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Effects of Difenzoquat on Photoreactions and Respiration in Wheat (Triticum aestivum) and Wild Oat (Avena fatua)

Published online by Cambridge University Press:  12 June 2017

Blaik P. Halling
Affiliation:
Dep. Agron. and Plant Genetics, Univ. of Minnesota, St. Paul, MN 55108
Richard Behrens
Affiliation:
Dep. Agron. and Plant Genetics, Univ. of Minnesota, St. Paul, MN 55108

Abstract

Experiments were conducted with isolated protoplasts of wild oat (Avena fatua L. # AVEFA) and isolated chloroplasts of wild oat and wheat (Triticum aestivum L.), to determine if the methyl sulfate salt of difenzoquat (1,2-dimethyl-3,5-diphenyl-1H-pyrazolium) might influence photoreactions in these species. Difenzoquat did not affect CO2 fixation, uncoupled electron transport, or proton uptake. At concentrations of 0.5 mM and 1 mM, difenzoquat caused a slight, but statistically significant, inhibition of photophosphorylation. Experiments assaying coupled electron transport indicated that inhibition of photophosphorylation occurred not through uncoupling, but by an energy-transfer inhibition. This same effect was observed in isolated mitocondria of both species, with about 50% inhibition of state 3 respiration rates occurring with 10 μM difenzoquat. However, no important differentials were observed in the relative susceptibilities of wheat and wild oat mitochondria. Difenzoquat also functioned as a weak autooxidizing electron acceptor in photosynthetic electron transport. Therefore, difenzoquat-induced leaf chlorosis and necrosis may result from a bipyridilium-type electron acceptor activity if sufficient herbicide is absorbed.

Type
Research Article
Copyright
Copyright © 1983 Weed Science Society of America 

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References

Literature Cited

1. Baldwin, B. C., Dodge, A. D., and Harris, N. 1968. Recent advances in studies of the mode of action of the bipyridilium herbicides. Proc. 9th Brit. Weed Control Conf. 639644.Google Scholar
2. Black, C. C. 1965. Chloroplast reactions with dipyridyl salts. Biochim. Biophys. Acta 120:332340.Google Scholar
3. Blank, S. E. and Behrens, R. 1974. Differential response of spring wheat varieties to difenzoquat. Proc. North Cent. Weed Control Conf. 29:37.Google Scholar
4. Calderbank, A. 1968. The bipryidilium herbicides. Adv. Pest Control Res. 8:127235.Google Scholar
5. Chow, P.N.P. 1976. Effects of post-emergence herbicides on growth, photosynthesis, and photosynthate translocation in wild oats. Can. J. Plant Sci. 56:429430.Google Scholar
6. Chow, P.N.P. 1982. Wild oat (Avena fatua) herbicide studies: I. Physiological response of wild oat to five postemergence herbicides. Weed Sci. 30.105.Google Scholar
7. Cohen, A. S., Morrison, I. N. 1982. Differential inhibition of potassium ion absorption by difenzoquat in wild oat and cereals. Pestic. Biochem. Physiol. 14:174179.Google Scholar
8. Dilley, R. A. 1972. Ion transport. (H+, K+, Mg2+ Exchange phenomena). Pages 6978 in Pietro, A. S., ed. Methods in Enzymology. Vol. 24. Academic Press, New York.Google Scholar
9. Edwards, G. E., Robinson, S. P., Tyler, N.J.C. and Walker, D. A. 1978. Photosynthesis by isolated protoplasts, protoplast extracts, and chloroplasts of wheat. Plant Physiol. 62:313319.Google Scholar
10. Friesen, H. A. and Litwin, O. B. 1975. Selective control of wild oats in barley with AC 84777. Can. J. Plant Sci. 55:927934.Google Scholar
11. Funderburk, H. H. and Lawrence, J. M. 1964. Mode of action and metabolism of diquat and paraquat. Weeds 12:259264.Google Scholar
12. Giannopolitis, C. N. and Ayers, G. S. 1978. Enhancement of chloroplast photooxidations with photosynthetic inhibiting herbicides and protection with NADH or NADPH. Weed Sci. 26:440443.Google Scholar
13. Hartree, E. F. 1972. Determination of protein: A modification of the Lowry method that gives a linear photometric response. Anal. Biochem. 48:422427.Google Scholar
14. Heath, R. L., and Packer, L. 1968. Photoperoxidation in isolated chloroplasts. II. Role of electron transfer. Arch. Biochem. Biophys. 125:850857.CrossRefGoogle ScholarPubMed
15. Knudson, L. L., Tibbits, T. W., and Edwards, G. E. 1977. Mechanisms of ozone injury by determination of leaf chlorophyll concentration. Plant Physiol. 60:606608.CrossRefGoogle Scholar
16. Krinsky, N. I. 1966. The role of carotenoid pigments as protective agents against photosensitized oxidations in chloroplasts. Pages 423430 in Goodwin, T. W., ed. Biochemistry of Chloroplasts. Vol. 1. Academic Press, New York.Google Scholar
17. Kunert, K. J. and Böger, P. 1981. The bleaching effect of the diphenyl ether oxyfluorfen. Weed Sci. 29:169173.Google Scholar
18. Machado, V. S., Arntzen, C. J., Bandeen, J. D. and Stephenson, G. R. 1978. Comparative triazine effects under system II photochemistry in chloroplasts of two common lambsquarters (Chenopodium album) biotypes. Weed Sci. 26:318322.Google Scholar
19. Matsunaka, S. 1969. Acceptor of light energy in photoinactivation of diphenyl ether herbicides. J. Agric. Food Chem. 17:171175.CrossRefGoogle Scholar
20. Miller, S. D., Nalewaja, J. D., Pudelko, J., and Adamczewski, K. A. Difenzoquat for wild oat (Avena fatua) control. Weed Sci. 26:571576.Google Scholar
21. Neumann, J. and Jagendorf, A. T. 1964. Light induced pH changes related to photophosphorylation by chloroplasts. Arch. Biochem. Biophys. 197:109119.Google Scholar
22. Nishimura, M., Ito, T., and Chance, B. 1962. Studies on bacterial photophosphorylation. III. A sensitive and rapid method of determination of photophosphorylation. Biochem. Biophys. Acta. 59:177182.Google Scholar
23. Pallet, K. E., Caseley, J. C. 1980. Differential inhibition of DNA synthesis in difenzoquat tolerant and susceptible United Kingdom spring wheat cultivars. Pestic. Biochem. Physiol. 14:144152.CrossRefGoogle Scholar
24. Pomeroy, M. K. 1974. Studies on the respiratory properties of mitochondria isolated from developing winter wheat seedlings. Plant Physiol. 53:653657.Google Scholar
25. Renger, G. and Wolff, C. 1977. Further evidence for dissipative energy migration via triplet states in photosynthesis. The protective mechanism of carotenoids in Rheudopseudomonas spheroides chromatophores. Biochem. Biophys. Acta 460:4757.Google Scholar
26. Sharma, M. P., Vanden Born, W. H., Friesen, H. A. and McBeath, D. K. 1976. Penetration, translocation, and metabolism of 14C-difenzoquat in wild oat and barley. Weed Sci. 24:379384.Google Scholar
27. Stanger, C. E. and Appleby, A. P. 1972. A proposed mechanism for diuron induced phytotoxicity. Weed Sci. 20:357363.Google Scholar
28. Takahma, U. and Nishimura, M. 1975. Formation of singlet molecular oxygen in illuminated chloroplasts. Effects on photoinactivation and lipid peroxidation. Plant Cell Physiol. 16:737748.Google Scholar
29. Vernon, L. P. 1960. Spectrophotometric determinations of chlorophylls and phaeophytins in plant extracts. Anal. Chem. 32:11441150.Google Scholar
30. West, K. R. and Wiskich, J. T. 1968. Photosynthetic control of isolated pea chloroplasts. Biochem. J. 109:527532.Google Scholar
31. Westra, P. H. and Wyse, D. L. 1981. Growth and development of quackgrass (Agropyron repens) biotypes. Weed Sci. 29:4452.Google Scholar