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Physicochemical and antioxidant capacity analysis of colored sweet potato genotypes: in natura and thermally processed

Análises físico-químicas e capacidade antioxidante de genótipos coloridos de batata-doce in natura e termicamente processados

ABSTRACT:

Sweet potato (Ipomoea batatas (L.) Lam) is one of the most popular and ancient roots of Brazil and it can be consumed at different forms such as boiled, roasted or as sweets. Its cooking can lead to physicochemical transformations altering the nutritional properties. The objective of this study was to evaluate the physicochemical characteristics, bioactive compounds and antioxidant capacity of twelve sweet potato genotypes of varying pulp color in natura and roasted. Soluble solids, acidity, sugars, carotenoids, anthocyanins, phenolic compounds and antioxidant capacity were analyzed in the following sweet potatoes genotypes: cream pulp (Rubissol, Cuia, ILS03, ILS10, ILS12, ILS24 and ILS44); orange pulp (Amelia and Beauregard); and purple pulp (ILS56, ILS16 and ILS71). According to the results, it was observed a wide variation among the sweet potato genotypes for all analyzed parameters, in both preparation forms. The antioxidant capacity was a parameter with wide variation among genotypes, 210.29 to 7870.57µg trolox equivalent/g in in natura form and 673.26 to 17306.22µg trolox equivalent/g in roasted form. Soluble solids, acidity, sugars and bioactive compounds, with the exception of carotenoids, tended to be concentrated, also increases the total antioxidant capacity, in roasted sweet potatoes. In conclusion, genotype and the color of sweet potatoes were parameters that had an influence on its chemical composition. Cultivars such as Amelia and Beauregard stood out by the amounts of total soluble solids and carotenoids, respectively. The selections ILS 16 and ILS 56 are recommended as sources of anthocyanins. Thermal process influenced the concentration of antioxidant compounds and changed some physicochemical characteristics.

Key words:
carotenoids; anthocyanins; processing; bioactive compounds; Ipomoea batatas

RESUMO:

A batata-doce (Ipomoea batatas (L.) Lam) é uma das raízes mais populares e antigas do Brasil, podendo ser consumida cozida, assada ou na forma de doces. A sua cocção pode levar à transformações físico-químicas alterando as propriedades nutricionais. O objetivo deste trabalho foi avaliar as características físico-químicas, compostos bioativos e atividade antioxidante de doze genótipos de batata-doce, de coloração de polpa variada, na forma in natura e assada. Foram determinados sólidos solúveis totais, acidez, açúcares, carotenoides, antocianinas, compostos fenólicos e atividade antioxidante nos seguintes genótipos de batatas-doces: polpa creme (Rubissol, Cuia, ILS03, ILS10, ILS12, ILS24 e ILS44); polpa laranja (Amélia e Beauregard) e polpa roxa (ILS56, ILS16 e ILS71). Quanto aos resultados foi observada ampla variação entre os genótipos de batata-doce, para todos os parâmetros analisados, em ambas as formas de preparo. A atividade antioxidante foi um parâmetro que demonstrou grande variação entre os genótipos, de 210,29 a 7870,57µg de equivalente trolox/g nos genótipos in natura e de 673,26 a 17306,22µg de equivalente trolox/g nos genótipos assados. Foi observado que em batatas-doces assadas os sólidos solúveis, acidez, açúcares e os compostos bioativos, com exceção dos carotenoides, tenderam a ser concentrados, elevando também a atividade antioxidante total. Em conclusão, o genótipo e a coloração da batata-doce foram parâmetros que exerceram influência sob a sua composição química. Cultivares como Amélia e Beauregard se destacaram pela quantidade de sólidos solúveis totais e carotenoides, respectivamente. Como fonte de antocianinas, as seleções ILS 16 e ILS 56 são recomendadas. O processo térmico influenciou a concentração de compostos antioxidantes e alterou algumas características físico-químicas.

Palavras-chave:
carotenoides; antocianinas; processamento; compostos bioativos; Ipomoea batatas

INTRODUCTION:

Sweet potato (Ipomoea batatas (L.) Lam.), original from tropical America, is a very popular and ancient root in Brazil where its production reached 479000 tons in 2013 (FAO, 2013). Characteristics such as wide adaptability, high tolerance towards drought, rusticity and easiness cultivation enables the sweet potatoes production throughout the national territory. Thus, this crop is present in family farming and has been an important food supply for most needy population, since it is a source of calories and has high vitamins and minerals contents (SILVA et al., 2008SILVA, J.B.C. et al. Sweet-potato (Ipomoea batatas)/Batata-doce (Ipomoea batatas). Brasília, Embrapa Hortaliças, 2008. (Embrapa Hortaliças. Sistemas de Produção). Available from: http://sistemasdeproducao.cnptia.embrapa.br/FontesHTML/Batata-doce/Batata-doce_Ipomoea_batatas/introducao.html>. Accessed: 19 Jul. 2015.
http://sistemasdeproducao.cnptia.embrapa...
). Brazil possesses a great genetic diversity of sweet potatoes, where roots with different forms (AZEVEDO et al., 2015AZEVEDO, A.M. et al. Genetic parameters and gain with selection in sweet potato/Parâmetros genéticos e ganho com seleção em batata-doce. Horticultura Brasileira, v.33, n.01, p.84-90, 2015. Available from: http://www.horticulturabrasileira.com.br/editor/index.php/HB/article/view/279>. Accessed: 11 Jan. 2016. doi: 10.1590/hb.v33i01.279.
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) and colors can be found.

Besides vitamins and minerals, sweet potatoes also have high levels of bioactive compounds such as anthocyanins and β-carotene that are described with antioxidant and anti-mutagenic properties (BOVELL-BENJAMIN, 2007BOVELL-BENJAMIN, A.C. Sweet potato: a review of its past, present, and future role in human nutrition. Advances in food and nutrition research, v.52, p.1-59, 2007. Available from: http://www.sciencedirect.com/science/article/pii/S1043452606520017>. Accessed: 21 Oct. 2015. doi: 10.1016/S1043-4526(06)52001-7.
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). The concentration of nutrients in sweet potatoes pulp depends on their color; however, purple sweet potatoes have high levels of phenolic compounds, as anthocyanins, and consequently, high antioxidant capacity (LIM et al., 2013LIM, S. et al. Role of anthocyanin-enriched purple-fleshed sweet potato p40 in colorectal cancer prevention. Molecular Nutrition & Food Research, v.57, n.11, p.1908-1917, 2013. Available from: http://onlinelibrary.wiley.com/enhanced/doi/10.1002/mnfr.201300040/>. Accessed: 24 Oct. 2015. doi: 10.1002/mnfr.201300040.
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). This fact shows the potential of purple varieties as healthy food and also as source of natural colorants. Conversely, orange sweet potatoes are an excellent source of carotenoids that are responsible for the yellow, orange and red pigments of plants and some animals (TANAKA et al., 2012TANAKA, T. et al. Cancer chemoprevention by carotenoids. Molecules, v.17, n.3, p.3202-3242, 2012. Available from: http://www.mdpi.com/1420-3049/17/3/3202>. Accessed: 05 Nov. 2015. doi: 10.3390/molecules17033202.
http://www.mdpi.com/1420-3049/17/3/3202...
). The main characteristic of carotenoids present in sweet potatoes is their provitamin A activity (BURRI, 2011BURRI, B.J. Evaluating sweet potato as an intervention food to prevent vitamin A deficiency. Comprehensive Reviews in Food Science and Food Safety, v.10, n.2, p.118-130, 2011. Available from: http://onlinelibrary.wiley.com/enhanced/doi/10.1111/j.1541-4337.2010.00146.x/>. Accessed: 25 Jul. 2015. doi: 10.1111/j.1541-4337.2010.00146.x.
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).

Antioxidants compounds, normally reported in functional food, are capable of inhibit or delay injuries caused by free radicals, which are molecules with one or more unpaired electron that reacts rapidly with different cellular targets causing damages that are associated with degenerative diseases and aging (PEREIRA & CARDOSO, 2012PEREIRA, R.J.; CARDOSO, M.G. Secondary plant metabolites and antioxidant benefits/Metabólitos secundários vegetais e benefícios antioxidantes. Journal of Biotechnology and Biodiversity, v.3, n.4, p.146-152, 2012. Available from: http://revista.uft.edu.br/index.php/JBB/article/viewArticle/386>. Accessed: 02 Nov. 2015.
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). The reactions caused by free radicals can be compensated by the action of antioxidants obtained through the diet, such as ascorbic acid, α-tocopherol, carotenoids, and polyphenols (CERQUEIRA et al., 2007CERQUEIRA, F.M. et al. Dietetic antioxidants: controversies and perspectives/Antioxidantes dietéticos: controvérsias e perspectivas. Química Nova, v.30, n.2, p.441, 2007. Available from: http://www.scielo.br/pdf/qn/v30n2/35.pdf>. Accessed: 25 Jul. 2015. doi: 10.1590/S0100-40422007000200036.
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), some of these antioxidants are abundant in sweet potatoes.

The literature has demonstrated the potential use of sweet potatoes for health maintenance. For instance, extracts of purple sweet potatoes, rich in anthocyanins, may protect against colorectal cancer due to different mechanism such as cell cycle arrest, anti-proliferative activity, and apoptosis (LIM et al., 2013LIM, S. et al. Role of anthocyanin-enriched purple-fleshed sweet potato p40 in colorectal cancer prevention. Molecular Nutrition & Food Research, v.57, n.11, p.1908-1917, 2013. Available from: http://onlinelibrary.wiley.com/enhanced/doi/10.1002/mnfr.201300040/>. Accessed: 24 Oct. 2015. doi: 10.1002/mnfr.201300040.
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).

Sweet potatoes can be consumed at different forms, such as cooked, roasted or as sweet; however, preparation of sweet potatoes for consumption, such as cooking, provides chemical, physical and structural changes due to heat effect which may alter the content of bioactive compounds and consequently the antioxidant capacity (MIRANDA et al., 1995MIRANDA, J.E.C. et al. The sweet-potatoe crop/A cultura da batata-doce, Brasília, Embrapa Hortaliças, 1995. 89p.; CAMPOS et al., 2008CAMPOS, F.M. et al. Stability of antioxidant compounds in processed vegetables: a review/Estabilidade de compostos antioxidantes em hortaliças processadas: uma revisão. Revista Alimentos e Nutrição, Araraquara, v.19, n.4, p.481-490, 2008. Available in: <Available in: http://serv-bib.fcfar.unesp.br/seer/index.php/alimentos/article/view/659/555 >. Accessed: 25 Jul. 2015.
http://serv-bib.fcfar.unesp.br/seer/inde...
).

The goal of this study was to determine the physicochemical characteristics, the content of bioactive compounds and the antioxidant capacity in genotypes (cultivars and advanced selections) of sweet potatoes in natura and the alterations after the heat process (roasting).

MATERIALS AND METHODS:

The following cultivars of sweet potatoes were studied: Rubissol (white pulp), Cuia (cream pulp), Amélia (yellow pulp) and Beauregard (orange pulp) and also the following advanced selections: ILS 03 (white pulp), ILS 10 (white pulp), ILS 12 (white pulp), ILS 24 (white pulp), ILS 44 (cream pulp), ILS 56 (purple pulp), ILS 16 (purple pulp) and ILS 71 (purple pulp). Samples were cultivated on the experimental field of the Embrapa Clima Temperado (31° 42'S; 52° 24'W; altitude 7m).

Planting was carried out in the first half of January 2013, using seedlings with high sanity, obtained from vegetative multiplication of matrices derived from the meristem culture. The spacing used for the production of roots in the seedbed was 0.80 to 1.00m between furrows, and 0.25 to 0.50m between plants, and spacing of 2.00 to 3.00 meters between different cultivars seedbeds. Only chemical fertilizer was applied, insecticides, fungicides and herbicides were not used. The crop was harvested approximately 140 days after planting. The climatic characteristics of this period had an average rainfall of 142.1, 177.3, 109.0, 133.6 and 113.9mm from January to May, and average maximum temperatures of 27.8, 28.1, 25.3, 24.3 and 19.5°C for the same period.

Sweet potatoes were collected and stored under refrigeration, between 7°C to 9°C, for approximately three months. The preparation of roasted sweet potatoes with peel was carried out in a conventional oven, at 250°C for approximately 90 minutes. All analyzes were performed in triplicate.

For physicochemical analysis of fresh samples, each genotype were sliced and weighed, and the amount of juice, enough to perform the analysis, was obtained in domestic centrifuge. The roasted samples were weighed and homogenized for analysis procedures. All analysis was carried out on peeled sweet potatoes.

For phytochemical analysis, equatorial portions were used (1.5 to 2.0cm) for both in natura and roasted forms, samples were peeled of, and radial sliced (for each slice cuts were made from the center until the extremity).

Physicochemical analysis

Soluble solids content: It was carried out according to AOAC "2005"AOAC INTERNATIONAL. Official methods of analysis of AOAC International. Rockville, USA. AOAC International, 2005., based on direct reading of samples on digital refractometer at 20ºC and results expressed in ºBrix. Total acidity: carried by titration and expressed in percentage (%) of citric acid according to method AOAC, 2005AOAC INTERNATIONAL. Official methods of analysis of AOAC International. Rockville, USA. AOAC International, 2005.. Sugars: sugar content was obtained using the method described by NELSON (1944NELSON, N.A. A photometric adaptation of Somogyi method for the determination of glucose. Journal of Biology Chemistry, v.153, p.375-80, 1944. Available from: http://citeseerx.ist.psu.edu/viewdoc/download&rep=rep1&type=pdf>. Accessed: 22 Feb. 2015. doi: 10.1.1.453.9073.
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).

Phytochemical analysis

Total carotenoids: carotenoids were quantified according to the method adapted from TALCOTT & HOWARD (1999TALCOTT, T.S.; HOWARD, R.L. Phenolic autoxidation is responsible for color degradation in processed carrot pure. Journal of Agriculture and Food Chemistry , v.47, p.2109-2115, 1999. Available from: http://www.mdpi.com/1420-3049/17/3/3202?trendmd-shared=1>. Accessed: 20 Fev. 2015. doi: 10.3390/molecules17033202.
http://www.mdpi.com/1420-3049/17/3/3202?...
). Total carotenoid content was measured spectrophotometrically at 470nm. β-Carotene was used as reference for the calibration curve (0-0.01mg mL-1) and results were expressed as mg of equivalent in β-carotene per 100g of sample. Total anthocyanins: the quantification was carried out according to the method adapted from FULEKI & FRANCIS (1968FULEKI, T.; FRANCIS, F.J. Quantitative methods for anthocyanins. Extraction and determination of total anthocyanin in cranberries. Journal Food Science, v.33, p.72-77, 1968. Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2621.1968.tb01365.x/abstract>. Accessed: 20 Feb. 2015. doi 10.1111/j.1365-2621.1968.tb00887.x.
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). Determination was made with spectrophotometer at 535nm. Cyanidin-3-glucoside was used as reference for the calibration curve (0-0.04mg mL-1) and results were expressed as mg of equivalent in cyanidyn-3-glucoside per 100g of sample. Total phenolic compounds: phenolic compounds were quantified according to the method adapted from SWAIN & HILLIS (1959SWAIN, T.; HILLIS, W.E. The phenolic constituents of Prunus domestica I. The quantitative analysis of phenolic constituents. Journal Science of Food Agriculture, v.10, n.1, p.63-68, 1959. Available from: http://onlinelibrary.wiley.com/doi/10.1002/jsfa.2740100110/abstract>. Accessed: 20 Fev. 2015. doi: 10.1002/jsfa.2740100110.
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). The absorbance at 725nm was read in a spectrophotometer. Chlorogenic acid was used as reference for the calibration curve (0-0.35mg mL-1). Total phenolic compounds content was expressed as mg of equivalents in chlorogenic acid per 100g of sample.

Total antioxidant capacity

Total antioxidant capacity was determined by the method adapted from BRAND-WILLIAMS et al. (1995BRAND-WILLIAMS, W. et al. Use of a free radical method to evaluate antioxidant activity. Lebensmittel-Wissenschaft & Technologie, v.28, p.25-30, 1995. Available from: http://www.sciencedirect.com/science/article/pii/S0023643895800085>. Accessed: 20 Feb. 2015. doi 10.1016/S0023-6438(95)80008-5.
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) using the stable radical 2,2-difenil-1-picrilhidrazil (DPPH). Absorbance at 515nm was read in a spectrophotometer. Trolox was used as reference for the calibration curve (0-0.8mg mL-1) and results were expressed as µg of equivalent of trolox per g of sample.

Statistical analysis

Obtained results were submitted to variance analyses and variables with significant effect for the genotype factor and preparation form (mean values) were further compared by Tukey test at 5% confidence level. Statistical analysis was run using Winstat - 2.11 version.

RESULTS AND DISCUSSION:

Soluble solids content (ºBrix) (Table 1), varied from 7.30 (ILS 24) to 14.57 (ILS 03), in sweet potato in natura, and the ILS 03 showed significant higher values among the genotypes (P<0.05). The obtained results were lower than those reported by SILVEIRA et al. (2011SILVEIRA, L.R. et al. Physical-chemical characterization and clones of sweet potato of orange pulp in the conditions of Palmas-TO / Caracterização físico-química e clones de batata-doce de polpa alaranjada nas condições de Palmas-TO. Estudos, v.38, n.2, p.365-380, 2011. Available from: http://anais.pucgoias.edu.br/index.php/estudos/article/download/2198/1358>. Accessed: 15 Oct. 2015.
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), which studied 10 clones of orange sweet potatoes in natura (9°Brix to 17.33°Brix). Superior values were reported in the roasted sweet potatoes, with values varying from 23.26ºBrix (Beauregard) to 42.23ºBrix (Amélia). Amelia cultivar showed the highest value among the studied genotypes.

Table 1
Total soluble solids (TSS), total titrible acidity (TTA) and total sugars (TS) in sweet potatoes genotypes in natura and roasted forms.

In relation to the cooking method effect on soluble solids, a significant increase in its content was observed for all genotypes of sweet potatoes after roasting, due to their concentration. The combination of high temperatures and time of processing promotes alterations on the cell wall structure leading to water loss and consequently accumulation of sugars (TONON et al., 2006TONON, R.V. et al. Study of the osmotic dehydration of tomatoes in ternary solutions by surface response methodology/Estudo da desidratação osmótica de tomate em soluções ternárias pela metodologia de superfície de resposta. Ciência e Tecnologia de Alimentos, v.26, n.3, p.715-723, 2006. Available from: http://www.scielo.br/pdf/cta/v26n3/31780>. Accessed: 05 Nov. 2015. doi: 10.1590/S0101-20612006000300036.
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).

Acidity, expressed as citric acid percentage, ranged from 0.12 (Beauregard and ILS 44) to 0.18 (ILS 16) in sweet potatoes in natura and from 0.09 (Cuia) to 0.32 (ILS 16) in the roasted form. Values of acidity were higher in roasted sweet potatoes, for the majority of the genotypes, than in sweet potatoes in natura form. The exceptions were Cuia and the selection ILS 56 that showed higher values in in natura form, while Amélia and Beauregard did not change with processing (Table 1). Roasted sweet potatoes tended to show higher values for acidity, which can be related to the concentration of compounds caused by loss of moisture and changes in the cellular structure.

Concentration of sugars, expressed as percentage (%), varied from 0.42 (ILS 16) to 1.96 (Beauregard) in sweet potatoes in natura form. In contrast, all genotypes showed higher values for the roasted form with concentrations ranging from 1.60 (ILS 12) to 2.24 (ILS 24). Beauregard cultivar showed the highest value of sugars among all genotypes for in natura form; however, no significant difference was observed for the selections ILS 24, ILS 71 and ILS 16 after roasting. Cooking in dry heat (roasting process) leads to the concentration of both energy and mineral values due to water loss, which is characteristic in this type of preparation (ORNELLAS, 2007ORNELLAS, L.H. Dietary technique - selection and preparation of food/Técnica dietética - seleção e preparo de alimentos. 8ed. São Paulo: editora Atheneu, 2007. 296p. ).

Anthocyanins, expressed in mg of equivalent of cyanidin-3-glucoside per 100g of sample (fresh weight), were detected in three selections with concentrations varying from 149.53 (ILS 71) to 229.20 (ILS 16) for sweet potatoes in in natura form, with high values reported for ILS 16 (Table 2). The concentration of anthocyanins reported in this study for purple sweet potatoes in natura was superior to those reported in the literature (JIAO et al., 2012JIAO, Y. et al. Studies on antioxidant capacity of anthocyanin extract from purple sweet potato (Ipomoea batatas L.). African Journal of Biotechnology, v.11, n.27, p.7046-7054, 2012. Available from: http://www.ajol.info/index.php/ajb/article/view/102125/92168>. Accessed: 20 Oct. 2015. doi: 10.5897/AJB11.3859.
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).

Table 2
Total anthocyanins and carotenoids in sweet potatoes genotypes in natura and roasted forms.

Concentration of anthocyanins in the roasted sweet potatoes varied from 106.51 (ILS 71) to 328.92 (ILS 16), and ILS 16 and ILS 56 were not statistically different (P<0.05). It could be observed that the dry heat process leads to the concentration of anthocyanins for the sweet potatoes selections ILS 16 and ILS 56, due to the elimination of free water. In the case of the ILS 71 there was a decrease in the concentration of these compounds, which could be attributed to a degradation process for a specific anthocyanin present in this genotype. According to the literature the main anthocyanins identified in colored sweet potatoes are acylated cyanidins and peonidins and its glycosides (GODA et al., 1997GODA, Y. et al. Two acylated anthocyanins from purple sweet potato. Phytochemistry, v.44, n.1, p.183-186, 1997. Available from: http://www.sciencedirect.com/science/article/pii/S003194229600533X>. Accessed: 20 Oct. 2015. doi: 10.1016/S0031-9422(96)00533-X.
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; GOULD et al., 2009GOULD, K. et al. Anthocyanins: biosynthesis, functions, and applications. New Zealand: editor Springer, 2009. 1v. ).

Results reported in the literature regarding the anthocyanins present after and before thermal process were divergent. The concentration of anthocyanins can increase after the roasting process (LACHMAN et al., 2012LACHMAN, J. et al. Impact of selected factors-cultivar, storage, cooking and baking on the content of anthocyanins in coloured-flesh potatoes. Food chemistry , v.133, n.4, p.1107-1116, 2012. Available from: http://www.sciencedirect.com/science/article/pii/S0308814611010387>. Accessed: 28 Oct. 2015. doi: 10.1016/j.foodchem.2011.07.077.
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), or a slight reduction can occur (KIM et al., 2012KIM, H.W. et al. Anthocyanin changes in the Korean purple-fleshed sweet potato, Shinzami, as affected by steaming and baking. Food chemistry, v.130, n.4, p.966-972, 2012. Available from: http://www.sciencedirect.com/science/article/pii/S0308814611011630>. Accessed: 23 Oct. 2015. doi: 10.1016/j.foodchem.2011.08.031.
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).

The variation of carotenoids in sweet potatoes in natura, expressed as mg of equivalent of β-carotene per 100g of sample (fresh weight), was from 0.21 (ILS 16 e ILS 24) to 21.79 (Beauregard). This genotype presented the higher values of β-carotene equivalent (Table 2). Beauregard is a biofortified sweet potato cultivar where carotenoids concentration can be 10 times higher than other cultivars (white and cream pulp). According to HAYASE & KATO (1984HAYASE, F.; KATO, H. Antioxidative components of sweet potatoes. Journal of Nutritional Science and Vitaminology, v.30, n.1, p.37-46, 1984. Available from: Available from: https://www.jstage.jst.go.jp/article/jnsv1973/30/1/30_1_37/_article . Accessed: 21 Oct. 2015. doi: 10.3177/jnsv.30.37.
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), β-carotene is the major carotenoid reported in orange sweet potatoes and it is responsible for their pulp orange color, this compound is transformed in the organism in vitamin A, which is important for health promotion (LIMA et al., 2012LIMA, J.P.D. et al. Activity and bioavailability of carotenoids in the organism/Atividade e biodisponibilidade dos carotenóides no organismo. Revista Ciências em Saúde, v.2, n.1, p.65-73, 2012. Accessed: 23 Oct. 2015. doi: 10.21876/rcsfmit.v2i1.75.
https://doi.org/10.21876/rcsfmit.v2i1.75...
).

These results are in agreement with other studies comparing genotypes of different colors, where high amounts of total carotenoids were reported for orange cultivars when compared with sweet potatoes with lighter colors (ROSE & VASANTHAKAALAM, 2011ROSE, I.M.; VASANTHAKAALAM, H. Comparison of the nutrient composition of four sweet potato varieties cultivated in Rwanda. American Journal of Food and Nutrition, v.1, p.34-38, 2011. Available from: http://www.scihub.org/AJFN/PDF/2011/1/AJFN-1-1-34-38.pdf>. Accessed: 05 Nov. 2015. doi: 10.5251/ajfn.2011.1.1.34.38.
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).

Concentration of carotenoids in roasted sweet potatoes ranged from 0.14 (Cuia) to 23.97 (Beauregard) (Table 2). No difference was observed between sweet potatoes in natura and roasted in relation to the concentration of carotenoid in most genotypes, except for Amelia and Beauregard cultivars, where, for the former there was a decrease after dry heat, and for the last, there was the concentration of these compounds.

Studies related to this theme are divergent, since the carotenoid content can be reduced (GAYATHRI et al., 2004GAYATHRI, G.N. et al. Influence of antioxidant spices on the retention of β-carotene in vegetables during domestic cooking processes. Food Chemistry, v.84, n.1, p.35-43, 2004. Available from: http://www.sciencedirect.com/science/article/pii/S030881460300164X>. Accessed: 20 Oct. 2015. doi: 10.1016/S0308-8146(03)00164-X.
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), do not change, or even increase (VIMALA et al., 2011VIMALA, B. et al. Retention of carotenoids in orange-fleshed sweet potato during processing. Journal of food science and technology, v.48, n.4, p.520-524, 2011. Available from: http://link.springer.com/article/10.1007/s13197-011-0323-2>. Accessed: 19 Oct. 2015. doi: 10.1007/s13197-011-0323-2.
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) after cooking. Normally, heat processing method can reduce the carotenoid content as a result of the susceptibility of these compounds to degradation and isomerization under high temperatures. At the same time, the heating process can be beneficial for the release and solubilization of carotenoids, once the matrix is breakdown, thus increasing their bioavailability (MAIANI et al., 2009MAIANI, G. et al. Carotenoids: actual knowledge on sources, intakes, stability and bioavailability and their protective role in humans. Molecular Nutrition & Food Research , v.53, n.2, p.194-218, 2009. Available from: http://onlinelibrary.wiley.com/doi/10.1002/mnfr.200800053/epdf>. Accessed: 20 Oct. 2015. doi: 10.1002/mnfr.200800053.
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).

Concentration of phenolic compounds, expressed as mg of equivalent in chlorogenic acid per 100 grams of sweet potato (fresh weight), varied from 51.26 (Amélia) to 663.48 (ILS 16) for samples in natura. Selection ILS 16, purple pulp, stood out with higher concentrations of phenolic compounds for both forms, in natura and roasted (Table 3). A great genetic variability concerning the phenolic compounds concentration has been already reported for sweet potatoes (JUNG et al., 2011JUNG, J.K. et al. Distribution of phenolic compounds and antioxidative activities in parts of sweet potato (Ipomoea batatas L.) plants and in home processed roots. Journal of food composition and analysis, v.24, n.1, p.29-37, 2011. Available from: http://www.sciencedirect.com/science/article/pii/S0889157510001729>. Accessed: 23 Oct. 2015. doi: 10.1016/j.jfca.2010.03.025.
http://www.sciencedirect.com/science/art...
), and the highest concentrations are usually observed in purple sweet potato (AMARO et al., 2013AMARO, F.S.; et al. Bioactive compounds and antioxidant activity in two sweet potato landraces (Ipomoea batatas) grown in organic system/Compostos bioativos e atividade antioxidante em duas etnovariedades de batata doce (Ipomoea batatas) cultivadas em sistema orgânico. Cadernos de Agroecologia, v.8, n.2, p.1-5, 2013. Available from: http://www.aba-agroecologia.org.br/revistas/index.php/cad/article/view/14295>. Accessed: 08 Oct. 2015.
http://www.aba-agroecologia.org.br/revis...
).

Table 3
Total phenolic compounds and antioxidant activity in sweet potatoes genotypes in natura and roasted forms.

Sweet potato processing using dry heat influenced the concentration of phenolic compounds that ranged from 124.39 (ILS 24) to 1268.33 (ILS 16). As previously mentioned, these compounds can be concentrated by water loss after dry heat cooking. Presence of anthocyanins in selections ILS 16 and ILS 56, purple selections, can influenced the reading of total phenolic compounds (LIMA et al., 2000LIMA, V.L.A.G. et al. Physical-chemical and sensorial characterization of purple cherry/Caracterização físico-química e sensorial de pitanga roxa. Revista Brasileira de Fruticultura, v.22, p.382-385, 2000. Available from: http://www.scielo.br/scielo.php?script=sci_nlinks&ref=000070&pid=S0101-2061200500010 001500014&lng=en>. Accessed: 19 Oct. 2015.
http://www.scielo.br/scielo.php?script=s...
). Chlorogenic acid is reported as the major phenolic compound in sweet potatoes (HAYASE & KATO, 1984HAYASE, F.; KATO, H. Antioxidative components of sweet potatoes. Journal of Nutritional Science and Vitaminology, v.30, n.1, p.37-46, 1984. Available from: Available from: https://www.jstage.jst.go.jp/article/jnsv1973/30/1/30_1_37/_article . Accessed: 21 Oct. 2015. doi: 10.3177/jnsv.30.37.
https://www.jstage.jst.go.jp/article/jns...
).

Antioxidant capacity, expressed in µg of equivalent of Trolox per gram of sample (fresh weight), is presented in table 3, indicating a variation from 210.29 (Cuia) to 7870.57 (ILS 16) for sweet potatoes in natura and from 673.26 (ILS 24) to 17306.22 (ILS 16) for the roasted samples.

The selection ILS 16 showed higher antioxidant capacity for both forms (in natura and roasted), confirming the results obtained for phenolic compounds. Regarding the antioxidant capacity a wide variation was reported among the sweet potato genotypes, although samples of purple pulps can be highlighted, fact that was confirmed by TEOW (2006TEOW, C.C. Antioxidant activity and bioactive compounds of sweet potatoes, 2006. 89f. Doutorado em ciência de alimentos - Curso de Pós-graduação em Ciência dos Alimentos, Universidade do Estado da Carolina do Norte.).

In a general way, dry heat processing do not influence or increase the sweet potato antioxidant capacity. This occurs due to the concentration of various bioactive compounds during processing, caused by water loss, characteristic of this type process.

Besides, the cell wall disruption during the cooking process can facilitated the release of bioactive compounds promoting their extraction as reported by (KAO et al., 2014KAO, F.J. et al. Effect of water cooking on antioxidant capacity of carotenoid-rich vegetables in Taiwan. Journal of Food and Drug Analysis, v.22, n.2, p.202-209, 2014. Available from: http://www.sciencedirect.com/science/article/pii/S1021949813000744>. Accessed: 23 Oct. 2015. doi: 10.1016/j.jfda.2013.09.010.
http://www.sciencedirect.com/science/art...
). This fact was observed by the increase of total phenolic compounds content and it was positively correlated with the antioxidant capacity.

The different genotypes of sweet potatoes under analysis showed varied characteristics. Cultivars Amélia and Beauregard can be highlighted due to their high concentrations of carotenoids which can have health benefits, and also the purple sweet potatoes, with high levels of anthocyanins in combination with good physicochemical characteristics. Purple sweet potatoes can be good sources of anthocyanins for both colorant extraction and for food consumption by the population. In addition, it is an accessible source of bioactive compounds well known as health promoters that can improve the human quality of life.

CONCLUSION:

The sweet potato genotype influenced the concentration of analyzed compounds. Amélia cultivar stood out by their high levels of total soluble solids in roasted sweet potatoes. Color is a factor responsible for the differentiation of genotypes and their quality characteristics. Beauregard cultivar stood out regarding carotenoids, followed by Amélia, and both can be indicated as a source of provitamin A. Genotypes ILS 16 and ILS 56 can be indicated as sources of anthocyanins. Heat processing affects the concentration of the antioxidant compounds and changes the physicochemical characteristics

ACKNOWLEDGEMENTS

Authors thank the project Quintais orgânicos de frutas (CGTEE / FINEP) for the financial support of this research and the scholarships

REFERENCES:

  • 1
    CR-2015-1385.R3

Publication Dates

  • Publication in this collection
    2017

History

  • Received
    05 Oct 2015
  • Accepted
    17 Oct 2016
  • Reviewed
    22 Dec 2016
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