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8<strong>of</strong>9<br />

Ding et al.<br />

metabolism. Further study on allelochemical uptake,<br />

compartmentalization, and detoxification is necessary to<br />

elucidate the mechanism involved in this specific recognition<br />

ability.<br />

Acknowledgements<br />

We are grateful to JM Vivanco and H Ye for their critical reading<br />

and revision <strong>of</strong> the manuscript. This work was supported by the<br />

National Natural Science Foundation <strong>of</strong> China (30235029;<br />

300070522) and the National Outstanding Youth Foundation<br />

(30230250).<br />

References<br />

An M, Pratley JE, Haig T. 2001a. Phytotoxicity <strong>of</strong> vulpia<br />

residues. III. Biological activity <strong>of</strong> identified alleochemicals from<br />

Vulpia myuros. Journal <strong>of</strong> Chemical Ecology 27, 381–392.<br />

An M, Pratley JE, Haig T. 2001b. Phytotoxicity <strong>of</strong> vulpia<br />

residues. IV. Dynamics <strong>of</strong> allelochemicals during decomposition<br />

<strong>of</strong> vulpia residues and their corresponding phytotoxicity. Journal<br />

<strong>of</strong> Chemical Ecology 27, 395–409.<br />

Asao T, Umeyama M, Ohta K, Hosoki T, Ito N, Ueda H. 1998.<br />

Decrease <strong>of</strong> yield <strong>of</strong> <strong>cucumber</strong> by non-renewal <strong>of</strong> the nutrient<br />

hydroponic solution and its reversal by supplementation <strong>of</strong><br />

activated charcoal. Journal <strong>of</strong> the Japanese Society for Horticultural<br />

Science 67, 99–105.<br />

Bais HP, Vepachedu R, Gilroy S, Callaway RM, Vivanco JM.<br />

2003. Allelopathy and exotic plant invasion: from molecules and<br />

genes to species interactions. Science 301, 1377–1380.<br />

Bais HP, Weir TL, Perry LG, Gilroy S, Vivanco JM. 2006. The<br />

role <strong>of</strong> root exudates in rhizosphere interactions with plants and<br />

other organisms. Annual Review <strong>of</strong> Plant Biology 57, 233–266.<br />

Baziramakenga R, Leroux GD, Simard RR. 1995. Effects <strong>of</strong><br />

benzoic and cinnamic acids on membrane permeability <strong>of</strong><br />

soybean roots. Journal <strong>of</strong> Chemical Ecology 21, 1271–1285.<br />

Bertin C, Yang XH, Weston LA. 2003. The role <strong>of</strong> root exudates<br />

and allelochemicals in the rhizosphere. Plant and Soil 256,<br />

67–83.<br />

Blum U. 2005. Relationships between phenolic acid concentrations,<br />

transpiration, water utilization, leaf area expansion, and uptake <strong>of</strong><br />

phenolic acids: nutrient culture studies. Journal <strong>of</strong> Chemical<br />

Ecology 31, 1907–1932.<br />

Bradford MM. 1976. A rapid and sensitive method for the<br />

quantitation <strong>of</strong> microgram quantities <strong>of</strong> protein utilizing the<br />

principle <strong>of</strong> protein–dye binding. Analytical Biochemistry 72,<br />

248–254.<br />

Cakmak I, Marschner H. 1992. Magnesium deficiency and high<br />

light intensity enhance activities <strong>of</strong> superoxide dismutase ascorbate<br />

peroxidase, and glutathione reductase in bean leaves. Plant<br />

Physiology 98, 1222–1227.<br />

Canals RM, Emeterio LS, Peralta J. 2005. Autotoxicity in<br />

Lolium rigidum: analysing the role <strong>of</strong> chemically mediated<br />

interactions in annual plant populations. Journal <strong>of</strong> Theoretical<br />

Biology 235, 402–407.<br />

Elstner EF, Heupel A. 1976. Inhibition <strong>of</strong> nitrite formation from<br />

hydroxylammoniumchloride: a simple assay for superoxide<br />

dismutase. Analytical Biochemistry 70, 616–620.<br />

Ezaki B, Gardner RC, Ezaki Y, Matsumoto H. 2000. Expression<br />

<strong>of</strong> aluminum-induced genes in transgenic Arabidopsis plants can<br />

ameliorate aluminum stress and/or oxidative stress. Plant Physiology<br />

122, 657–665.<br />

Forman HJ, Torres M, Fukuto J. 2002. Redox signaling.<br />

Molecular and Cellular Biochemistry 234, 49–62.<br />

Friebe A, Roth U, Kuck P. 1997. Effects <strong>of</strong> 2,4-dihydroxy-1,4-<br />

benzoxazin-3-ones on the activity <strong>of</strong> plasma membrane H + -<br />

ATPase. Phytochemistry 44, 979–983.<br />

Fryer MJ, Oxborough K, Mullineaux PM, Baker NR. 2002.<br />

Imaging <strong>of</strong> photo-oxidative stress responses in leaves. Journal <strong>of</strong><br />

Experimental Botany 53, 1249–1254.<br />

Giannopolitis N, Ries SK. 1977. Superoxide dismutase. I.<br />

Occurrence in higher plants. Plant Physiology 59, 309–314.<br />

Halliwell B. 2006. Reactive species and antioxidants. Redox<br />

biology is a fundamental theme <strong>of</strong> aerobic life. Plant Physiology<br />

141, 312–322.<br />

Hejl AM, Koster KL. 2004. The allelochemical sorgoleone<br />

inhibits root H + -ATPase and water uptake. Journal <strong>of</strong> Chemical<br />

Ecology 30, 2181–2191.<br />

Herrig V, De Lourdes M, Ferrarese MDL, Suzuki LS,<br />

Rodrigues JD, Ferrarese O. 2002. Peroxidase and phenylalanine<br />

ammonia-lyase activities, phenolic acid contents, and<br />

allelochemicals-inihibited root growth <strong>of</strong> soybean. Biological<br />

Research 35, 59–66.<br />

Inderjit, Duke SO. 2003. Ecophysiological aspect <strong>of</strong> allelopathy.<br />

Planta 217, 529–539.<br />

Kasamo K. 1986. Comparison <strong>of</strong> plasma membrane and tonoplast<br />

H + -translocating ATPase in Phaseolus mungo L. Plant Cell<br />

Physiology 27, 49–59.<br />

Keller T, Damude HG, Werner D, Doerner P, Dixon RA,<br />

Lamb C. 1998. A plant homolog <strong>of</strong> the neutrophil NADPH<br />

oxidase gp91(phox) subunit gene encodes a plasma membrane<br />

protein with Ca 2+ binding motifs. The Plant Cell 10, 255–266.<br />

Lara-Nunez A, Romero-Romero T, Ventura JL, Blancas V,<br />

Anaya AL, Cruz-Ortega R. 2006. Allelochemical stress causes<br />

inhibition <strong>of</strong> growth and oxidative damage in Lycopersicon<br />

esculentum Mill. Plant, Cell and Environment 29, 2009–2016.<br />

Larsson C, Widell S, Kjellbom P. 1987. Preparation <strong>of</strong> high-purity<br />

plasma membranes. Methods in Enzymology 148, 558–568.<br />

Laloi C, Apel K, Danon A. 2004. Reactive oxygen signalling: the<br />

latest news. Current Opinion in Plant Biology 7, 323–328.<br />

MacNevin WM, Uron PF. 1953. Separation <strong>of</strong> hydrogen peroxide<br />

from organic hydroperoxide. Analytical Biochemistry 25,<br />

1760–1761.<br />

Mehdy MG, Sharma YK, Sathasivan K, Bays NW. 1996. The<br />

role <strong>of</strong> activated oxygen species in plant disease resistance.<br />

Physiologia Plantarum 98, 365–374.<br />

Mittler R, Vanderauwere S, Gollery M, Breusegem FV. 2004.<br />

Reactive oxygen gene network <strong>of</strong> plants. Trends in Plant Science<br />

9, 490–498.<br />

Nakano Y, Asada K. 1981. Hydrogen peroxide is scavenged by<br />

ascorbate specific peroxidase in spinach chloroplasts. Plant Cell<br />

Physiology 22, 679–690.<br />

Ohinishi T, Gall RS, Mayer ML. 1975. An improved assay <strong>of</strong><br />

inorganic phosphate in the presence <strong>of</strong> extralabile phosphate<br />

compounds: application to the ATPase assay in the presence <strong>of</strong><br />

phosphocreatine. Analytical Biochemistry 69, 261–267.<br />

Pinton R, Cakmak I, Marschner H. 1994. Zinc deficiency<br />

enhanced NAD(P)H-dependent superoxider radical production in<br />

plasma membrane vesicles isolated from roots <strong>of</strong> bean plants.<br />

Journal <strong>of</strong> Experimental. Botany 45, 45–50.<br />

Politycka B. 1996. Peroxidase activity and lipid peroxidation in<br />

roots <strong>of</strong> <strong>cucumber</strong> seedlings influenced by derivatives <strong>of</strong> cinnamic<br />

and benzoic acids. Acta Physiologiae Plantarum 18, 365–370.<br />

Rhoads DM, Umbach AL, Subbaiah CC, Siedow JN. 2006.<br />

Mitochondrial reactive oxygen species. Contribution to oxidative<br />

stress and interorganellar signaling. Plant Physiology 141,<br />

357–366.<br />

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