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ANTIOXIDANT DEFENSES OF IRRIGATED FORAGE SORGHUM WITH SALINE AQUACULTURE EFFLUENT 1 1 Paper extracted from the masters dissertation of the first author.

DEFESAS ANTIOXIDATIVAS DO SORGO FORRAGEIRO SOBRE O CULTIVO IRRIGADO COM EFLUENTE SALINO DE PISCICULTURA

ABSTRACT

The objective of this work was to evaluate the biomass production and antioxidant enzymatic system activity of irrigated forage sorghum with saline aquaculture effluent under different leaching fractions. The experiment was conducted in the Caatinga Experimental Field of the Embrapa Semiarido, in Petrolina, State of Pernambuco, Brazil. The experimental design was a complete randomized block in a split-plot arrangement with four replications, consisting of three forage sorghum varieties (Volumax, F305 and Sudan) and four leaching fractions (0, 5, 10 and 15%). The vegetal materials were collected when the plants were at the soft-dough stage. The biomass production and activity of the enzymes superoxide dismutase, catalase and ascorbate peroxidase were evaluated. Irrigation with saline aquaculture effluent with leaching fraction of 15% results in low salinity level in the root zone and higher biomass production of forage sorghum Sudan and F305, in semiarid conditions. The antioxidant system was activated in the three sorghum varieties to prevent accumulation of reactive oxygen species, with the synchrony between the enzymes superoxide dismutase and catalase resulting in a better productive response of the varieties Sudan and F305.

Keywords:
Enzymes; Oxidative stress; Sorghum bicolor (L.); Moench.

RESUMO

Objetivou-se com este trabalho avaliar o desempenho da cultura do sorgo forrageiro irrigado com efluente salino da piscicultura sob diferentes frações de lixiviação em relação à produção de biomassa e a atividade do sistema enzimático antioxidativo. O estudo foi realizado no Campo Experimental Caatinga, pertencente à Embrapa Semiárido, em Petrolina - PE. O delineamento experimental foi blocos ao acaso, com quatro repetições, em parcelas subdivididas, composto por três variedades de sorgo forrageiro (Volumax, F305 e Sudão) e quatro frações de lixiviação (0; 5; 10 e 15%). A coleta do material vegetal foi realizada quando os grãos da porção central da panícula apresentaram aspecto leitoso a pastoso. Foi avaliada a produção de biomassa e a atividade das enzimas superóxido dismutase, catalase e ascorbato peroxidase. O uso de 15 % de fração de lixiviação para irrigação com efluentes salinos da piscicultura proporciona um menor nível de salinidade da zona radicular e promove uma melhor produção de biomassa do sorgo forrageiro Sudão e F305 em condições semiáridas. O sistema antioxidativo foi ativado nas três variedades de sorgo para evitar o acúmulo de ROS, sendo a sincronia entre as enzimas superóxido dismutase e catalase que refletiu numa melhor resposta produtiva das variedades Sudão e F305.

Palavras-chave:
Enzimas; Estresse oxidativo; Sorghum bicolor (L.); Moench.

INTRODUCTION

Saline water is often the only water found in arid and semiarid regions. The greater the amount of salts in the water, the more severe is this abiotic stress and damage to plants, therefore, techniques to minimize this stress through irrigation is very important. Irrigation with saline water considering the leaching fraction aims to leach salts and prevent salinization in the root zone, which limits crop yield (ARAGÜÉSA et al., 2014ARAGÜÉSA, R. et al. Regulated deficit irrigation, soil salinization and soil sodification in a table grape vineyard drip-irrigated with moderately saline waters. Agricultural Water Management, Gangtok, v. 134, n. 1, p. 84-93, 2014.).

More tolerant species and cultivars to the adverse conditions of semiarid regions have been used to increase the productive potential of these regions. In this context, forage sorghum production has increasing in recent years in the Brazilian semiarid region, since it is a typical hot climate plant, with xerophilous characteristics, low soil fertility requirement and tolerance to abiotic stresses, such as water deficit and salinity (GUIMARÃES et al., 2016GUIMARÃES, M. J. M. et al. Cultivation of forage sorghum varieties irrigated with saline effluent from fish-farming under semiarid conditions. Revista Brasileira de Engenharia Agrícola e Ambiental , Campina Grande, v. 20, n. 5, p. 461-465, 2016.; HEFNY; ABDEL-KADER, 2009HEFNY, M.; ABDEL-KADER, D. Z. Antioxidant-enzyme system as selection criteria for salt tolerance in forage sorghum genotypes (Sorghum bicolor L. Moench). International Journal of Plant Breeding and Genetics, Faisalabad, v. 1, n. 2, p. 38-53, 2009. ).

Semiarid regions usually have high temperatures, water deficit and high salt rates in soil and water. These factors can cause mild to severe changes in plant metabolism, depending on the intensity and interaction between them (NILSEN; ORCUTT, 1996NILSEN, E.; ORCUTT, D. The physiology of plants under stress. New York: John Wiley & Sons, 1996. p. 704.).

Saline stress causes morphological and physiological changes in plants, reducing their growth and trigging oxidative stress, which increase reactive oxygen species (ROS) (GILL; TUTEJA, 2010GILL, S.; TUTEJA, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, Bari, v. 48, n. 12, p. 909-930, 2010.). ROS can damage macromolecules and cellular structures and lead to the plant death (BARBOSA et al., 2014BARBOSA, M. R. et al. Geração e desintoxicação enzimática de espécies reativas de oxigênio em plantas. Ciência Rural, Santa Maria, v. 44, n. 3, p. 453-460, 2014.). Plants have an efficient antioxidant defense mechanism to these physiological and biochemical effects, with activation of a complex enzymatic system (BARBOSA et al., 2014BARBOSA, M. R. et al. Geração e desintoxicação enzimática de espécies reativas de oxigênio em plantas. Ciência Rural, Santa Maria, v. 44, n. 3, p. 453-460, 2014.). Oxidative stress is an imbalance between the endogenous rates of antioxidant and oxidant compounds (ROS) (SHARMA et al., 2012SHARMA, P. et al. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. Journal of Botany, London, v. 2012, s/n., p. 1-26, 2012.).

The antioxidant system of plants produces a large number of compounds that regulate redox homeostasis, such as the superoxide dismutase (SOD), catalase (CAT) and ascorbate peroxidase (APX) (MILLER et al., 2010MILLER, G. et al. Reactive oxygen species homeostasis and signaling during drought and salinity stresses. Plant, Cell and Environment, Medford, v. 33, n. 4, p. 453-467, 2010.). According to Gill and Tuteja (2010GILL, S.; TUTEJA, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, Bari, v. 48, n. 12, p. 909-930, 2010.), SOD is the first defense against ROS, with dismutation of the superoxide radical (O2 •-) to form hydrogen peroxide (H2O2) and molecular oxygen (O2). This H2O2 is then converted to H2O by the APX and CAT, since H2O2 accumulation is also toxic to plants. The balance of these enzymes is essential for homeostasis. However, the increase in the antioxidant system activity alone does not result in high crop yields, as reported by Hefny and Abdel-Kader (2009HEFNY, M.; ABDEL-KADER, D. Z. Antioxidant-enzyme system as selection criteria for salt tolerance in forage sorghum genotypes (Sorghum bicolor L. Moench). International Journal of Plant Breeding and Genetics, Faisalabad, v. 1, n. 2, p. 38-53, 2009. ), who evaluated 26 sorghum genotypes.

In this context, the objective of this work was to evaluate the biomass production and antioxidant enzymatic system activity of irrigated forage sorghum with saline aquaculture effluent under different leaching fractions.

MATERIAL AND METHODS

The study was conducted in the Caatinga Experimental Field of the Embrapa Semiarido, in Petrolina, State of Pernambuco, Brazil, in the Sub-mid São Francisco Valley (9°8'8.9''S, 40°18'33.6''W and altitude of 373 m) from February to July 2013. The climate of the region is classified as semiarid, type BSwh', according to the classification of Köppen. The experimental period had average relative air humidity of 63.86%, average temperature of 25.46 °C, maximum evapotranspiration of 6.97 mm dia-1 (average of 5.85 mm day-1), main precipitation events concentrated in the first 10 days after planting (DAP) and at the 74th DAP, totaling 32.7 mm.

The experimental design was a complete randomized block in a split-plot arrangement with four replications, consisting of three forage sorghum varieties (Volumax, F305 and Sudan) and four leaching fractions (0, 5, 10 and 15%). Each experimental unit (subplot) was formed by five 5-meter rows in an area of 5.0 x 0.50 m (12.5 m²) with 10 plants per linear meter, considering the plants within the central 3-meters of the rows for evaluation.

The soil of the experimental area was classified as a Red Yellow Argissolo (EMBRAPA, 2013EMPRESA BRASILEIRA DE PESQUISA AGROPECUÁRIA - EMBRAPA. Sistema brasileiro de classificação de solos. 3. ed. Brasília, DF: EMBRAPA, 2013. 353 p.) (Ultisol) of medium texture and plane relief. Soil preparation was according to the crop requirements, with plowing and harrowing. Soil fertilization was based on a previous soil analysis (Table 1), with application of nitrogen (30 kg ha-1), phosphorus (60 kg ha-1) and potassium (20 kg ha-1). An additional nitrogen fertilization (30 kg ha-1) was performed 30 DAP. Sowing was carried out in April 2013, and seedling emergency occurred at 7 DAP. A manual weeding was performed at 30 DAP and preventive application of insecticide was carried out at 40 and 60 DAP.

Irrigations were carried out daily with saline aquaculture effluent through a surface drip irrigation system connected to fish tanks containing black tilapia (population density of 40 fish m-3). Fifty percent of the water of the tanks were pumped daily to storage tanks for irrigation, and the tanks were replenished. The chemical characteristics of the aquaculture effluent used for irrigation were determined and its electrical conductivity (EC) was monitored with a portable digital conductivity meter, which remained at approximately 2.57 dS m-1 (Table 2).

Table 1
Soil chemical, physical and granulometry parameters of the experimental area.

Table 2
Chemical characteristics of the aquaculture effluent used for irrigation.

Irrigation water depths were calculated according to crop evapotranspiration (ETo×Kc×Kl), using the Kc indicated by FAO (2006FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS - FAO. Sweet Sorghum in China. Rome. 2006.), measured in the period between irrigations, according to the water application efficiency of the system and the leaching fractions tested, using the Equation 1,

Wd= ETo x Kc x Kl-PEf x (1+LF)
, in which Wd is the water depth (mm), ETo is the evapotranspiration measured in the period (mm), Kc is the crop coefficient, Kl is the coefficient of localization (BERNARDO et al., 2006BERNARDO, S. et al. Manual de irrigação. 8. ed. Viçosa, MG: UFV, 2006. 625 p.), P is the precipitation measured in the period (mm), Ef is the efficiency of the irrigation system (0.9) and LF is the leaching fraction applied (decimal).

Soil moisture was monitored with PR2 probes (Profile Probe PR2, Delta-T Devices Ltd), which are based on frequency domain reflectometry (FDR), previously configured to measure soil moisture at depths of 10, 20, 30, 40, 60 and 100 cm. Moisture readings were performed weekly, approximately two hours after each irrigation. Simple soil samples from the layers 0-5, 5-20, 20-40, 40-60 and 60-80 cm were collected when the sorghum was harvested to determine the EC through the saturated soil paste extract in each layer.

The vegetal material was collected for biochemical analyzes in July, when the plants were at the soft-dough stage. Samples of the leaf blade of the third fully expanded leaf from the apex were collected, stored in aluminum foil envelopes and immersed in liquid nitrogen (N2), then, they were stored at -80ºC until the enzymatic analyzes.

The plants were harvested shortly after the leaf material was collected to determine their shoot biomass production. Plants from the evaluation area of the plots were cut at 10 cm from the soil, weighted to determine their fresh biomass, and dried in an oven at 60 ºC to a constant weight, to determine their dry biomass.

The catalase (CAT) activity was assessed by a method based on Havir and Mchale (1987HAVIR, E. A.; MCHALE, N. A. Biochemical and developmental characterization of multiple forms of catalase in tobacco leaves. Plant Physiology , Rockville, v. 84, n. 2, p. 450-455, 1987.). A solution of 1.0 mL of potassium phosphate buffer (100 mM at pH 7.5) and 25 μL of hydrogen peroxide (H2O2) (1.0 mM) reacted with 25 μL of the protein extract. The CAT activity was determined by the decomposition of H2O2 for 60 seconds with spectrophotometric readings at 240 nm and 25 °C.

The ascorbate peroxidase (APX) activity was determined as described by Nakano and Asada (1981NAKANO, Y; ASADA, K. Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplast. Plant Cell Physiol, Nagoya, v. 22, n. 5, p. 867-880, 1981.). A solution of 650 μl of potassium phosphate buffer (80 mM at pH 7.5), 100 μl of ascorbate (5.0 mM), 100 μl of EDTA (1.0 M), 100 μL of H2O2 (1.0 mM) reacted with 50 μL of the protein extract. The APX activity was determined by monitoring the ascorbate oxidation rate for 60 seconds using a spectrophotometer at 290 nm and 30 °C.

The superoxide dismutase (SOD) activity was determined by the protocol of Giannopolitis and Ries (1977GIANNOPOLITIS, C. N.; RIES, S. K. Superoxide Dismutases: I. Occurrence in Higher Plants. Plant Physiology, Rockville, v. 59, n. 2, p. 309-314, 1977.), determining the inhibition of the reduction of nitro blue tetrazolium (NBT) by the enzyme extract to avoiding formation of chromophore. A solution (3.0 mL) of consisted of 85 mM phosphate buffer (pH 7.8), 75 μM of NBT, 5.0 μM of riboflavin, 13.0 mM of methionine, 0.1 mM EDTA reacted with 50 μl of the enzyme extract. This solution was placed in glass tubes, irradiated by a white light (15-W fluorescent lamp) for 5 min and then analyzed in a spectrophotometer at 560 nm.

The data were subjected to analysis of variance (ANOVA), test of means (Tukey) and regression, using the program Sisvar 5.0. When significant interactions between varieties and leaching fractions were found, the variables within each factor were considered, otherwise the independent effect of the factors on the variables was considered.

RESULTS AND DISCUSSION

The shoot fresh and dry biomass of the plants increased with increasing leaching fractions (Figure 1). Increases in dry biomass as a function of leaching fractions has been reported in peanut (SANTOS et al., 2012SANTOS, D. B. et al. Produção e parâmetros fisiológicos do amendoim em função do estresse salino. Idesia, Arica, v. 30, n. 2, p. 69-74. 2012.), sorghum (GUIMARÃES et al., 2016GUIMARÃES, M. J. M. et al. Cultivation of forage sorghum varieties irrigated with saline effluent from fish-farming under semiarid conditions. Revista Brasileira de Engenharia Agrícola e Ambiental , Campina Grande, v. 20, n. 5, p. 461-465, 2016.) and maize (CARVALHO et al., 2012CARVALHO, J. F. et al. Produção e biometria do milho verde irrigado com água salina sob frações de lixiviação. Revista Brasileira de Engenharia Agrícola e Ambiental, Campina Grande, v. 16, n. 4, p. 368-374, 2012.), and increases in fresh and dry biomass was also found by Carvalho Junior et al. (2010CARVALHO JUNIOR, S. B. et al. Produção e avaliação bromatológica de espécies forrageiras irrigadas com água salina. Revista Brasileira de Engenharia Agrícola e Ambiental , Campina Grande, v. 14, n. 10, p. 1045-1051, 2010.), who describe the irrigation management with leaching fractions as an efficient alternative to make irrigation with saline water possible.

Figure 1
Shoot fresh (A) and dry (B) biomass of irrigated forage sorghum with saline aquaculture effluent, subjected to different leaching fractions.

However, the crop tolerance level to salt to determine the appropriate leaching fraction are directly related to the irrigation water salinity and the efficiency of this application depends on physical-chemical and biological interactions of agricultural systems (LETEY et al., 2011LETEY, J. et al. Evaluation of soil salinity leaching requirement guidelines. Agricultural Water Management , Gangtok, v. 98, n. 2, p. 502-506, 2011.). A proper irrigation management is essential for crop efficiency, since high leaching fractions can reduce crop yield, as observed by Carvalho et al. (2012CARVALHO, J. F. et al. Produção e biometria do milho verde irrigado com água salina sob frações de lixiviação. Revista Brasileira de Engenharia Agrícola e Ambiental, Campina Grande, v. 16, n. 4, p. 368-374, 2012.), who evaluated irrigated corn yield with saline water (3.3 dS m-1), applying leaching fractions of up to 20%.

The variety Sudan stood out with the highest fresh biomass production, and the variety F305 with the highest dry biomass production. The variety Volumax had the lowest fresh and dry biomass (Table 3).

Table 3
Average fresh and dry biomass production of irrigated forage sorghum varieties with saline aquaculture effluent.

Treatments with leaching fractions of 5, 10 and 15% increased the water availability in the soil layer 0-40 cm to 0.02, 0.05 and 0.11 cm3 cm-3, respectively, above the field capacity (FC) (Figure 2). This result denotes the low water flow in this soil, which hinders the drainage and leaching of salts, thus making the application of leaching fractions an even more important factor for irrigated sorghum crops with saline water, since about 80% of its effective root system is distributed in the first 30 cm of soil (MAGALHÃES et al., 2000MAGALHÃES, P. C. et al. Fisiologia da planta de sorgo. 1. ed. Sete Lagoas, MG: EMBRAPA, 2000, 46 p. (EMBRAPA - CNPMS: Circular Técnica, 3).).

Figure 2
Moisture (A) and electrical conductivity (B) along the soil profile under crops of irrigated forage sorghum varieties with saline aquaculture effluent, subjected to leaching fractions of 0, 5, 10 and 15%. FC = moisture at field capacity.

The largest leaching fractions had the lowest electrical conductivity (EC) (Figure 2). Studies on beetroot (SIMÕES et al., 2016SIMÕES, W. L. et al. Beet cultivation with saline effluent from fish farming. Revista Brasileira de Engenharia Agrícola e Ambiental , Campina Grande, v. 20, n. 1, p. 62-66, 2016.) and peanut (SANTOS et al., 2012SANTOS, D. B. et al. Produção e parâmetros fisiológicos do amendoim em função do estresse salino. Idesia, Arica, v. 30, n. 2, p. 69-74. 2012.) crops also showed increases in leaching fraction reducing EC and sodium accumulation in the surface layer, and improving salt distribution in the soil profile, confirming the use of leaching fractions as an effective practice to reduce excess soluble salts in the root zone of crops. Reducing EC of the soil increases the area available to plant roots, thus reducing the stress caused by the accumulation of salts.

Reducing EC of the soil with high leaching fractions resulted, in general, in a lower activity of the antioxidant enzymes catalase (CAT) and ascorbate peroxidase (APX) (Figure 3). An additional daily irrigation leach salts accumulate in the root zone, since the soil retains water only until reaching field capacity (FC) (ASSOULINE; OR, 2014ASSOULINE, S.; OR, D. The concept of field capacity revisited: Defining intrinsic static and dynamic criteria for soil internal drainage dynamics. Water Resource Research, Malden, v. 50, n. 6, p. 4787-4802, 2014.). Thus, this decrease in soil salinity reduces the stress intensity and consequently, the generation of reactive oxygen species (ROS), decreasing the need for activation of the enzyme antioxidant defense systems.

The low activity of CAT in high EC, as found with the sorghum variety F305 in treatment without leaching fraction (CE>5 dS m-1) was also found with the variety CSF-20 subjected to salinity of 4.0 to 8.0 dS m-1 (FREITAS et al., 2011FREITAS, V. S. et al. Changes in physiological and biochemical indicators associated with salt tolerance in cotton, sorghum and cowpea. African Journal of Biochemistry Research, Durban, v. 5, n. 8, p. 264-271, 2011.). Similar results were found in Boehmeria nivea plants subjected to progressive levels of NaCl (2 to 8 g kg-1) in the soil (HUANG et al., 2014HUANG, C. et al. Effects of concentrations of sodium chloride on photosynthesis, antioxidative enzymes, growth and fiber yield of hybrid ramie. Plant Physiology and Biochemistry, Dorchester, v. 76, n. 1, p. 86-93, 2014.). The activity of CAT in the varieties Sudan and F305 increased with salinity, however, subsequently decreasing with increasing salt stress, confirming that the activity of CAT in low saline stress (4 g kg-1 NaCl) could extinguish H2O2, while under high stress (6 g kg-1 NaCl), the capacity of this this enzyme to eliminate H2O2 is reduced (HUANG et al., 2014HUANG, C. et al. Effects of concentrations of sodium chloride on photosynthesis, antioxidative enzymes, growth and fiber yield of hybrid ramie. Plant Physiology and Biochemistry, Dorchester, v. 76, n. 1, p. 86-93, 2014.). Very high concentrations of NaCl, especially above 100 mM, cause inhibition of a wide range of enzymes (MUNNS et al., 2002MUNNS, R. et al. Avenues for increasing salt tolerance of crops, and the role of physiologically based election traits. Plant and Soil, Crawley, v. 247, n. 1, p. 93-105, 2002.).

The enzyme APX is also responsible for eliminate H2O2. The difference in the activity of the enzymes CAT and APX in the three varieties evaluated denotes the different behavior of these varieties in saline environments.

The APX activity in the variety F305 decreased with increasing leaching fractions, denoting a gradual reduction in plant stress. The APX activity did not vary depending on the treatments in the variety Sudan, denoting that this enzyme was not affected in these saline levels. That APX activity in the variety Volumax, which had the lowest biomass production, was inversely proportional to SOD (Figure 4), this asynchrony between the enzymes APX and SOD indicates a probable accumulation of O2 •-. The low activity of SOD in this cultivar (Table 4) and the high activity of APX and CAT, which eliminate H2O2, indicate the existence of other sources of H2O2, especially without leaching fraction. The low SOD activity without leaching fraction can be an important parameter, since it results in accumulation of O2 •- and, like other ROS, causes oxidation of proteins, amino acids, nucleic acids and carbohydrates, resulting in cell damage (SHARMA et al., 2012SHARMA, P. et al. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. Journal of Botany, London, v. 2012, s/n., p. 1-26, 2012.) and reduced crop yields.

Figure 3
Activity of catalase (CAT-A, C and E) and ascorbate peroxidase (APX-B, D and F) in irrigated forage sorghum varieties with saline aquaculture effluent, subjected to different leaching fractions.

The SOD regression curve of the varieties Sudan and F305 (Figure 4), as well as the curve of the CAT (Figure 3) were parabolic, denoting the synchrony of these enzymes. The highest biomass production of these varieties (Table 3) coincided with the highest SOD activity (Table 4), and the lowest biomass production coincided with the lower activities of SOD and CAT, which occurred without leaching fraction, resulting in a higher accumulation of salts in the soil. Carrasco-Ríos and Pinto (2014CARRASCO-RÍOS, L.; PINTO, M. Effect of salt stress on antioxidant enzymes and lipid peroxidation in leaves in two contrasting corn, ‘Lluteño’ and ‘Jubilee’. Chilean Journal of Agricultural Research, Chillan, v. 74, n. 1, p. 89-95, 2014.) and Gill and Tuteja (2010GILL, S.; TUTEJA, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, Bari, v. 48, n. 12, p. 909-930, 2010.) also found high SOD activities for more tolerant genotypes to salinity.

Although SOD is not the only H2O2-producing enzyme in plant tissues, the balance between the activity of this enzyme and those responsible for the elimination of H2O2 in the cells is considered essential for the balance between O2 •- and H2O2 levels, preventing the formation of hydroxyl radical (OH) (GILL; TUTEJA, 2010GILL, S.; TUTEJA, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, Bari, v. 48, n. 12, p. 909-930, 2010.). The relationship between SOD activity and H2O2 elimination in sorghum is an important biochemical marker to determine the tolerance of this species to salinity (COSTA et al., 2005COSTA, P. H. A. et al. Antioxidant-enzymatic system of two sorghum genotypes differing in salt tolerance. Brazilian Journal of Plant Physiology, Campinas, v. 17, n. 4, p. 353-362, 2005.).

Figure 4
Enzymatic activity of superoxide dismutase (SOD) in irrigated forage sorghum varieties with saline aquaculture effluent, subjected to different leaching fractions.

Table 4
Enzymatic activity of superoxide dismutase (SOD) in irrigated forage sorghum varieties with saline aquaculture effluent.

The enzymatic synchrony of SOD and CAT, observed in the varieties Sudan and F305, is essential to regulate the level of ROS produced in the plant cell, since as the O2 •- are generated, dismutation occurs by SOD to H2O2, which is eliminated by the CAT, converting it to water and oxygen.

The efficiency of this process reduces the level of oxidative stress (ASHRAF, 2009ASHRAF, M. Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnology Advances, Rehovot, v. 27, n. 1, p. 84-93, 2009. ). Researches with the sorghum variety IPA-1011 in saline conditions indicate that activity of APX is not important to protect this variety against oxidative stress damage (OLIVEIRA et al., 2012OLIVEIRA, A. B. et al. Seed priming effects on growth, lipid peroxidation, and activityof ROS scavenging enzymes in NaCl-stressed sorghum seedlings from aged seeds. Journal of Plant Interactions, Turim, v. 7, n. 2, p. 151-159, 2012.).

CONCLUSIONS

Irrigation with saline aquaculture effluent with leaching fraction of 15% results in lower salinity level in the root zone and higher biomass production of forage sorghum Sudan and F305, in semiarid conditions. The antioxidant system was activated in the three sorghum varieties evaluated to prevent accumulation of reactive oxygen species, with the synchrony between the enzymes superoxide dismutase and catalase resulting in a better productive response of the varieties Sudan and F305.

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  • 1
    Paper extracted from the masters dissertation of the first author.

Publication Dates

  • Publication in this collection
    Jan-Mar 2018

History

  • Received
    27 Mar 2017
  • Accepted
    18 July 2017
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