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ρ-Cymene Inhibits Growth and Induces Oxidative Stress in Rice Seedling Plants

Published online by Cambridge University Press:  20 January 2017

Fengjuan Zhang ,
Fengxin Chen ,
Wanxue Liu ,
Jianying Guo  and
Fanghao Wan
Fengjuan Zhang
Affiliation:
College of life Science, Hebei University, Baoding, Hebei, 071002, China State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
Fengxin Chen
Affiliation:
College of life Science, Hebei University, Baoding, Hebei, 071002, China
Wanxue Liu
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
Jianying Guo
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
Fanghao Wan*
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
*
Corresponding author's E-mail: [email protected]
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Abstract

ρ-Cymene was one of the major components of volatiles released by croftonweed. The allelopthy of ρ-cymene on the growth of upland rice seedlings was performed. Hydrogen peroxide generation, malondialdehyde (MDA) content, proline content, total ascorbate (ascorbate/dehydroascorbate), reduced/oxidized glutathione, and the levels of induction of antioxidant enzyme were studied in the seedlings of upland rice. ρ-Cymene inhibited the growth of upland rice seedlings. Exposure of upland rice seedlings to ρ-cymene increased levels of H2O2, MDA, and proline, indicating lipid peroxidation and induction of oxidative stress. Activities of the antioxidant enzymes superoxide dismutase, catalase, peroxidase, guaiacol peroxidase, ascorbate peroxidase, and glutathione reductase were significantly elevated during the treatment period (7–15 d) compared with enzymes in the upland rice seedlings unexposed to ρ-cymene, thereby indicating the enhanced generation of reactive oxygen species (ROS) upon ρ-cymene exposure. These results suggest that activation of the antioxidant system by ρ-cymene led to the formation of ROS that resulted in cellular damage and decreased growth of upland rice seedlings.

Keywords

Croftonweed, Ageratina adenophora (Sprenge) King & H.E. Robins. (synonym: Eupatorium adenophora Sprenge)rice, Oryza sativa Lρ-Cymenereactive oxygen speciesantioxidant enzymes
Type
Weed Biology and Ecology
Information
Weed Science , Volume 60 , Issue 4 , December 2012 , pp. 564 - 570
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Ain-Lhout, F., Zunzunegui, F. A., Diaz Barradas, M. C., Tirado, R., Clavijio, A., and Novo, Garcia. F. 2001. Comparison of proline accumulation in two Mediterranean shrubs subjected to natural and experimental water deficit. Plant Soil. 230:175–183.Google Scholar
Amaral, J. A. and Knowles, R. 1998. Inhibition of methane consumption in forest soils by monoterpenes. J. Chem. Ecol. 24:723–734.Google Scholar
Apel, K. and Hirt, H. 2004. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Ann. Review. Plant Biol. 55:373–399.Google Scholar
Asada, K. 2006. Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol. 141:391–396.Google Scholar
Asao, T., Kitazawa, H., Tomita, K., Suyama, K., Yamamoto, H., Hosoki, T., and Pramanik, M. H. R. 2004. Mitigation of cucumber autotoxicity in hydroponic culture using microbial strain. Sci. Hort. 99:207–214.Google Scholar
Azevedo Neto, A. D., Prisco, J. T., Eneas-Filho, J., Braga de Abreu, C. E., and Gomes-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.Google Scholar
Bai, R., Zhao, X., Ma, F. W., and Li, C. Y. 2009. Identification and bioassay of allelopathic substances from the root exudates of Malus prunifolia . Allelopathy J. 23:477–484.Google Scholar
Bais, H. P., Vepachedu, R., Gilroy, S., Callaway, R. M., and Vivanco, J. M. 2003. Allelopathy and exotic plant invasion: from molecules and genes to species interactions. Science. 301:1377–1380.Google Scholar
Baruah, N. C., Sarma, S., and Shara, R. P. 1994. Seed germination and growth inhibitory cadinenes from Eupatorium adenophorum Spreng. J. Chem. Ecol. 20:1885–1892.Google Scholar
Bates, L. S., Walderen, R. D., and Taere, I. D. 1973. Rapid determination of free proline for water stress studies. Plant Soil. 39:205–207.Google Scholar
Batish, D. R., Singh, H. P., Kaur, S., Kohli, R. K., and Yadav, S. S. 2008. Caffeic acid affects early growth, and morphogenetic response of hypocotyl cuttings of mung bean (Phaseolus aureus). J. Plant Physiol. 165:297–305.Google Scholar
Beauchamp, C. and FridovichI, I. 1971. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal. Biochem. 44:276–286.Google Scholar
Becana, M., Dalton, D. A., Moran, J. F., Iturbe-Ormaetxe, I., Matamoros, M. A., and Rubio, M. C. 2000. Reactive oxygen species and antioxidants in legume nodules. Physiol. Plant. 109:372–381.Google Scholar
Blokhina, O., Virolanen, E., and Fagerstedt, K. V. 2003. Antioxidants, oxidative damage and oxygen deprivation stress: a review. Ann. Bot. 91:179–194.Google Scholar
Cakmak, I. and Marschner, H. 1992. Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase and glutathione reductase in bean leaves. Plant Physiol. 98:1222–1227.Google Scholar
Dalton, D. A., Russell, S. A., Hanus, F. J., Pascoe, G. A., and Evans, H. J. 1986. Enzymatic reactions of ascorbate and glutathione that prevent peroxide damage in soybean root nodules. Proc. Natl. Acad. Sci. U. S. A. 83:3811–3815.Google Scholar
Dayan, F. E. and Watson, S. B. 2011. Plant cell membrane as a marker for light-dependent and light-independent herbicide mechanisms of action. Pestic. Biochem. Physiol. 101:182–190.Google Scholar
Egley, G. H., Paul, R. N., Vaughn, K. C., and Duke, S. O. 1983. Role of peroxidase in the development of water-impermeable seed coats in Sida spinosa L. Planta. 157:224–232.Google Scholar
Foyer, C. H. and Halliwell, B. 1976. Presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta. 133:21–25.Google Scholar
Foyer, C. H., Lelandais, M., Edwards, E. A., and Mullineaux, P. M. 1991. The role of ascorbate in plants, interactions with photosynthesis and regulatory significance. Pp. 131–144 in Pell, E. and Steffen, K., eds. Proceedings of the 6th Annual Penn State Symposium in Plant Physiology. Rockville, MD American Society of Plant Physiologists.Google Scholar
Foyer, C. H. and Noctor, G. 2003. Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiol. Plant. 119:355–364.Google Scholar
Foyer, C. H. and Noctor, G. 2009. Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications. Pp. 861–905 in Buchanan, B., Dietz, K. J., and Pfannschmidt, T., eds. Antioxidants and Redox Signaling. Volume 11. New Rochelle, NY Mary Ann Liebert.Google Scholar
Foyer, C. H., Trebst, A., and Noctor, G. 2006. Protective and signalling functions of ascorbate, glutathione and tocopherol in chloroplasts. Pp. 241–268 in Demmig-Adams, B., Adams, W. W., and Mattoo, A. K., eds. Advances in Photosynthesis and Respiration. Volume 21. Photoprotection, Photoinhibition, Gene Regulation, and Environment. Dordrecht, the Netherlands Kluwer Academic Publishers.Google Scholar
Grant, J. J. and Loake, G. J. 2000. Role of ROIs and cognate redox signaling in disease resistance. Plant Physiol. 124:21–29.Google Scholar
Griffith, O. W. 1980. Determination of glutathione and glutathione disulphide using glutathione reductase and 2-vinyl pyridine. Anal. Biochem. 106:207–212.Google Scholar
Hammondkosack, K. E. and Jones, J. D. G. 1996. Resistance gene-dependent plant defense responses. Plant Cell. 8:1773–1791.Google Scholar
Hare, P. D., Cress, W. A., and van Staden, J. 1998. Dissecting the roles of osmolyte accumulation during stress. Plant Cell Environ. 21:535–553.Google Scholar
Heath, R. L. and Packer, L. 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch. Biochem. Biophys. 125:189–198.Google Scholar
Hernandez, J. A., Jimenez, A., Mullineaux, P., and Sevilla, F. 2000. Tolerance of pea plants (Pisum sativum) to long-term salt stress is associated with induction of antioxidant defences. Plant Cell Environ. 23:853–862.Google Scholar
Hierro, J. L. and Callaway, R. M. 2003. Allelopathy and exotic plant invasion. Plant Soil. 256:29–39.Google Scholar
Jones, M. A. and Smirnoff, N. 2005. Reactive oxygen species in plant development and pathogen defence. Pp. 53–86 in Smirnoff, N., ed. Antioxidants and Reactive Oxygen Species in Plants. Oxford, UK Blackwell Publishing.Google Scholar
Knight, K. S., Kurylo, J. S., Endress, A. G., Stewart, J. R., and Reich, P. B. 2007. Ecology and ecosystem impacts of common buckthorn (Rhamnus cathartica): a review. Biol. Invasions. 9:925–937.Google Scholar
Lee, D. H., Kim, Y. S., and Lee, C. B. 2001. The inductive responses of the antioxidant enzymes by salt stress in rice (Oryza sativa L.). J. Plant Physiol. 158:737–745.Google Scholar
Lowry, O. H., Rosebrough, N. T., Farr, A. L., and Randall, R. J. 1951. Protein measurement with the folin–phenol reagent. J. Biol. Chem. 193:265–275.Google Scholar
Meloni, D. A., Oliva, M. A., Martinez, C. A., and Cambraia, J. 2003. Photosynthesis and activity of superoxide dismutase, peroxidase and glutathione reductase in cotton under salt stress. Environ. Exp. Bot. 49:69–76.Google Scholar
Miake, C. and Asada, K. 1992. Thylakoid-bound ascorbate peroxidase in spinach chloroplasts and photoreduction of its primary oxidation product monodehydroascorbate radicals in thylakoids. Plant Cell Physiol. 33:541–553.Google Scholar
Nakano, Y. and Asada, K. 1981. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 22:867–880.Google Scholar
Nishida, N., Tamotsu, S., Nagata, N., Saito, C., and Sakai, A. 2005. Allelopathic effects of volatile monoterpenoids produced by Salvia leucophylla: inhibition of cell proliferation and DNA synthesis in the root apical meristem of Brassica campestris seedlings. J. Chem. Ecol. 31:1187–1203.Google Scholar
Pala'-Pau'l, J., Pe'rez-Alonso, M. J., Velasco-Negueruela, A., and Sanz, J. 2002. Analysis by gas chromatography–mass spectrometry of the volatile components of Ageratina adenophora Spreng., growing in the Canary Islands. J. Chromatogr. A. 947:327–331.Google Scholar
Romagni, J. G., Allen, S. N., and Dayan, F. E. 2000. Allelopathic effects of volatile cineoles on two weedy plant species. J. Chem. Ecol. 26:303–313.Google Scholar
Romero-Romero, T., Sanchez-Nieto, S., San Juan-Badillo, A., Anaya, A. L., and Cruz-Ortega, R. 2005. Comparative effects of allelochemical and water stress in roots of Lycopersicon esculentum Mill. (Solanaceae). Plant Sci. 168:1059–1066.Google Scholar
Singh, H. P., Batish, D. R., Kaur, S., Arora, K., and Kohli, R. K. 2006. α-Pinene inhibits growth and induces oxidative stress in roots. Ann. Bot. 98:1261–1269.Google Scholar
Sofo, A., Dichio, B., Xiloynnis, C., and Masia, A. 2004. Effects of different irradiance levels on some antioxidant enzymes and on malondialdehyde content during rewatering in olive tree. Plant Sci. 166:293–302.Google Scholar
Song, Q. S., Fu, J., Tang, J. W., Feng, Z. L., and Yang, C. R. 2000. Allelopathic potential of Eupatorium adenophorum Spreng. Acta Phytoecol. Sin. 24:362–365.Google Scholar
Smirnoff, N. 1996. The function and metabolism of ascorbic acid in plants. Ann. Bot. 78:661–669.Google Scholar
Sreenivasulu, N., Grimm, B., Wobus, U., and Weschke, W. 2000. Differential response of antioxidant compounds to salinity stress in salt-tolerant and salt-sensitive seedlings of fox-tail millet (Setaria italica). Physiol. Plant. 109:435–442.Google Scholar
Testa, B. 1995. The Metabolism of Drugs and Other Xenobiotics. New York Academic Press. 471 p.Google Scholar
Tripathi, R. S., Singh, R. S., and Pai, J. P. N. 1981. Allelopathic potential of Eupatorium adenophorum, a dominant ruderal weed of Meghalaya. Proc. Indian Natl. Sci. Acad. Part B Biol. Sci. 47:458–465.Google Scholar
Vaughn, S. F. and Spencer, G. F. 1993. Volatile monoterpenes as potential parent structures for new herbicides. Weed Sci. 41:114–119.Google Scholar
Velikova, V., Yordanov, I., and Edreva, A. 2000. Oxidative stress and some antioxidant systems in acid rain-treated bean plants. Plant Sci. 151:59–66.Google Scholar
Wang, S. Y., Jiao, H. J., and Faust, M. 1991. Changes in ascorbate, glutathione, and related enzyme activities during thidiazuron-induced bud break of apple. Physiol. Plant. 82:231–236.Google Scholar
Weir, T. L., Park, S-W., and Vivanco, J. M. 2004. Biochemical and physiological mechanisms mediated by allelochemicals. Curr. Opin. Plant Biol. 7:472–479.Google Scholar
Yu, J. Q., Ye, S. F., Zhang, M. F., and Hu, W. H. 2003. Effects of root exudates and aqueous root extracts of cucumber (Cucumis sativus) and allelochemicals on photosynthesis and antioxidant enzymes in cucumber. Biochem. Syst. Ecol. 31:129–139.Google Scholar
Yu, X. J., Yu, D., Lu, Z. J., and Ma, K. P. 2005. A new mechanism of invader success: exotic plant inhibits natural vegetation restoration by changing soil microbe community. Chin. Sci. Bull. 50:1105–1112.Google Scholar
Zhang, F. J., Guo, J. Y., Chen, F. X., Liu, W. X., and Wan, F. H. 2012. Identification of volatile compounds released by leaves of the invasive plant croftonweed (Ageratina adenophora, Compositae), and their inhibition of rice seedling growth. Weed Sci. 60:205–211.Google Scholar
Zhang, J. H., Mao, Z. Q., Wang, L. Q., and Shu, H. R. 2007. Bioassay and identification of root exudates of three fruit tree species. J. Integr. Plant Biol. 49:257–261.Google Scholar