Skip to main content
Log in

Comparison of the effects of white light and the growth retardant paclobutrazol on the ethylene production in bean hypocotyls

  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

At a concentration of 17 µmol·L−1, paclobutrazol (PP), a triazole plant growth retardant, effectively reduced the elongation and increased the thickness of hypocotyls in 6-day-old Phaseolus vulgaris L. cv. Juliska seedlings, both in the light and in the dark. PP treatment did not increase the cell number in transverse sections of hypocotyls. The diameter of hypocotyls was uniform from the zone of intensive elongation along the whole hypocotyl in etiolated plants, but those grown in the light exhibited an additional lateral expansion at the base. Ethylene evolution was not reduced by PP in etiolated hypocotyls, and did not differ significantly in the elongating apical and fully grown basal zones. PP reduced the ethylene release by the growing zones in green hypocotyls, but not in the basal parts, which resulted in an increasing ethylene gradient towards the hypocotyl base. The level of 1-aminocyclopropane-1-carboxylic acid (ACC), the immediate precursor of ethylene, was much higher in retardant-treated hypocotyls than in the controls, which was due in part to the reduced malonylation. The swelling of the hypocotyl bases could be eliminated by inhibitors of ethylene biosynthesis or action, or could be induced by 10 µmol·L−1ACC in control plants in the light. None of these treatments had a significant effect on the lateral expansion of hypocotyls in etiolated seedlings. PP treatment induced a similar effect to that of white light in etiolated seedlings, and amplified the effect of light in green plants with respect to the ACC distribution, and consequently, the ethylene production in the hypocotyls of 6-day-old bean seedlings. It can be concluded that the lateral expansion of hypocotyl bases in PP-treated green plants is controlled by ethylene.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Bandurski RS, Schulze A and Cohen DJ (1977) Photoregulation of the ratio of ester to free indole-3-acetic acid. Biochem Biophys Res Commun. 79: 1219–1223

    Google Scholar 

  2. Bernáth J, Tischner T and Ábrányi A (1982) Növénykörnyezet és Szabályozása (Control of Plant Environment, in Hungarian), pp 59. Budapest: Academic Press

    Google Scholar 

  3. Dalziel J and Lawrence DK(1984) Biochemical and biological effects of kaurene oxidase inhibitors, such as paclobutrazol. British Plant Growth Regulator Group Monograph 11: 43–57

    Google Scholar 

  4. Dicks JW (1980) Mode of action of growth retardants. British Plant Growth Regulator Group Monograph 4: 1–14

    Google Scholar 

  5. Eisinger, W (1983) Regulation of pea internode expansion by ethylene. Ann Rev Plant Physiol 34: 225–240

    Google Scholar 

  6. Foster KR, Miller FR, Childs KL and Morgan PW (1994) Genetic regulation of development in Sorghum bicolor. Plant Physiol 105: 941–948

    Google Scholar 

  7. Furuya M, Pyon CJ, Fujii T and Ito M (1969) Phytochrome action in Oryza sativa L. III. The separation of photoperceptive site and the growing zone in coleoptiles, and auxin transport as effector system. Devel Growth Diff 11: 62–76

    Google Scholar 

  8. Goodwin RH and Owens OH (1951) The effectiveness of the spectrum in Avena internode inhibition. Bull Torrey Bot Club 78: 11–21

    Google Scholar 

  9. Graebe J (1987) Gibberellin biosynthesis and control. Annu Rev Plant Physiol 38: 419–465

    Google Scholar 

  10. Grossmann K (1990) Plant growth retardants as tools in physiological research. Physiol Plant 78: 640–648

    Google Scholar 

  11. Grossmann K (1992) Plant growth retardants: Their mode of action and benefit for physiological research. In: CM Karssen, LC Van Loon and D Vreugdenhil (eds) Progress in Plant Growth Regulation, pp 788–797. Dordrecht: Kluwer Academic Publishers

    Google Scholar 

  12. Haughan PA, Burden RS, Lenton JR and Goad LJ (1989) Inhibition of celery cell growth and sterol biosynthesis by the enantiomers of paclobutrazol. Phytochemistry 28: 781–787

    Google Scholar 

  13. Iino M (1982a) Action of red light on IAA status and growth in coleoptiles of etiolated maize seedlings. Planta 156: 21–32

    Google Scholar 

  14. Iino M (1982b) Inhibitory action of red light on the growth of the maize mesocotyl: Evaluation of the auxin hypothesis. Planta 156: 388–395

    Google Scholar 

  15. Kao CH and Yang SF (1982) Light inhibition of the conversion of 1-aminocyclopropane-1-carboxylic acid to ethylene in leaves is mediated through carbon dioxide. Planta 155: 261– 266

    Google Scholar 

  16. Kende H (1993) Ethylene biosynthesis. Annu Rev Plant Physiol Plant Mol Biol 44: 283–307

    Google Scholar 

  17. Kraus TE, Murr DP, Hofstra G and Fletcher RA (1992) Regulation of ethylene synthesis in acotyledonous soybean and wheat seedlings. J Plant Growth Regul 11: 47–53

    Google Scholar 

  18. Lizada MCC and Yang SF (1979) A simple and sensitive assay for 1-aminocyclopropane-1-carboxylic acid. Anal Biochem 100: 140–146

    Google Scholar 

  19. Nagy M and Tari I (1987) Gibberellin and auxin contents and ethylene production in hypocotyls of green and etiolated bean plants treated with chlorocholine chloride. Biol Plant 29: 28– 33

    Google Scholar 

  20. Nagy M, Tari I and Bubán T (1991) IAA distribution in the hypocotyls and primary leaves of Phaseolus vulgaris L. treated with paclobutrazol in relation to their rooting capacity. Biochem Physiol Pflanzen 187: 447–451

    Google Scholar 

  21. Osborne DJ (1982) The ethylene regulation of cell growth in specific target tissues of plants. In: PF Wareing (ed) Plant Growth Substances, pp 279–290. London: Academic Press

    Google Scholar 

  22. Rademacher W (1991) Inhibitors of gibberellin biosynthesis: Applications in agriculture and horticulture. In: N Takahashi, BO Phinney and J MacMillan (eds) Gibberellins, pp 296–310. New York: Springer-Verlag

    Google Scholar 

  23. Ross JJ, Willis CL, Gaskin P and Reid JB (1992) Shoot elongation in Lathyrus elongatus L.: gibberellin levels in light and dark-grown tall and dwarf seedlings. Planta 187: 10–13

    Google Scholar 

  24. Snedecor GW and Cohran WG (1956) Statistical Methods 5th ed., pp 237–254. Ames, IA: Iowa State Univ. Press

    Google Scholar 

  25. Tari I and Nagy M (1994) Enhancement of extractable ethylene at light/dark transition in primary leaves of paclobutrazol-treated Phaseolus vulgaris seedlings. Physiol Plant 90: 353– 357

    Google Scholar 

  26. Zacarías L, Tudela D and Primo-Millo E (1990) Stimulation of ACC-dependent ethylene production in citrus leaf discs by light. Physiol Plant 80: 89–94

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tari, I., Mihalik, E. Comparison of the effects of white light and the growth retardant paclobutrazol on the ethylene production in bean hypocotyls. Plant Growth Regulation 24, 67–72 (1998). https://doi.org/10.1023/A:1005902515559

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1005902515559

Navigation