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Role of IAA conjugates in inducing ethylene production by tobacco leaf discs

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Abstract

Indole-3-acetic acid (IAA) labeled in its carboxyl group was metabolized by tobacco leaf discs (Nicotiana tabacum L. cv. Xanthi) into three metabolites, two of which were preliminarily characterized as a peptide and an ester-conjugated IAA. Reapplication of each of the three metabolites (at 10 μM) resulted in a marked stimulation of ethylene production and decarboxylation by the leaf discs. Similarly, these three IAA metab olites could induce elongation of wheat coleoptile segments, which was accompanied by decarboxylation. Both the exogenously supplied esteric and peptidic IAA conjugates were converted by the leaf discs into the same metabolites as free IAA. (1-14C)IAA, applied to an isolated epidermis tissue, was completely metabolized to the esteric and peptidic IAA conjugates. This epidermis tissue showed much higher ethylene production rates and lower decarboxylation rates than did the whole leaf disc.

The results suggest that the participation of IAA conjugates in the regulation of various physiological processes depends on the release of free IAA, which is obtained by enzymatic hydrolysis of the conjugates in the tissue. The present study demonstrates biological activity of endogenous IAA conjugates that were synthesized by tobacco leaf discs in response to exogenously supplied IAA.

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References

  • Abdul-Baki AA (1974) Pitfalls in using sodium hypochlorite as a seed disinfectant in14C incorporation studies. Plant Physiol 53:768–771

    PubMed  CAS  Google Scholar 

  • Abeles FB (1973) Ethylene in plant biology. Academic Press, New York.

    Google Scholar 

  • Aharoni N, Lieberman M, Sisler HD (1979) Patterns of ethylene production in senescing leaves. Plant Physiol 64:796–800

    PubMed  CAS  Google Scholar 

  • Aharoni N, Yang SF (1983) Auxin-induced ethylene production as related to auxin metabolism in leaf discs of tobacco and sugar beet. Plant Physiol 73:598–604

    PubMed  CAS  Google Scholar 

  • Andreae WA, Good NE (1955) The formation of indoleacetylaspartic acid in pea seedlings. Plant Physiol 30:380–382

    PubMed  CAS  Google Scholar 

  • Andreae WA, Van Ysselstein MW (1960) Studies on 3-indoleacetic acid metabolism. I. Effect of calcium ions on IAA uptake and metabolism by pea roots. Plant Physiol 35:220–224

    PubMed  CAS  Google Scholar 

  • Bandurski RS, Schulze A (1977) Concentration of indole-3-acetic acid and its derivatives in plants. Plant Physiol 60:211–213.

    PubMed  CAS  Google Scholar 

  • Bandurski RS, Schulze A, Cohen JD (1977) Photo-regulation of the ratio of ester to free indole-— acetic acid. Biochem Biophys Res Commun 79:1219–1223

    Article  PubMed  CAS  Google Scholar 

  • Cohen JD, Bandurski RS (1978) The bound auxins: Protection of indole-3-acetic acid from peroxidase-catalyzed oxidation. Planta 139:203–208

    Article  CAS  Google Scholar 

  • Ehmann A (1977) The Van Urk-Salkowski reagent—a sensitive and specific chromogenic reagent for silica gel thin-layer chromatographic detection and identification of indole derivatives. J Chromatogr 132:267–276

    Article  PubMed  CAS  Google Scholar 

  • Epstein E, Cohen JD, Bandurski RS (1980) Concentration and metabolic turnover of indoles in germinating kernels ofZea mays L. Plant Physiol 65:415–421

    PubMed  CAS  Google Scholar 

  • Feung CS, Hamilton RH, Mumma RO (1977) Metabolism of indole-3-acetic acid. IV. Biological properties of amino acid conjugates. Plant Physiol 59:91–93

    PubMed  CAS  Google Scholar 

  • Hangarter RP, Good NE (1981) Evidence that IAA conjugates are slow-release sources of free IAA in plant tissues. Plant Physiol 68:1424–1427

    PubMed  CAS  Google Scholar 

  • Hangarter RP, Peterson MD, Good NE (1980) Biological activities of indoleacetylamino acids and their use as auxins in tissue culture. Plant Physiol 65:761–767

    PubMed  CAS  Google Scholar 

  • Imaseki H, Kondo K, Watanabe A (1975) Mechanism of cytokinin action and auxin-induced ethylene production. Plant Cell Physiol 16:777–787

    CAS  Google Scholar 

  • Kang BO, Newcomb W, Burg SP (1971) Mechanism of auxin-induced ethylene production. Plant Physiol 47:504–509

    Article  PubMed  CAS  Google Scholar 

  • Lau OL, Yang SF (1973) Mechanism of a synergistic effect of kinetin on auxin-induced ethylene production. Plant Physiol 51:1011–1014

    PubMed  CAS  Google Scholar 

  • Lieberman M (1979) Biosynthesis and action of ethylene. Annu Rev Plant Physiol 30:533–591

    Article  CAS  Google Scholar 

  • Liu ST, Gruenert D, Knight CA (1978) Bound form indole-3-acetic acid synthesis in tumorous and non-tumorous species ofNicotiana. Plant Physiol 61:50–53

    PubMed  CAS  Google Scholar 

  • Nitsch JP, Nitsch C (1956) Studies on the growth of coleoptile and first internode sections. A new, sensitive, straight-growth test for auxins. Plant Physiol 31:94–111

    Article  PubMed  CAS  Google Scholar 

  • Reinecke DM, Bandurski RS (1981) Metabolic conversion of14C-indole-3-acetic acid to14C-oxindole-3-acetic acid. Biochem Biophys Res Commun 103:429–433

    Article  PubMed  CAS  Google Scholar 

  • Sakai S, Imaseki H (1973) Properties of the proteinaceous inhibitor of ethylene synthesis: Action on ethylene production and indoleacetyl aspartate formation. Plant Cell Physiol 14:881–892

    CAS  Google Scholar 

  • Yang SF, Adams DO, Lizada C, Yu YB, Bradford KJ, Cameron AC, Hoffman NE (1980) Mechanism and regulation of ethylene biosynthesis. In: Skoog F (ed) Plant growth substances 1979. Springer-Verlag, Berlin, pp 219–229

    Google Scholar 

  • Young RE, Pratt HK, Biale JB (1952) Manometric determination of low concentration of ethylene. Anal Chem 24:551–555

    Article  CAS  Google Scholar 

  • Yu YB, Adams DO, Yang SF (1979) Regulation of auxin-induced ethylene production in mung bean hypocotyls: Role of 1-aminocyclopropane-1-carboxylic acid. Plant Physiol 63:589–590

    PubMed  CAS  Google Scholar 

  • Yu YB, Yang SF (1979) Auxin-induced ethylene production and its inhibition by aminoethoxyvinylglycine and cobalt ion. Plant Physiol 64:1074–1077

    Article  PubMed  CAS  Google Scholar 

  • Zenk MH (1964) Isolation, biosynthesis and function of indoleacetic acid conjugates. In: Regulateurs naturels de la croissance vègètable. Fifth International Conference on Plant Growth Substances. Centre Nationale de la Recherche Scientifique, Paris, pp 241–249

    Google Scholar 

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Contribution No. 952-E, 1983 series, from the Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel.

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Meir, S., Philosoph-Hadas, S. & Aharoni, N. Role of IAA conjugates in inducing ethylene production by tobacco leaf discs. J Plant Growth Regul 3, 169–181 (1984). https://doi.org/10.1007/BF02042001

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  • DOI: https://doi.org/10.1007/BF02042001

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