| Literature DB >> 31187106 |
Domitille Chambre1, Christine Guérard-Hélaine1, Ekaterina Darii2, Aline Mariage2, Jean-Louis Petit2, Marcel Salanoubat2, Véronique de Berardinis2, Marielle Lemaire1, Virgil Hélaine1.
Abstract
We explored a collection of 2-deoxyribose-5-phosphate aldolases (DERAs) from biodiversity for their nucleophile substrate promiscuity. The DERAs were screened using as nucleophiles propanone, propanal, cyclobutanone, cyclopentanone, dihydroxyacetone, and glycolaldehyde with l-glyceraldehyde-3-phosphate as an electrophile in aldol addition. A DERA from Arthrobacter chlorophenolicus (DERAArthro) efficiently allowed the synthesis of the corresponding aldol adducts in good yields, displaying complementarity in terms of configuration and substrate specificity with fructose-6-phosphate aldolase, the only previously known aldolase with a large nucleophile tolerance.Entities:
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Year: 2019 PMID: 31187106 DOI: 10.1039/c9cc03361k
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222