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. 1980 Oct;66(4):656–659. doi: 10.1104/pp.66.4.656

Effect of Glyphosate on Intact Bean Plants (Phaseolus vulgaris L.) and Isolated Cells 1

Barry J Brecke 1,2, William B Duke 1
PMCID: PMC440698  PMID: 16661497

Abstract

Whole bean (var. “Eastern Butterwax”) plants and isolated cells were used to investigate possible mechanisms of action of glyphosate [N-(phosphonomethyl)glycine]. Results showed that glyphosate was quickly absorbed by the whole plant but not by individual cells and that it caused a rapid reduction in leaf dry matter accumulation, leaf expansion, leaf angle, and stomatal aperture without affecting the water status of the plant. Glyphosate also caused a rapid reduction in cellular uptake of 86Rb and 32P which preceded its detrimental effects on photosynthesis, RNA and protein synthesis, and respiration of isolated cells. This reduction in ion absorption was not due to a loss of membrane integrity, decrease in energy supply or chelation of ions. It was concluded that glyphosate was directly inhibiting the ion absorption process of bean leaf cells.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Francki R. I., Zaitlin M., Jensen R. G. Metabolism of Separated Leaf Cells: II. Uptake and Incorporation of Protein and Ribonucleic Acid Precursors by Tobacco Cells. Plant Physiol. 1971 Jul;48(1):14–18. doi: 10.1104/pp.48.1.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Haderlie L. C., Widholm J. M., Slife F. W. Effect of glyphosate on carrot and tobacco cells. Plant Physiol. 1977 Jul;60(1):40–43. doi: 10.1104/pp.60.1.40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Humble G. D., Raschke K. Stomatal opening quantitatively related to potassium transport: evidence from electron probe analysis. Plant Physiol. 1971 Oct;48(4):447–453. doi: 10.1104/pp.48.4.447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Jensen R. G., Francki R. I., Zaitlin M. Metabolism of separated leaf cells: I. Preparation of photosynthetically active cells from tobacco. Plant Physiol. 1971 Jul;48(1):9–13. doi: 10.1104/pp.48.1.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Leonard R. T., Hotchkiss C. W. Cation-stimulated Adenosine Triphosphatase Activity and Cation Transport in Corn Roots. Plant Physiol. 1976 Sep;58(3):331–335. doi: 10.1104/pp.58.3.331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Moreland D. E., Hussey G. G., Shriner C. R., Farmer F. S. Adenosine Phosphates in Germinating Radish (Raphanus sativus L.) Seeds. Plant Physiol. 1974 Oct;54(4):560–563. doi: 10.1104/pp.54.4.560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Roisch U., Lingens F. Effect of the herbicide N-phosphonomethylglycine on the biosynthesis of aromatic amino acids. Angew Chem Int Ed Engl. 1974 Jun;13(6):400–400. doi: 10.1002/anie.197404001. [DOI] [PubMed] [Google Scholar]
  8. SKOU J. C. Preparation from mammallian brain and kidney of the enzyme system involved in active transport of Na ions and K ions. Biochim Biophys Acta. 1962 Apr 9;58:314–325. doi: 10.1016/0006-3002(62)91015-6. [DOI] [PubMed] [Google Scholar]
  9. Scholander P. F., Bradstreet E. D., Hemmingsen E. A., Hammel H. T. Sap Pressure in Vascular Plants: Negative hydrostatic pressure can be measured in plants. Science. 1965 Apr 16;148(3668):339–346. doi: 10.1126/science.148.3668.339. [DOI] [PubMed] [Google Scholar]
  10. de la Roche A. I. Increase in linolenic Acid is not a prerequisite for development of freezing tolerance in wheat. Plant Physiol. 1979 Jan;63(1):5–8. doi: 10.1104/pp.63.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]

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