Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-27T01:27:57.221Z Has data issue: false hasContentIssue false

Auxinlike Activity and Metabolism of Mefluidide in Corn (Zea mays) and Soybean (Glycine max) Tissue

Published online by Cambridge University Press:  12 June 2017

Scott Glenn
Affiliation:
Univ. of Kentucky, Lexington, KY 40546
Charles E. Rieck
Affiliation:
Univ. of Kentucky, Lexington, KY 40546

Abstract

Mefluidide {N-[2,4-dimethyl-5-[[(trifluoromethyl) sulfonyl] amino] phenyl] acetamide} was evaluated for effects on corn [Zea mays (L.) ‘Pioneer 3535’] coleoptile elongation. Mefluidide at 10-8 M, 10-7 M, and 10-6 M stimulated elongation approximately equal to growth stimulations with 10-6 M indoleacetic acid (IAA). Polar transport of 14C-IAA from donor agar blocks through corn coleoptiles and into receiver agar blocks after 12 h was increased 246% by 10-4 M mefluidide and inhibited 82% by 10-3 M mefluidide. Mefluidide-related chemicals (10-4 M) lacking a trifluoromethyl-sulfonyl-amino chain at the 1-position of the phenyl ring did not alter 14C-IAA transport. IAA transport was increased 97% when the acetamide chain at the 5-position was absent and 255% when the methyl in the 4-position was absent, and it decreased 65% when the methyl at the 2-position was absent. Polar transport of 14C-IAA through soybean [Glycine max (L.) Merr. ‘Williams’] hypocotyls was not altered by 10-4 M mefluidide; however, 10-3 M mefluidide increased IAA transport 116%. After 6 h, corn coleoptiles metabolized 14% of the mefluidide absorbed and soybean metabolized 54% of the mefluidide absorbed from 14C-mefluidide solutions (10-6 M). Differences in the rate of metabolism of mefluidide in meristematic tissue of corn and soybean may explain differences in mefluidide effects on auxin transport in corn and soybean.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1985 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. Bloomberg, J. R. and Wax, L. M. 1978. Absorption and translocation of mefluidide by soybean (Glycine max), common cocklebur (Xanthium pensylvanicum), and giant foxtail (Setaria faberi). Weed Sci. 26:434440.Google Scholar
2. Cardenas, J., Slife, F. W., Hanson, J. B., and Butler, H. 1968. Physiological changes accompanying the death of cocklebur plants treated with 2,4-D. Weed Sci. 16:96100.CrossRefGoogle Scholar
3. Frear, D. S. 1968. Herbicide metabolism in plants-I. Purification and properties of UDP-glucose:arylamine N-glucosyl-transferase from soybean. Phytochemistry 7:381390.Google Scholar
4. Frear, D. S. and Swanson, H. R. 1970. Biosynthesis of S-(4-ethylamino-6-isopropylamino-2-S-triazine)glutathione: partial purification and properties of a glutathione S-transferase from corn. Phytochemistry 9:21232132.CrossRefGoogle Scholar
5. Glenn, S., Rieck, C. E., Ely, D. G., and Bush, L. P. 1980. Quality of tall fescue forage affected by mefluidide. J. Agric. Food Chem. 28:391393.Google Scholar
6. Glenn, S., Glenn, B. P., Rieck, C. E., Ely, D. G., and Bush, L. P. 1981. Chemical quality, in vitro cellulose digestion, and yield of tall fescue forage affected by mefluidide. J. Agric. Food Chem. 29:11581161.CrossRefGoogle Scholar
7. Goldsmith, M. H.M. and Wilkins, M. B. 1964. Movement of auxin in coleoptiles of Zea mays during geotropic stimulation. Plant Physiol. 39:151162.Google Scholar
8. Hook, B. J. and Glenn, S. 1984. Mefluidide and acifluorfen interactions of ivyleaf morningglory (Ipomoea hederacea), velvetleaf (Abutilon theophrasti), and common cocklebur (Xanthium pensylvanicum). Weed Sci. 32:198201.Google Scholar
9. Keitt, G. W. Jr. and Baker, R. A. 1966. Auxin activity of substituted benzoic acids and their effect on polar auxin transport. Plant Physiol. 41:15611569.Google Scholar
10. Lay, Mih-Muh and Casida, J. E. 1976. Dichloroacetamide antidotes enhance the thiocarbamate sulfoxide detoxification by elevating corn root glutathione content and glutathione S-transferase activity. Pestic. Biochem. Physiol. 6:442456.Google Scholar
11. McWhorter, C. G. and Barrentine, W. L. 1979. Weed control in soybeans (Glycine max) with mefluidide applied postemergence. Weed Sci. 27:4247.Google Scholar
12. McWhorter, C. G. and Wills, G. D. 1978. Factors affecting the translocation of 14C-mefluidide in soybeans (Glycine max), common cocklebur (Xanthium pensylvanicum), and johnsongrass (Sorghum halepense). Weed Sci. 26:382388.Google Scholar
13. Naqvi, S. M., Dedolph, R. R., and Gordon, S. A. 1965. Auxin transport and geoelectric potential in corn coleoptile sections. Plant Physiol. 40:966968.Google Scholar
14. Rao, S. R. and Harger, T. R. 1981. Mefluidide-bentazon interactions on soybeans (Glycine max) and red rice (Oryza sativa). Weed Sci. 29:208212.Google Scholar
15. Ray, P. M., Dohrmann, U., and Hertel, R. 1977. Specificity of auxin-binding sites on maize coleoptile membranes as possible receptor sites for auxin action. Plant Physiol. 60:585591.Google Scholar
16. Swisher, B. A. and Kapusta, G. 1980. Selective postemergence herbicidal control of johnsongrass (Sorghum halepense) in soybeans (Glycine max). Weed Sci. 28:529533.Google Scholar
17. Truelove, B., Davis, D. E., and Pillai, G.C.P. 1971. Mefluidide effects on growth of corn (Zea mays) and the synthesis of protein by cucumber (Cucumis sativus) cotyledon tissue. Weed Sci. 25:360363.Google Scholar
18. Watschke, T. L. 1976. Growth regulation of Kentucky bluegrass with several growth retardants. Agron. J. 68:787791.Google Scholar
19. Wilkinson, R. E. 1982. Mefluidide inhibition of sorghum growth and giberellin precursor biosynthesis. J. Plant Growth Regul. 1:8594.Google Scholar
20. Zaerr, J. B. and Mitchell, J. W. 1976. Polar transport related to mobilization of plant constituents. Plant Physiol. 42:863874.Google Scholar