography. Heliyon. 2020 Oct;6(10):e05307. Doi: 10.1016/j.heliyon.2020.e05307.
    » https://doi.org/10.1016/j.heliyon.2020.e05307.
  • 12
    Assis RCD, Siqueira ACP, Oliveira JPDS, Silva FLFD, Matos WO, Gouveia ST, et al. Characterization of Mineral Content in Fruits of Northeast Agrobiodiversity of Brazil. Braz. Arch. Biol. Technol. 2022 Jan; 65:e22200759. Doi: 10.1590/1678-4324-2022200759.
    » https://doi.org/10.1590/1678-4324-2022200759.
  • 13
    Jacob MCM, Medeiros MFA, Albuquerque UP. 2020. Biodiverse food plants in the semiarid region of Brazil have unknown potential: A systematic review. Plos One, 15(5): e0230936. Doi: 10.1371/journal.pone.0230936
    » https://doi.org/10.1371/journal.pone.0230936
  • 14
    Greenfield H, Southgate DAT. 2003. Food Composition Data: Production, Management and Use. FAO: Rome. Available from: http://www.fao.org/docrep/pdf/008/y4705e/y4705e.pdf
    » http://www.fao.org/docrep/pdf/008/y4705e/y4705e.pdf
  • 15
    AOAC-Association of Official Analytical Chemists. 2005. Official Methods of Analysis of the AOAC International. In Horwitz, W., & Latimer, G. W. (Eds.). (18th ed.). Gaithersburg, MD. AOAC International.
  • 16
    Bligh EG, Dyer WJ. Canadian Journal of Biochemistry and Physiology. Can. J. Biochem. 1959;37(8):911-7.
  • 17
    Hartman L. Rapid preparation of fatty acid methyl esters from lipids. Lab.Pract. 1973;22(7):475-6.
  • 18
    Adams RP. Identification of essential oil components by gas chromatography/mass spectrometry, 4th Ed. Biochem. Syst. Ecol. 1995;24(6):594.
  • 19
    Hanai T, Hong C. Structure‐retention correlation in CGC. J. High Resolut Chromatogr. 1989; 12(5):327-32.
  • 20
    Silva UFD, Borba EL, Semir J, Marsaioli AJ. A simple solid injection device for the analyses of Bulbophyllum (Orchidaceae) volatiles. Phytochemistry. 1999;50(1):31-4.
  • 21
    Grzeszczuk M, Wesolowska A, Jadczak D, Jakubowska B. Nutritional value of Chili edible flowers. ActaSci Pol-Hortoru. 2011;10,85-94.
  • 22
    Kim JS. GC-MS Analysis of the Volatile Components in Dried Boxthorn (Lyciumchinensis) Fruit. J Korean SocAppl Bi. 2009 Sept;52(5):516-24. Doi: 10.3839/jksabc.2009.088.
    » https://doi.org/10.3839/jksabc.2009.088.
  • 23
    Tret'yakov KV. 2007. Retention Data. NIST Mass Spectrometry Data Center. Available from: https://webbook.nist.gov/cgi/cbook.cgi?ID=C506172&Units=SI&Mask=2000
    » https://webbook.nist.gov/cgi/cbook.cgi?ID=C506172&Units=SI&Mask=2000
  • 24
    Pino JA, Mesa J, Muñoz Y, Martí MP, Marbot R. Volatile components from mango (Mangifera indica L.) cultivars. J. Agric. Food Chem. 2005;53(6):2213-23.
  • 25
    Vedernikov DN, Roshchin VI. Extractive compounds of birch buds (Betula pendula Roth.): I. Composition of fatty acids, hydrocarbons, and esters. Russ J Bioorg Chem. 2010;36(7):894-8.
  • 26
    Andriamaharavo NR. 2014a. Retention Data. NIST Mass Spectrometry Data Center. Available from: https://webbook.nist.gov/cgi/cbook.cgi?ID=C506309&Units=SI&Mask=3F92
    » https://webbook.nist.gov/cgi/cbook.cgi?ID=C506309&Units=SI&Mask=3F92
  • 27
    Andriamaharavo NR. 2014b. Retention Data. NIST Mass Spectrometry Data Center. Available from: https://webbook.nist.gov/cgi/cbook.cgi?ID=C929771&Units=SI&Mask=3F92
    » https://webbook.nist.gov/cgi/cbook.cgi?ID=C929771&Units=SI&Mask=3F92
  • 28
    Andriamaharavo NR. 2014c. Retention Data. NIST Mass Spectrometry Data Center. Available from: https://webbook.nist.gov/cgi/cbook.cgi?ID=C2442491&Units=SI&Mask=3F92
    » https://webbook.nist.gov/cgi/cbook.cgi?ID=C2442491&Units=SI&Mask=3F92
  • 29
    Barbagallo RN, Di Silvestro I, Patanè C. Yield, physicochemical traits, antioxidant pattern, polyphenol oxidase activity and total visual quality of field-grown processing tomato cv. Brigade as affected by water stress in Mediterranean climate. J Sci Food Agric. 2013;93(6):1449-57.
  • 30
    FDA - Food and Drug Administration. 2018. Hazard Analysis and Risk-Based Preventive Controls for Human Food: Guidance for Industry. Available from: https://www.fda.gov/downloads/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/UCM517610.pdf/
    » https://www.fda.gov/downloads/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/UCM517610.pdf
  • 31
    Alezandro MR, Dubé P, Desjardins Y, Lajolo FM, Genovese MI. Comparative study of chemical and phenolic compositions of two species of jaboticaba: Myrciaria jaboticaba (Vell.) Berg and Myrciaria cauliflora (Mart.) O. Berg. Food Res Int. 2013 Nov;54(1):468-77. Doi: 10.1016/j.foodres.2013.07.018.
    » https://doi.org/10.1016/j.foodres.2013.07.018.
  • 32
    Souza VRD, Pereira PAP, Silva TLT, Lima LCO, Pio R, Queiroz F. Determination of the bioactive compounds, antioxidant activity and chemical composition of Brazilian blackberry, red raspberry, strawberry, blueberry and sweet cherry fruits. Food Chem. 2014 Aug; 156:362-8. Doi: 10.1016/j.foodchem.2014.01.125.
    » https://doi.org/10.1016/j.foodchem.2014.01.125.
  • 33
    Abdualrahman MAY, Ma H, Zhou C, Yagoub AEA, Ali AO, Tahir HE, et al. Postharvest physicochemical properties of the pulp and seed oil from Annona squamosa L. (Gishta) fruit grown in Darfur region, Sudan. Arab. J. Chem. 2019 Dec;12(8):4514-21.
  • 34
    Beckles DM. Factors affecting the postharvest soluble solids and sugar content of tomato (Solanumly copersicum L.) fruit. Postharvest Biol Tec. 2012 Jan;63(1):129-40. Doi: 10.1016/j.postharvbio.2011.05.016.
    » https://doi.org/10.1016/j.postharvbio.2011.05.016.
  • 35
    Navarro JM, Botía P, Pérez-Pérez JG. Influence of deficit irrigation timing on the fruit quality of grapefruit (Citrus paradisi Mac.). Food Chem. 2015 Dec; 175:329-36. Doi: 10.1016/j.foodchem.2014.11.152.
    » https://doi.org/10.1016/j.foodchem.2014.11.152.
  • 36
    Barbosa HA, Kumar TVL, Paredes F, Elliott S, Ayuga JG. Assessment of Caatinga response to drought using Meteosat-SEVIRI Normalized Difference Vegetation Index (2008-2016). ISPRS J Photogramm. 2019 Feb; 148:235-52. Doi: 10.1016/j.isprsjprs.2018.12.014.
    » https://doi.org/10.1016/j.isprsjprs.2018.12.014.
  • 37
    Sales CH, Fontanelli MDM, Vieira DAS, Marchioni DM, Fisberg RM. Inadequate dietary intake of minerals: Prevalence and association with socio-demographic and lifestyle factors. Brit J Nutr. 2017 Jan;117(2):267-77. Doi: 10.1017/S0007114516004633.
    » https://doi.org/10.1017/S0007114516004633.
  • 38
    Sena A, Ebi KL, Freitas C, Corvalan C, Barcellos C. Indicators to measure risk of disaster associated with drought: Implications for the health sector. PLoS One. 2017 Jul; 12(7). Doi: 10.1371/journal.pone.0181394.
    » https://doi.org/10.1371/journal.pone.0181394.
  • 39
    Hossain A, Begum P, Zannat MS, Rahman MH, Ahsan M, Islam SN. Nutrient composition of strawberry genotypes cultivated in a horticulture farm. Food Chem. 2016 May; 199:648-52. Doi: 10.1016/j.foodchem.2015.12.056.
    » https://doi.org/10.1016/j.foodchem.2015.12.056.
  • 40
    Nascimento-Silva NRR, Mendes NSR, Silva FA. Nutritional composition and total phenolic compounds content of pequi pulp (Caryocar brasiliense Cambess.). J. Bioen. Food Sci. 2020; 07:1-10.
  • 41
    Barazzoni R, Deutz NEP, Biolo G, Bischoff S, Boirie Y, Cederholm T, et al. Carbohydrates and insulin resistance in clinical nutrition: Recommendations from the ESPEN expert group. Clin Nutr. 2017 Apr;36(2):355-63. Doi: 10.1016/j.clnu.2016.09.010.
    » https://doi.org/10.1016/j.clnu.2016.09.010.
  • 42
    Souza VRD, Pereira PAP, Queiroz F, Borges SV, Carneiro JDS. Determination of bioactive compounds, antioxidant activity and chemical composition of Cerrado Brazilian fruits. Food Chem. 2012 Sept;134(1):381-386. Doi: 10.1016/j.foodchem.2012.02.191.
    » https://doi.org/10.1016/j.foodchem.2012.02.191.
  • 43
    Wu JHY, Micha R, Mozaffarian D. Dietary fats and cardiometabolic disease: mechanisms and effects on risk factors and outcomes. Nat. Rev. Cardiol. 2019 Oct;16(10):581-601. Doi:10.1038/s41569-019-0206-1.
    » https://doi.org/0.1038/s41569-019-0206-1.
  • 44
    Mozaffarian D, Wu JHY. Flavonoids, dairy foods, and cardiovascular and metabolic health: a review of emerging biologic pathways. Circ. Res. 2018 Jan;122(2):369-84. Doi: 10.1161/CIRCRESAHA.117.309008.
    » https://doi.org/10.1161/CIRCRESAHA.117.309008.
  • 45
    Rees A, Dodd GF, Spencer JPE. The effects of flavonoids on cardiovascular health: A review of human intervention trials and implications for cerebrovascular function. Nutrients. 2018 Dec;10(12):1852. Doi: 10.3390/nu10121852.
    » https://doi.org/10.3390/nu10121852.
  • 46
    May CY, Nesaretnam K. Research advancements in palm oil nutrition. Eur J Lipid Sci Tech. 2014 Oct; 116(10):1301-15. Doi: 10.1002/ejlt.201400076.
    » https://doi.org/10.1002/ejlt.201400076.
  • 47
    Mendes-Oliveira AC, Peres CA, Maués PCRDA, Oliveira GL, Mineiro IGB, Silva de Maria SL, et al. Oil palm monoculture induces drastic erosion of an Amazonian forest mammal fauna. PLoS One. 2017 Nov;12(11):1-19. Doi: 10.1371/journal.pone.0187650.44.
    » https://doi.org/10.1371/journal.pone.0187650.44.
  • 48
    Handl J, Meloun M, Muzáková V. Inflammatory markers in dependence on the plasma concentration of 37 fatty acids after the coronary stent implantation. J Pharmaceut Biomed. 2018 Feb;149,96-105. Doi: 10.1016/j.jpba.2017.10.033.
    » https://doi.org/10.1016/j.jpba.2017.10.033.
  • 49
    Ganesan B, Brothersen C, McMahon DJ. Fortification of Foods with Omega-3 Polyunsaturated Fatty Acids. Crit Rev Food Sci. 2014;54(1),98-114. Doi: 10.1080/10408398.2011.578221.
    » https://doi.org/10.1080/10408398.2011.578221.
  • 50
    Ercisli S. Chemical composition of fruits in some rose (Rosa spp.) species. Food Chem. 2007;104(4):1379-84. Doi: 10.1016/j.foodchem.2007.01.053.
    » https://doi.org/10.1016/j.foodchem.2007.01.053.
  • 51
    Rockett FC, Schmidt HO, Pagno CH, Fochezatto ES, Oliveira VR, Silva VL, et al. Native fruits from southern Brazil: Physico‐chemical characterization, centesimal composition, and mineral content. J. Food Process. Preserv. 2020 May;44(8):e14582. Doi: 10.1111/jfpp.14582.
    » https://doi.org/10.1111/jfpp.14582.
  • 52
    TACO. [Brazilian Food Composition Table]. 1ª ed. Campinas: NEPA - UNICAMP, 2004. 42 p.
  • 53
    Guedes AMM, Antoniassi R, Faria-Machado AF. Pequi: A Brazilian fruit with potential uses for the fat industry. EDP Sciences, 2017 Sep;24(5):1-4. Doi: 10.1051/ocl/2017040.
    » https://doi.org/10.1051/ocl/2017040.
  • 54
    Cunha MC, Cunha MC, Lago RC, Melo RS, Almeida LC, Pereira J, et al. Using Response Surface Methodology to evaluate the effect of pequi flour, and pulp and by-product on sweet bread development. Acta Scientiarum. Technology 2021 Apr;43(1): e51850. Doi:. 10.4025/actascitechnol.v43i1.51850.
    » https://doi.org/10.4025/actascitechnol.v43i1.51850.
  • 55
    Sousa EO, Santos AMM, Duarte AMS, Silva MTG. [Use of residual flour from pequi pulp cake (Caryoca rcoriacium Wittm) in the development and characterization of sequilho biscuits]. Rev. Bras. Eng. Biossistemas. 2021 Dec;15(4):632-643. Doi: 10.18011/bioeng2021v15n4p632-643.
    » https://doi.org/10.18011/bioeng2021v15n4p632-643.
  • 56
    Alves-Silva GF, Romani VP, Martins GV. Different crosslinking as a strategy to improve films produced from external mesocarp of pequi (Caryocar brasiliense). Food Chem. 2024Jun; 432:137202. Doi: 10.1016/j.foodchem.2023.137202.
    » https://doi.org/10.1016/j.foodchem.2023.137202.
  • 57
    Ribeiro J, Barros HEA, Viana EBM, Gualberto S, Silva A, Souza C, et al. Composition, Antinutrients and Antioxidant Capacity of Genipap (Genipa americana L.): Activity of Phenolic Constituents on the Thermal Stability of β-carotene. J. Culin. Sci. Technol. 2023 Apr;21(2):215-37. Doi: 10.1080/15428052.2021.1914263.
    » https://doi.org/10.1080/15428052.2021.1914263.
  • 58
    Silva MS. Evaluation of the chemical composition and antioxidant activity of Genipa americana L. (jenipapo) from the brazilian cerrado. Top Acad. J. of Environ. Agric. Sci. 2021 Oct;6(5):27-35.
  • 59
    Altamirano-Fortoul R, Avdić G, Al-Dmoor HM, Babić J, Balaž D, Balestra F, et al. Flour - Bread '13: Proceedings of the 7th International Congress Flour - Bread '13 and 9th Croatian Congress of Cereal Technologists. In: Hassan CZ, Jamal AF, Kal-kausar MA, Ismail S. UDC 664.782: 28-442-027.568 2014. 119p
  • 60
    Butke W, Amaral LA, Santos EF, Novello D. [Addition of jenipapo flour in cookie alters physico-chemical composition and sensory acceptability among children]. Multitemas. 2019 Jun;24(56):247-60. Doi: 10.20435/multi.v24i56.2084.
    » https://doi.org/10.20435/multi.v24i56.2084.

Edited by

Editor-in-Chief:

Bill Jorge Costa

Associate Editor:

Bill Jorge Costa

Publication Dates

  • Publication in this collection
    24 June 2024
  • Date of issue
    2024

History

  • Received
    19 Apr 2023
  • Accepted
    11 Jan 2024
Instituto de Tecnologia do Paraná - Tecpar Rua Prof. Algacyr Munhoz Mader, 3775 - CIC, 81350-010 Curitiba PR Brazil, Tel.: +55 41 3316-3052/3054, Fax: +55 41 3346-2872 - Curitiba - PR - Brazil
E-mail: babt@tecpar.br