| Literature DB >> 29542859 |
Victor Laurent1, Ekaterina Darii2, Angelina Aujon1, Marine Debacker1, Jean-Louis Petit2, Virgil Hélaine1, Tibor Liptaj3, Martin Breza3, Aline Mariage2, Lionel Nauton1, Mounir Traïkia1, Marcel Salanoubat2, Marielle Lemaire1, Christine Guérard-Hélaine1, Véronique de Berardinis2.
Abstract
Dihydroxyacetone phosphate (DHAP)-dependent rhamnulose aldolases display an unprecedented versatility for ketones as electrophile substrates. We selected and characterized a rhamnulose aldolase from Bacteroides thetaiotaomicron (RhuABthet) to provide a proof of concept. DHAP was added as a nucleophile to several α-hydroxylated ketones used as electrophiles. This aldol addition was stereoselective and produced branched-chain monosaccharide adducts with a tertiary alcohol moiety. Several aldols were readily obtained in good to excellent yields (from 76 to 95 %). These results contradict the general view that aldehydes are the only electrophile substrates for DHAP-dependent aldolases and provide a new C-C bond-forming enzyme for stereoselective synthesis of tertiary alcohols.Entities:
Keywords: aldolases; biocatalysis; branched-chain sugars; carboligation; tertiary alcohols
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Year: 2018 PMID: 29542859 DOI: 10.1002/anie.201712851
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336