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Synthesis of Specially Designed Probes to Broaden Transketolase Scope.

Authors :
Simon, G.
Eljezi, T.
Legeret, B.
Charmantray, F.
Castillo, J. A.
Guérard‐Hélaine, C.
Lemaire, M.
Bouzon, M.
Marlière, P.
Hélaine, V.
Hecquet, L.
Source :
ChemCatChem; Mar2013, Vol. 5 Issue 3, p784-795, 12p
Publication Year :
2013

Abstract

Efficient, biocompatible, stereospecific strategies were developed to prepare eight probes to assay transketolase (TK) variants with new substrate specificities. The structure of these probes combines a sugar moiety ( D- threo or L- erythro ketose, or D- threo aldose) with the side chain of an amino acid (Ala, Leu, Val, Met, Thr) for in vivo detection of new TK activities using amino acid auxotrophs. To obtain D- threo ketose probes, biocatalysts, such as transketolase and fructose-6-phosphate aldolase Ala129Ser, were used whereas L- erythro ketoses and D- threo aldose probes were synthesized by the way of organocatalysis or Sharpless dihydroxylation as sustainable alternative key steps to biocatalysis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18673880
Volume :
5
Issue :
3
Database :
Complementary Index
Journal :
ChemCatChem
Publication Type :
Academic Journal
Accession number :
85713810
Full Text :
https://doi.org/10.1002/cctc.201200479