2015
DOI: 10.1039/c5ra14414k
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A new concept for production of (3S,4R)-6-[(benzyloxycarbonyl)amino]-5,6-dideoxyhex-2-ulose, a precursor of d-fagomine

Abstract: A novel cascade reaction for the production of aldol adduct (3S,4R)-6-[(benzyloxycarbonyl)amino]-5,6dideoxyhex-2-ulose was studied in this work. The strategy combines three enzymes in one pot: (i) horse liver alcohol dehydrogenase for the oxidation of N-Cbz-3-aminopropanol to the corresponding aldehyde, (ii) NADH oxidase for the regeneration of coenzyme NAD + and (iii) D-fructose-6-phosphate aldolase from E. coli A129S variant for the aldol addition of dihydroxyacetone to N-Cbz-3aminopropanal. On the basis of … Show more

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Cited by 13 publications
(15 citation statements)
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References 36 publications
(96 reference statements)
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“…In contrast, a vast number of different aldehydes are accepted . Aldehydes are very strong electrophiles, which can undergo different side reactions, such as the irreversible formation of a Schiff base with the free amino group of the lysine in the active site (class I aldolase), overoxidation to the corresponding carboxylic acid in the presence of alcohol dehydrogenases (ADHs), or polymerization . Such obstacles can be overcome by the in situ production of the aldehyde species, which can be converted concomitantly, in the presence of a donor molecule, to the corresponding aldol adduct.…”
Section: Introductionmentioning
confidence: 89%
See 1 more Smart Citation
“…In contrast, a vast number of different aldehydes are accepted . Aldehydes are very strong electrophiles, which can undergo different side reactions, such as the irreversible formation of a Schiff base with the free amino group of the lysine in the active site (class I aldolase), overoxidation to the corresponding carboxylic acid in the presence of alcohol dehydrogenases (ADHs), or polymerization . Such obstacles can be overcome by the in situ production of the aldehyde species, which can be converted concomitantly, in the presence of a donor molecule, to the corresponding aldol adduct.…”
Section: Introductionmentioning
confidence: 89%
“…Thus, the aldehyde concentration will be low and side reactions can be reduced. The groups of Clapés and Turner successfully demonstrated this approach in a biocatalytic in vitro cascade composed of an alcohol oxidase/chloroperoxidase or ADH, wild‐type FSA, and a cofactor recycling system for the synthesis of a precursor of d ‐fagomine …”
Section: Introductionmentioning
confidence: 89%
“… 31 The same precursor was prepared with high isolated yields (79%) in a three-enzyme cascade, employing FSA-A129S, horse-liver dehydrogenase (HLADH) for the oxidation of the achiral starting material as well as the cofactor recycling enzyme NADH-oxidase (NOX). 32 …”
Section: C–c-bond Formation Leading To 12-diols Employing Aldolasesmentioning
confidence: 99%
“…A two-step chemo-enzymatic synthesis of D-fagomine has been described based on an aldol reaction catalyzed by D-Fructose-6-phosphate aldolase (FSA) from Escherichia coli [4][5][6]. FSA is a decameric protein of 230 kDa that accepts unphosphorylated dihydroxyacetone (DHA) as a donor substrate [7,8].…”
Section: Introductionmentioning
confidence: 99%