Enzymatic acylation of polar dipeptides: Influence of reaction media and molecular environment of functional groups
Fiche publication
Date publication
avril 2009
Auteurs
Membres identifiés du Cancéropôle Est :
Dr VANDERESSE Régis
Tous les auteurs :
Husson E, Hurneau C, Paris C, Vanderesse R, Framboisier X, Marc I, Chevalot I
Lien Pubmed
Résumé
The enzymatic acylation of polar dipeptides was investigated. First, the Novozym435 (R)-catalyzed acylation of Lys-Ser, HCl exhibiting three potential acylable sites was carried out in organic media (2-methyl-2-butanol, oleic acid) and in an ionic liquid ([Bmim](+)[PF6](-)). in these reactions, the chemoselectivity of the acylation was exclusively in favour of the NE-lysine acylation and the efficiency (Substrate conversion) was demonstrated to be under control of the peptide solubility. The use of [Bmim](+)[PF6](-) permitted to significantly improve the dipeptide solubility, and to enhance both substrates conversion and initial rates of acylation reaction. In the three reaction media used, the O-acylated derivative of the dipeptide was never detected suggesting a weak reactivity of the serine hydroxyl group due to its molecular environment and particularly to the presence of a free carboxylic group known for its electroattractor property. Last, the acylation of a natural dipeptide (carnosine), exhibiting a very low solubility in organic solvents, was also performed. Carnosine was Successfully N-acylated in 2-methyl-2-butanol, and a yield of 39% was obtained when improving the substrate solubility: a better dispersibility was obtained by application of a high pressure on the reaction medium just before starting the reaction. (C) 2008 Elsevier Ltd. All rights reserved.
Référence
Process Biochem. 2009 Apr;44(4):428-34