ORIGINAL ARTICLE Chemical composition of potato tubers: the effect of cultivars and growth conditions Magali Leonel1 • Ezequiel Lopes do Carmo2 • Adalton Mazetti Fernandes1 • Rogério Peres Soratto3 • Juliana Aparecida Marques Ebúrneo1 • Émerson Loli Garcia1 • Thaı́s Paes Rodrigues dos Santos1 Accepted: 28 April 2017 / Published online: 30 May 2017 � Association of Food Scientists & Technologists (India) 2017 Abstract The aim of the study involved evaluating the chemical composition of tubers of five potato cultivars that were grown under the same cultural practices in soils with low, medium, and high availability of phosphorus. The experimental designs corresponded to a randomized block with four replicates. Tuber samples were analyzed in terms of moisture, ash, protein, lipid, total sugar, fiber, starch, and phosphorus contents. The results suggested that increased availability of phosphorus in soil allowed the production of tubers with higher dry matter content, lower total sugar content, and a higher percentage of starch and protein. Hence, the aforementioned parameters constitute important factors corresponding to the nutritional and industrial quality of potatoes. Increased phosphorus availability in soil can promote significant changes in the composition of potato tubers, and thereby in potential uses of tubers. Keywords Solanum tuberosum � Tuber quality � Nutrients � Soil fertility Introduction Productive efficiency of a potato ensures high use of areas for the production of food, and this is an important feature in a global scenario of constant population growth. A potato is the fourth most important food crop, and it con- tains a wide variety of phytochemicals compounds (Brown 2008; Marwaha et al. 2010; Ezekiel et al. 2013). In Brazil, a potato is the main horticultural crop in terms of area and food preference (Streck et al. 2007), and the planted area in 2013 corresponded to 127 thousand hectares with an agricultural production of 3.5 million tons (FAO 2016). The potato production in Brazil is concentrated in a limited number of cultivars. The cultivars Agata, Asterix, Atlantic, Markies, and Mondial constitute the most planted cultivars in Brazil and represent the largest portion of the total area planted with potatoes. The chemical composition of potatoes determines pro- cessing quality and is influenced by several factors, including production area, cultivars, soil and climate, agricultural practice, storage, and commercialization con- ditions (Arvanitoyannis et al. 2008). Differences in the potato crop between genotypes for shoot growth rate and dry matter production are attributed to differences in phosphorus (P) uptake efficiency and in the use efficiency of phosphorus absorbed (Balemi and Schenk 2009). Potato crops possess a high requirement for soil available P and this indicates a low P uptake efficiency. Low P use efficiency in potato was reported as primarily related to a relatively low root to shoot ratio and especially to a relatively low proportion of root hairs (Dechassa et al. 2003; Westermann 2005; Iwama 2008; Thornton et al. 2014; Hopkins et al. 2014). The phosphorus following absorption by a plant participates in various metabolic processes including energy transfer, synthesis of nucleic & Magali Leonel mleonel@cerat.unesp.br 1 Tropical Root and Starches Center (CERAT), São Paulo State University (UNESP), Botucatu, São Paulo 18610-307, Brazil 2 Federal Institute of Mato Grosso, Campo Novo Do Parecis, Brazil 3 School of Agriculture (FCA), São Paulo State University (UNESP), Botucatu, São Paulo 18610-307, Brazil 123 J Food Sci Technol (July 2017) 54(8):2372–2378 DOI 10.1007/s13197-017-2677-6 http://crossmark.crossref.org/dialog/?doi=10.1007/s13197-017-2677-6&domain=pdf http://crossmark.crossref.org/dialog/?doi=10.1007/s13197-017-2677-6&domain=pdf acids and starch, respiration, synthesis and stability of membranes, activation and deactivation of enzymes, redox reactions and carbohydrate metabolism (Vance et al. 2003). Starch is the main carbohydrate of potato tubers and phosphorylation of starch during its biosynthesis process has important effects on technological properties of potato starch (Lu et al. 2011). Leonel et al. (2016) examined the characteristics of starches of different potato cultivars grown in soils with three levels of phosphorus (P) avail- ability and found that higher contents of P in starch were observed when potatoes were grown in soils with higher P availability. Additionally, increased starch phosphorylation promoted significant changes in amylose content as well as thermal and pasting properties. Potatoes are among most widely cultivated crops in the world, and thus it is extremely important to understand the impact of grown conditions on qualitative parameters of potatoes in terms of the importance of phosphorus in potato plant metabolism. Therefore, an objective of this study involved investigating the impact of three levels of phos- phorus availability in soil on the composition of tubers of five potato cultivars that were grown in Brazil. Materials and methods Growing of potatoes The study involved three experiments that were conducted under field conditions in commercial potato production areas. Soil samples consisting of 20 subsamples were col- lected at a depth corresponding to a 0–0.20 m layer to determine chemical properties of the soil prior to the installation of the experimental tests. The experiments were conducted in the following soils with different P availabilities: low (14 mg dm-3), medium (36 mg dm-3) and high (70 mg dm-3) P availability soils. The available phosphorus was extracted using ion exchange resin and was determined by atomic absorption spectrophotometry (Van Raij et al. 2001). The experiments were conducted in a randomized block design with four replications. The treatments consisted of five potato cultivars, and each plot consisted of five rows of 5 m of length. With respect to the evaluations, central rows disregarding 0.5 m were considered at the end of each row of plants and a row on each side of the plot. The species of potato cultivars used in all the experiments included Agata, Asterix, Atlantic, Markies, and Mondial. Potatoes were grown by following traditional potato pro- duction technology.Mineral fertilization at the planting phase of all experiments consisted of the application of 62 kg ha-1 N and 124 kg ha-1 K2O for all cultivars in the form of ammonium sulfate and potassium chloride, respectively. Topdressing fertilization in areas with low, medium, and high phosphorus availability was performed 22, 24, and 28 days after planting (DAP), respectively. Specifically, 43, 64, and 41 kg ha-1 N of fertilizer was applied in areas with low, medium, and high phosphorus availability, respectively. Pest control was performed in all the exper- iments based on technical recommendations for the potato crop. The plants in all areas were desiccated with diquat (331 g a.i. ha-1) at approximately 100 DAP, and the tubers were harvested after 21 days for performing evaluations. Analysis of potato tubers The samples for qualitative examinations (8–10 kg of potato tubers) were collected from four field replications for each plot by using standard methods. Washed and peeled potato tubers were comminuted, and the following indices were determined with respect to the potato pulp: moisture, ash, total protein, total lipids, total sugar, fibers, starch (AOAC 2012), and phosphorus (Noda et al. 2004). Statistical analysis Experimental data were collectively analyzed by consid- ering the potato cultivars and phosphorus availability of the three soil types. The data were subjected to analysis of variance using SAS statistical software. Blocks and all block interactions were considered as random effects. The cultivars and P availability were considered as fixed effects. The means were separated by using Tukey’s test at a 0.05 probability level. Results and discussion The importance of tuber moisture (or dry matter) in potato processing industries is widely known. Dry matter content of tubers is the most important character that determines the quality and yield of fried and dehydrated products. Increased dry matter or solid content results in the increased recovery of processed products, lower oil absorption, lesser energy consumption, and imparts a crispy texture to a product (Marwaha et al. 2010; Rommens et al. 2010). A dry matter content corresponding to 18–20% is considered as acceptable for chips, French fries, and dehydrated products (Ezekiel et al. 1999). The results of the present study revealed that the moisture of potato tubers was influenced by the investi- gated combination of soil P availability and cultivars and corresponded to a range of 78.17 to 88.11 g 100 g-1 (11.89–21.83 g 100 g-1 of dry matter) (Table 1). Braun et al. (2010) cited 16.54, 16.63, and 21.45% of dry matter content for Agata, Asterix, and Atlantic cultivars, J Food Sci Technol (July 2017) 54(8):2372–2378 2373 123 respectively. Zorzella et al. (2003) analyzed thirteen potato genotypes and reported levels of dry matter ranging from 16.37 to 24.51 g 100 g-1, and observed a content corre- sponding to 23.51 g 100 g-1 of dry matter for the cultivar Atlantic. Similar levels of dry matter in the potato cultivars were observed in the current study with respect to condi- tions of higher P availability (Table 1). Data analysis showed that the increase in P soil avail- ability led to an increase in dry matter content of tubers (Table 1). This revealed that the adequate availability of this nutrient in the soil significantly influenced the pro- duction and allocation of assimilates in the tubers. The interference of growth conditions on the composition of potato tubers was also observed in other studies. Specifically, Jenkins and Ali (1999) used different potato cultivars and doses of phosphorus (0–400 kg P2O5 ha-1) in their experiments and concluded that P deficiency decreased dry matter production by reducing the radiation intercepted during the crop cycle (RI). However, the sen- sitivity of RI to phosphorus deficiency potentially varied with the genotype. Daily RI constitutes a product of the daily fraction of radiation intercepted (FRI) by a crop and daily incident solar radiation (Sandaña and Kalazich 2015). Sandaña (2016) investigated phosphorus uptake and utilization efficiency in response to potato genotype and phosphorus availability and observed that tuber dry matter yield was positively related to total P uptake in two growth conditions corresponding to P fertilization rates of 0 and 130 kg ha-1 P. The potato is considered as a plant with low P use efficiency and with a limited ability to absorb in soils with low phosphorus availability, and this is typically attributed to low density roots of a potato that are concentrated mainly in first 30 cm of depth below the seed tubers (Dechassa et al. 2003; Iwama 2008). The differences observed between the varieties in the three soils could be due to their mechanisms of adaptation to the growing conditions. Plants growing at low P con- centrations develop adaptive mechanisms including chan- ges in morphology and architecture of the root system as well as in physiological characteristics of roots. Root sys- tems with larger root surfaces, lengths, and densities Table 1 Chemical composition of tubers of potato cultivars culti- vated in soil with different P availability Cultivars Soil P availability 14 mg dm-3 36 mg dm-3 70 mg dm-3 Moisture (g 100 g-1) Agata 88.11Aa 85.22Ba 85.67Ba Asterix 85.52Ab 83.39Bb 83.04Cb Atlantic 82.47Ad 81.43Bc 78.17Cc Markies 84.00Ac 80.86Bc 78.38Cc Mondial 85.54Ab 83.37Bb 82.10Cb Starch (g 100 g-1) Agata 8.89Bd 11.78Ac 11.33Ac Asterix 11.47Cc 13.60Bb 14.94Ab Atlantic 14.53Ca 15.57Ba 18.83Aa Markies 13.00Cb 16.14Ba 18.62Aa Mondial 11.46Cc 13.63Bb 14.90Ab Protein (g 100 g-1) Agata 1.59ABc 1.71Ac 1.45Bd Asterix 1.91Ab 1.71Bc 1.65Bc Atlantic 2.28Aa 1.97Bb 1.91Bb Markies 2.17Aa 2.35Aa 1.93Bb Mondial 2.17Aa 1.68Bc 1.50Bd Fibers (g 100 g-1) Agata 0.66Ab 0.57Ab 0.60Aa Asterix 0.74Aa 0.74Aa 0.62Ba Atlantic 0.71Aa 0.48Bb 0.34Bb Markies 0.49Ac 0.41ABc 0.39Bb Mondial 0.80Aa 0.50Bb 0.46Bb Total sugars (g100 g-1) Agata 0.72Aa 0.58Ba 0.36Ca Asterix 0.54Ab 0.65Aa 0.28Ba Atlantic 0.76Aa 0.19Bc 0.11Bb Markies 0.20Ac 0.12ABc 0.08Bb Mondial 0.45Ab 0.44Ab 0.34Aa Ash (g 100 g-1) Agata 0.87Ab 0.81Ac 0.81Ad Asterix 1.07Aa 0.86Bbc 0.99Ac Atlantic 1.09Ba 1.10Ba 1.38Aa Markies 1.08 Ba 0.94Cb 1.20Ab Mondial 0.95Ab 0.92Ab 0.97Ac Lipids (g 100 g-1) Agata 0.28Bb 0.94Aa 0.94Aa Asterix 0.95Aa 0.91Aa 0.88Aa Atlantic 1.04Aa 0.74Bb 0.60Bb Markies 0.25Cc 0.43Bc 0.82Aa Mondial 0.90Aa 0.75ABb 0.66Bb Phosphorus (mg 100 g-1) Agata 19.75Aab 25.80Aab 23.32Ab Asterix 18.70Bab 25.53Aab 22.90ABb Atlantic 21.27Bab 27.88ABab 29.63Aab Table 1 continued Cultivars Soil P availability 14 mg dm-3 36 mg dm-3 70 mg dm-3 Markies 24.05Ba 30.95Aa 35.27Aa Mondial 14.10Bb 22.77Ab 24.10Ab Means followed by the same capital letters in the row do not differ at 5% level by Tukey test. Means followed by the same lowercase letters in the column do not differ at 5% by Tukey test 2374 J Food Sci Technol (July 2017) 54(8):2372–2378 123 usually exhibit high P uptake efficiency when P availability is low (Hu et al. 2010; López-Bucio et al. 2003; Ragho- thama and Karthikeyan 2005). With respect to the starch content in the potato tubers, the results indicated differences among cultivars and also revealed the interference of P in the soil with respect to this component for all cultivars (Table 1). The starch content ranged from 8.89 to 18.83 g 100 g-1. All cultivars accumulated higher starch content in soil with higher P availability. This result occurreddue toPparticipating in a number of key enzymes that are involved in the regulation of starch synthesis. Additionally, phosphorus is also part of starch composition and is connected to the amylopectin frac- tion in the form of phosphate ester (Nielsen et al. 1994). The cultivar Agata did not exhibit an increase in the content of starch with increases in phosphorus availability, and this shows that this cultivar does not require increased P availability in the soil to synthesize and accumulate amounts of starch in tubers (Table 1). This result could be related to an increased development of the root system of the cultivar Agata that resulted in higher P uptake under conditions of medium P availability, and thereby in increased starch accumulation in the tubers. The results indicate that the P availability in soil can affect the starch content of tubers and could thereby interfere in the quality of potatoes with respect to the industry. Kita (2002) correlated texture of potatoes with their starch content as intended for the chips industry and found that levels exceeding 15 g 100 g-1 (wet basis) of starch provided greater crispness in terms of the slices. Following carbohydrates, proteins constitute the second major components of dry matter in potato tubers with content ranging between 2.7 and 14.6 g 100 g-1 of dry matter. (Bárta and Bártová 2008; Bártová and Bárta 2009; Bárta et al. 2012; Bártová et al. 2012). The results showed a variation of 1.45–2.35 g 100 g-1 with respect to the protein content in potato tubers (Table 1). The data analysis revealed that lower protein levels were observed in soils with high P availability, and this behavior was not observed for the cultivar Agata. The fiber content of potatoes is relatively low when compared with that of other commonly used vegetables. Results with respect to the potato tubers showed variations ranging from 0.34 to 0.80 g 100 g-1 (wet basis). The effects of cultivars and soil on this component were observed as listed in Table 1. With the exception of the Agata cultivar, potatoes cultivated in soil with increased P availability exhibited less fiber in the composition. The cultivar Markies displayed a lower content of fiber in soil with low and medium P availabilities. Reistad and Hagen (1986) examined dietary fiber in potato and observed 3.5 g 100 g-1 of soluble fiber, 4.0 g 100 g-1 of insoluble fiber, and 7.5 g 100 g-1 of total fiber (dry weight). A study by Mulling and Smith (1991) revealed values of 2.5 g 100 g-1 with respect to soluble fiber, 4.3 g 100 g-1 with respect to insoluble fiber, and 6.8 g 100 g-1 with respect to total fiber in peeled potatoes, and the aforementioned contents exceeded those for potato cultivars grown in the three soils examined in the current study. Conversely, the fiber content for potato cultivars in the experiment in the present study are close to those observed by Garcia et al. (2015) in their study with eight potato cultivars planted in Brazil that presented a variation of 0.31–0.66 g 100 g-1 of total fiber. The potato sugar content is an important quality parameter. Non-enzymatic browning or Maillard reaction that occurs in tubers with high levels of reducing sugars constitutes a serious problem in potato products including flakes, chips and French fries. This is the largest contrib- utor to the dark color of foodstuffs in which the pigments melanoidins correspond to end products (Marwaha et al. 2008). Total sugars in potato tubers ranged from 0.11 to 0.76 g 100 g-1 (Table 1). With the exception of the cul- tivar Mondial, the total sugar content was lower in potatoes cultivated in soil with higher P availability. The limit established as the sugar content was almost consensual and was in the range corresponding to 0.2 and 0.3 g 100 g-1 for tubers intended for frying. Thus, only Agata and Mondial cultivars exceeded this limit in the soil with higher P availability. Low sugar levels in tubers cultivated in soil with high availability of P constitutes very interesting information for potato cultivars destined for the production of chips or French fries. Thus, in these cultivation conditions, cultivars such as Atlantic, Asterix, and Markies are considered as more valuable in the market because they result in products with better quality. The ash contents of potato tubers ranged from 0.81 to 1.38 g 100 g-1. The results showed differences between cultivars grown in the same soil as well with respect to the same cultivar grown in different soils (Table 1). Lower values for this component were observed with respect to the Agata cultivar and did not differ from those observed for the Mondial cultivar in soils with low P availability. The lipid content ranged from 0.25 to 1.04 g 100 g-1 for potato tubers (Table 1). Statistical analysis of the data showed that differences between cultivars in the same soil as well as with respect to cultivation of the same cultivar in different soils. A significant increase in this component in tubers of cultivar Markies was observed when the P availability in soil was higher. J Food Sci Technol (July 2017) 54(8):2372–2378 2375 123 The absorption of phosphorus by the roots resulted from interactions between the morphological and physiological characteristics of the roots as well as the rhizosphere sur- rounding the root system and the soil characteristics that determine the movement of P to the soil-root interface. Differences exist between potato cultivars in terms of the length and surface area of roots and the uptake kinetic parameters that affect the P uptake from soil (Fernandes et al. 2014). The availability of phosphorus in the soil interfered in the content of the P uptake from the soil component in potato tubers, and this effect was not observed for the cultivar Agata (Table 1). With respect to the other evalu- ated cultivars, an increase in the available phosphorus in the soil led to an increase in this mineral in the composition of the tubers. This result is important because phosphorus in root and tubers is covalently linked to starch in the form of phosphorus esters and the degree of starch phosphory- lation influences the qualitative properties of this polymer (Noda et al. 2007). Conversely, the variation observed for the potato culti- vars indicates differences in the absorption efficiency, and this is very important since the use of genotypes with high P efficiency is an option for sustainable production in low- P soils. Balemi and Schenk (2009) examined genotypic varia- tion for phosphorus efficiency related to the simulation of P uptake and revealed that the processes involved in P transport and morphological root characteristic affect the P uptake. Significant differences exist in terms of the root mass (dry weight and length) in the plow layer between potato cultivars, breeding lines, and wild relatives. The differ- ences are generally stable across different environmental Table 2 Pearson correlation coefficients for tuber composition 1 2 3 4 5 6 7 8 Soil (p = 14 mg dm-3) 1-Fiber 1 0.88*** Ns Ns -0.65** Ns Ns Ns 2-Total sugar 1 -0.59* Ns -0.81*** Ns 0.72** -0.54* 3-Protein 1 Ns 0.72** 0.85*** -0.89*** 0.66*** 4-Lipids 1 Ns Ns Ns Ns 5-Starch 1 0.87*** -0.95*** Ns 6-Ash 1 -0.95*** Ns 7-Moisture 1 Ns 8- Phosphorus 1 Soil (p = 36 mg dm-3) 1-Fiber 1 0.52* 0.54* Ns Ns Ns -0.52* -0.59* 2-Total sugar 1 Ns 0.83*** Ns Ns Ns Ns 3-Protein 1 Ns 0.66*** 0.85*** -0.93*** Ns 4-Lipids 1 -0.56* Ns Ns Ns 5-Starch 1 Ns -0.84*** Ns 6-Ash 1 -0.70** Ns 7-Moisture 1 Ns 8- Phosphorus 1 Soil (p = 70 mg dm-3) 1-Fiber 1 0.65** -0.60* 0.68*** Ns -0.71*** 0.61* -0.56* 2-Total sugar 1 -0.89*** 0.56* -0.94*** -0.90*** 0.95*** -0.74*** 3-Protein 1 Ns 0.89*** 0.73** -0.86*** 0.80*** 4-Lipids 1 Ns -0.81*** 0.62* Ns 5-Starch 1 0.84*** -0.95*** 0.68** 6-Ash 1 -0.96*** 0.57* 7-Moisture 1 -0.65*** 8- Phosphorus 1 Ns = not significant (p[ 0.05), * p\ 0.05; ** p\ 0.01; *** p\ 0.001 2376 J Food Sci Technol (July 2017) 54(8):2372–2378 123 conditions including locations with different soil types, fertilizer rates, and planting densities. Under favorable environmental conditions without severe water and nutrient shortages, root mass differences between genotypes are related to maturity class wherein late genotypes continue root growth for longer periods and attain larger root mass and deeper rooting when compared with those of early genotypes (Iwama 2008). Results of the Pearson correlation indicated that when the average values of all potatoes were considered it is possible to observe more significant correlations between the components in the tubers cultivated in soils with high availability of phosphorus (Table 2). Typically, the fiber content was positively correlated with total sugar content and negatively correlated with starch, ash and phosphorus contents. The moisture displayed a negative correlation with protein, starch, ash, and phosphorus contents in soils with the increased availability of phosphorus (Table 2). Conclusion The results of the present study indicated that the main potato cultivars planted in Brazil differ in terms of nutri- tional composition. The P availability in the soil plays an important role in the composition of potato tubers. Soils with higher phosphorus concentrations allow the produc- tion of tubers with increased dry matter content, decreased total sugar content, and increased percentages of starch and protein, which constitute important parameters influencing the nutritional and industrial qualities of potatoes. The cultivar Agata exhibited distinct behavior that differed from those of other cultivars, thereby indicating possible differences in the absorption system and use of available phosphorus in the soil. The Pearson analysis indicated that moisture content displays a primarily negative correlation with the levels of starch, ash, and protein and is indepen- dent of the type of cultivar and soil. Starch and protein were positively correlated in addition to fiber and total sugar. References AOAC (2012) Official method of analysis, 19th edn. Association of Official Analytical Chemists, Washington, DC Arvanitoyannis I, Vaitsi O, Mavromatis A (2008) Potatoes: a comparative study of the effect of cultivars and cultivation conditions and genetic modification on the physico-chemical properties of potato tubers in conjunction with multivariate analysis towards authenticity. Crit Rev Food Sci Nutr 48:799–823 Balemi T, Schenk MK (2009) Genotypic variation of potato for phosphorus efficiency and quantification of phosphorus uptake with respect to root characteristics. J Plant Nutr Soil Sci 172:669–677 Bárta J, Bártová V (2008) Patatin, the major protein of potato (Solanum tuberosum L.) tubers, and its occurrence as genotype effect: processing versus table potatoes. CJFS 26:347–359 Bárta J, Bátová V, Zdráhal Z, Sedo O (2012) Cultivar variability of patatin biochemical characteristics: table versus processing potatoes (Solanum tuberosum L.). J Agric Food Chem 60:4369–4378 Bártová V, Bárta J (2009) Chemical composition and nutritional value of protein concentrates isolated from potato (Solanum tuberosum L.) fruit juice by precipitation with ethanol or ferric chloride. J Agric Food Chem 57(19):9028–9034 Bártová V, Bárta J, Svajner J, Divis J (2012) Soil nitrogen variability in relation to seasonal nitrogen cycling and accumulation of nitrogenous components in starch processing potatoes. Acta Agri. Scand 62:70–79 Braun H, Fontes PCR, Finger FL, Busato C, Cecon PR (2010) Carbohydrates and dry matter in tubers of potato cultivars as affected by nitrogen doses. Cienc Agrotecn 34(2):285–293 Brown CR (2008) Breeding for phytonutrient enhancement of potato. AJPR 85(4):298–307 Dechassa N, Schenk M, Claassen N, Steingrobe B (2003) Phosphorus efficiency of cabbage (Brassica oleraceae L. var. capitata), carrot (Daucuscarota L.), and potato (Solanum tuberosum L.). Plant Soil 250(1):215–224 Ezekiel R, Verma SC, Sukumaran NP, Shekhawat GS (1999) A guide to potato processors. Tech Bull 48, Cent Potato Res Inst, Shimla Ezekiel R, Singh N, Sharma S, Kaur A (2013) Beneficial phyto- chemicals in potato—a review. Food Res Int 50(2):487–496 FAO (2016) Food and agriculture organization of the united nations. FAOSTAT: Production-Crops. http://faostat3.fao.org/home/E. Accessed 5 Jan 2016 Fernandes AM, Soratto RP, Gonsales JR (2014) Root morphology and phosphorus uptake by potato cultivars grown under deficient and sufficient phosphorus supply. Sci Hortic 180(1):190–198 Garcia EL, Carmo EL, Pádua JG, Leonel M (2015) Industrial processing potential of potato cultivars. Cienc Rural 10(10):1742–1747 Hopkins B, Horneck D, MacGuidwin E (2014) Improving phosphorus use efficiency through potato rhizosphere modification and extension. Am J Potato Res 91:161–174 Hu Y, Ye X, Shi L, Duan H, Fangsen X (2010) Genotypic differences in root morphology and phosphorus uptake kinetics in Brassica napus under low phosphorus supply. J Plant Nutr 33(6):889–901 Iwama K (2008) Physiology of the potato: new insights into root system and repercussions for crop management. Potato Res 51(1):333–353 Jenkins PD, Ali H (1999) Growth of potato cultivars in response to application of phosphate fertiliser. Ann Appl Biol 135:431–438 Kita A (2002) The influence of potato chemical composition on crisp texture. Food Chem 76(2):173–179 Leonel M, Carmo EL, Fernandes AM, Franco CML, Soratto RP (2016) Physicochemical properties of starches isolated from potato cultivars grown in soils with different phosphorus availability. J Sci Food Agric 96:1900–1905 López-Bucio J, Cruz-Ramı́rez A, Herrera-Estrella L (2003) The role of nutrient availability in regulating root architecture. Curr Opin Plant Biol 6(1):280–287 Lu Z-L, Yada RY, Liu Q, Bizimungu B, Murphy A, De Koeyer, Lid X-Q, Pinhero RG (2011) Correlation of physicochemical and nutritional properties of dry matter and starch in potatoes grown in different locations. Food Chem 126:1246–1253 Marwaha RS, Kumar D, Singh SV, Pandey SK (2008) Influence of blanching of slices of potato varieties on chipping quality. J Food Sci Technol 45:364–367 J Food Sci Technol (July 2017) 54(8):2372–2378 2377 123 http://faostat3.fao.org/home/E Marwaha R, Pandey SK, Kumar D, Singh SV, Kumar P (2010) Potato processing scenario in India: industrial constraints, future projections, challenges ahead and remedies—a review. J Food Sci Technol 47(2):137–156 Mulling WJ, Smith JM (1991) Dietary fiber in raw and cooked potatoes. J Food Compos Anal 4(2):100–106 Nielsen TH, Wischmann B, Enevoldren K, Moller BL (1994) Starch phosphorylation in potato tubers proceeds concurrently with de novo biosynthesis of starch. Plant Physiol 105(1):111–117 Noda T, Tsuda S, Mori M, Takigawa S, Matsuura-Endo C, Saito K, Mangalika WHA, Hanaoka A, Suzuki Y, Yamauchi H (2004) The effect of harvest dates on the starch properties in various potato cultivars. Food Chem 86(1):119–125 Noda T, Kottearachchi NS, Tsuda S, Mori M, Takigawa S, Matsuura- Endo C, Kim S-J, Hashimoto N, Yamauchi H (2007) Starch phosphorus content in potato (Solanum tuberosum L.) cultivars and its effect on other starch properties. Carbohydr Polym 68:793–796 Raghothama KG, Karthikeyan AS (2005) Phosphate acquisition. In: Lambers H, Colmer TD (eds) Root physiology: from gene to function, series plant ecophysiology. Springer, Netherlands, pp 37–49 Reistad R, Hagen BF (1986) Dietary fibre in raw and cooked potatoes. Food Chem 19(3):189–196 Rommens CM, Shakya R, Heap M, Fesseden K (2010) Tastier and healthier alternatives to French Fries. J Food Sci 75(4):109–115 Sandaña P (2016) Phosphorus uptake and utilization efficiency in response to potato genotype and phosphorus availability. Eur J Agron 76:95–106 Sandaña P, Kalazich J (2015) Ecophysiological determinants of tuber yield as affected by potato genotype and phosphorus availability. Field Crops Res 180:21–28 Streck NA, Lago I, Paula FLM, Bisognin DA, Helddwein AB (2007) Improving predictions of leaf appearance in field grown potato. Sci Agric 64(1):12–18 Thornton M, Novy R, Stark J (2014) Improving phosphorus use efficiency in the future. Am J Potato Res 91:175–179 Van Raij B, Andrade JC, Cantarella H, Quaggio JA (2001) Análise quı́mica para avaliação da fertilidade de solos tropicais. Instituto Agronômico, Campinas Vance CP, Uhde-Stone C, Allan DL (2003) Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenew- able resource. New Phytol 157(3):423–447 Westermann DT (2005) Nutritional requirements of potatoes. Am J Potato Res 82:301–307 Zorzella CA, Vendruscolo JLS, Treptow RO, Almeida TL (2003) Physical, chemical and sensory characterization of different potato genotypes, processed in the form of chips. Braz J Food Technol 6(1):15–24 2378 J Food Sci Technol (July 2017) 54(8):2372–2378 123 Chemical composition of potato tubers: the effect of cultivars and growth conditions Abstract Introduction Materials and methods Growing of potatoes Analysis of potato tubers Statistical analysis Results and discussion Conclusion References