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Metabolism of [14C]indole-3-acetic acid by the cortical and stelar tissues of Zea mays L. roots

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Abstract

Reverse-phase high-performance liquid chromatography was used to analyse 14C-labelled metabolites of indole-3-acetic acid (IAA) formed in the cortical and stelar tissues of Zea mays roots. After a 2-h incubation in [14C]IAA, stelar segments had metabolised between 1–6% of the methanol-extractable radioactivity compared with 91–92% by the cortical segments. The pattern of metabolites produced by cortical segments was similar to that produced by intact segments bathed in aqueous solutions of [14C]IAA. In contrast, when IAA was supplied in agar blocks to stelar tissue protruding from the basal ends of segments, negligible metabolism was evident. On the basis of its retention characteristics both before and after methylation, the major metabolite of [14C]IAA in Zea mays root segments was tentatively identified by high-performance liquid chromatography as oxindole-3-acetic acid.

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Abbreviations

HPLC:

High-performance liquid chromatography

IAA:

Indole-3-acetic acid

References

  • Bowen, M.R., Wilkins, M.B., Cane, A.R., McCorquodale, I. (1972) Auxin transport in roots. VIII. The distribution of radioactivity in the tissues of Zea root segments. Planta 105, 273–292

    Google Scholar 

  • Bridges, I.G., Hillman, J.R., Wilkins, M.B. (1973) Identification and localisation of auxin in primary roots of Zea mays by mass spectrometry. Planta 115, 189–192

    Google Scholar 

  • Crozier, A., Loferski, K., Zaerr, J.B., Morris, R.O. (1980) Analysis of picogram quantities of indole-3-acetic acid by highperformance liquid chromatography-fluorescence procedures. Planta 150, 366–376

    Google Scholar 

  • Greenwood, M.S., Hillman, J.R., Shaw, S., Wilkins, M.B. (1973) Localisation and identification of auxin in roots of Zea mays. Planta 109, 369–374

    Google Scholar 

  • Hinman, R.L., Bauman, C.P. (1964) Reaction of N-bromosuccinimide and indoles, a simple synthesis of 3-bromo-oxindoles. J. Org. Chem. 29, 1206–1215

    Google Scholar 

  • Klämbt, H.D. (1959) Die 2 Hydroxy-indol-3-essigsäure, ein pflanzliches Indolderivat. Naturwissenschaften 46, 649

    Google Scholar 

  • Nonhebel, H.M., Crozier, A., Hillman, J.R. (1983) Analysis of [14C]-indole-3-acetic acid metabolites from the primary roots of Zea mays seedlings using reverse-phase high-performance liquid chromatography. Physiol. Plant. 57, 129–134

    Google Scholar 

  • Nonhebel, H.M., Hillman, J.R., Crozier, A., Wilkins, M.B. (1985) Metabolism of [14C]indole-3-acetic acid by coleoptiles of Zea mays L. J. Exp. Bot. 36, 99–109

    Google Scholar 

  • Reeve, D.R., Crozier, A. (1977) Radioactivity monitor for highperformance liquid chromatography. J. Chromatogr. 137, 271–282

    Google Scholar 

  • Reinicke, D.M., Bandurski, R.S. (1981) Metabolic conversion of 14C-indole-3-acetic acid to 14C-oxindole-3-actic acid. Biochem. Biophys. Res. Commun. 103, 429–433

    Google Scholar 

  • Reinicke, D.M., Bandurski, R.S. (1983) Oxindole-3-acetic acid, an indole-3-acetic acid catabolite in Zea mays. Plant Physiol. 71, 211–213

    Google Scholar 

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Nonhebel, H.M., Hillman, J.R., Crozier, A. et al. Metabolism of [14C]indole-3-acetic acid by the cortical and stelar tissues of Zea mays L. roots. Planta 164, 105–108 (1985). https://doi.org/10.1007/BF00391033

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  • DOI: https://doi.org/10.1007/BF00391033

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