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The Pantothenate-Synthesizing Enzyme, A Metabolic Site in the Herbicidal Action of Chlorinated Aliphatic Acids

Published online by Cambridge University Press:  12 June 2017

J. L. Hilton
Affiliation:
Crops Research Division, Agricultural Research Service, U. S. Department of Agriculture, Beltsville, Maryland
J. S. Ard
Affiliation:
Eastern Utilization Research and Development Division, Agricultural Research Service, U. S. Department of Agriculture, Philadelphia 18, Pennsylvania
L. L. Jansen
Affiliation:
Crops Research Division, Agricultural Research Service, U. S. Department of Agriculture, Beltsville, Maryland
W. A. Gentner
Affiliation:
Crops Research Division, Agricultural Research Service, U. S. Department of Agriculture, Beltsville, Maryland
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Extract

Evidence that β-alanine or calcium pantothenate partially reversed the inhibitory action of several chlorinated aliphatic acids on yeast growth (4) suggested the hypothesis that synthesis of pantothenate is one of the metabolic pathways sensitive to this group of herbicides. The objectives of the experiments reported herein were (a) to determine the mechanism by which the enzymatic synthesis of pantothenate was inhibited by these compounds, (b) to seek evidence for the contributions of this mechanism, in vivo, to the herbicidal effects of 2,2-dichloropropionic acid (dalapon), (c) to determine whether pantothenate treatments could overcome the effects of dalapon in plants and (d) to test chloro-substituted analogs of pantoate for herbicidal activity. To achieve the last objective it was necessary to synthesize several new chemicals.

Type
Research Article
Information
Weeds , Volume 7 , Issue 4 , October 1959 , pp. 381 - 396
Copyright
Copyright © 1959 Weed Science Society of America 

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References

Literature Cited

1. Darzens, G. Nouvelle méthode d'éthérification des alcools par les hydracides. Comptes Rendus 152:13141317. 1911.Google Scholar
2. Eaton, F. M. Selective gametocide opens way to hybrid cotton. Science 126:11741175. 1957.Google Scholar
3. Gerrard, W. Studies of the esters of sulphurous, chlorosulphinic, and chlorosulphonic acids. J. Chem. Soc. (London) 99103. 1939.Google Scholar
4. Hilton, J. L., Jansen, L. L., and Gentner, W. A. Beta-alanine protection of yeast growth against the inhibitory action of several chlorinated aliphatic acid herbicides. Plant Physiol. 33:4345. 1958.CrossRefGoogle ScholarPubMed
5. Kirkwood, S., and Phillips, P. H. The antiinositol effect of γ-hexachlorocyclohexane. J. Biol. Chem. 163:251254. 1946.Google Scholar
6. Levene, P. A., and Mori, T. On Walden inversion. XII. Part II. Levo–ethyl–γ–chlorovalerate. J. Biol. Chem. 78:1617. 1928.Google Scholar
7. Lineweaver, H., and Burk, D. The determination of enzyme dissociation constants. Jour. Am. Chem. Soc. 56:658666. 1934.Google Scholar
8. Maas, W. K. Pantothenate Studies. III. Description of the extracted pantothenate-synthesizing enzyme of Escherichia coli . J. Biol. Chem. 198:2332. 1952.CrossRefGoogle ScholarPubMed
9. Novelli, G. D. Pantothenate-synthesizing enzyme. In Colowick, S. P. and Kaplan, N. O., Editors. Methods in Enzymology Vol. II, 619622. Academic Press Inc., New York, New York. 1955.Google Scholar
10. Shaw, W. C., and Swanson, C. R. Techniques and equipment used in evaluating chemicals for their herbicidal properties. Weeds 1:352365. 1952.CrossRefGoogle Scholar
11. Slade, R. E. The γ-isomer of hexachlorocyclohexane (Gammexane). Chem. and Ind. 64:314319. 1945.Google Scholar
12. Williams, R. J., and Wenner, W. Pantothenic Acid. In Kirk, R. E. and Othmer, D. F., Editors. Encyclopedia of Chemical Technology. 9:807808. Interscience Publishers, 250 Fifth Ave. New York 1, N. Y. 1952.Google Scholar