Involvement of antioxidant capacity in quinclorac tolerance in Eleusine indica

Environmental and Experimental Botany

Volumn 74, Issue 1, 2011, Pages 74-81

  Sunohara, Yukari ^a   Shirai, Shinjiro ^a   Yamazaki, Hiroki ^a   Matsumoto, Hiroshi ^a  

^a UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

Antioxidant capacity; Auxinic herbicide; Digitaria adscendens; Eleusine indica; Quinclorac; Quinclorac tolerance; Reactive oxygen species; Superoxide anion

Indexed keywords

ANION; ANTIOXIDANT; CHLOROPHYLL; ENZYME ACTIVITY; GRASS; HERBICIDE; PESTICIDE RESISTANCE; PHYTOTOXICITY; SCAVENGING (CHEMISTRY); TOLERANCE;

DIGITARIA CILIARIS; ELEUSINE; ELEUSINE INDICA;

EID: 80955177157     PISSN: 00988472     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.envexpbot.2011.05.001     Document Type: Article

References (54)

1. Abdallah I., Fischer A.J., Elmore C.L., Saltveit M.E., Zaki M. Mechanism of resistance to quinclorac in smooth crabgrass (Digitaria ischaemum). Pest. Biochem. Physiol. 2006, 84:38-48.
2. Aebi H.E. Catalase. Methods of Enzymatic Analysis 1983, vol. 3:273-286. Verlag Chemie Weinheim, Deerfield Beach, FL.
3. Apel K., Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 2004, 55:373-399.
4. Azevedo Neto A.D., Prisco J.T., Eneas-Filho J., Medeiros J.R., Gomes-Filho E. Hydrogen peroxide pre-treatment induces salt stress acclimation in maize plants. J. Plant Physiol. 2005, 162:1114-1122.
5. Becker L.B., Hoek T.L.V., Shao Z.H., Li C.Q., Schumacker P.T. Generation of superoxide in cardiomyocytes during ischemia before reperfusion. Am. J. Physiol. Heart. Circ. Physiol. 1999, 277:2240-2246.
6. Berghaus R., Wuerzer B. The mode of action of the new experimental herbicide quinclorac (BAS 514 H). Proc. 11th Asian-Pac. Weed Sci. Soc. Conf., vol. 1 1987, 81-87.
7. Carter W.O., Narayanan P.K., Robinson J.P. Intracellular hydrogen peroxide and superoxide anion detection in endothelial cells. J. Leukoc. Biol. 1994, 55:253-258.
8. Casano L.M., Gomez L.D., Lascano H.R., Gonzalez C.A., Trippi V.S. Inactivation and degradation of CuZn-SOD by active oxygen species in wheat chloroplasts exposed photo oxidative stress. Plant Cell Physiol. 1997, 38:433-440.
9. Chappelle E.W., Kim M.S., McMurtrey J.E. Ratio analysis of reflectance spectra (RARS): an algorithm for the remote estimation of the concentrations of chlorophyll a, chlorophyll b, and carotenoids in soybean leaves. Remote Sens. Environ. 1992, 39:239-247.
10. Chism W.J., Bingham S.W., Shaver R.L. Uptake, translocation and metabolism of quinclorac in two grass species. Weed Technol. 1991, 5:771-775.
11. Davies K.J.A. Protein damage and degradation by oxygen radicals. J. Biol. Chem. 1987, 262:9895-9901.
12. Foyer C.H., Lopez-Delgado H., Dat J.F., Scott I.M. Hydrogen peroxide- and glutathione-associated mechanisms of acclimatory stress tolerance and signaling. Physiol. Plant 1997, 100:241-254.
13. Fridovich I. Biological effects of the superoxide radical. Arch. Biochem. Biophys. 1986, 247:1-11.
14. Grant J.J., Loake G.J. Role of reactive oxygen intermediates and cognate redox signaling in disease resistance. Plant Physiol. 2000, 124:21-29.
15. Grossmann K. Quinclorac belongs to a new class of highly selective auxin herbicides. Weed Sci. 1998, 46:707-716.
16. Grossmann K., Kwiatkowski J. Selective induction or ethylene and cyanide biosynthesis appears to be involved in the selective of the herbicide quinclorac between rice and barnyard grass. J. Plant Physiol. 1993, 142:457-465.
17. Grossmann K., Kwiatkowski J. Evidence for a causative role of cyanide, derived from ethylene biosynthesis, in the herbicidal mode of action of quinclorac in barnyard grass. Pest. Biochem. Physiol. 1995, 51:150-160.
18. Grossmann K., Kwiatkowski J. The mechanism of quinclorac selectivity in grasses. Pest. Biochem. Physiol. 2000, 66:83-91.
19. Grossmann K., Scheltrup F. Selective induction of 1-aminocyclopropane-1-carboxylate acid (ACC) synthase activity is involved in the selectivity of the auxin herbicide quinclorac between barnyard grass and rice. Pest. Biochem. Physiol. 1997, 58:145-153.
20. Gupta A.S., Heinen J.L., Holaday A.S., Burke J., Allen R.D. Increased resistance to oxidative stress in transgenic plants that overexpress chloroplastic Cu/Zn superoxide dismutase. Proc. Natl. Acad. Sci. U.S.A. 1993, 90:1629-1633.
21. Halliwell B., Foyer C.H. Properties and physiological function of a glutathione reductase purified from spinach leaves by affinity chromatography. Planta 1978, 139:9-17.
22. Imlay J.A., Linn S. DNA damage and oxygen radical toxicity. Science 1988, 240:1302-1309.
23. Koo S.J., Kwon Y.W., Cho K.Y. Differences in herbicidal activity, phytotoxic symptoms and auxin activity of quinclorac among plant species compared with 2,4-D. Weed Res. Jpn. 1991, 36:311-317.
24. Koo S.J., Neal J.C., DiTomaso J.M. 3,7-dichloroquinolinecarboxylic acid inhibits cell-wall biosynthesis in maize roots. Plant Physiol. 1996, 112:1383-1389.
25. Lopez-Martinez N., Shimabukuro R.H., Prado R.D. Effect of quinclorac on auxin-induced growth, transmembrane proton gradient and ethylene biosynthesis in Echinochloa spp. Aust. J. Plant Physiol. 1998, 25:851-857.
26. Meloni D.A., Oliva M.A., Martinez C.A., Cambraia J. Photosynthesis and activity of superoxide dismutase, peroxidase and glutathione reductase in cotton under salt stress. Environ. Exp. Bot. 2003, 49:69-76.
27. Menck B.H., Rosebrock H., Unglaub W., Kibler E. BAS514. H-quinclorac field experience to control Echinochloa crus-galli in rice. Proc. 10th Asian-Pac. Weed Sci. Soc. Conf., vol. 1 1985, 107-113.
28. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 2002, 7:405-410.
29. Nakano Y., Asada K. Purification of ascorbate peroxidase in spinach chloroplasts; its inactivation in ascorbate-depleted medium and reactivation by monodehydroascorbate radical. Plant Cell Physiol. 1987, 28:131-140.
30. Nagata T., Todoriki S., Masumizu T., Suda I., Furuta S., Du Z., Kikuchi S. Levels of active oxygen species are controlled by ascorbic acid and anthocyanin in Arabidopsis. J. Agric. Food Chem. 2003, 51:2992-2999.
31. Neill S.J., Desikan R., Clarke A., Hurst R.D., Hancock J.T. Hydrogen peroxide and nitric oxide as signaling molecules in plants. J. Exp. Bot. 2002, 53:1237-1247.
32. Niki E. Action of ascorbic acid as a scavenger of active and stable oxygen radicals. Am. J. Clin. Nutr. 1991, 54:1119-1124.
33. Noctor G., Foyer C.H. Ascorbate and glutathione: Keeping active oxygen under control. Annu. Rev. Plant Physiol. Plant Mol. 1998, 49:249-279.
34. Ohta Y., Yamamoto K., Deguchi M. Effect of calcium supply and plant age on the distribution of calcium salts in rice. Jpn. J. Soil Sci. Plant Nutr. 1970, 41:19-26. (in Japanese).
35. Rosen G.M., Freeman B.A. Detection of superoxide generated by endothelial cells. Proc. Natl. Acad. Sci. U.S.A. 1984, 81:7269-7273.
36. Scandalios J.G., Guan L., Polidoros A.N. Catalases in plants: gene structure, properties, regulation and expression. Oxidative Stress and the Molecular Biology of Antioxidant Defenses 1997, 343-406. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. J.G. Scandalios (Ed.).
37. Schabenberger O., Tharp B., Kells J., Penner D. Statistical tests for hormesis and effective dosages in herbicide dose-response. Agronomy J. 1999, 91:713-721.
38. Seefeldt S.S., Jensen J.E., Fuerst E.P. Log-logistic analysis of herbicide dose-response relationships. Weed Technol. 1995, 9:218-227.
39. Solomanson L.P. Cyanide as a metabolic inhibitor. Cyanide in Biology 1981, 11-28. Academic Press, London. B. Vennesland, E.E. Conn, C.J. Knowles, J. Westley, F. Wissing (Eds.).
40. Sunohara Y., Kobayashi M., Matsumoto H. Light effect on induction of 1-aminocyclopropane-1-carboxylic acid synthase activity in quinclorac- or 2,4-D-treated maize seedlings. Proc. 19th Asian-Pac. Weed Sci. Soc. Conf. II 2003, 828-836.
41. Sunohara Y., Kobayashi M., Matsumoto H. Light induction of 1-aminocyclopropane-1-carboxylic acid synthase activity in quinclorac-treated maize seedlings. J. Pest. Sci. 2003, 28:18-23.
42. Sunohara Y., Matsumoto H. Comparative physiological effects of quinclorac and auxins, and light involvement in quinclorac-induced chlorosis in corn leaves. Pest. Biochem. Physiol. 1997, 58:125-132.
43. Sunohara Y., Matsumoto H. Oxidative injury induced by the herbicide quinclorac on Echinochloa oryzicola Vasing. and the involvement of antioxidative ability in its highly selective action in grass species. Plant Sci. 2004, 167:597-606.
44. Sunohara Y., Matsumoto H. Quinclorac-induced cell death is accompanied by generation of reactive oxygen species in maize root tissue. Phytochemistry 2008, 69:2312-2319.
45. Sunohara Y., Shirai S., Wongkantrakorn N., Matsumoto H. Sensitivity and physiological responses of Eleusine indica and Digitaria adscendens to herbicide quinclorac and 2, 4-D. Environ. Exp. Bot. 2010, 68:157-164.
46. Takematsu T., Ichizen N. Monocotyledoneae. Weeds of the World 1997, vol. 3. Zenkoku Noson Kyoiku Kyokai, Tokyo, (in Japanese).
47. Tresch S., Grossmann K. Quinclorac does not inhibit cellulose (cell wall) biosynthesis in sensitive barnyard grass and maize roots. Pest. Biochem. Physiol. 2003, 75:73-78.
48. Tresch S., Grossmann K. Erratum to " Quinclorac does not inhibit cellulose (cell wall) biosynthesis in sensitive barnyard grass and maize roots" Pest. Biochem. Physiol. 2003, 76:70-71.
49. Vaidyanathan H., Sivakumar P., Chakrabarty R., Thomas G. Scavenging of reactive oxygen species in NaCl-stressed rice (Oryza sativa L.)-differential response in salt-tolerant and sensitive varieties. Plant Sci. 2003, 165:1411-1418.
50. Vranová E., Inzé D., van Breusegem F. Signal transduction during oxidative stress. J. Exp. Bot. 2002, 53:1227-1236.
51. Wei-Feng X., Wei-Ming S., Ueda A., Takabe T. Mechanisms of salt tolerance in transgenic Arabidopsis thaliana carrying a peroxisomal ascorbate peroxidase gene from barley. Pedosphere 2008, 18:486-495.
52. Wuerzer B., Berghaus R. Substituted quinoline carboxylic acid-new elements in herbicide systems. Proc. 10th Asian-Pac. Weed Sci. Soc. Conf., vol. 1 1985, 177-184.
53. Yamamoto Y., Kobayashi Y., Devi S.R., Rikiishi S., Matsumoto H. Aluminum toxicity is associated with mitochondrial dysfunction and the production of reactive oxygen species in plant cells. Plant Physiol. 2002, 128:63-72.
54. Zawierucha J.E., Penner D. Absorption, translocation, metabolism, and spray retention of quinclorac in Digitaria sanguinalis and Eleusine indica. Weed Sci. 2000, 48:296-301.