Abstracts
Leaf lipoxygenases (LOX) are involved with important physiological processes such as plant growth and development, senescence, biosynthesis of regulatory molecules, and response to pathogens and insects. We did a biochemical evaluation of the LOX pathway of soybean leaves submitted to wounding in a normal genotype (IAC-100) and its counterpart lacking seed LOX (IAC-100 TN). Our results indicate that LOX activities in the different pHs and temperatures tended to be higher in the wounded plants compared to their respective controls. The K M app values at 168 h after wounding reached a minimum in both genotypes indicating that the plants respond by changing the leaf LOX pool. There was an increase on protease inhibitor levels in all time points after wounding, for both cultivars. The levels of hexanal and total aldehydes are similar for the wounded plants at different times after wounding and their respective controls for both genotypes. Our results strongly suggest that the LOX pathway is activated during the wound response leading to jasmonate by the initial action of hydroperoxide cyclase. In addition, the results show that the genetic removal of seed LOX does not interfere with the plant’s ability to respond to wound via the LOX pathway.
Lipoxygenases; soybean; mechanical wounding
Lipoxigenases (LOX) de folhas estão envolvidas em importantes processos fisiológicos, tais como: crescimento e desenvolvimento, senescência, biossíntese de moléculas regulatórias e resposta a patógenos e a insetos. Neste trabalho, foi feita uma avaliação da via bioquímica das lipoxigenases em folhas de soja submetidas a ferimento em um genótipo normal (IAC-100) e em uma linhagem avançada derivada de IAC-100, mas isenta de LOX na semente (IAC-100 TN). De um modo geral, as atividades de LOX em diferentes valores de pH e temperaturas foram maiores em plantas feridas com relação a seus respectivos controles. Os valores de K M app, 168h após ferimento, atingiram o seu mínimo em ambos os genótipos, indicando que as plantas responderam ao ferimento por meio da alteração no "pool" de LOX da folha. Em ambos os genótipos houve um aumento nos níveis de inibidores de proteases após o ferimento. Os níveis de hexanal e de aldeídos totais foram similares em plantas feridas em diferentes tempos, após ferimento, com relação a seus respectivos controles para ambos os genótipos. Pelos resultados, infere-se fortemente que a via das lipoxigenases é ativada durante a resposta a ferimento, levando à síntese de jasmonato pela ativação inicial da hidroperóxido ciclase. Além disso, por esses mesmos resultados, constata-se que a remoção genética de LOX das sementes não interfere com a capacidade de a planta responder a ferimentos por meio da via bioquímica das lipoxigenases.
Lipoxigenases; soja; ferimento mecânico
BIOCHEMICAL EVALUATION OF LIPOXYGENASE PATHWAY OF SOYBEAN PLANTS SUBMITTED TO WOUNDING
ANGÉLICA APARECIDA VIEIRA1 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) , MARIA GORETI DE ALMEIDA OLIVEIRA2 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) , INES CHAMEL JOSÉ1 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) , NEWTON DENIZ PIOVESAN1 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) , SEBASTIÃO TAVARES DE REZENDE2 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) , MAURILIO ALVES MOREIRA2 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) AND EVERALDO GONÇALVES DE BARROS3 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br) ,* 1 Received: 25/10/99 - Accepted: 20/9/2000 . BIOAGRO 2 . Depto. de Bioquímica e Biologia Molecular/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil 3 . Depto. de Biologia Geral/BIOAGRO, UFV, 36571-000, Viçosa, MG, Brazil. * Author to whom correspondence should be addressed (email: ebarros@mail.ufv.br)
BIOAGRO, Universidade Federal de Viçosa (UFV), 36571-000, Viçosa, MG, Brazil
ABSTRACT - Leaf lipoxygenases (LOX) are involved with important physiological processes such as plant growth and development, senescence, biosynthesis of regulatory molecules, and response to pathogens and insects. We did a biochemical evaluation of the LOX pathway of soybean leaves submitted to wounding in a normal genotype (IAC-100) and its counterpart lacking seed LOX (IAC-100 TN). Our results indicate that LOX activities in the different pHs and temperatures tended to be higher in the wounded plants compared to their respective controls. The KM app values at 168 h after wounding reached a minimum in both genotypes indicating that the plants respond by changing the leaf LOX pool. There was an increase on protease inhibitor levels in all time points after wounding, for both cultivars. The levels of hexanal and total aldehydes are similar for the wounded plants at different times after wounding and their respective controls for both genotypes. Our results strongly suggest that the LOX pathway is activated during the wound response leading to jasmonate by the initial action of hydroperoxide cyclase. In addition, the results show that the genetic removal of seed LOX does not interfere with the plants ability to respond to wound via the LOX pathway.
ADDITIONAL INDEX TERMS: Lipoxygenases, soybean, mechanical wounding.
AVALIAÇÃO BIOQUÍMICA DA VIA DAS LIPOXIGENASES EM PLANTAS DE SOJA SUBMETIDAS A FERIMENTO
RESUMO - Lipoxigenases (LOX) de folhas estão envolvidas em importantes processos fisiológicos, tais como: crescimento e desenvolvimento, senescência, biossíntese de moléculas regulatórias e resposta a patógenos e a insetos. Neste trabalho, foi feita uma avaliação da via bioquímica das lipoxigenases em folhas de soja submetidas a ferimento em um genótipo normal (IAC-100) e em uma linhagem avançada derivada de IAC-100, mas isenta de LOX na semente (IAC-100 TN). De um modo geral, as atividades de LOX em diferentes valores de pH e temperaturas foram maiores em plantas feridas com relação a seus respectivos controles. Os valores de KM app, 168h após ferimento, atingiram o seu mínimo em ambos os genótipos, indicando que as plantas responderam ao ferimento por meio da alteração no pool de LOX da folha. Em ambos os genótipos houve um aumento nos níveis de inibidores de proteases após o ferimento. Os níveis de hexanal e de aldeídos totais foram similares em plantas feridas em diferentes tempos, após ferimento, com relação a seus respectivos controles para ambos os genótipos. Pelos resultados, infere-se fortemente que a via das lipoxigenases é ativada durante a resposta a ferimento, levando à síntese de jasmonato pela ativação inicial da hidroperóxido ciclase. Além disso, por esses mesmos resultados, constata-se que a remoção genética de LOX das sementes não interfere com a capacidade de a planta responder a ferimentos por meio da via bioquímica das lipoxigenases.
TERMOS ADICIONAIS PARA INDEXAÇÃO: Lipoxigenases, soja, ferimento mecânico.
INTRODUCTION
Lipoxygenases (LOX) (linoleate:oxygen oxidoreductase, E.C. 1.13.11.12) are dioxygenases that catalyze the addition of molecular oxygen to polyunsaturated fatty acids containing the group cis, cis -1,4-pentadiene. Linolenic acid (C18:3) contains such group and is the most abundant fatty present in the majority of plant tissues. Linoleic acid (C18:2) which also contains the cis, cis-1,4-pentadiene group is found in high concentrations in seeds and embryos (Hildebrand et al., 1988).
Several studies have been conducted aiming to elucidate the physiological role of LOX in plant tissues. LOX have been studied in soybeans (Axelrod et al., 1981; Peterman and Siedow, 1985; Park and Pollaco, 1989; Grayburn et al., 1991; Saravitz and Siedow, 1995; Saravitz and Siedow, 1996), in wheat (Bohland et al., 1997), barley (Reinbothe et al., 1997), tobacco (Rickauear et al., 1997), tomato (Farmer and Ryan, 1992), and potato (Bell and Mullet, 1993), among others. These studies suggest that LOX are related to plant growth and development, senescence, plant defense against pathogens and insects, and biosynthesis of regulatory molecules.
In soybeans, LOX have been studied mostly in seeds and leaves. It has been suggested that 10 to 12 genes encoding LOX are present in the soybean genome. Three LOX isozymes have been extensively characterized by Axelrod et al. (1981) in soybean seeds. Despite the extensive characterization, the physiological roles of these enzymes have not been fully understood. However, recent data show that these enzymes affect the levels of protease inhibitors in the seed suggesting that they have an important function during seed development (Carvalho et al., 1999). In leaves, it has been observed that LOX expression increases considerably as a result of reproductive sink removal (Kato et al., 1990), pod removal (Bunker et al., 1995), and mechanical wounding (Saravitz and Siedow, 1996), indicating that LOX can be considered a vegetative storage protein as well as an important component of the plant response system to pathogen and insect attack.
The main goal of this work was to biochemically characterize the LOX pool present in leaves of soybean plants submitted to wounding. Wild type genotypes and mutant lines lacking seed LOX were used to determine if these two genetic materials respond to wounding by activating the LOX pathway.
MATERIAL AND METHODS
Genetic material
Soybean (Glycine max L.) leaves at development stage V3 (Fehr et al., 1971) were obtained from commercial cultivar IAC-100 and from an advanced line derived from IAC-100 but lacking seed LOX (IAC-100 TN). Seeds from IAC-100 were obtained from the Germplasm Bank of the Department of Plant Sciences of the Federal University of Viçosa (UFV), MG, Brazil. IAC-100 TN was developed by conventional breeding after five cycles of backcrossing in our Breeding Program conducted at the UFV Biotechnology Institute (BIOAGRO). The high genetic simarility between IAC-100 and IAC-100 TN was confirmed by analysis of DNA fingerprinting with random amplified polymorphic DNA (RAPD) markers and phenotypic characteristics. The plants were cultivated in the greenhouse in 4 kg pots containing three plants each.
Mechanical wounding
Seven mechanical wounds were inflicted in each of the three leaflets of the first trifoliolate leaf with the aid of a pincer. After 0, 6, 12, 24, 48, and 168 h the wounded leaflets (local response) and the leaflets of the second fully expanded trifoliolate leaf (systemic response) were collected, immediately immersed in liquid nitrogen and kept at 80o C for the biochemical analyses. Leaves from control plants, not submitted to wounding, were also collected in all time points.
Leaf extract
Leaf extract for biochemical determinations were obtained according to Ohta et al. (1986) with the following modifications: the extraction buffer was 0.05 mol.L-1 sodium phosphate pH 6.5 with no Triton X-100. Protein determination was by the bicinchoninic acid assay (Smith et al., 1985).
Lipoxygenase activity
LOX activity in the leaf extracts was determined using linolenic acid as substrate according to Axelrod et al. (1981). This method determines the increase on absorbance at 234 nm as a result of the formation of conjugate double bonds in the linoleic acid hydroperoxide. For optimum pH determination different buffer systems at a final concentration of 50 mmol.L-1 were used covering the range of pH 2 to 10. For determination of optimum temperature enzyme activity was determined in 50 mmol.L-1 sodium phosphate pH 6.0 in the range of 20 to 50 oC. All determinations were done in triplicate.
Kinetic parameters
LOX activity was determined in 50 mmol.L-1 phosphate buffer pH 6.0, at 25 oC, using linoleic acid in the following concentrations: 10, 20, 40, 80, 160, 320, 640, and 1,280 mmol.L-1. The kinetic parameters, in the steady state, were obtained by non-linear regression analyses using the program Enzifitter (Leatherbarrow, 1987). All determinations were done in triplicate.
Protease Inhibitors
Determination of protease inhibitor contents in the leaf extracts was based on the inhibition of trypsin activity upon N-benzoyl-D,L-arginine-p-nitroanilide (D,L-BapNA) (Kakade et al., 1974).
Hexanal determination
Hexanal production by leaf extracts was determined by gas chromatography based on the procedure developed by Utumi et al. (1998). The column used was a carbowax (25 m x 0.53 mm). The initial column temperature of 45 oC was raised 7 oC per minute until 70 oC and kept at this temperature for 5 min. Then it was raised 15 oC per minute until 200 oC. The temperatures of the injector and detector were 200 oC and 250 oC, respectively. Nitrogen was used as the carrier gas at a flow rate of 5.7 ml per min.
Total aldehyde determination
Total aldehyde content in leaf extracts was determined according to Wilson and McDonald (1986) using 3-methyl-2-benzothiozolinone hydrazone (MBTH).
RESULTS AND DISCUSSION
To biochemically characterize the LOX pool present in soybean leaves submitted to mechanical wounding, we first determined pH and temperature effects on the activity of these enzymes. Figure 1 shows the pH profiles of enzyme activities (systemic response) analyzed in extracts from cultivar IAC-100 and respective control at 168 h after wounding. At this time point the KM app value reached a minimum in relation to the control (Table 1). Two prominent activity peaks are seen around pHs 4.5 and 6.0, with and without wounding, indicating the existence of at least two LOX isoenzymes. The activity profiles for all time points analyzed for IAC-100 and IAC-100 TN, local and systemic response, followed the same trend observed in this time point (data not shown). Our data are similar to those observed for leaf LOX from other soybean cultivars (Lanna et al., 1996), from potato tubers (Galliard et al., 1971), sunflower seeds (Leoni et al., 1985), and green pepper (Minguez-Mosqueira et al., 1993).
Figure 2 shows the temperature profiles of enzyme activities (local response) analyzed in extracts from cultivar IAC-100 and respective control at 168 h after wounding. Optimum temperature was around 25 oC, with or without wounding. The activity profiles for all time points analyzed for IAC-100 and IAC-100 TN, local and systemic responses, followed the same trend observed in this time point (data not shown). Lanna et al. (1996), working with cultivars IAC-100 and Cristalina, both wild type and LOX minus, at vegetative stage V4, found the same temperature optimum for leaf LOX.
As a whole, considering that the protein concentrations in all extracts analyzed were very close to each other, our data suggest that LOX activities in the different pHs and temperatures tended to be higher in the wounded plants compared to their respective controls. This indicates that both genotypes (wild type and LOX minus) respond to wounding by activating the LOX pathway.
The leaf LOX pool activities present in the two genotypes analyzed using the linoleic acid concentrations defined in our experiments, at pH 6.0, follow the Michaelis-Menten kinetics. Figure 3 shows the Michaelis-Menten for LOX activity 48 h after wounding using IAC-100 TN extract (local response). The activity profiles for all time points analyzed for both cultivars, wild type and LOX minus, local and systemic response, followed the same trend observed in this time point (data not shown). Table 1 presents the KM app values obtained for IAC-100 and IAC-100 TN, respectively, local and systemic responses, at different times after wounding. The local response shows that KM app values increased 6 h after wounding for both genotypes in relation to the control plants (not wounded). The KM app values at 12, 24, and 48 h after wounding are similar to the respective controls. However, at 168 h after wounding the KM app values reached a minimum in both genotypes.
The LOX pool in the systemic response does not show the same profile for the two genotypes. In cultivar IAC-100, KM app values decreased 12 h after wounding reaching its minimum after 168 h in relation to the controls. In the case of cultivar IAC-100 TN, KM app values were greater than the controls from 6 to 48 h after wounding, but dropped again to a value similar to the control 168 h after wounding. These data suggest an alteration on the leaf LOX pool at 168 h after wounding, indicating that the plant responds to wounding by activating the LOX pathway.
Saravitz and Siedow (1996) determined the local and systemic responses of soybean plants to wounding in the same vegetative stage analyzed in this work. In that work, they analyzed the variation in transcript levels for LOX 7 and 8 in the first (local response) and the second trifoliate leaves (systemic response). Transcripts for LOX 7 were detected only transiently at 8 h after wounding in both types of responses while LOX 8 transcripts were detected from 8 to 72 h only in the local response. The changes in KM app values observed in our work at 6 h after wounding in the local responses of IAC-100 and IAC-100 TN and in the systemic response of IAC-100 (Table 1) coincide with the alterations observed for LOX 7 by Saravitz and Siedow (1996).
Although the KM app values vary differently during the systemic response when cultivar IAC-100 is compared to IAC-100 TN, as a whole these values are very close to each other in both types of genotypes, indicating that the genetic removal of seed LOX does not interfere with the plant response to wounding. Consequently, the expression of seed LOX genes in the cultivar analyzed does not interfere with the expression of genes coding for the LOX pool present in the leaves.
Tables 2 and 3 depict the protease inhibitor levels (expressed in mg of trypsin inhibited per mg of protein) of IAC-100 and IAC-100 TN submitted to wounding, local and systemic responses. The data show that there was an increase on protease inhibitor levels in all time points after wounding, for both cultivars, in both types of responses. These data indicate that the plant respond to wounding by activating transcription of genes encoding protease inhibitors, most probably through the LOX pathway. This suggestion is in accordance to the model proposed by Farmer and Ryan (1992) working with tomato leaves. In this model, hydroperoxides derived from LOX activity are converted into jasmonic acid by a series of enzymatic steps. This plant hormone would finally cause the activation of genes coding for protease inhibitors.
The LOX pathway can have two alternative branches, one starting with the hydroperoxide cyclase leading to jasmonates, and the other starting with hydroperoxide lyase leading to aldehydes. To test if there is a major branch used during the wound response, we determined the levels of hexanal and total aldehydes in IAC-100 and IAC-100 TN. However, our data showed that the levels of these compounds are similar for the wounded plants at different times after wounding and their respective controls for both genotypes (data not shown). This result suggests that the wound response through the LOX pathway does not occur via aldehyde production.
Our results involving the determination of LOX enzymatic parameters, and products of the LOX pathway in soybean leaves submitted to mechanical wounding strongly suggest that this pathway is activated during the wound response leading to jasmonate by the initial action of hydroperoxide cyclase. In addition, the results show that the genetic removal of seed LOX does not interfere with the plants ability to respond to wound via the LOX pathway.
ACKNOWLEDGEMENTS
This work was supported by BID/FINEP and FAPEMIG.
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Publication Dates
-
Publication in this collection
20 Nov 2002 -
Date of issue
2001
History
-
Accepted
20 Sept 2000 -
Received
25 Oct 1999