PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
1997 | 44 | 2 |

Tytuł artykułu

Transformation of 1-O-[indole-3-acetyl]-beta-D-glucose into di-O-[indole-3-acetyl]-D-glucose catalysed by enzyme preparations from corn seedlings

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
A new enzymatic activity, which catalyses formation in vitro of di-O-(indole-3-acetyl)-D-glucose from 1-O-(indole-3-acetyl)-beta-D-glucose has been found in extracts of Zea mays seedlings. The structure of di-O-(indole-3-acetyl)-D-glucose, not as yet described, has been assigned by GC-MS, 1H NMR and ammonolysis.

Wydawca

-

Rocznik

Tom

44

Numer

2

Opis fizyczny

p.215-220,fig.

Twórcy

  • Nicholas Copernicus University, Gagarina 9, PL-87-100 Torun, Poland
autor
autor

Bibliografia

  • 1. Bandurski, R.S., Desrosies, M.F., Jensen, P., Pawlak, M. & Schulze, A. (1991) Genetics, chemistry, and biochemical physiology in the study of hormonal homeostasis; in Progress in Plant Growth Regulation (Karssen, C.M., van Loon, L.C. & Vreugdenhil, D., eds.) pp. 1-12, Kluwer Academic Pub., Netherlands.
  • 2. Michalczuk, L. & Bandurski, R.S. (1982) En­zymatic synthesis of l-O-indol-3-ylacetyl-D- glucose and indol-3-ylacetyl-myo-inositol. Biochem. J. 207, 273-281.
  • 3. Keglevic, D. & Pokorny, M. (1969) The chemi­cal synthesis of l-0-(indol-3'-ylacetyl)-p-D- glucopyranose. Biochem. J. 114, 827-832.
  • 4. Zenk, M.N. (1961) l-(Indole-3-acetyl)-D-glu- cose, a new compound in the metabolism of indole-3-acetic acid in plants. Nature 191, 493-494.
  • 5. Kowaiczyk, S. & Bandurski, R.S. (1990) Isomerization of l-O-indol-3-ylacetyl-glucose. Enzymatic hydrolysis of l-0,4-0, and 6-O-in- dol-3-ylacetyl-n-glucose and enzymatic syn­thesis of indole-3-acetyl glycerol by hormone metabolizing complex. Plant Physiol. 94, 4-12.
  • 6. Szmidt-rJaworska, A., Kcsy, J. & Bandurski, R.S. (1996) l-0-(Indol-3-ylacetyl)-D-glucopy- ranoside. Plant Physiol. Ill (Suppl.), 115.
  • 7. Ehmann, A. (1977) The Van Urk-Salkowski reagent — a sensitive and specific chromo- genic reagent for silica thin layer chroma­tographic detection and identification of in­dole derivatives. J. Chromatogr. 132, 267-276.
  • 8. Ehmann, A. & Bandurski, R.S. (1972) Purifi­cation of indol-3-acetic acid myo-inositol es­ters on polystyrene-divinylbenzcnc resins. J. Chromatogr. 72, 61-70.
  • 9. Ehmann, A. & Bandurski, R.S. (1974) Identi­fication of 2-0-(indole-3-acetyl)-D-glucose, 4-0-(indole-3-acetyl)-D-glucose, and 6-0-(indo- le-3-acetyl)-D-glucose from kernel of Zea mays by gas-liquid chromatography-mass spectro­metry. Carbohydr. Res. 34, 99-114.
  • 10. Saul, R., Chambers, J.P., Molyneux, R.J. & Elbein, A.D. (1983) Castanospermine, a tetra- hydroxylated alkaloid that inhibits ^-glucosi- dasc and p-glucocerebrosidase. Arch. Blo­chem. Biophys. 221, 593-597.
  • 11. Ehmann, A. & Bandurski, R.S. (1974) The isolation of di-0-(indole-3-acetyl)-myo-inosi- tol and tri-0-(indole-3-acetyl)-myo-inositol from mature kernels of Zea mays. Carbohydr. Res. 36,1-12.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-1934c5b1-17ac-43cd-9672-d39f694bc130
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.