Hostname: page-component-788cddb947-55tpx Total loading time: 0 Render date: 2024-10-19T08:19:25.722Z Has data issue: false hasContentIssue false

Reversal of Fluridone-Reduced Chlorophyll Accumulation in Cucumber (Cucumus sativus) Cotyledons by Stimulatory Compounds

Published online by Cambridge University Press:  12 June 2017

Ronald A. Fletcher
Affiliation:
Dep. Environmental Biol., Univ. of Guelph, Guelph, Ontario, Canada N1G 2W1
Sarma V. Meru
Affiliation:
Dep. Environmental Biol., Univ. of Guelph, Guelph, Ontario, Canada N1G 2W1
Satindra N. Bhardwaj
Affiliation:
Div. Plant Physiol., Indian Agric. Res. Instit., New Delhi 110012, India

Abstract

Pretreatment of etiolated cucumber cotyledons with potassium (K), benzyladenine (BA), or δ-aminolevulinic acid (ALA) for 20 h in the dark, followed by exposure to light for 24 h, increased chlorophyll and carotenoid content. A similar treatment with fluridone {1-methyl-3-phenyl-5-[3-(trifluoromethyl)phenyl]-4(1H)-pyridinone} decreased the levels of these photosynthetic pigments. However, when the etiolated cotyledons were pretreated with either BA or ALA for 20 h in the dark, followed by fluridone during a 24-h light period, the inhibitory effects of fluridone on chlorophyll content were reversed and the values were higher than the controls. In these treatments, ALA did not counteract the inhibitory effects of fluridone on carotenoids, but BA reduced the effects. In the cucumber cotyledon greening system, K was found to be most effective in stimulating both chlorophyll and carotenoid accumulation. When K was administered to the cotyledons either together with, prior to, or after the fluridone treatment, the inhibitory effect of fluridone on chlorophyll accumulation was totally eliminated and the stimulatory effects due to K were still maintained. Although K increased carotenoid content, it did not reverse the inhibitory effect of fluridone on carotenoids. From these findings it is concluded that the inhibition of chlorophyll and carotenoid accumulation by fluridone may be mediated via unrelated mechanisms at fluridone concentrations that do not totally eliminate or drastically reduce carotenoid content.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1984 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. Bartels, P. G. and Watson, C. W. 1978. Inhibition of carotenoid synthesis by fluridone and norflurazone. Weed Sci. 26:198203.Google Scholar
2. Britton, G. 1979. Carotenoid biosynthesis–A target for herbicide activity. Z. Naturforsch. 34C:979985.CrossRefGoogle Scholar
3. Castelfranco, P. A. 1983. Chlorophyll biosynthesis: Recent advances and areas of current interest. Annu. Rev. Plant Physiol. 34:241278.CrossRefGoogle Scholar
4. Devlin, R. M., Saras, C. N., Kisiel, M. J., and Kostusiak, A. S. 1978. Influence of fluridone on chlorophyll content of wheat (Triticum aestivum) and corn (Zea mays). Weed Sci. 26:432433.CrossRefGoogle Scholar
5. Drexler, D. M. and Fletcher, R. A. 1981. Inhibition of photosynthetic pigments in cucumber cotyledons as a principle for a bioassay with fluridone. Weed Res. 21:7176.Google Scholar
6. Fletcher, R. A. and McCullagh, D. 1971. Cytokinin-induced chlorophyll formation in cucumber cotyledons. Planta 101:8890.Google Scholar
7. Fletcher, R. A., Teo, C., and Ali, A. 1973. Stimulation of chlorophyll synthesis in cucumber cotyledons by benzyladenine. 51:937939.Google Scholar
8. Fletcher, R. A., Kallidumbil, V., and Steele, P. 1982. An improved bioassay for cytokinins using cucumber cotyledons. Plant Physiol. 69:675677.CrossRefGoogle ScholarPubMed
9. Fletcher, R. A., Venkatarayappa, T., and Kallidumbil, V. 1983. Comparative effects of abscisic acid and methyl jasmonate in greening cucumber cotyledons and its application to a bioassay for abscisic acid. Plant Cell Physiol. 24:10571064.Google Scholar
10. Green, J. F. and Muir, R. M. 1978. The effect of potassium on cotyledon expansion induced by cytokinins. Physiol. Plant. 43:213218.Google Scholar
11. Kirk, J. T. O. and Allen, R. L. 1965. Dependence of chloroplast pigment synthesis on protein synthesis: effect of actidione. Biochem. Biophys. Res. Commun. 21:523530.Google Scholar
12. Kirk, J. T. O. 1968. Studies on the dependence of chlorophyll synthesis on protein synthesis in Euglena gracillis, together with a nomogram for determination of chlorophyll concentration. Planta 78:200207.Google Scholar
13. Kunert, K. J. and Boger, P. 1979. Influence of bleaching herbicides on chlorophyll and carotenoids. Z. Naturforsch. 34C: 10471051.CrossRefGoogle Scholar
14. Moreland, D. E. 1980. Mechanism of action of herbicides. Annu. Rev. Plant Physiol. 31:597638.Google Scholar
15. Rafii, Z. E., Ashton, F. M., and Glenn, R. K. 1979. Metabolic sites of action of fluridone in isolated mesophyll cells. Weed Sci. 27:422426.Google Scholar
16. Rudiger, W. and Benz, J. 1979. Influence of aminotriazol on the biosynthesis of chlorophyll and phytol. Z. Naturforsch. 34C:10551057.CrossRefGoogle Scholar
17. Weinberg, M. B. and Castelfranco, P. A. 1975. Effect of EPTC on plastid membrane constituents in germinating cucumber cotyledons. Weed Sci. 3:185187.Google Scholar