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Effect of salt on malondialdehyde and antioxidant enzymes in seedling roots of Jerusalem artichoke (Helianthus tuberosus L.)

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Abstract

Two cultivars of Jerusalem artichoke (Helianthus tuberosus L.) differing in genotype, Red skin (cv. R., salt-tolerant but low-yield) and White skin (cv. W., salt-sensitive but high-yield), were used to investigate malondialdehyde (MDA) content and antioxidant enzyme activity changes in their roots under a hydroponic culture system with 250 mM NaCl. The results showed that MDA contents in roots of the two genotypes increased, but MDA content of cv. R. was higher than that of cv. W. Changes in all antioxidant enzymes in roots of both varieties exhibited a similar trend, namely increased initially and then decreased. However, there were still some differences existing between the two cultivars. In other words, activities of the other two antioxidant enzymes except catalase (CAT) and peroxidase (POD) in roots of cv. R. were less than controls at 48 h, while all others except ascorbate peroxidase (APX) in roots of cv. W. were greater than controls. The peak of superoxide dismutase (SOD) activity of cv. W. was observed to appear earlier than that of cv. R. CAT activity of cv. W. was significantly greater than the value of cv. R. and the latter showed a moderate trend. POD activity of cv. R. obtained the maximum at 6 h, whereas the peak of cv. W. displayed at 24 h. APX activity of cv. R. declined more than that of cv. W. These results suggested that there was a lower efficiency of scavenging reactive oxygen species (ROS) in cv. R. roots. Concomitantly, salt stress caused more severe damage to roots of cv. R. Antioxidant enzymes in roots were inadequate to elucidate salt-tolerance mechanisms of the whole plant.

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Abbreviations

APX:

Ascorbate peroxidase

AsA:

Ascorbate

CAT:

Catalase

H2O2 :

Hydrogen peroxide

MDA:

Malondialdehyde

POD:

Peroxidase

ROS:

Reactive oxygen species

SOD:

Superoxide dismutase

References

  • Ashraf M (2009) Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotech Adv 27:84–93

    Article  CAS  Google Scholar 

  • Ashraf M, Ali Q (2008) Relative membrane permeability and activities of some antioxidant enzymes as the key determinants of salt tolerance in canola (Brassica napus L.). Environ Exp Bot 63:266–273

    Article  CAS  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  • Cavalcanti FR, Oliveira JTA, Martins-Miranda AS, Viégas RA, Silveira JAG (2004) Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt-stressed cowpea leaves. New Phytol 163:563–571

    Article  CAS  Google Scholar 

  • Chen JX, Wang XF (eds) (2006) Experiment guide of plant physiology. (China’s) South China University of Technology Press, Guangzhou (in Chinese)

    Google Scholar 

  • Giannopolitis CN, Ries SK (1977) Superoxide dismutases. I. Occurrence in higher plants. Plant Physiol 59:309–314

    Article  CAS  PubMed  Google Scholar 

  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198

    Article  CAS  PubMed  Google Scholar 

  • Hernandez JA, Corpas FJ, Gomez M, Del Rio LA, Sevilla F (1993) Salt-induced oxidative stress mediated by activated oxygen species in pea leaf mitochondria. Physiol Plant 89:103–110

    Article  CAS  Google Scholar 

  • Hernandez JA, Ferrer MA, Jimenez A, Ros-Barcelo A, Sevilla F (2001) Antioxidant systems and O ·−2 /H2O2 production in the apoplast of Pisum sativum L. leaves: its relation with NaCl-induced necrotic lesions in minor veins. Plant Physiol 27:817–831

    Article  Google Scholar 

  • Katsuhara M, Otsuka T, Ezaki B (2005) Salt stress-induced lipid peroxidation is reduced by glutathione S-transferase, but this reduction of lipid peroxides is not enough for a recovery of root growth in Arabidopsis. Plant Sci 169:369–373

    Article  CAS  Google Scholar 

  • Khan MH, Panda SK (2008) Alterations in root lipid peroxidation and antioxidative responses in two rice cultivars under NaCl-salinity stress. Acta Physiol Plant 30:81–89

    Article  CAS  Google Scholar 

  • Liu ZP, Liu L, Chen MD, Deng LQ, Zhao GM, Tang QZ, Xia TX (2003) Study on the irrigation systems in agriculture by seawater. J Nat Resour 18:423–429 (in Chinese)

    Google Scholar 

  • Long XH, Chi JH, Liu L, Li Q, Liu ZP (2009) Effect of seawater stress on physiological and biochemical responses of five Jerusalem artichoke ecotypes. Pedosphere 19(2):208–216

    Article  CAS  Google Scholar 

  • Mandhania S, Madan S, Sawhney V (2006) Antioxidant defense mechanism under salt stress in wheat seedlings. Biol Plant 50:227–231

    Article  CAS  Google Scholar 

  • Neto ADA, Prisco JT, Eneas-Filho J, Abreu CEB, Gomez-Filho E (2006) Effect of salt stress on antioxidative enzymes and lipid peroxidation in leaves and roots of salt-tolerant and salt-sensitive maize genotypes. Environ Exp Bot 56:87–94

    Article  Google Scholar 

  • Rahnama H, Ebrahimzadeh H (2005) The effect of NaCl on antioxidant enzyme activities in potato seedlings. Biol Plant 49:93–97

    Article  CAS  Google Scholar 

  • Shabala S, Cuin TA (2007) Potassium transport and plant salt tolerance. Physiol Plant 133:651–669

    Article  Google Scholar 

  • Shalata A, Tal M (1998) The effect of salt stress on lipid peroxidation and antioxidants in the leaf of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiol Plant 104:169–174

    Article  CAS  Google Scholar 

  • Shi LH (2008) High-yield cultivation techniques of Jerusalem artichoke in the alpine and cold region. North Hortic 4:136 (in Chinese)

    Google Scholar 

  • Singh BK, Sharma SR, Singh B (2010) Antioxidant enzymes in cabbage: variability and inheritance of superoxide dismutase, peroxidase and catalase. Sci Hortic 124:9–13

    Article  CAS  Google Scholar 

  • Xue YF, Liu ZP (2008) Antioxidant enzymes and physiological characteristics in two Jerusalem artichoke cultivars under salt stress. Russ J Plant Physiol 55(6):776–781

    Article  CAS  Google Scholar 

  • Zhang YK, Han XJ, Chen XL, Jin H, Cui XM (2009) Exogenous nitric oxide on antioxidative system and ATPase activities from tomato seedlings under copper stress. Sci Hortic 123:217–223

    Article  CAS  Google Scholar 

  • Zhao SJ, Shi GA, Dong XC (eds) (2002) Techniques of plant physiological experiment. China Agricultural Science and Technology Press, Beijing (in Chinese)

    Google Scholar 

Download references

Acknowledgments

This work was supported by Knowledge Innovation Program of the Chinese Academy of Sciences (KSCX2-YW-G-035, KSCX2-YW-G-027-2).

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Correspondence to Shihua Shen.

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Communicated by W. Filek.

Q. Chen and M. Zhang contributed equally to this work.

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Chen, Q., Zhang, M. & Shen, S. Effect of salt on malondialdehyde and antioxidant enzymes in seedling roots of Jerusalem artichoke (Helianthus tuberosus L.). Acta Physiol Plant 33, 273–278 (2011). https://doi.org/10.1007/s11738-010-0543-5

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  • DOI: https://doi.org/10.1007/s11738-010-0543-5

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