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Effect of Chlorimuron and Quizalofop on Fatty Acid Biosynthesis

Published online by Cambridge University Press:  12 June 2017

Leslie A. Bjelk
Affiliation:
Dep. Hortic. Sci., North Carolina State Univ., Raleigh, NC 27695-7609
Thomas J. Monaco
Affiliation:
Dep. Hortic. Sci., North Carolina State Univ., Raleigh, NC 27695-7609

Abstract

Chlorimuron antagonized the activity of quizalofop on broadleaf signalgrass when applied in greenhouse studies as a postemergence tank mix. In vitro leaf disc assays utilizing 14C-acetate or 14C-pyruvate as substrates were conducted to ascertain the effect of clorimuron and quizalofop on fatty acid biosynthesis and to determine if antagonism between the two herbicides occurs at the biochemical sites of action. Incorporation of 14C-acetate in control treatments was linear with time to 120 min. Acetate incorporation in the presence of quizalofop (1.1 μM) was also linear but was inhibited 30 min after initialization of the reaction. The concentration of quizalofop that inhibited 14C-acetate incorporation 50% (I50) was 0.54 μM. Chlorimuron, up to 155 μM, had no effect on 14C-acetate incorporation. A mixture of quizalofop (1.1 μM) and chlorimuron (4.8 μM) inhibited 14C-acetate incorporation similar to that of quizalofop alone at 1.1 μM. Quizalofop I50 for incorporation of 14C-pyruvate was 1.1 μM, and clorimuron at 4.8 μM decreased incorporation 15%. Excess unlabeled pyruvate (5 μM) had no effect on either 14C-acetate or 14C-pyruvate incorporation in the presence of both herbicides. It is believed that antagonism of quizalofop by clorimuron is not due to an excess pool of pyruvate resulting from inhibition of acetolactate synthase by chlorimuron.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1992 by the Weed Science Society of America 

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References

Literature Cited

1. Burton, J. D., Gronwald, J. W., Somers, D. A., Connelly, J. A., Gengenbach, B. G., and Wyse, D. L. 1988. Inhibition of plant acetylcoenzyme A carboxylase by the herbicides sethoxydim and haloxyfop. Biochem. Biophys. Res. Commun. 148:10391044.CrossRefGoogle Scholar
2. Chow, P.N.P. 1988. Effect of chlorsulfuron on four graminicides for weed control and wheat yield. Weed Res. 28:145150.CrossRefGoogle Scholar
3. Croon, K. A., Ketchersid, M. L., and Merkle, M. G. 1989. Effect of bentazon, imazaquin, and chlorimuron on the absorption and translocation of the methyl ester of haloxyfop. Weed Sci. 37:645650.Google Scholar
4. Croon, K. A. and Merkle, M. G. 1988. Effects of bentazon, imazaquin, or chlorimuron on haloxyfop or fluazifop-p efficacy. Weed Technol. 2:3640.CrossRefGoogle Scholar
5. Gerwick, B. C., Thompson, P., and Noveroske, R. 1988. Potential mechanisms in antagonism with aryloxyphenoxypropionate herbicides. Abstr. Weed Sci. Soc. Am. 28:100.Google Scholar
6. Hahn, K. L. 1989. Characterization of the antagonistic interaction between quizalofop and chlorimuron. Ph.D. Dissertation. Dep. Crop Sci., North Carolina State Univ., Raleigh, NC 27695.Google Scholar
7. Hall, C., Edgington, L. V., and Switzer, C. M. 1982. Effects of chlorsulfuron or 2,4-D upon diclofop-methyl efficacy in oat (Avena sativa). Weed Sci 30:672676.Google Scholar
8. Homeyer, U., Schulze-Siebert, D., and Schultz, G. 1985. Control of pyruvate metabolism in spinach chloroplasts by exogenously added products and coenzymes. J. Plant Physiol. 119:8791.Google Scholar
9. Homeyer, U., Schulze-Siebert, D., and Schultz, G. 1985. On the specificity of the herbicide chlorsulfuron in intact spinach chloroplasts. Z. Naturforsch. 40c:917918.Google Scholar
10. LaRossa, R. A., Van Dyk, T. K., and Smulski, D. R. 1987. Toxic accumulation of α-ketobutyrate caused by inhibition of the branchedchain amino acid biosynthetic enzyme acetolactate synthase in Salmonella typhimurium . J. Bacteriol. 169:13721378.CrossRefGoogle ScholarPubMed
11. Liebl, R. and Worsham, A. D. 1987. Effect of chlorsulfuron on diclofop phytotoxicity to Italian ryegrass (Lolium multiflorum). Weed Sci. 35:383387.Google Scholar
12. Liebl, R. and Worsham, A. D. 1987. Effect of chlorsulfuron on the movement and fate of diclofop in Italian ryegrass (Lolium multiflorum) and wheat (Triticum aestivum). Weed Sci. 35:623628.CrossRefGoogle Scholar
13. Murphy, D. J. and Stumpf, P. K. 1981. The origin of chloroplastidic acetyl coenzyme A. Arch. Biochem. Biophys. 212:730739.Google Scholar
14. Nakahira, K., Uchiyama, M., and Ikai, T. 1988. Effect of (R)-(+)- and (S)-(-)-quizalofop-ethyl on lipid metabolism in excised corn stem-base meristems. J. Pestic. Sci. 13:269276.Google Scholar
15. Nikolau, B. J., Hawke, J. C., and Slack, C. R. 1981. Acetyl-coenzyme A carboxylase in maize leaves. Arch. Biochem. Biophys. 211:605612.Google Scholar
16. O'Sullivan, P. A. and Kirkland, K. J. 1984. Chlorsulfuron reduced control of wild oat (Avena fatua) with diclofop, difenzoquat, and flamprop. Weed Sci. 32:285289.Google Scholar
17. Parsells, A. J. 1985. Assure—a new postgrass herbicide from Du Pont. Weeds Today. 16:910.Google Scholar
18. Ray, T. B. 1986. Sulfonylurea herbicides as inhibitors of amino acid biosynthesis in plants. Trends Biochem. Sci. 11:180183.Google Scholar
19. Ray, T. B. 1985. The site of action of the sulfonylurea herbicides. Proc. Br. Crop Prot. Conf.—Weeds. 1985. 3A–1:131138.Google Scholar
20. Rhodes, D., Hogan, A. L., Deal, L., Jamieson, G. C., and Haworth, P. 1987. Amino acid metabolism of Lemna minor L. Plant Physiol. 84:775780.Google Scholar
21. Roughan, P. G., Holland, R., and Slack, C. R. 1978. Acetate is the preferred substrate for long-chain fatty acid synthesis in isolated spinach chloroplasts. Biochem. J. 184:565569.Google Scholar
22. Sakata, G., Makino, K., Kawamura, Y., and Ikai, T. 1985. Syntheses and selective herbicidal activities of ethyl 2-[4-(6-chloro-2-quinoxalinyloxy) phenoxy]propanoate and its related compounds. J. Pestic. Sci. 10:6167.Google Scholar
23. Schulze-Siebert, D., Heineke, D., Scharf, H., and Schultz, G. 1984. Pyruvate-derived amino acids in spinach chloroplasts. Plant Physiol. 76:465471.CrossRefGoogle ScholarPubMed
24. Secor, J. and Cséke, C. 1988. Inhibition of acetyl-CoA carboxylase activity by haloxyfop and tralkoxydim. Plant Physiol. 86:1012.Google Scholar
25. Secor, J., Cséke, C., and Owen, W. J. 1989. Aryloxyphenoxypropionate and cyclohexanedione herbicides inhibit acetyl CoA carboxylase. Am. Chem. Soc. Symp. Ser. 389:265276.Google Scholar