Title of article :
Towards the biotechnological isomerization of branched sugars: d-tagatose-3-epimerase equilibrates both enantiomers of 4-C-methyl-ribulose with both enantiomers of 4-C-methyl-xylulose
Author/Authors :
Rao، نويسنده , , Devendar and Yoshihara، نويسنده , , Akihide and Gullapalli، نويسنده , , Pushpakiran and Morimoto، نويسنده , , Kenji and Takata، نويسنده , , Goro and da Cruz، نويسنده , , Filipa P. and Jenkinson، نويسنده , , Sarah F. and Wormald، نويسنده , , Mark R. and Dwek، نويسنده , , Raymond A. and Fleet، نويسنده , , George W.J. and Izumori، نويسنده , , Ken، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2008
Pages :
6
From page :
3316
To page :
3321
Abstract :
Microbial oxidation of 2-C-methyl-d-ribitol and 2-C-methyl-d-arabinitol by Gluconobacter thailandicus NBRC 3254 produces 4-C-methyl-l-ribulose and 4-C-methyl-d-ribulose, respectively. Further, 4-C-methyl-l-ribulose and 4-C-methyl-d-ribulose were equilibrated by d-tagatose-3-epimerase (DTE) with 4-C-methyl-l-xylulose and 4-C-methyl-d-xylulose, respectively. These transformations demonstrate that polyol dehydrogenase and DTE act on branched synthetic sugars. The green preparation of all of the stereoisomers of 4-C-methyl pentuloses illustrates the ability of biotechnology to generate novel branched monosaccharides.
Journal title :
Tetrahedron Letters
Serial Year :
2008
Journal title :
Tetrahedron Letters
Record number :
1859262
Link To Document :
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