| Literature DB >> 28266745 |
Raquel Roldán1, Israel Sanchez-Moreno2, Thomas Scheidt3, Virgil Hélaine2, Marielle Lemaire2, Teodor Parella4, Pere Clapés1, Wolf-Dieter Fessner3, Christine Guérard-Hélaine2.
Abstract
d-Fructose-6-phosphate aldolase (FSA) was probed for extended nucleophile promiscuity by using a series of fluorogenic substrates to reveal retro-aldol activity. Four nucleophiles ethanal, propanone, butanone, and cyclopentanone were subsequently confirmed to be non-natural substrates in the synthesis direction using the wild-type enzyme and its D6H variant. This exceptional widening of the nucleophile substrate scope offers a rapid entry, in good yields and high stereoselectivity, to less oxygenated alkyl ketones and aldehydes, which was hitherto impossible.Entities:
Keywords: aldolization; biocatalysis; enzymes; fructose-6-phosphate aldolase; phosphorylated compounds
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Year: 2017 PMID: 28266745 DOI: 10.1002/chem.201701020
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236