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Enzyme expression in indica and japonica rice cultivars under saline stress/Expressao de enzimas em cultivares de arroz indica e japonica sob estresse salino.

Introduction

Although total affected area by salinity in Brazil is 2% (MENEZES-BENAVENTE et al., 2004), it has become a major obstacle to crop productivity (DASGAN et al., 2002), especially in the southern State of Rio Grande do Sul, Brazil, where Oryza sativa L. culture is irrigated by flooding. Saline water comes from the Laguna dos Patos and coastal rivers which are subjected to salinization due to the introduction of sea water when water levels are low (MARCOLIN et al., 2005). This fact mainly occurs during the summer when low rainfall and high evaporation-transpiration coincide with the culture's reproduction phase.

Rice is moderately tolerant to salinity. However, the widespread use of indica rice cultivars in RS may be one of the most impairing factors in the process, since japonica cultivars have a higher salt tolerance than that of indica cultivars (LIMA et al., 2004). The plant needs osmosis adjustments to adapt itself to stress which involves increased energy expenditure due to the synthesis of organic solutes (FLOWERS et al., 2010). The latter act as enzymatic protection (GREENWAY; MUNNS, 1980) and cause disturbances in the general metabolic activity (MANSOUR; SALAMA, 2004), including photosynthesis (WILLADINO et al., 2011), enzymatic activity (MENEZES-BENAVENTE et al., 2004; SOUZA FILHO et al., 2003) and respiration (TAIZ; ZEIGER, 2004). Thus, enzymes involved in respiration may somehow provide a carbon source for regulating ionic and osmotic adjustment (TAIZ; ZEIGER, 2004), synthesis of new molecules) and removal of toxic substances during anaerobic respiration (FARIA et al., 2003). Moreover, they have an important role in Krebs cycle through photorespiration (MANCHENKO, 2000).

Isozyme analysis is employed to characterize rice cultivars (BONOW et al., 2001) and mobility differences in an electric field are the result of differences at DNA sequence levels that encode the enzymes. When band patterns of two individuals differ, it is presumed that that these differences have a genetic basis (MURPHY et al., 1990). The presence or absence of bands and changes in their intensity significantly differentiate the plants' isozymes (ORASMO; MACHADO, 2003). In fact, the environment is an important factor in the modulation of gene expression. The monitoring of such changes may be done by molecular markers. They not only provide useful data on the structure and genetic diversity of plant populations, but also visualize enzyme activity at the plant's different stages (ALFENAS, 1991).

It is therefore highly important that farmers understand the mechanisms of adaptation and acclimation to salt stress through a combined biochemical and physiological research and thus, the development and use of tolerant cultivars (SHINOZAKI; DENNIS, 2003), coupled to the reuse of degraded areas and the employment of low quality water.

Current research evaluates the respiration enzymes expression in Oryza sativa spp. japonica S. Kato and Oryza sativa spp. indica S. Kato cultivars under salt stress.

Material and methods

Subspecies of Oryza sativa spp. japonica, tolerant to salinity, and Oryza sativa spp. indica, susceptible to salt stress, were used in the experiment (LIMA et al., 2004, 2005). Whereas cultivars of Oryza sativa L. spp. japonica S. Kato comprised BRS Bojuru, IAS 12-9 Formosa and Goyakuman, cultivars of Oryza sativa L. spp. indica S. Kato comprised BRS-7 Taim, BRS Querencia and BRS Atalanta.

The seedlings were obtained by sowing in plastic trays containing washed sand as a substrate. Ten days after emergency (DAE) seedlings were transferred to a greenhouse with controlled temperature and humidity, and placed in 15L-basins containing 12 L Hoagland nutrient solution (HOAGLAND; ARNON, 1950), 50%, with concentrations 0, 25, 50, 75 and 100 mM NaCl, based on previous research with the same cultivars, and changed at a 4-day interval. Styrofoam plates were used to prop the 30 seedlings fixed with cotton. They were kept in the basins for 42 days after transfer (DAT). During this period 3 sample collections were undertaken every 14 days. The plants were harvested at 14, 28 and 42 DAT, packed in identified plastic bags, with wet cotton, and placed in styrofoam boxes with ice for transport to the laboratory. They were immediately stored at -70[degrees]C in an ultrafreezer until further analysis.

The tests were conducted in the BioSeeds Laboratory, Department of Phytotechnology of the Eliseu Maciel Faculty of Agronomy, Federal University of Pelotas, Pelotas, State of Rio Grande do Sul, Brazil. Plant tissues (the last three leaves from the base to the apex) were ground in a porcelain mortar with ice. Aliquots ranging between 200 and 300 mg of the plant extract were placed in an eppendorf tube with an extractor gel buffer solution (Tris 0.051 M, 0.0076 M citric acid and water qsp 1 L), electrode buffer (Lithium hydroxide 0.38 M, 0.192 M boric acid and water qsp 1 L) and 0.15% of 2-mercaptoethanol at 9:1:2 (w [v.sup.-1]) (SCANDALIOS, 1969). They were then stored in a refrigerator for 24 hours for enzyme extraction after centrifuged at 16,100 g for 5 min., at 4[degrees]C. Electrophoresis was undertaken in 7% polyacrylamide gels by placing 20 [micro]L of each sample in acrylic comb-produced wells. The enzymatic patterns were analyzed by the buffer system (SCANDALIOS, 1969). Gels were placed in vertical electrophoretic vats and kept in a cold chamber at 4-6[degrees]C. The electrophoretic migrations were undertaken with a potential difference of 1.0 V [mm.sup.-1], until the front line formed by bromophenol blue reached 90 mm from the point of application.

Bands were revealed for the enzyme systems esterase (EST), according to Scandalios (1969), alcohol dehydrogenase (ADH), phosphoglucose isomerase (PGI), malate dehydrogenase (MDH) and malic enzyme (ME), described by Alfenas (1991), and alpha amylase ([alpha] - AMY), according to Alfenas (1998). Electrophoresis gels were fixed in the solution of distilled water: methanol: acetic acid at 5:5:1 (v [v.sup.-1]). Taking into account the presence / absence and intensity of each electrophoretic band, results' interpretation was based on visual analysis of electrophoresis gels.

[FIGURE 1 OMITTED]

Results and discussion

Although esterase electrophoretic patterns (EST - EC 3.1.1.1) revealed the presence of the enzyme in the three tillage periods (14, 28 and 42 DAT), highest intensity of bands was reported at 28 DAT. In first harvest, at 14 DAT, the japonica cultivars Bojuru (B); Formosa (F) and GoyaKuman (G), tolerant to salinity, and the indica cultivar Taim (T), susceptible to salinity, had a higher esterase expression. Bands' intensity among the tolerant Formosa cultivars increased in salinity accordingly. This fact suggested higher enzyme activity when subjected to salt stress. The same pattern was obtained for all japonica varieties tested at 28 DAT (Figure 1).

With the exception of differential expressions between tolerant and susceptible genotypes, no variation in response intensity to different salt concentrations occurred. In the third collection, the bands' intensity decreased in all cultivars when compared to that of previous periods. However, bands in Querencia and Taim cultivars were more intense up to 50 mM NaCl treatment. Cultivar Formosa showed a more intense band with higher salt concentrations (100 mM) and may indicate the involvement of esterase in the cultivar's possible tolerance to salt stress (Figure 1).

The change in enzyme expression in proportion to salinity level is possibly related to some mechanism of plant defense. In fact, esterase is involved in lipid catabolism. Such degradation may be a carbon source for the synthesis of new molecules (FLOWERS et al., 2010) which would justify a differential standard in the japonica Formosa cultivar. When Lima et al. (2004) researched the effect of salt stress on rice seedlings, they reported higher salinity tolerance in O. sativa spp. japonica cultivars. Environmental factors affect plants' metabolism, influence the activity of isoenzymes, especially esterase, peroxidases, phosphatases and phenolases, and cause different enzyme patterns or activities (MALONE et al., 2006).

Alcohol dehydrogenase (ADH-EC 1.1.1.1) showed activity only in the first collection, at 14 DAT (Figure 2), in all japonica cultivars and in the Taim indica cultivar. The presence of more highlighted bands in the japonica Bojuru cultivar than in other genotypes has been reported. In fact, there was an increase in their intensity in proportion to increase in NaCl concentrations.

ADH is an enzyme that acts on the respiratory process by removing toxic substances, such as acetaldehyde and ethanol, produced when cells start anaerobic respiration (FARIA et al., 2003). Therefore, when the aerobics path is impaired, the anaerobic respiration route is activated and cells' toxic substances, such as acetaldehyde and ethanol, are produced. In anaerobic metabolism (alcohol fermentation), pyruvate, primarily produced in glycolysis, is transformed into acetaldehyde by pyruvate decarboxylase enzyme and the acetaldehyde is reduced to ethanol by ADH. Plants with increased resistance to salinity compartimentize salt to reduce its harmful effects (FLOWERS et al., 2010). Compartmentalization may have occurred in cytosol and not in vacuoles of leaves of more resistant cultivars.

[FIGURE 2 OMITTED]

This fact possibly triggered the fermentation process. ADH activation for ethanol production occurred to minimize salt damage to the cell and the detrimental effect of acetaldehyde accumulation. Evidence exists that acetaldehyde accumulation may be more detrimental to cell metabolism that ethanol accumulation (DREW, 1997). Moreover, since lipids are soluble in ethanol, their diffusion to the external environment through the membrane in which it would be diluted or metabolized by microorganisms, is possible.

Malate dehydrogenase (MDH-EC 1.1.1.37) zymograms showed enzyme activity in the three collection periods even though greater intensity of MDH has been verified at first sampling (14 DAT) in all cultivars. Among the japonica cultivars (Figure 3B, F and G), Bojuru had more intense bands in the three collections and in the more saline treatments. Cultivars Formosa and GoyaKuman showed a similar enzymatic pattern in the first and second collections. The bands in the GoyaKuman cultivar were more intense according to increasing NaCl concentrations. Indica cultivars (Figure 3A, Q and T) showed similar expression pattern among themselves in three tillages. However, the Atalanta cultivar had more intense bands in the three lower doses in the first collection and virtually no activity in the third one. It is an indication of higher susceptibility to increased saline concentrations.

Enzyme MDH occurs in the mitochondrial matrix and in cell cytoplasm and functions in the mitochondrial during the two final reactions of the citric acid cycle. NADH is thus oxidized in the mitochondrial respiratory chain to produce ATP by oxidative phosphorylation (TAIZ; ZEIGER, 2004). In the cytoplasm, MDH catalyzes the reaction of OAA reduction, producing NAD+ required for glycolysis, and may also oxidize mitochondria-transported malate, to produce sucrose by glyconeogenic pathway. MDH has an important role in Krebs cycle (MANCHENKO, 2000) since it participates in the malate movement through the mitochondrial membrane and CO2 fixation. Further, it also has a metabolic function in NADPH production, in photorespiration, ionic regulation and osmotic adjustment (TAIZ; ZEIGER, 2004).

[FIGURE 3 OMITTED]

Since it is a constitutive enzyme, MDH is important because it shows activity in all evaluated cultivars and sampling periods. Plants under salt stress make osmotic adjustments by the accumulation of ions in the vacuole and by the synthesis of compatible solutes in the cytosol, such as glycine-betaine, sorbitol, mannitol, sucrose and proline (SZABADOS; SAVOURE, 2009). They all have the protective function of the plasma membrane (MANSOUR; SALAMA, 2004) and the cytosol enzymes. The amount of carbon used for the synthesis of organic solutes is high and carbon diversion for the adjustment of water potential reduces growth, total biomass and crop productivity. MDH pattern suggests increased activity of the enzyme in cultivars when the environment's salinity increases. Tolerant rice cultivars have an increased MDH activity as salinity increases (KUMAR et al., 2000). These data corroborate the findings of current research.

[FIGURE 4 OMITTED]

The Atalanta cultivar showed phosphoglicoisomerase expression (PGI - EC 5.3.1.9) only in the first sampling of treatments 0, 25 and 50 mM NaCl (Figure 4).

While Bojuru cultivar revealed bands with similar intensity patterns for all treatments, bands in the Formosa cultivar were detected during the first collection at concentrations 50, 75 and 100 mM NaCl and at concentrations of 0, 25 and 50 mM in the second collection. Bands in GoyaKuman cultivar were more intense in the second collection and at salinity levels 25 and 100 mM.

Operating in glycolysis, PGI enzyme catalyzes the reversible isomerization from G6P to F6P (MANCHENKO, 2000; TAIZ; ZEIGER, 2004). Consequently, its presence in japonica cultivars may indicate an alternative mechanism to compensate the demand for carbon skeletons for the production of organic solutes that act in osmotic adjustment. According to Greenway and Munns (1980) and others, it is a strategy employed by salinity-tolerant species.

[FIGURE 5 OMITTED]

The [alpha]-amylase ([alpha]-AMY-EC 3.2.1.1) enzyme was not detected in all cultivars, concentrations and stages under analysis (unpublished data). Cultivars have probably shown enzyme expression in a period previous to plants' exposure to salinity. This is due to the fact that the enzyme causes starch hydrolysis during the germination process and early growth, which may justify the non-formation of bands. Highest enzyme activity in seeds occurs approximately ten days after germination. Within the initial phase, growth is slow and photo-assimilates demand is high in roots and new leaves growth. Starch accumulation that would favor [alpha]-amylase synthesis fails to occur (BEWLEY; BLACK, 1994).

Malic enzyme (EM-EC 1.1.1.40) zymograms indicate that it had activities during the three sampling periods, or rather, 14, 28 and 42 DAT (Figure 5). Bands of enzyme activities in the first collection were greater than those in indica Taim cultivar and in japonica GoyaKuman and Formosa cultivars. The latter had more intense bands according to increasing salinity. Bands in the second collection showed a higher intensity in japonica Bojuru and GoyaKuman cultivars at concentrations 50, 75 and 100 mM NaCl. As a rule, Formosa had similar activity in the different treatments. Within the context of indica cultivars, Atalanta exhibited bands at higher concentrations, although the others showed activity in control and in 25 mM NaCl. Only the japonica Bojuru, Formosa and GoyaKuman cultivars expressed any activity in the third collection, whereas bands in the Formosa cultivar showed uniformity in intensity either in control or in the other treatments.

A band in the Atalanta cultivar was detected at the highest salt concentration although with less intensity than that obtained at 28 DAT. Moreover, in the GoyaKuman cultivar, enzyme expression decreased with increasing salinity. Malic enzyme decarboxylates malate into pyruvate with mitochondria operating alternative pathways for the metabolism of glycolysis-derived phosphoenolpyruvate (PEP) and providing metabolic flexibility to plants (TAIZ; ZIEGER, 2004). This mechanism suggests that plants undergoing salinity transform pyruvate into ethanol under anaerobic conditions, as mentioned earlier (Figure 3). In its absence or lack, the plants oxidize malate or citrate in alternative routes without the involvement of glycolysis-derived pyruvate. Consequently, flexibility is provided to saline-stressed plants as a response to such environment.

Current research was undertaken to identify which rice genotypes belonging to the subspecies indica and japonica were susceptible and tolerant to salinity. In the first place, there was a positive response of the subspecies japonica cultivars. The information triggered the search for adaptation mechanisms of the two subspecies and how they responded to salt stress. This search became the focus of current study. The evaluation of certain enzymes' expression involved in respiration becomes interesting since respiration is the source of energy for plants to support growth and development. These factors comprise the overcoming of difficulties in the environment, often due to anthropogenic issues brought about by the misuse of natural resources.

Conclusion

Although some are constitutive enzymes, results may imply that the enzymatic systems ADH, MDH, ME and PGI at 14 DAT, and EST and ME at 28 DAT are more expressed and that japonica cultivars have more intense bands in proportion to increasing salinity. Evaluated enzyme expression suggests that the above-mentioned cultivars resort to these mechanisms to tolerate stress. In fact, they are employed as an alternative route for metabolism, carbon and energy source for the synthesis of new molecules, in toxic substances removal and in ionic regulation and/or osmotic adjustment.

Doi: 10.4025/actascibiolsci.v34i4.8535

Acknowledgements

We would like to thank the Coordination for the Improvement of University Personnel (CAPES) for the scholarship given to the first author, and for the financial support for current research provided by PROAP/CAPES.

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Received on October 19, 2009.

Accepted on February 8, 2011.

Maria da Graca de Souza Lima (1) *, Nei Fernandes Lopes (1), Paulo Dejalma Zimmer (2), Geri Eduardo Meneghello (2), Cristina Rodrigues Mendes (1) and Luciano do Amarante (3)

(1) Departamento de Botanica Instituto de Biologia, Universidade Federal de Pelotas, Campus Universitario Capao do Leao, s/n, 96010-900, Cx. Postal 354, Pelotas, Rio Grande do Sul, Brazil. (2) Departamento de Fitotecnia, Faculdade de Agronomia Eliseu Maciel, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul, Brazil. (3) Departamento de Bioquimica, Instituto de Quimica e Geociencias, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul, Brazil. * Author for correspondence. E-mail: peccoli@gmail.com
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Author:Lima, Maria da Graca de Souza; Lopes, Nei Fernandes; Zimmer, Paulo Dejalma; Meneghello, Geri Eduardo
Publication:Acta Scientiarum. Biological Sciences (UEM)
Date:Oct 1, 2012
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