Abstracts
The objective of this work was to investigate the germination of hybrid sunflowers BRS191 and C11 as a means of lowering phytic acid (PA) content by enhancing the activity of endogenous phytase and acid phosphatase. The concentration of PA in hybrid sunflower achenes varied from 2.16 to 2.83g/100g of sample (p < 0.05). The phytase and acid phosphatase activities of sunflowers BRS191 and C11 were the highest on the 4th and 5th days of germination, respectively, with the release of the phosphorus. These results indicated that hybrid sunflower PA reduced and enhance phytase activity at distinct germination periods, which could open up the possibility of applying these enzymes in the control of PA content in cereals, thus improving their nutritional value.
germination; sunflower hybrids; phytic acid; phytase; acid phosphatase
O objetivo deste trabalho foi investigar a germinação de girassóis híbridos BRS 191 e C11 com finalidade de reduzir o teor de AF e aumentar as atividades de phytases e fosfatases endógenas. A concentração do AF nos aquênios de girassóis híbridos variou de 2,16 a 2,83 g /100g de amostra (p< 0,005). As atividades de fitases e fosfatases de girassóis BRS191 e C11 foram elevadas no 4º e 5º dia de germinação, respectivamente, com liberação do fósforo necessário para o desenvolvimento da semente. Estes resultados indicam que o AF do girassol hibrido reduz e a atividade de phytase aumenta em períodos distintos da germinação, possibilitando assim a aplicação desta enzima no controle do teor de AF em cereais, melhorando o seu valor nutricional.
FOOD/FEED SCIENCE AND TECHNOLOGY
Lowering of phytic acid content by enhancement of phytase and acid phosphatase activities during sunflower germination
Juliana da Silva Agostini; Rosicler Balduíno Nogueira; Elza Iouko Ida* * Author for correspondence: elida@uel.br
Departamento de Ciência e Tecnologia de Alimentos; Centro de Ciências Agrárias; Universidade Estadual de Londrina; C. P.: 6001; 86051-970; Londrina - PR - Brasil
ABSTRACT
The objective of this work was to investigate the germination of hybrid sunflowers BRS191 and C11 as a means of lowering phytic acid (PA) content by enhancing the activity of endogenous phytase and acid phosphatase. The concentration of PA in hybrid sunflower achenes varied from 2.16 to 2.83g/100g of sample (p < 0.05). The phytase and acid phosphatase activities of sunflowers BRS191 and C11 were the highest on the 4th and 5th days of germination, respectively, with the release of the phosphorus. These results indicated that hybrid sunflower PA reduced and enhance phytase activity at distinct germination periods, which could open up the possibility of applying these enzymes in the control of PA content in cereals, thus improving their nutritional value.
Key words: germination, sunflower hybrids, phytic acid, phytase, acid phosphatase
RESUMO
O objetivo deste trabalho foi investigar a germinação de girassóis híbridos BRS 191 e C11 com finalidade de reduzir o teor de AF e aumentar as atividades de phytases e fosfatases endógenas. A concentração do AF nos aquênios de girassóis híbridos variou de 2,16 a 2,83 g /100g de amostra (p< 0,005). As atividades de fitases e fosfatases de girassóis BRS191 e C11 foram elevadas no 4º e 5º dia de germinação, respectivamente, com liberação do fósforo necessário para o desenvolvimento da semente. Estes resultados indicam que o AF do girassol hibrido reduz e a atividade de phytase aumenta em períodos distintos da germinação, possibilitando assim a aplicação desta enzima no controle do teor de AF em cereais, melhorando o seu valor nutricional.
INTRODUCTION
Sunflower production has increased worldwide and Brazil presents excellent production prospects. Sunflower grain has been used for extracting high quality cooking oil and its residue is normally used as a meal in animal feeds and alternatively as an isolated protein to enrich the baking flour and meat products for human consumption (Reyes et al., 1985; Rossi, 1997). However, as other grains, sunflower contains from 0.4 to 6.4% phytic acid (PA) (Harland and Oberleas, 1987; Egli, et al., 2002). About 70-80% of the total phosphorus present in grains derives from phytates, and PA is the main form of phosphorus storage (Reddy et al., 1982). Due to its chemical structure, PA chelates certain essential minerals, which decreases its bioavailability. In contrast, monogastric animals such as birds, pigs, and humans eat various types of cereals that contain phosphate in the form of phosphorus-phytate, which is unavailable for intestinal phytase activity (Wodzinsk and Ullah, 1996). Some in vitro reports state that phytates can complex with proteins, making them insoluble and, thus, biologically unavailable under normal human physiological conditions (Cheryan, 1980). Furthermore, protein-phytate complexes are less sensitive to enzymatic activity in relation to free proteins (Cheryan, 1980). PA has also been described as a potent natural antioxidant in food (Graf and Eaton, 1990) and to have anticarcinogenic effects (Zhou and Erdman, 1995; Oatway et al., 2001; Minihane and Rimbach, 2002). Other beneficial antioxidizing effects have been observed as an exogenous additive in fresh broiler breast meat (Soares et al., 2003) and as an endogenous ingredient in swine diet (Harbach et al., 2007). All these reports show the controversial biological role of PA. PA enzymatic hydrolysis has been put forward as an alternative to improve the nutritional value of grain food (Sandberg et al., 1996; Egli et al., 2002) and to decrease the amount of phosphorus in excreta, which is considered to cause pollution in intensive farming (Simons and Verteegh, 1990).
Agostini and Ida (2006a) investigated the germination of hybrid sunflower M734 by response surface methodology and observed minimal phytate and acid phosphatase activity on the 6th day of germination at 30º C. The best conditions for phytase activity were the 4th day of germination at the same temperature. Other studies by different techniques suggest a decrease or control in PA content (Reddy et al., 1982; Coelho et al., 2008). Phytases or mio-inositolhexaphosphate phosphohydrases (EC 3.1.3.26) or 6-phytases are phytate-specific phosphatases that hydrolyze PA or mio-inositol hexaphosphate to inositols and phosphates (Reddy et al., 1982). Some reports state that the physiological function of phytases in grains is related to the release of inorganic phosphorus (Pi) from phytate, being mostly incorporated in nucleic acids (Houde et al., 1990; Wodzinsk and Ullah, 1996; Lopez et al., 2002). These works pointed out that phytases are were responsible for the enzymatic degradation of phytates, and their activity increased during seed germination, and that free Pi might be connected to cell energy production. Phytases also play a practical role as an additive and the reduction of PA residues in the animal feed and the improvement of food consumption as a consequence of their nutritive value (Greiner et al., 1998). Hybrid sunflower M734 phytase is heat-stable at 50ºC for 10 min. When added to deffated sunflower flour after 8h of incubation, it hydrolyzed 92% of phytate (Agostini and Ida, 2006b). Thus, the objective of this work was to investigate the reduction of the PA content in two hybrid sunflowers by enhancing the phytase and acid phosphatase activities during natural germination.
MATERIAL AND METHODS
Samples and germination
Hybrid sunflower (Hilianthus annus) BRS191 and C11 seeds were kindly donated by Embrapa-Soja, Londrina, PR, Brazil. The seeds were previously sanitized by the method of Konietzny et al. (1995) and copiously washed with sterilized distilled water to remove the sanitizer residues of each hybrid. Thus 50 seeds were distributed on a paper sheet, wrapped, and placed in a germination chamber at 25ºC under fluorescent illumination for 8 days. After 2, 4, 5, 6, and 8 days of germination, the new cotyledons were separated, freeze dried and triturated in mill in order to determine the amount of PA, soluble proteins, and phytase and acid phosphatase activities in triplicate.
Quantification of PA
The quantity of PA in g in 100 g of dry basis sample was determined by the Latta and Eskin (1980) technique with some modification by using Dowex-AGX-4 resin as in Ellis and Morris (1986).
Determination of phytase and acid phosphatase activity
Enzyme extraction and fractionation were carried out according to the Lolas and Markakis technique (1977). Essentially, enzyme was extracted from the sunflower meal homogenized in 2.0g/100 of CaCl2 solution at 1:10 (w:v) for 1h at 4ºC. To the filtered supernatant after centrifugation at 20,000x g ammonium sulphate was added up to 35g/100g of saturation, followed by centrifugation. The ammonium sulphate was added to the filtered supernatant up to 80g/100g of saturation. After centrifugation, the pellet was suspended in 5 mL tris-maleato 0.01M buffer (pH 6.5) dialyzed for 48 h with several buffer exchanges at 2ºC. Phytase and acid phosphatase activities were evaluated in this final extract.
Phytase activity was evaluated as described in Lolas and Markakis (1977) using sodium phytate as a substrate. Pi was determined by the ammonium molibdate method as described in Heinonen and Lahti (1981). One unit of phytase activity (1U PA) was defined as µmoles of Pi liberated per minute. Acid phosphatase activity was measured by the release of p-nitrophenol from p-nitrophenylphosphate (Ullah and Gibson, 1988). One unit of acid phosphatase activity (1U APA) was defined as ηmoles of p-nitrophenol released per minute.
Protein quantification
The amount of soluble protein was determined by the Lowry's method (1951).
Statistical analysis
PA content was submitted to variance analysis and Tukey test (p<0.05) under Statistical Analysis Systems (SAS, 1989).
RESULTS AND DISCUSSION
Hybrid sunflower PA
PA contents of the achenes of the two hybrids varied significantly (p<0.05) from 2.16 to 2.83g/100g of sample probability as a consequences of seed variety and production area, since the soil phosphorus level could influence the PA content in the plants (Asada et al., 1969). The results were in accordance with Saeed and Cheryan (1988) that investigated the sunflower protein concentrates and isolates free of polyphenols and/or low phytate.
PA and enzyme activity in germination
The presence of PA and enzyme activities were observed particularly in cotyledons in germination under illumination at 25 ºC for 8 days, but absent in the axial parts of BRS 191 and C11 plantules. Figures 1 and 2 show the relationship between the PA content and phytase activity throughout the experiment. As can be seen, taking the first day of germination as control, on the 4th day, the PA content decreased to 70.42 and 75.26% in BRS191 and C11, respectively, which was in agreement with Agostini and Ida (2006a) who observed the germination of hybrid sunflower M734, and previously reported by Egli et al. (2002) who investigated the germination of several grains and seeds. On the other hand, Coelho et al. (2008), from in vitro synthesis of phytate in culturing bean fruit explants concluded that different concentrations of phosphorus, sucrose, abscisic acid, glutamine and methionine caused an increase in the phytate of bean seed, showing that it could be possible to alter its content.
Phytases activities in non-germinated seeds varied from 0.08 UI/g for both BRS191 and C11, which demonstrated the correlation between the PA content and both enzyme activities. Thus, the common pattern was maximum phytase activity around the 4th day of germination. In contrast, the lowest amount of PA was reached approximately on the same day of germination, indicating the hydrolysis of PA by this enzyme.
All the hybrids presented an acid phosphatase activity pattern similar to that shown in Figure 3. C11 presented maximum activity of 72.59 UI/g of sample on the 5th day of germination, while for BRS191, the maximum activity was 64.63 UI/g of sample on the 6th of germination. According to Agostini and Ida, (2006a) M734 presented maximum activity of 75.13 UI/g of sample and germination similar to that of C11. The maximum increase in the phosphatase activity was 30-40-fold higher than in non-germinated seeds. Silva and Trugo (1996) observed that maximum activity on the 8th day of germination in plants like lupine was 45-fold higher than in non-germinating seeds. In contrast, acid phosphatase activity was about 50-fold higher than that of phytases, and Greiner et al. (2000) reported acid phosphatase activity 10fold higher than those of phytases in germinated barley. Lolas and Markakis (1977) reported that phytase and phosphatase hydrolyzed PA and other phosphorylated esters, indicating that phytates were not the only source of Pi under the activity of these two enzymes. The results of this experiment indicated that endogenous phytase partially acted upon PA, giving rise to the liberation of phosphorus and other minerals necessary for sunflower seed germination.
CONCLUSIONS
The germination of hybrid sunflowers is a natural biological process in which the decrease in phytic acid content by the enhancement of endogenous phytase and acid phosphatase activities. The highest enzymatic activities were at the 4th and 5th days of germination.
ACKNOWLEDGMENTS
The authors are grateful to Embrapa-Soja-Londrina-PR/Brazil for the kind donation of sunflower seeds. JSA and RBN were under postgraduate scholarships from Conselho Nacional de Desenvolvimento Científico e Tecnológico-CNPq. EII is a CNPq Research Fellow. This project was partially financed by CNPq.
Received: November 18, 2008; Revised: February 13, 2009; Accepted: October 21, 2009.
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Publication Dates
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Publication in this collection
06 Aug 2010 -
Date of issue
Aug 2010
History
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Received
18 Nov 2008 -
Accepted
21 Oct 2009 -
Reviewed
13 Feb 2009