Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1990 Dec;94(4):1598–1604. doi: 10.1104/pp.94.4.1598

Partial Purification and Characterization of Indol-3-Ylacetylglucosemyo-Inositol Indol-3-Ylacetyltransferase (Indoleacetic Acid-Inositol Synthase) 1

Jacek Marcin Kesy 1,2, Robert S Bandurski 1
PMCID: PMC1077426  PMID: 11537469

Abstract

A procedure is described for the purification of the enzyme indol-3-ylacetylglucose:myo-inositol indol-3-ylacetyltransferase (IAA-myo-inositol synthase). This enzyme catalyzes the transfer of indol-3-ylacetate from 1-0-indol-3-ylacetyl-β-d-glucose to myo-inositol to form indol-3-ylacetyl-myo-inositol and glucose. A hexokinase or glucose oxidase based assay system is described. The enzyme has been purified approximately 16,000-fold, has an isoelectric point of pH 6.1 and yields three catalytically inactive bands upon acrylamide gel electrophoresis of the native protein. The enzyme shows maximum transferase activity with myo-inositol but shows some transferase activity with scyllo-inositol and myo-inosose-2. No transfer of IAA occurs with myo-inositol-d-galactopyranose, cyclohexanol, mannitol, or glycerol as acyl acceptor. The affinity of the enzyme for 1-0-indol-3-ylacetyl-β-d-glucose is, Km = 30 micromolar, and for myo-inositol is, Km = 4 millimolar. The enzyme does not catalyze the exchange incorporation of glucose into IAA-glucose indicating the reaction mechanism involves binding of IAA glucose to the enzyme with subsequent hydrolytic cleavage of the acyl moiety by the hydroxyl of myo-inositol to form IAA myo-inositol ester.

Full text

PDF
1600

Images in this article

Selected References

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

  1. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  2. Chisnell J. R., Bandurski R. S. Translocation of radiolabeled indole-3-acetic acid and indole-3-acetyl-myo-inositol from kernel to shoot of Zea mays L. Plant Physiol. 1988;86:79–84. doi: 10.1104/pp.86.1.79. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Corcuera L. J., Bandurski R. S. Biosynthesis of Indol-3-yl-acetyl-myo-inositol Arabinoside in Kernels of Zea mays L. Plant Physiol. 1982 Dec;70(6):1664–1666. doi: 10.1104/pp.70.6.1664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Corcuera L. J., Michalczuk L., Bandurski R. S. Enzymic synthesis of indol-3-ylacetyl-myo-inositol galactoside. Biochem J. 1982 Nov 1;207(2):283–290. doi: 10.1042/bj2070283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Corcuera L. J., Michalczuk L., Bandurski R. S. Enzymic synthesis of indol-3-ylacetyl-myo-inositol galactoside. Biochem J. 1982 Nov 1;207(2):283–290. doi: 10.1042/bj2070283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Domagalski W., Schulze A., Bandurski R. S. Isolation and characterization of esters of indole-3-acetic acid from the liquid endosperm of the horse chestnut (Aesculus species). Plant Physiol. 1987;84:1107–1113. doi: 10.1104/pp.84.4.1107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ehmann A. Identification of 2-O (indole-3-acetyl)-D-glucopyranose, 4-O-(indole-3-acetyl)-D-glucopyranose and 6-O-(indole-3-acetyl)-D-glucopyranose from kernels of Zea mays by gas-liquid chromatography-mass spectrometry. Carbohydr Res. 1974 May;34(1):99–114. doi: 10.1016/s0008-6215(00)80374-2. [DOI] [PubMed] [Google Scholar]
  8. Ehmann A. 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. 1977 Feb 11;132(2):267–276. doi: 10.1016/s0021-9673(00)89300-0. [DOI] [PubMed] [Google Scholar]
  9. Epstein E., Cohen J. D., Bandurski R. S. Concentration and Metabolic Turnover of Indoles in Germinating Kernels of Zea mays L. Plant Physiol. 1980 Mar;65(3):415–421. doi: 10.1104/pp.65.3.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hall P. J., Bandurski R. S. [3H]Indole-3-acetyl-myo-inositol hydrolysis by extracts of Zea mays L. vegetative tissue. Plant Physiol. 1986;80:374–377. doi: 10.1104/pp.80.2.374. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Keglević D., Pokorny M. The chemical synthesis of 1-O-(indol-3'-ylacetyl)-beta-D-glucopyranose. The higher activity of the glucoside in comparison with exogenous indol-3-ylacetic acid in plant-section elongation tests. Biochem J. 1969 Oct;114(4):827–832. doi: 10.1042/bj1140827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Keglević D. Synthesis of 1-O-(indol-3-ylacetyl)- -D-glucopyranose and its rearrangement into 2-O-(indol-3-ylacetyl)-D-glucopyranose. Carbohydr Res. 1971 Dec;20(2):293–298. doi: 10.1016/s0008-6215(00)81383-x. [DOI] [PubMed] [Google Scholar]
  13. Komoszynski M., Bandurski R. S. Transport and metabolism of indole-3-acetyl-myo-inositol-galactoside in seedlings of Zea mays. Plant Physiol. 1986;80:961–964. doi: 10.1104/pp.80.4.961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kopcewicz J., Ehmann A., Bandurski R. S. Enzymatic Esterification of Indole-3-acetic Acid to myo-Inositol and Glucose. Plant Physiol. 1974 Dec;54(6):846–851. doi: 10.1104/pp.54.6.846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kowalczyk S., Bandurski R. S. Isomerization of 1-O-indol-3-ylacetyl-beta-D-glucose. Enzymatic hydrolysis of 1-O, 4-O, and 6-O-indol-3-ylacetyl-beta-D-glucose and the enzymatic synthesis of indole-3-acetyl glycerol by a hormone metabolizing complex. Plant Physiol. 1990;94:4–12. doi: 10.1104/pp.94.1.4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Labarca C., Nicholls P. B., Bandurski R. S. A partial characterization of indoleacetylinositols from ZEA mays. Biochem Biophys Res Commun. 1965 Sep 8;20(5):641–646. doi: 10.1016/0006-291x(65)90448-1. [DOI] [PubMed] [Google Scholar]
  17. Leznicki A. J., Bandurski R. S. Enzymic synthesis of indole-3-acetyl-1-O-beta-d-glucose. I. Partial purification and characterization of the enzyme from Zea mays. Plant Physiol. 1988;88:1474–1480. doi: 10.1104/pp.88.4.1474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Leznicki A. J., Bandurski R. S. Enzymic synthesis of indole-3-acetyl-1-O-beta-d-glucose. II. Metabolic characteristics of the enzyme. Plant Physiol. 1988;88:1481–1485. doi: 10.1104/pp.88.4.1481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nowacki J., Bandurski R. S. Myo-Inositol Esters of Indole-3-acetic Acid as Seed Auxin Precursors of Zea mays L. Plant Physiol. 1980 Mar;65(3):422–427. doi: 10.1104/pp.65.3.422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Ogita Z. I., Markert C. L. A miniaturized system for electrophoresis on polyacrylamide gels. Anal Biochem. 1979 Nov 1;99(2):233–241. doi: 10.1016/s0003-2697(79)80001-9. [DOI] [PubMed] [Google Scholar]
  21. Piskornik Z., Bandurski R. S. Purification and Partial Characterization of a Glucan Containing Indole-3-acetic Acid. Plant Physiol. 1972 Jul;50(1):176–182. doi: 10.1104/pp.50.1.176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Strack D., Gross W. Properties and Activity Changes of Chlorogenic Acid:Glucaric Acid Caffeoyltransferase From Tomato (Lycopersicon esculentum). Plant Physiol. 1990 Jan;92(1):41–47. doi: 10.1104/pp.92.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. ZENK M. H. I-(Indole-3-acetyl)-beta-D-glucose, a new compound in the metabolism of indole-3-acetic acid in plants. Nature. 1961 Jul 29;191:493–494. doi: 10.1038/191493a0. [DOI] [PubMed] [Google Scholar]

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

RESOURCES