Conversion of D-hamamelose into 2-carboxy-D-arabinitol and 2-carboxy-D-arabinitol 1-phosphate in leaves of Phaseolus vulgaris L.

CA --> CA1P. -->
Substance Nomenclature: 0 (2-carboxyarabinitol)
0 (Anions)
0 (Carbon Radioisotopes)
0 (Hexoses)
0 (Pentosephosphates)
0 (Sugar Alcohols)
106777-19-9 (2-carboxyarabinitol 1-phosphate)
3107IMR9FU (hamamelose)
Entry Date(s): Date Created: 19961025 Date Completed: 19961216 Latest Revision: 20210210
Update Code: 20231215
DOI: 10.1074/jbc.271.43.26803
PMID: 8900161
Autor: Andralojc PJ; Department of Biochemistry and Physiology, IACR-Rothamsted, Harpenden, Hertfordshire AL5 2JQ, United Kingdom., Keys AJ, Martindale W, Dawson GW, Parry MA
Jazyk: angličtina
Zdroj: The Journal of biological chemistry [J Biol Chem] 1996 Oct 25; Vol. 271 (43), pp. 26803-9.
DOI: 10.1074/jbc.271.43.26803
Abstrakt: [1-14C]Hamamelose (2-hydroxymethyl-D-ribose) was synthesized by reaction of ribulose 5-phosphate with potassium [14C]cyanide, catalytic hydrogenation of the resulting cyanohydrin, and dephosphorylation of the product. Its identity was established by a chromatographic comparison with hamamelose isolated from the bark of witch hazel (Hamamelis virginiana L.). Following vacuum infiltration of the [1-14C]hamamelose into leaf discs from Phaseolus vulgaris L., 14C-labeled 2carboxy-D-arabinitol (CA) and 2-carboxy-D-arabinitol 1-phosphate (CA1P) were formed, in the dark. Conversion of hamamelose to both CA and CA1P in the leaf discs was inhibited by dithiothreitol and sodium fluoride, although at high concentrations of these inhibitors conversion into CA was still evident when conversion into CA1P was totally inhibited. Wheat (Triticum aestivum L.) leaves converted hamamelose into CA without formation of CA1P. Leaves from P. vulgaris contained 68 nmol.g-1 fresh weight of hamamelose in the light and 35 nmol.g-1 fresh weight in the dark. A pathway for the biosynthesis of CA1P from Calvin cycle intermediates is proposed which includes the sequence: hamamelose --> CA --> CA1P.
Databáze: MEDLINE