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Comptes Rendus

Plant biology and pathology
Changes in antioxidant and lignifying enzyme activities in sunflower roots (Helianthus annuus L.) stressed with copper excess
[Variations des activités enzymatiques anti-oxydantes et lignifiantes dans les racines de tournesol (Helianthus annuus L.) traitées par un excès de cuivre]
Comptes Rendus. Biologies, Volume 326 (2003) no. 7, pp. 639-644.

Résumés

Treatment with 50 μM CuSO4 for five days caused significant decrease in dry-matter production and protein level of ten-day-old sunflower seedling roots. An increase of lipoperoxidation product rate was also observed. The involvement of some enzyme activities in the sunflower root defence against Cu-induced oxidative stress was studied. Copper treatment induced several changes in antioxidant enzymes. SOD (superoxide dismutase, EC 1.15.1.1) activity was reduced but CAT (catalase, EC 1.11.1.6) and GPX (guaiacol peroxidase, EC 1.11.1.7) activities were significantly enhanced. The lignifying peroxidase activities, assayed using coniferyl alcohol and syringaldazine, were also stimulated. Analysis by native gel electrophoresis of syringaldazine peroxidase activity showed the stimulation of an isoform (A2) and the induction of another one (A1) under cupric stress conditions. On the other hand, the activity of PAL (phenylalanine ammonia lyase, EC 4.3.1.5), which plays an important role in plant defence, was also activated. The possible mechanisms by which Cu-induced growth delay and changes in enzymatic activities involved in plant defence processes are discussed.

Des jeunes plantules de tournesol (Helianthus annuus L.) cultivées sur un milieu nutritif de base en conditions contrôlées et âgées de 10 jours sont traitées par une dose de 50 μmol l−1 de CuSO4 pendant cinq jours. Les effets du stress métallique sont déterminés, au niveau des racines, sur la croissance, la teneur en protéines totales, la lipoperoxydation membranaire et les activités de certaines enzymes impliquées dans la défense contre les stress abiotiques. Concernant la croissance, l'application de 50 μmol l−1 de CuSO4 dans le milieu de culture se traduit par une nette réduction de la biomasse sèche racinaire, estimée à 41 % par rapport aux témoins. La longueur des racines traitées ainsi que leur teneur en eau sont également réduites de 20 % et de 53 %, respectivement. L'effet du stress cuprique se manifeste encore par une diminution de 53 % de la teneur des protéines totales solubles et une stimulation significative de la production de MDA (malondialdéhyde), un des produits majeurs de la lipoperoxydation membranaire. Parallèlement à ces perturbations, des modulations de quelques activités enzymatiques ont été notées. En effet, les racines traitées présentent une importante stimulation de l'activité de la CAT (catalase, EC 1.11.1.11) et la GPX (gaı̈acol peroxydase, EC 1.11.1.7) (267 % et 163 %, respectivement par rapport aux témoins). Quant à la SOD (superoxyde dismutase, EC 1.15.1.1), son activité se trouve plutôt inhibée dans les extraits de racines traitées par le cuivre en excès. L'étude a porté aussi sur l'activité de certaines enzymes impliquées dans le processus de lignification : les peroxydases lignifiantes et la PAL (phénylalanine ammonia-lyase, EC 4.3.1.5), l'enzyme clé de la voie de biosynthèse des phénylpropanoı̈des, aboutissant à la formation des monolignols. L'activité des peroxydases lignifiantes a été testée par leurs substrats spécifiques : l'alcool coniférylique et la syringaldazine. Le dosage de l'alcool coniférylique peroxydase montre une stimulation importante de son activité (245 %). De même, la révélation de l'activité de la syringaldazine peroxydase par électrophorèse native sur gel de polyacrylamide a montré la stimulation d'un isoforme (A2) et l'induction d'un autre isoforme (A1). Cette stimulation de l'activité des peroxydases lignifiantes a été accompagnée, en outre, d'une activation de la PAL dans les racines traitées par le cuivre. L'ensemble des modifications des activités enzymatiques étudiées est discuté en relation avec le retard de croissance enregistré dans les racines de tournesol traitées par 50 μmol l−1 de CuSO4.

Métadonnées
Reçu le :
Accepté le :
Publié le :
DOI : 10.1016/S1631-0691(03)00157-4
Keywords: catalase, peroxidases, Helianthus annuus L., PAL, SOD
Mot clés : catalase, Helianthus annuus L., PAL, peroxydases, SOD

Hager Jouili 1 ; Ezzedine El Ferjani 1

1 Laboratoire de biologie et physiologie cellulaires, faculté des sciences de Bizerte, 7021 Zarzouna, Tunisia
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     title = {Changes in antioxidant and lignifying enzyme activities in sunflower roots {(\protect\emph{Helianthus} annuus} {L.)} stressed with copper excess},
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Hager Jouili; Ezzedine El Ferjani. Changes in antioxidant and lignifying enzyme activities in sunflower roots (Helianthus annuus L.) stressed with copper excess. Comptes Rendus. Biologies, Volume 326 (2003) no. 7, pp. 639-644. doi : 10.1016/S1631-0691(03)00157-4. https://comptes-rendus.academie-sciences.fr/biologies/articles/10.1016/S1631-0691(03)00157-4/

Version originale du texte intégral

1 Introduction

The aim of this study is to investigate the possible relationship between the toxic effect of copper and the changes of some enzyme activities involved in defence mechanisms.

In plants, excess of copper can easily catalyse the generation of harmful free radicals [1] and might therefore cause oxidative stress [2]. This injurious effect may be alleviated by enzymatic reactions scavenging oxygen free radicals and including SOD, CAT and peroxidases. The activities of these enzymes are increased by copper excess treatment [3,4].

Copper can also affect membrane properties by oxidation of membrane lipids [5]. The injurious membrane effect can however be estimated from the increase of MDA, one of lipid peroxidation product [2].

Moreover, increased activities of lignifying peroxidases and PAL are known to be related to environmental injury in both biotic and abiotic stimuli [6]. In plants, lignifying peroxidases were involved in polymerization of hydroxy cinnamyl alcohols to lignin. PAL is responsible for the conversion of l-phenylalanine to trans-cinnamic acid, a key intermediate in the pathway of lignin production.

In the present study, we investigated the changes of SOD, CAT, GPX, CAPX (coniferyl alcohol peroxidase), SPX (syringaldazine peroxidase) and PAL activities in sunflower roots exposed to cupric stress.

2 Materials and methods

2.1 Plant material and growth conditions

Sunflower seeds (Helianthus annuus L.) were germinated and grown in a controlled chamber, as previously described by Mazhoudi et al. [7]. Ten-day-old seedlings, previously grown on a non-contamined nutrient medium, were treated for five days by addition of 50 μM CuSO4 on the nutrient solution.

2.2 Malondialdehyde determination

Lipid peroxidation was measured as the amount of MDA determined by the thiobarbituric acid (TBA) reaction, as described by Heath and Packer [8]. The assay was carried out according to Baccouche et al. [9].

2.3 Enzyme preparations and assays

Plant material was extracted in 50 mM potassium phosphate buffer (pH 7.0) containing 5 mM sodium ascorbate and 0.2 mM EDTA. The homogenate was centrifuged at 13 000 g for 15 min. The resulting supernatant was used for assays of CAT, SOD and peroxidases. CAT and SOD activities were determined as described by Aebi [10] and Polle et al. [11], guaiacol peroxidase and coniferyl alcohol peroxidase were assayed, respectively, according to Fielding and Hall [12] and Sato et al. [13].

For determination of PAL activity, fresh material was homogenized in 100 mM borate buffer (pH 8.8) containing 0.5 mM EDTA and 17 mM β-mercaptoethanol. The homogenate was centrifuged at 20 000 g for 20 min and the supernatant was immediately assayed for PAL activity. The reaction mixture (3 ml), containing 100 mM borate buffer (pH 8.8), 20 mM l-phenylalanine and 200 μl of extract, was incubated at 40° for 1 h. Production of cinnamic acid was measured as an increase in absorbance at 290 nm.

2.4 Electrophoretic analysis

Anionic isoperoxidases were separated on 10% polyacrylamide gel electrophoresis. The syringaldazine isoperoxidases were stained by incubation of the gel with a solution of syringaldazine as described by Tadeo and Primo-Millo [14].

2.5 Protein determination

Protein content was determined according to Bradford [15] using bovine serum albumin as standard.

2.6 Statistical analysis

The results presented are the mean values±standard errors obtained from at least five replicates. Significant differences between treated and control plants are determined using ANOVA test (P<0.05).

3 Results

3.1 Seedling growth, water content and protein level

Under 50 μM CuSO4, sunflower roots showed a reduced length (Fig. 1A) and a delay of ramification. Also, matter production and water content were reduced by 41% and 53%, respectively, in treated roots compared to the control (Fig. 1B and  1C). The amount of total protein has decreased by 53% in Cu treatment conditions (Fig. 2A).

Fig. 1

Root length (A), dry weight (B) and water content (C) from 10-day-old sunflower seedlings grown in control nutrient medium (□) or supplemented with 50 μM CuSO4 (■) for five days. The values given are the means of ten experiments. Standard errors are indicated by vertical bars.

Fig. 2

Total protein content (A) and MDA level (B) in roots from 10-day-old sunflower seedlings grown in control nutrient medium (□) or supplemented with 50 μM CuSO4 (■) for five days. The values given are the means of five experiments. Standard errors are indicated by vertical bars.

3.2 Lipid peroxidation

An increase in the level of lipid peroxidation products, measured as thiobarbituric acid reactive metabolites, was observed in sunflower roots after copper treatment. The MDA content was increased by 22% in treated roots compared to the control (Fig. 2B).

3.3 Enzyme activities

The catalase and guaiacol peroxidase activities were significantly enhanced by copper treatment (Fig. 3A and  3B). By contrast, data showed a notable reduction of superoxide dismutase activity in treated roots compared with control (Fig. 3C).

Fig. 3

CAT (A), GPX (B) and SOD (C) activities in roots from 10-day-old sunflower seedlings grown in control nutrient medium (□) or supplemented with 50 μM CuSO4 (■) for five days. The values given are the means of five experiments. Standard errors are indicated by vertical bars.

Fig. 4A showed that coniferyl alcohol peroxidase activity was strongly enhanced (245% increase over the control). In the same way, PAL activity has increased in treated roots with respect to control (Fig. 4B).

Fig. 4

CAPX (A) and PAL (B) activities in roots from 10-day-old sunflower seedlings grown in control nutrient medium (□) or supplemented with 50 μM CuSO4 (■) for five days. The values given are the means of five experiments. Standard errors are indicated by vertical bars.

Native gel electrophoretic analysis of syringaldazine peroxidase activity in control roots showed only one isoform (A2). In treated roots, the isoform A2 was increased and another putative isoform A1 is displayed and seems to be induced, or its amount increased (Fig. 5).

Fig. 5

Native PAGE of syringaldazine peroxidase isozymes in root extracts from 10-day-old sunflower seedlings grown in control nutrient medium (control) or supplemented with 50 μM CuSO4 (Cu) for five days. The same protein amount (75 μg) is deposed in each lane.

4 Discussion

In the present work, we have examined the effect of copper excess on growth and several physiological processes in roots of sunflower seedlings.

A significant reduction of dry matter production, root length and water content are observed in roots exposed to copper treatment (41, 33 and 53%, respectively, Fig. 1). In fact, copper has been identified as being a powerful inhibitor at high levels [2,7,16,17]. Our findings indicate again a significant decrease in protein level by cupric stress (53%, Fig. 2A). This reduction of protein amount could be related to the ability of Cu to interfere with thiol groups of a wide range of enzymes [16] and might therefore produce disorder in protein metabolism. Moreover, cupric ion is considered as an efficient generator of toxic oxygen species that caused protein degradation [18].

Our results also show an increase in the MDA level in roots of Cu-treated sunflower seedlings compared with controls (Fig. 2B). Lipid peroxidation was already demonstrated in roots [5] and leaf segments [19] treated by excess of copper. In fact, it is well known that copper initiates the lipoperoxidation process, which generates free radicals and is recognized to affect membrane integrity [1], leading to the alteration of ion transports [20].

These damaging membrane effects could explain, in part, the reduction of water content in treated sunflower roots (Fig. 1C) affecting cellular turgor and thereafter cell enlargement. So, growth delay could be related to the inhibition of cellular turgor, the reduction of total protein amount and to the generated free radicals by lipoperoxidation.

Generally, it is known that growth inhibition, noted in plants under heavy metals uptake, is related to some physiological process alterations owing to generated oxidative stress. Such damages could be mitigated and repaired by antioxidative enzymes like CAT, SOD and peroxidases.

In fact, our results show a stimulation of CAT and guaiacol peroxidase activities in treated roots. De Vos et al. [5] and Wecks and Clijsters [2] also reported an increase in the capacity of CAT by toxic concentrations of Cu in roots. Copper-induced guaiacol peroxidase activity was also shown by Mazhoudi et al. [7] and Chen et al. [21]. In the case of SOD, the inhibition of its activity after copper treatment (Fig. 3C) is confirmed by Palma et al. [22] and Wecks and Clijsters [2]. Thus, it seems that in sunflower treated roots CAT and guaiacol peroxidase take part in defence mechanisms against oxidative stress caused by copper, while SOD does not.

Finally, we have examined the effect of cupric stress on lignifying peroxidases (coniferyl alcohol and syringaldazine peroxidases) and PAL. Lignifying peroxidases were assayed using specific electron donors, coniferyl alcohol and syringaldazine. It appears that copper enhances coniferyl alcohol peroxidase activity (Fig. 3B). Qualitative and quantitative changes in isoenzymatic profile of syringaldazine peroxidase were investigated (Fig. 5). Our findings show a stimulation of isoform A2 and an induction of isoform A1. In the same way, Chen et al. [21] reported that copper excess induced lignifying peroxidase activities in radish roots, which are correlated with growth reduction. Thus, we can also propose that, in sunflower roots, growth reduction could be caused by Cu-enhanced lignifying peroxidase activities.

PAL, a key intermediate of phenylpropanoid pathway, is also activated by cupric stress (Fig. 4B). It was shown that PAL is generally stimulated in plant tissues exposed to several environmental stresses [6]. The same authors indicated that PAL enhancement in these stress conditions is due to H2O2 generation, which occurs as primary reaction in response to stress. So, it seems that, in sunflower roots, the enhancement of PAL activity could be related to the implication of this enzyme in the plant response to cupric stress.

In conclusion, activities of antioxidant enzymes, lignifying peroxidases and PAL increased when sunflower roots were treated with 50 μM CuSO4. This indicates that sunflower roots mobilize several enzymatic defence processes in order to mitigate Cu-stress damages.


Bibliographie

[1] B. Halliwell; J.M.C. Gutteridge Oxygen toxicity, oxygen radicals, transition metals and disease, Biochem. J., Volume 219 (1984), pp. 1-14

[2] J.E.J. Weckx; H.M.M. Clijsters Oxidative damage and defence mechanisms in primary leaves of Phaseolus vulgaris as a result of root assimilation of toxic amounts of copper, Physiol. Plant., Volume 96 (1996), pp. 506-512

[3] F. Van Assche; H.M.M. Clijsters Effects of metals on enzyme activity in plants, Plant Cell Environ., Volume 13 (1990), pp. 195-206

[4] K. Asada Ascorbate peroxidase-a hydrogen peroxide-scavenging enzyme in plant, Physiol. Plant., Volume 85 (1992), pp. 235-241

[5] C.H.R. De Vos; W.M. Ten Bookum; R. Voojs; H. Schat; L.J. De Kok Effect of copper on fatty acid composition and peroxidation of lipids in the roots of copper tolerant and sensitive Silene cucubalus, Plant Physiol. Biochem., Volume 31 (1993), pp. 151-158

[6] S. Dorey; M. Kopp; P. Geoffroy; B. Friting; S. Kauffman Hydrogen peroxide from the oxidative burst is neither necessary nor sufficient for hypersensitive cell death induction. Phenylalanine ammonia lyase stimulation salicylic acid accumulation, or scopoletin consumption in cultured tobacco cells treated with elicitin, Plant Physiol., Volume 121 (1999), pp. 163-171

[7] S. Mazhoudi; A. Chaoui; M.H. Ghorbal; E. El Ferjani Response of antioxidant enzymes to excess copper in tomato (Lycopersicon esculentum, Mill.), Plant Sci., Volume 127 (1997), pp. 129-137

[8] R.L. Heath; L. Packer Photoperoxidation in isolated chloroplast. I. Kinetics and stoiciometry of fatty acid peroxidation, Arch. Biochem. Biophys., Volume 125 (1968), pp. 189-198

[9] S. Baccouch; A. Chaoui; E. El Ferjani Nickel induced oxidative damage and antioxidative responses in Zea mays shoots, Plant Physiol. Biochem., Volume 36 (1998), pp. 689-694

[10] H. Aebi Catalase in vitro, Methods Enzymol., Volume 105 (1984), pp. 121-126

[11] A. Polle; B. Krings; H. Rennenberg Superoxide dismutase activity in needles of Norwegian spruce trees (Picea abies L.), Plant Physiol., Volume 90 (1989), pp. 1310-1315

[12] J.L. Fielding; J.L. Hall A biochemical and cytochemical study of peroxidase activity in roots of Pisum sativum, J. Exp. Bot., Volume 29 (1978), pp. 969-981

[13] Y. Sato; M. Sugiyama; A. Komamine; H. Fukuda Separation and characterization of the isoenzymes of wall-bound peroxidase from cultured Zinnia cells during tracheary element differentiation, Planta, Volume 196 (1995), pp. 141-147

[14] F.R. Tadeo; E. Primo-Millo Peroxidase activity changes and lignin deposition during the senescence process in Citrus stigmas and styles, Plant Sci., Volume 68 (1990), pp. 47-56

[15] M.M. Bradford A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding, Anal. Biochem., Volume 72 (1976), pp. 248-254

[16] J.C. Fernandes; F.S. Henriques Biochemical, physiological and structural effects of excess copper in plants, Bot. Rev., Volume 57 (1990), pp. 246-273

[17] B. Mocquot; J. Vangrosveld; H.M.M. Clijsters; M. Mench Copper toxicity in young maize (Zea mays L.) plants, Plant and Soil, Volume 182 (1996), pp. 287-300

[18] J.M. Palma; L.M. Sandalio; F.J. Corpas; M.C. Romero-Puertas; I. McCarthy; L.A. del Rı́o Plant proteases, protein degradation and oxidative stress: role of peroxisomes, Plant Physiol. Biochem., Volume 40 (2002), pp. 521-530

[19] C.M. Luna; C.A. Gonzalez; V.S. Trippi Oxidative damage caused by excess of copper in oat leaves, Plant Cell Physiol., Volume 35 (1994), pp. 11-15

[20] L.F. De Filippis The effect of heavy metal compounds on the permeability of Chlorella cells, Z. Pflanzenphysiol., Volume 92 (1979), pp. 39-49

[21] E.L. Chen; Y.A. Chen; L.M. Chen; Z.H. Liu Effect of copper on peroxidase activity and lignin content in Raphanus sativus, Plant Physiol. Biochem., Volume 40 (2002), pp. 439-444

[22] J.M. Palma; M. Gómez; J.L.A. Yánez del Rı́o Increased levels of peroxisomal active oxygen-related enzymes in copper tolerant pea plants, Plant Physiol., Volume 85 (1987), pp. 570-574


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