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-...

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Main Authors: Rao, D, Yoshihara, A, Gullapalli, P, Morinioto, K, Takata, G, da Cruz, F, Jenkinson, S, Wormald, M, Dwek, R, Fleet, G, Izumori, K
格式: Journal article
语言:English
出版: 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.
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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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