Abstract
When the esterase substrate α-naphthyl acetate is added to segments from coleoptiles of oat (Avena sativa L., var. Victory) or corn (Zea mays L., Bear hybrid WF 9 × 38) or to roots of lentil (Lens culinaris Med.), it is rapidly taken up and hydrolyzed to α-naphthol and acetic acid. This technique was used to generate intracellular acid and to study the effect of its efflux on growth. With corn coleoptile segments, treatment with α-naphthyl acetate induced more rapid and more prolonged growth than did exposure to external acidic buffers. Dose—response studies of α-naphthyl acetate induction of H+ secretion and growth indicated the existence of a distinct threshold rate of H+ efflux below which growth is not enhanced. The rate of H+ efflux induced by optimal levels of auxin appears to be at or below this threshold level in corn coleoptile tissue. These data indicate that the relationship between external acidification and elongation is not a simple one and that the effectiveness of H+ entering the cell wall may depend on factors not directly correlated with the appearance of H+ in the external medium.
Keywords: auxin, acid growth, cycloheximide, coleoptiles, roots
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- Cleland R. Auxin-induced hydrogen ion excretion from Avena coleoptiles. Proc Natl Acad Sci U S A. 1973 Nov;70(11):3092–3093. doi: 10.1073/pnas.70.11.3092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Evans M. L. A New Sensitive Root Auxanometer: Preliminary Studies of the Interaction of Auxin and Acid pH in the Regulation of Intact Root Elongation. Plant Physiol. 1976 Oct;58(4):599–601. doi: 10.1104/pp.58.4.599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- GOMORI G. Human esterases. J Lab Clin Med. 1953 Sep;42(3):445–453. [PubMed] [Google Scholar]
- Haschke H. P., Lüttge U. Stoichiometric Correlation of Malate Accumulation with Auxin-dependent K-H Exchange and Growth in Avena Coleoptile Segments. Plant Physiol. 1975 Nov;56(5):696–698. doi: 10.1104/pp.56.5.696. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacobs M., Ray P. M. Rapid Auxin-induced Decrease in Free Space pH and Its Relationship to Auxin-induced Growth in Maize and Pea. Plant Physiol. 1976 Aug;58(2):203–209. doi: 10.1104/pp.58.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson K. D., Daniels D., Dowler M. J., Rayle D. L. Activation of Avena coleoptile cell wall glycosidases by hydrogen ions and auxin. Plant Physiol. 1974 Feb;53(2):224–228. doi: 10.1104/pp.53.2.224. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson K. D., Rayle D. L. Enhancement of CO(2) Uptake in Avena Coleoptiles by Fusicoccin. Plant Physiol. 1976 May;57(5):806–811. doi: 10.1104/pp.57.5.806. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poole R. J., Thimann K. V. Uptake of Indole-3-acetic Acid and Indole-3-acetonitrile by Avena Coleoptile Sections. Plant Physiol. 1964 Jan;39(1):98–103. doi: 10.1104/pp.39.1.98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rayle D. L., Cleland R. Control of plant cell enlargement by hydrogen ions. Curr Top Dev Biol. 1977;11:187–214. doi: 10.1016/s0070-2153(08)60746-2. [DOI] [PubMed] [Google Scholar]
- Rayle D. L., Cleland R. Enhancement of wall loosening and elongation by Acid solutions. Plant Physiol. 1970 Aug;46(2):250–253. doi: 10.1104/pp.46.2.250. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vesper M. J., Evans M. L. Time-dependent Changes in the Auxin Sensitivity of Coleoptile Segments: Apparent Sensory Adaptation. Plant Physiol. 1978 Feb;61(2):204–208. doi: 10.1104/pp.61.2.204. [DOI] [PMC free article] [PubMed] [Google Scholar]