Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-10T03:12:06.482Z Has data issue: false hasContentIssue false

Enhancement of Chloroplast Photooxidations with Photosynthesis-Inhibiting Herbicides and Protection with NADH or NADPH

Published online by Cambridge University Press:  12 June 2017

C. N. Giannopolitis
Affiliation:
Pesticide Res. Center, Michigan State Univ., East Lansing, MI 48824
G. S. Ayers
Affiliation:
Pesticide Res. Center, Michigan State Univ., East Lansing, MI 48824

Abstract

Representative herbicides of the substituted ureas, uracils, s-triazines, benzonitriles, and bipyridyls, which are potent inhibitors of photosynthetic electron transport, markedly accelerated photooxidations (chlorophyll bleaching and lipid peroxidation) normally occurring in isolated intact chloroplasts. Other herbicides, which are not potent inhibitors of photosynthesis, did not accelerate photooxidations. The photooxidations, whether in the presence or absence of herbicides, were completely prevented by exogenously supplied NADH or NADPH but not by sucrose or mannitol. Herbicide-induced injury to barley (Hordeum vulgare L.) seedlings treated with paraquat (1,1′-dimethyl-4,4′-bipyridinium ion) was diminished by allowing the seedlings to absorb NADPH. These results provide additional support to the hypothesis that depletion of the source of reducing potential (NADPH) is responsible for chloroplast photooxidations and plant death following treatment with photosynthesis-inhibiting herbicides.

Type
Research Article
Copyright
Copyright © 1978 by the Weed Science Society of America 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Literature Cited

1. Arnon, D. I. 1949. Copper enzymes in isolated chloroplasts: Polyphenoloxidase in Beta vulgaris . Plant Physiol. 24:115.Google Scholar
2. Ashton, F. M., Gifford, E. M., and Bisalputra, T. 1963. Structural changes in Phaseolus vulgaris induced by atrazine. II. Effects on fine structure of chloroplasts. Bot. Gaz. 124:336343.CrossRefGoogle Scholar
3. Ashton, F. M. and Crafts, A. S. 1973. Mode of Action of Herbicides. Wiley, New York, 504 pp.Google Scholar
4. Baldwin, B. C., Dodge, A. D., and Harris, N. 1968. Recent advances in studies of the mode of action of the bipyridilium herbicides. Proc. Brit. Weed Control Conf. 639644.Google Scholar
5. Davis, E. A. 1966. The role of starvation in fenuron injury to shrub live oak. Weeds 14:1017.Google Scholar
6. Gast, A. 1958. Uber pflanzen wash stums regulatoren: beitrage zur kenntmis der phytotoxischen wirkung von triazinen. Experientia 14:134136.Google Scholar
7. Good, N. E. 1962. Inhibitors of photosynthesis as herbicides. World Rev. Pest Control 1:1928.Google Scholar
8. Heath, R. L. and Packer, L. 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of the fatty acid peroxidation. Arch. Biochem. Biophys. 125:189198.Google Scholar
9. Heath, R. L. and Packer, L. 1968. Photoperoxidation in isolated chloroplasts. II. Role of electron transfer. Arch. Biochem. Biophys. 125:850857.Google Scholar
10. Hill, E. R., Putala, E. C., and Vengris, J. 1968. Atrazine induced ultrastructural changes of barnyardgrass chloroplasts. Weed Sci. 16:377380.Google Scholar
11. 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. I, Academic Press, New York.Google Scholar
12. Mees, G. C. 1960. Experiments on the herbicidal action of 1,1-ethylene-2,2-dipyridilium dibromide. Ann. Appl. Biol. 48:601612.CrossRefGoogle Scholar
13. Moreland, D. E. 1967. Mechanisms of action of herbicides. Annu. Rev. Plant Physiol. 18:365386.Google Scholar
14. Stanger, C. E. and Appleby, A. P. 1972. A proposed mechanism for diuron-induced phytotoxicity. Weed Sci. 20:357363.CrossRefGoogle Scholar
15. Sweetser, P. B. and Todd, C. W. 1961. The effect of monuron on oxygen liberation in photosynthesis. Biochim. Biophys. Acta 51:504508.Google Scholar
16. Vernon, L. P. and Zaugg, W. S. 1960. Photoreductions by fresh and aged chloroplasts: Requirement for ascorbate and 2,6-dichlorophen with aged chloroplasts. J. Biol. Chem. 235:27282733.CrossRefGoogle ScholarPubMed
17. Wareing, P. F. and Phillips, I. D. J. 1970. The Control of Growth and Differentiation in Plants, Pergamon Press, Oxford, 303 pp.Google Scholar