Physiological basis of different allelopathic reactions of cucumber ...

More documents

Recommendations

Info

8of9 Ding et al. metabolism. Further study on allelochemical uptake, compartmentalization, and detoxification is necessary to elucidate the mechanism involved in this specific recognition ability. Acknowledgements We are grateful to JM Vivanco and H Ye for their critical reading and revision of the manuscript. This work was supported by the National Natural Science Foundation of China (30235029; 300070522) and the National Outstanding Youth Foundation (30230250). References An M, Pratley JE, Haig T. 2001a. Phytotoxicity of vulpia residues. III. Biological activity of identified alleochemicals from Vulpia myuros. Journal of Chemical Ecology 27, 381–392. An M, Pratley JE, Haig T. 2001b. Phytotoxicity of vulpia residues. IV. Dynamics of allelochemicals during decomposition of vulpia residues and their corresponding phytotoxicity. Journal of Chemical Ecology 27, 395–409. Asao T, Umeyama M, Ohta K, Hosoki T, Ito N, Ueda H. 1998. Decrease of yield of cucumber by non-renewal of the nutrient hydroponic solution and its reversal by supplementation of activated charcoal. Journal of the Japanese Society for Horticultural Science 67, 99–105. Bais HP, Vepachedu R, Gilroy S, Callaway RM, Vivanco JM. 2003. Allelopathy and exotic plant invasion: from molecules and genes to species interactions. Science 301, 1377–1380. Bais HP, Weir TL, Perry LG, Gilroy S, Vivanco JM. 2006. The role of root exudates in rhizosphere interactions with plants and other organisms. Annual Review of Plant Biology 57, 233–266. Baziramakenga R, Leroux GD, Simard RR. 1995. Effects of benzoic and cinnamic acids on membrane permeability of soybean roots. Journal of Chemical Ecology 21, 1271–1285. Bertin C, Yang XH, Weston LA. 2003. The role of root exudates and allelochemicals in the rhizosphere. Plant and Soil 256, 67–83. Blum U. 2005. Relationships between phenolic acid concentrations, transpiration, water utilization, leaf area expansion, and uptake of phenolic acids: nutrient culture studies. Journal of Chemical Ecology 31, 1907–1932. Bradford MM. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Analytical Biochemistry 72, 248–254. Cakmak I, Marschner H. 1992. Magnesium deficiency and high light intensity enhance activities of superoxide dismutase ascorbate peroxidase, and glutathione reductase in bean leaves. Plant Physiology 98, 1222–1227. Canals RM, Emeterio LS, Peralta J. 2005. Autotoxicity in Lolium rigidum: analysing the role of chemically mediated interactions in annual plant populations. Journal of Theoretical Biology 235, 402–407. Elstner EF, Heupel A. 1976. Inhibition of nitrite formation from hydroxylammoniumchloride: a simple assay for superoxide dismutase. Analytical Biochemistry 70, 616–620. Ezaki B, Gardner RC, Ezaki Y, Matsumoto H. 2000. Expression of aluminum-induced genes in transgenic Arabidopsis plants can ameliorate aluminum stress and/or oxidative stress. Plant Physiology 122, 657–665. Forman HJ, Torres M, Fukuto J. 2002. Redox signaling. Molecular and Cellular Biochemistry 234, 49–62. Friebe A, Roth U, Kuck P. 1997. Effects of 2,4-dihydroxy-1,4- benzoxazin-3-ones on the activity of plasma membrane H + - ATPase. Phytochemistry 44, 979–983. Fryer MJ, Oxborough K, Mullineaux PM, Baker NR. 2002. Imaging of photo-oxidative stress responses in leaves. Journal of Experimental Botany 53, 1249–1254. Giannopolitis N, Ries SK. 1977. Superoxide dismutase. I. Occurrence in higher plants. Plant Physiology 59, 309–314. Halliwell B. 2006. Reactive species and antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiology 141, 312–322. Hejl AM, Koster KL. 2004. The allelochemical sorgoleone inhibits root H + -ATPase and water uptake. Journal of Chemical Ecology 30, 2181–2191. Herrig V, De Lourdes M, Ferrarese MDL, Suzuki LS, Rodrigues JD, Ferrarese O. 2002. Peroxidase and phenylalanine ammonia-lyase activities, phenolic acid contents, and allelochemicals-inihibited root growth of soybean. Biological Research 35, 59–66. Inderjit, Duke SO. 2003. Ecophysiological aspect of allelopathy. Planta 217, 529–539. Kasamo K. 1986. Comparison of plasma membrane and tonoplast H + -translocating ATPase in Phaseolus mungo L. Plant Cell Physiology 27, 49–59. Keller T, Damude HG, Werner D, Doerner P, Dixon RA, Lamb C. 1998. A plant homolog of the neutrophil NADPH oxidase gp91(phox) subunit gene encodes a plasma membrane protein with Ca 2+ binding motifs. The Plant Cell 10, 255–266. Lara-Nunez A, Romero-Romero T, Ventura JL, Blancas V, Anaya AL, Cruz-Ortega R. 2006. Allelochemical stress causes inhibition of growth and oxidative damage in Lycopersicon esculentum Mill. Plant, Cell and Environment 29, 2009–2016. Larsson C, Widell S, Kjellbom P. 1987. Preparation of high-purity plasma membranes. Methods in Enzymology 148, 558–568. Laloi C, Apel K, Danon A. 2004. Reactive oxygen signalling: the latest news. Current Opinion in Plant Biology 7, 323–328. MacNevin WM, Uron PF. 1953. Separation of hydrogen peroxide from organic hydroperoxide. Analytical Biochemistry 25, 1760–1761. Mehdy MG, Sharma YK, Sathasivan K, Bays NW. 1996. The role of activated oxygen species in plant disease resistance. Physiologia Plantarum 98, 365–374. Mittler R, Vanderauwere S, Gollery M, Breusegem FV. 2004. Reactive oxygen gene network of plants. Trends in Plant Science 9, 490–498. Nakano Y, Asada K. 1981. Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiology 22, 679–690. Ohinishi T, Gall RS, Mayer ML. 1975. An improved assay of inorganic phosphate in the presence of extralabile phosphate compounds: application to the ATPase assay in the presence of phosphocreatine. Analytical Biochemistry 69, 261–267. Pinton R, Cakmak I, Marschner H. 1994. Zinc deficiency enhanced NAD(P)H-dependent superoxider radical production in plasma membrane vesicles isolated from roots of bean plants. Journal of Experimental. Botany 45, 45–50. Politycka B. 1996. Peroxidase activity and lipid peroxidation in roots of cucumber seedlings influenced by derivatives of cinnamic and benzoic acids. Acta Physiologiae Plantarum 18, 365–370. Rhoads DM, Umbach AL, Subbaiah CC, Siedow JN. 2006. Mitochondrial reactive oxygen species. Contribution to oxidative stress and interorganellar signaling. Plant Physiology 141, 357–366. Downloaded from http://jxb.oxfordjournals.org/ by guest on August 30, 2013
Ridenour WM, Callaway RM. 2001. The relative importance of allelopathy in interference: the effects of an invasive weed on a native bunchgrass. Oecologia 126, 444–450. Tsuchiya D. 1990. Problems on allelopathy in vegetable cropping. Agriculture and Horticulture 65, 9–16(in Japanese). Weir TL, Park SW, Vivanco JM. 2004. Biochemical and physiological mechanisms mediated by allelochemicals. Current Opinion in Plant Biology 7, 472–479. Weir TL, Bais HP, Stull VJ, Callaway RM, Thelen GC, Ridenour WM, Bhamidi S, Stermitz FR, Vivanco JM. 2006. Oxalate contributes to the resistance of Gaillardia grandiflora and Lupinus sericeas to a phytotoxin produced by Centaurea maculosa. Planta 223, 785–795. Weir TL, Bais HP, Vivanco JM. 2003. Intraspecific and interspecific interactions mediated by a phytotoxin, (-)-catechin, secreted by the roots of Centaurea maculosa (spotted knapweed). Journal of Chemical Ecology 29, 2397–2412. Yamamoto Y, Kobayashi Y, Devi SR, Rikiishi S, Matsumono H. 2003. Oxidative stress triggered by aluminum in plant roots. Plant and Soil 255, 239–243. Ye SF, Zhou YH, Sun Y, Zou LY, Yu JQ. 2006. Cinnamic acid causes oxidative stress in cucumber roots, and promotes incidence Different response to allelochemical between species 9of9 of Fusarium wilt. Environmental and Experimental Botany 56, 255–262. Ye SF, Yu JQ, Peng YH, Zheng JH, Zou LY. 2004. Incidence of Fusarium wilt in Cucumis sativus L. is promoted by cinnamic acid, an autotoxin in root exudates. Plant and Soil 263, 143–150. Yu JQ, Matsui Y. 1994. Phytotoxic substances in the root exudates of Cucumis sativus L. Journal of Chemical Ecology 20, 21–31. Yu JQ, Matsui Y. 1997. Effects of root exudates of cucumber (Cucumis sativus) and allelochemicals on uptake by cucumber seedlings. Journal of Chemical Ecology 23, 817–827. Yu JQ, Shou SY, Qian YR, Hu WH. 2000. Autotoxic potential in cucurbit crops. Plant and Soil 223, 147–151. Yu JQ, Ye SF, Zhang MF, Hu WH. 2003. Effects of root exudates, aqueous root extracts of cucumber (Cucumis sativus L.) and allelochemicals on photosynthesis and antioxidant enzymes in cucumber. Biochemical and Systematics Ecology 31, 129–139. Zhou YH, Yu JQ, Huang LF, Nogues S. 2004. The relationship between CO 2 assimilation, photosynthetic electron transport, and water–water cycle in chill-exposed cucumber leaves under low light and subsequent recovery. Plant, Cell and Environment 27, 1503–1514. Downloaded from http://jxb.oxfordjournals.org/ by guest on August 30, 2013
Page 1 and 2: Journal of Experimental Botany Adva
Page 3 and 4: supernatant obtained was used for e
Page 5 and 6: Different response to allelochemica
Page 7: Different response to allelochemica

Physiological basis of different allelopathic reactions of cucumber ...

Create successful ePaper yourself

Delete template?

Save as template?