Plant cell membrane as a marker for light-dependent and light-independent herbicide mechanisms of action

Pesticide Biochemistry and Physiology

Volumn 101, Issue 3, 2011, Pages 182-190

  Dayan, Franck E ^a   Watson, Susan B ^a  

^a NATURAL PRODUCTS UTILIZATION RESEARCH UNIT   (United States)

Author keywords

Conductivity; Electrolyte leakage; Herbicide; Light dependent; Light independent; Mechanism of action; Mode of action; Peroxidation; Plasma membrane

Indexed keywords

CUCUMIS SATIVUS;

EID: 81555228728     PISSN: 00483575     EISSN: 10959939     Source Type: Journal    
DOI: 10.1016/j.pestbp.2011.09.004     Document Type: Article

References (74)

1. Joyard J., Teyssier E., Miege C., Berny-Seigneurin D., Marechal E., Block M.A., Dorne A.-J., Rolland N., Ajlani G., Douce R. The biochemical machinery of plastid envelope membranes. Plant Physiol. 1998, 118:715-723.
2. Newmeyer D.D., Ferguson-Miller S. Mitochondria: releasing power for life and unleashing the machineries of death. Cell 2003, 112:481-490.
3. Heese-Peck A., Raikhel N.V. The nuclear pore complex. Plant Mol. Biol. 1998, 38:145-162.
4. Maeshima M. Tonoplast transporters: organization and function. Annu. Rev. Plant Mol. Biol. 2001, 52:469-497.
5. Hayashi M., Nishimura M. Entering a new era of research on plant peroxisomes. Curr. Opin. Plant Biol. 2003, 6:577-582.
6. M.A. Jenks, S.D. Eigenbrode, B. Lemieux, Cuticular waxes of Arabidopsis, In The Arabidopsis Book, 1:e0016 (2002). doi:10.1199/tab.0016.
7. Samuels L., Kunst L., Jetter R. Sealing plant surfaces: Cuticular wax formation by epidermal cells. Annu. Rev. Plant Biol. 2008, 59:683-707.
8. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 2002, 7:405-410.
9. McKersie B.D., Hoekstra F.A., Krieg L.C. Differences in the susceptibility of plant membrane lipids to peroxidation. Biochim. Biophys. Acta 1990, 1030:119-126.
10. Gutteridge J.M.C. Lipid peroxidation and antioxidants as biomarkers of tissue damage. Clin. Chem. 1995, 41:1819-1828.
11. Triantaphylidès C., Havaux M. Singlet oxygen in plants: production. Detoxification signal. Trends Plant Sci. 2009, 14:219-228.
12. Duke S.O., Kenyon W.H. Peroxidizing activity determined by cellular leakage. Target Assays for Modern Herbicides, Related Compounds 1993, Lewis Publishers, Boca Raton, pp 61-66. P. Böger, G. Sandmann (Eds.).
13. Dayan F.E., Duke S.O., Grossmann K. Herbicides as probes in plant biology. Weed Sci. 2010, 58:340-350.
14. Zhen R.-G., Singh B.J. From inhibitors to target site genes and beyond-herbicidal inhibitors as powerful tools for functional genomics. Weed Sci. 2001, 49:266-272.
15. Falk J.S., Al-Khatib K., Peterson D.E. Rapid assay evaluation of plant response to protoporphyrinogen oxidase (protox)-inhibiting herbicides. Weed Technol. 2006, 20:104-112.
16. Jaspers P., Kangasjärvi J. Reactive oxygen species in abiotic stress signaling. Physiol. Plant. 2010, 138:405-413.
17. Hess F.D. Light-dependent herbicides: an overview. Weed Sci. 2000, 48:160-170.
18. Belbachir O., Matringe M., Tissut M., Chevallier D. Physiological actions of dinoterb, a phenol derivative: 1. Physiological effects on the whole plant and on tissue fragments of pea. Pestic. Biochem. Physiol. 1980, 14:303-308.
19. Senseman S.A. Herbicide Handbook. Weed Science Society of America 2007, Lawrence, KS. 9th.
20. Sachs R.M., Michael J.L. Comparative phytotoxicity among four arsenical herbicides. Weed Sci. 1971, 19:558-564.
21. Wauchope R.D. Uptake, translocation and phytoxicity of arsenic in plants. Arsenic: Industrial biomedical and environmental perspective. 1983, 348-375. Van Nostrand Reinhold, New York. W.H. Lederer, R.J. Fensterhein (Eds.).
22. Ellis J.P., Camper N.D. In vitro cultured cocklebur (Xanthium strumarium L.) responses to dimercaptopropanesulfonic acid and monosodium methanearsonate. J. Plant Growth Reg. 1995, 14:9-13.
23. Nimbal C.I., Shaw D.R., Duke S.O., Jr Byrd J.D. Response of MSMA-resistant and -susceptible common cocklebur (Xanthium strumarium) biotypes to cotton (Gossypium hirsutum) herbicides and cross-resistance to arsenicals and membrane disruptors. Weed Technol. 1995, 9:440-445.
24. Böger P., Sandmann G. Carotenoid biosynthesis inhibitor herbicides - mode of action and resistance mechanisms. Pestic. Outlook 1998, 9:29-35.
25. Chamovitz D., Sandmann G., Hirschberg J. Molecular and biochemical characterization of herbicide-resistant mutants of cyanobacteria reveals that phytoene desaturation is a rate-limiting step in carotenoid biosynthesis. J. Biol. Chem. 1993, 268:17348-17353.
26. Norris S.R., Barrette T.R., DellaPenna D. Genetic dissection of carotenoid synthesis in Arabidopsis defines plastoquinone as an essential component of phytoene desaturation. Plant Cell 1995, 7:2139-2149.
27. Pallett K.E., Little J.P., Sheekey M., Veerasekaran P. The mode of action of isoxaflutole I. Physiological effects, metabolism, and selectivity. Pestic. Biochem. Physiol. 1998, 62:113-124.
28. Lee D.L., Prisbylla M.P., Cromartie T.H., Dagarin D.P., Howard S.W., Provan W.M., Ellis M.K., Fraser T., Mutter L.C. The discovery and structural requirements of inhibitors of p-hydroxyphenylpyruvate dioxygenase. Weed Sci. 1997, 45:601-609.
29. Eisenreich W., Bacher A., Arigoni D., Rohdich F. Biosynthesis of isoprenoids via the non-mevalonate pathway. Cell. Mol. Life Sci. 2004, 61:1401-1426.
30. Ferhatoglu Y., Barrett M. Studies of clomazone mode of action. Pestic. Biochem. Physiol. 2006, 85:7-14.
31. Mueller C., Schwender J., Zeidler J., Lichtenthaler H.K. Properties and inhibition of the first two enzymes of the non-mevalonate pathway of isoprenoid bioynthesis. Biochem. Soc. Trans. 2000, 28:792-793.
32. Dayan F.E., Duke S.O. Phytotoxicity of protoporphyrinogen oxidase inhibitors: Phenomenology, mode of action, mechanisms of resistance. Herbicide Activity: Toxicology, Biochemistry, Molecular Biology 1997, IOS Press, Washington,DC, pp 11-35. R.M. Roe, J.D. Burton, R.J. Kuhr (Eds.).
33. Lehnen L.P., Sherman T.D., Becerril J.M., Duke S.O. Tissue and cellular localization of acifluorfen-induced porphyrins in cucumber cotyledons. Pestic. Biochem. Physiol. 1990, 37:239-248.
34. Sherman T.D., Becerril J.M., Matsumoto H., Duke M.V., Jacobs J.M., Jacobs N.J., Duke S.O. Physiological basis for differential sensitivities of plant species to protoporphyrinogen oxidase-inhibiting herbicides. Plant Physiol. 1991, 97:280-287.
35. Kenyon W.H. S.O.Duke, Effects of acifluorfen on endogenous antioxidants and protective enzymes in cucumber (Cucumis sativus L.) cotyledons. Plant Physiol. 1985, 79:862-866.
36. Dayan F.E., Rimando A.M., Duke S.O., Jacobs N.J. Thiol-dependent degradation of protoporphyrin IX by plant peroxidases. FEBS Lett. 1999, 444:227-230.
37. McCourt J.A., Pang S.S., King-Scott J., Guddat L.W., Duggleby R.G. Herbicide-binding sites revealed in the structure of plant acetohydroxyacid synthase. Proc. Nat. Acad. Sci. USA 2006, 130:569-573.
38. Michel A., Johnson R.D., Duke S.O., Scheffler B.E. Dose-response relationships between herbicides with different modes of action and growth of Lemna paucicostata: An improved ecotoxicological method, environment. Toxicol. Chem. 2004, 23:1074-1079.
39. Lydon J., Duke S.O. Inhibitors of glutamine synthesis. Plant Amino Acids 1999, Marcel Dekker, New York, NY, pp 445-464. B.K. Singh (Ed.).
40. Occhipinti A., Berlicki L., Gilberti S., Dzeidziola G., Wieczorek A., Kafarski P., Forlani G. Effectiveness and mode of action of phosphonate inhibitors of plant glutamine synthetase. Pest Manag. Sci. 2009, 66:51-58.
41. Forlani G. Purification and properties of a cytosolic glutamine synthetase expressed in Nicotiana plumbaginifolia cultured cells. Plant Physiol. Biochem. 2000, 38:201-207.
42. F.E. Dayan, J.G. Romagni, S.O. Duke, Herbicides: Cinmethylin, in: Encyclopedia of Agrochemicals, in: J.R. Plimmer, D.W. Gammon, D.W., N.N. Ragsdale (Eds.), John Wiley & Sons, New York, NY, 2003, pp 754-757.
43. K. Grossmann, J. Hutzler, S. Tresch, N. Christiansen, R. Looser, T. Ehrhardt, Using " physionomics and metabolomics" approaches to discovery of new modes of action. Proceedings of the annual meeting of the WSSA #303, 2011.
44. Penner D., Ashton F.M. Influence of dichlobenil, endothall, and bromoxynil on kinin control of proteiolytic activity. Weed Sci. 1968, 16:323-326.
45. Mann J.D., Jordan L.S., Day B.E. A survey of herbicides for their effect upon protein synthesis. Plant Physiol. 1965, 40:840-843.
46. Ayaydin F., Vissi E., Mészáros T., Miskolczi P., Kovács I., Fehér A., Dombrádi V., Erdödi F., Gergely P., Dudits D. Inhibition of serine/threonine-specific protein phosphatases causes premature activation of cdc2MsF kinase at G2/M transition and early mitotic microtubule organization in alfalfa. Plant J. 2000, 23:85-96.
47. Rikin A., Rubin B. Increase of cotton cotyledon resistance to the herbicide endothall by abscisic acid. Physiol. Plant 1993, 59:161-164.
48. Guerineau F., Brooks L., Meadows J., Lucy A., Robinson C., Mullineaux P. Sulfonamide resistance gene for plant transformation. Plant Mol. Biol. 1990, 15:127-136.
49. Konishi T., Shinohara K., Yamada K., Sasaki Y. Acetyl-CoA carboxylase in higher plants: most plants other than gramineae have both the prokaryotic and the eukaryotic forms of this enzyme. Plant Cell Physiol. 1996, 37:117-122.
50. Hausler R.E., Holtum J.A.M., Powles S.B. Cross-resistance to herbicides in annual ryegrass (Lolium rigidum) IV. Correlation between membrane effects and resistance to graminicides. Plant Physiol. 1991, 97:1035-1043.
51. Shimabukuro R.H., Hoffer B.L. Effect of diclofop on the membrane potentials of herbicide-resistant and -susceptible annual ryegrass root tips. Plant Physiol. 1992, 98:1415-1422.
52. Zheng H., Rowland O., Kunst L. Disruptions of the Arabidopsis enoyl-CoA reductase gene reveal an essential role for very-long-chain fatty acid synthesis in cell expansion during plant morphogenesis. Plant Cell 2005, 17:1467-1481.
53. McMurry L.M., McDermott P.F., Levy S.B. Triclosan targets lipid synthesis. Nature 1998, 394:531-532.
54. Villalain J., Mateo R., Aranda F.J., Shapiro S., Micol V. Membranotropic effects of the antibacterial agent triclosan. Arch. Biochem. Biophys. 2001, 390:128-136.
55. Böger P. Mode of action for chloroacetamides and functionally related compounds. J. Pestic. Sci. 2003, 28:324-329.
56. Böger P., Matthes B., Schmalfuß J. Towards the primary target of chloroacetamides - new findings pave the way. Pest Manag. Sci. 2000, 56:497-508.
57. Fukuda M.Y., Tsujino Y., Fujimori T., Wakabayashi K., Böger P. Phytotoxic activity of middle-chain fatty acids I: effects on cell constituents. Pestic. Biochem. Physiol. 2004, 80:143-150.
58. Lederer B., Fujimori T., Tsujino Y., Wakabayashi K., Böger P. Phytotoxic activity of middle-chain fatty acids II: peroxidation and membrane effects. Pestic. Biochem. Physiol. 2004, 80:151-156.
59. Sabba R.P., Vaughn K.C. Herbicides that inhibit cellulose biosynthesis. Weed Sci. 1999, 47:757-763.
60. Paredez A.R., Somerville C.R., Ehrhardt D.W. Visualization of cellulose synthase demonstrates functional association with microtubules. Science 2006, 312:1491-1495.
61. Fisher D.D., Cyr R.J. Extending the microtubule/microfibril paradigm. Cellulose synthesis is required for normal cortical microtubule alignment in elongating cells. Plant Physiol. 1998, 116:1043-1051.
62. Mutwil M., Debolt S., Persson S. Cellulose synthesis: a complex complex. Curr. Opin. Plant Biol. 2008, 11:252-257.
63. Rajangam A.S., Kumar M., Aspeborg H., Guerriero G., Arvestad L., Pansri P., Brown C.J.-L., Hober S., Blomqvist K., Divne C., Ezcurra I., Mellerowicz E., Sundberg B., Bulone V., Teeri T.T. MAP20, a microtubule-associated protein in the secondary cell walls of hybrid aspen, is a target of the cellulose synthesis inhibitor 2, 6-dichlorobenzonitrile. Plant Physiol. 2008, 148:1283-1294.
64. Grossmann K. Auxin herbicides: current status of mechanism and mode of action. Pest Manag. Sci. 2010, 66:113-120.
65. Dayan F.E., Duke S.O., Sauldubois A., Singh N., McCurdy C., Cantrell C.L. P-Hydroxyphenylpyruvate dioxygenase is a herbicidal target site for β-triketones from Leptospermum scoparium. Phytochemistry 2007, 68:2004-2014.
66. Abbas H.K., Paul R.N., Riley R.T., Tanaka T., Shier W.T. Ultrastructural effects of AAL-toxin T-A from the fungus Alternaria alternata on black nightshade (Solanum nigrum L.) leaf discs and correlation with biochemical measures of toxicity. Toxicon 1998, 36:1821-1832.
67. Abbas H.K., Tanaka T., Duke S.O., Boyette C.D. Susceptibility of various crop and weed species to AAL-Toxin, a natural herbicide. Weed Technol. 1995, 9:125-130.
68. Basja J., Pan Z., Duke S.O. Transcriptional responses to cantharidin, a protein phosphatase inhibitor, in Arabidopsis thaliana reveal the involvement of multiple signal transduction pathways. Physiol. Plant. 2011, 143:188-205.
69. Amagasa T., Paul R.N., Heitholt J.J., Duke S.O. Physiological effects of cornexistin on Lemna pausicostata. Pestic. Biochem. Physiol. 1994, 49:37-42.
70. Daub M.E., Hangarter R.P. Light-induced production of singlet oxygen and superoxide by the fungal toxin, cercosporin. Plant Physiol. 1983, 73:855-857.
71. Dayan F.E., Weete J.D., Duke S.O., Hancock H.G. Soybean (Glycine max) cultivar differences in response to sulfentrazone. Weed Sci. 1997, 45:634-641.
72. Dayan F.E., Ferreira D., Wang Y.-H., Khan I.A., McInroy J.A., Pan Z. A pathogenic fungi diphenyl ether phytotoxin targets plant enoyl (acyl carrier protein) reductase. Plant Physiol. 2008, 147:1062-1071.
73. Malev V.V., Kaulin Y.A., Bezrukov S.M., Gurnev P.A., Takemoto J.Y., Schagina L.V. Kinetics of opening and closure of syringomycin E channels from in lipid bilayers. Membr. Cell Biol. 2001, 14:813-829.
74. Galindo J.C.G., Hernández A., Dayan F.E., Tellez M.R., Macías F.A., Paul R.N., Duke S.O. Dehydrozaluzanin C, a natural sesquiterpenolide, causes rapid plasma membrane leakage. Phytochemistry 1999, 52:805-813.