Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1975 Apr;55(4):757–762. doi: 10.1104/pp.55.4.757

The Nature of Spontaneous Changes in Growth Rate in Isolated Coleoptile Segments 1

Michael L Evans a, Mark R Schmitt a,2
PMCID: PMC541701  PMID: 16659162

Abstract

About 4 hours after they are cut from the seedling, corn (Zea mays L.) coleoptile segments mounted vertically show a strong increase in growth rate. This increase occurs in water or various buffers near pH 7 and is not accompanied by the accumulation of a growth promoter in the medium. The increase in growth rate is prevented by 1 mmp-fluorophenylalanine and is strongly inhibited by 0.1 mmp-chlorophenoxyisobutyric acid.

The increased growth rate is accompanied by a 95% increase in the ability of tissue extracts to catalyze the conversion of 14C-tryptophan to 14C-indole-3-acetic acid and by a nearly 3-fold increase in indole-3-acetic acid oxidase activity. The increase in growth rate is also observed in segments from coleoptiles grown aseptically.

The spontaneous increase in growth rate is completely but reversibly inhibited by 1 μm indole-3-acetic acid. Cytokinins have little effect on the spontaneous growth response, whereas gibberellic acid is observed to extend the latent period and reduce the magnitude of the response. It is tentatively concluded that the increase in endogenous growth rate may result from increased auxin production upon derepression of the auxin biosynthesis pathway after isolating the tissue from the normal supply of auxin from the tip.

Full text

PDF
757

Selected References

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

  1. Black R. C., Hamilton R. H. Indoleacetic Acid biosynthesis in Avena coleoptile tips and excised bean shoots. Plant Physiol. 1971 Nov;48(5):603–606. doi: 10.1104/pp.48.5.603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. CLARKE A. J., MANN P. J. The oxidation of tryptamine to 3-indolylacetaldehyde by plant amine oxidase. Biochem J. 1957 Apr;65(4):763–774. doi: 10.1042/bj0650763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cheng T. Y. Induction of indoleacetic Acid synthetases in tobacco pith explants. Plant Physiol. 1972 Dec;50(6):723–727. doi: 10.1104/pp.50.6.723. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ecklund P. R., Moore T. C. Correlations of Growth Rate and De-etiolation with Rate of Ent-Kaurene Biosynthesis in Pea (Pisum sativum L.). Plant Physiol. 1974 Jan;53(1):5–10. doi: 10.1104/pp.53.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Evans M. L. Promotion of cell elongation in Avena coleoptiles by acetylcholine. Plant Physiol. 1972 Sep;50(3):414–416. doi: 10.1104/pp.50.3.414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Evans M. L., Ray P. M. Timing of the auxin response in coleoptiles and its implications regarding auxin action. J Gen Physiol. 1969 Jan;53(1):1–20. doi: 10.1085/jgp.53.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. HINMAN R. L., BAUMAN C., LANG J. The conversion of indole-3-acetic acid to 3-methyleneoxindole in the presence of peroxidase. Biochem Biophys Res Commun. 1961 Jul 26;5:250–254. doi: 10.1016/0006-291x(61)90156-5. [DOI] [PubMed] [Google Scholar]
  8. Hecht S. M., Bock R. M., Schmitz R. Y., Skoog F., Leonard N. J. Cytokinins: development of a potent antagonist. Proc Natl Acad Sci U S A. 1971 Oct;68(10):2608–2610. doi: 10.1073/pnas.68.10.2608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hopkins W. G., Bonnell K. F. Avena coleoptile elongation: stimulation by fluorophenylalanine. Plant Physiol. 1969 Feb;44(2):281–286. doi: 10.1104/pp.44.2.281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jordan W. R., Skoog F. Effects of cytokinins on growth and auxin in coleoptiles of derooted Avena seedlings. Plant Physiol. 1971 Jul;48(1):97–99. doi: 10.1104/pp.48.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lantican B. P., Muir R. M. Isolation and properties of the enzyme system forming indoleacetic Acid. Plant Physiol. 1967 Aug;42(8):1158–1160. doi: 10.1104/pp.42.8.1158. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Lee T. T. Promotion of indoleacetic Acid oxidase isoenzymes in tobacco callus cultures by indoleacetic Acid. Plant Physiol. 1971 Jul;48(1):56–59. doi: 10.1104/pp.48.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mills V. M., Todd G. W. Effects of water stress on the indoleacetic Acid oxidase activity in wheat leaves. Plant Physiol. 1973 Jun;51(6):1145–1146. doi: 10.1104/pp.51.6.1145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Noodén L. D., Thimann K. V. Action of inhibitors of RNA and protein synthesis on cell enlargement. Plant Physiol. 1966 Jan;41(1):157–164. doi: 10.1104/pp.41.1.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. RAY P. M. The destruction of indoleacetic acid. II. Spectrophotometric study of the enzymatic reaction. Arch Biochem Biophys. 1956 Sep;64(1):193–216. doi: 10.1016/0003-9861(56)90254-5. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES