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Breaking the Dogma of Aldolase Specificity: Simple Aliphatic Ketones and Aldehydes are Nucleophiles for Fructose-6-phosphate Aldolase.

Raquel RoldánIsrael Sanchez-MorenoThomas ScheidtVirgil HélaineMarielle LemaireTeodor ParellaPere ClapésWolf-Dieter FessnerChristine Guérard-Hélaine
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2017)
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.
Keyphrases
  • wild type
  • ionic liquid
  • genome wide
  • molecular dynamics simulations
  • gene expression
  • dna methylation
  • amino acid
  • quantum dots