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
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-...
Main Authors: | , , , , , , , , , , |
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格式: | Journal article |
语言: | English |
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2008
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author | Rao, D Yoshihara, A Gullapalli, P Morinioto, K Takata, G da Cruz, F Jenkinson, S Wormald, M Dwek, R Fleet, G Izumori, K |
author_facet | Rao, D Yoshihara, A Gullapalli, P Morinioto, K Takata, G da Cruz, F Jenkinson, S Wormald, M Dwek, R Fleet, G Izumori, K |
author_sort | Rao, D |
collection | OXFORD |
description | 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. © 2008 Elsevier Ltd. All rights reserved. |
first_indexed | 2024-03-06T18:55:46Z |
format | Journal article |
id | oxford-uuid:11c87647-8f07-4ab2-86fa-db44dba23e50 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-06T18:55:46Z |
publishDate | 2008 |
record_format | dspace |
spelling | oxford-uuid:11c87647-8f07-4ab2-86fa-db44dba23e502022-03-26T10:04:09ZTowards 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-xyluloseJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:11c87647-8f07-4ab2-86fa-db44dba23e50EnglishSymplectic Elements at Oxford2008Rao, DYoshihara, AGullapalli, PMorinioto, KTakata, Gda Cruz, FJenkinson, SWormald, MDwek, RFleet, GIzumori, KMicrobial 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. © 2008 Elsevier Ltd. All rights reserved. |
spellingShingle | Rao, D Yoshihara, A Gullapalli, P Morinioto, K Takata, G da Cruz, F Jenkinson, S Wormald, M Dwek, R Fleet, G Izumori, K 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 |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
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