Hostname: page-component-77c89778f8-5wvtr Total loading time: 0 Render date: 2024-07-16T12:12:25.488Z Has data issue: false hasContentIssue false

Effects of Haloxyfop on Corn (Zea mays) and Soybean (Glycine max) Cell Suspension Cultures

Published online by Cambridge University Press:  12 June 2017

Hyung-Yul Cho
Affiliation:
Dep. Agron., Univ. Illinois, 1102 S. Goodwin Avenue, Urbana, IL 61801
Jack M. Widholm
Affiliation:
Dep. Agron., Univ. Illinois, 1102 S. Goodwin Avenue, Urbana, IL 61801
Fred W. Slife
Affiliation:
Dep. Agron., Univ. Illinois, 1102 S. Goodwin Avenue, Urbana, IL 61801

Abstract

To investigate the mode of action of a grass-specific herbicide, haloxyfop {2-[4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl] oxy] phenoxy] propanoic acid} was added to corn and soybean cell suspension cultures containing metabolic intermediates such as sucrose [14C-U], sodium acetate [14C-1,2], or L-leucine [14C-U]. Death of the corn suspension cells occurred within 3 days after haloxyfop was added at a concentration of 1.0 μM to supplemented Murashige and Skoog's medium. At 0.1 μM haloxyfop, 14C-sucrose uptake and 14C loss due to respiration of the corn cells declined without a significant reduction in cell fresh weight, cell viability, cellular ATP level, free sugar content, cell wall materials, or level of glycolytic intermediates. The proportions of sucrose, glucose, and fructose in the free sugar fraction were not affected. However, the 14C-labeled free amino acid level was increased. During a 24-h incubation period, incorporation of leucine [14C] as a precursor revealed that haloxyfop did not inhibit protein synthesis. Incorporation of acetate [14C-1,2] showed that total lipid synthesis was inhibited by 42% at 0.1 μM haloxyfop (sublethal). Similar responses were observed in the soybean suspension cells; however, the calculated 50% lethal concentration (LC50) was 47 times higher than for corn cells. The results of this study suggest that the site of action of haloxyfop is located where metabolic intermediates enter the Kreb's cycle and lipid synthesis. Glycolysis is not inhibited.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1986 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. Asare-Boamah, N. K. and Fletcher, R. A. 1983. Physiological and cytological effects of BAS-9052-OH on corn (Zea mays) seedlings. Weed Sci. 31:4955.CrossRefGoogle Scholar
2. Choury, P. S. and Zurawski, D. B. 1981. Callus formation from protoplast of a maize cell culture. Theor. Appl. Genet. 59:341344.CrossRefGoogle Scholar
3. Chow, P.N.P. and LaBerge, D. E. 1978. Wild oat studies. 2. Physiological and chemical changes in barley and wild oat treated with diclofop-methyl herbicide in relation to plant tolerance. J. Agric. Food Chem. 26:11341137.CrossRefGoogle Scholar
4. Finney, D. J. 1971. Statistical methods in biological assay. 2d. ed. Griffin Press, London.Google Scholar
5. Gealy, D. R. and Slife, F. W. 1983. BAS 9052 effects on leaf photosynthesis and growth. Weed Sci. 31:457461.CrossRefGoogle Scholar
6. Giaquinta, R. T. and Beyer, E. Jr. 1977. 14C2H4: Distribution of 14C-labeled tissue metabolites in pea seedlings. Plant Cell Physiol. 18:141148.Google Scholar
7. Green, C. E. and Phillips, R. L. 1975. Plant regulation from tissue cultures of maize. Crop Sci. 15:417421.CrossRefGoogle Scholar
8. Hatzios, K. K. 1982. Effects of sethoxydim on the metabolism of isolated leaf cells of soybean [Glycine max (L.) Merr.]. Plant Cell Rep. 1:8790.CrossRefGoogle Scholar
9. Hoppe, H. H. 1981. Effect of diclofop-methyl on protein nucleic acid and lipid biosynthesis in tips of radicles from Zea mays L. Z. Pflanzenphysiol. Bd. 102:189197.CrossRefGoogle Scholar
10. Ishikawa, H., Okunuki, S., Kawana, T., and Hirono, Y. 1980. Histological investigation on herbicidal effect of alloxydimsodium in oat. J. Pestic. Sci. 5:547551.CrossRefGoogle Scholar
11. Murashige, T. and Skoog, F. 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15:473497.CrossRefGoogle Scholar
12. Stahl, E. 1969. Spray reagents: Preparation and application of the spray reagent. Pages 845905 in Thin-Layer Chromatography. Berlin.Google Scholar
13. Swisher, B. A. and Corbin, F. T. 1982. Behavior of BAS-9052-OH in soybean (Glycine max) and johnsongrass (Sorghum halepense) plant and cell culture. Weed Sci. 30:640650.CrossRefGoogle Scholar
14. Weber, E. J. 1969. Lipids of maturing grain of corn (Zea mays L.). I. Changes in lipid classes and fatty acid composition. J. Am. Oil Chem. Soc. 46:485488.CrossRefGoogle Scholar
15. Widholm, J. M. 1972. The use of fluorescein diacetate and phenosafarin for determining viability of cultured plant cells. Stain Technol. 47:189194.CrossRefGoogle ScholarPubMed