Modélisation moléculaire de l'acétylation de la quercétine par des lipases : étude des interactions enzyme-substrat

Abstract : Quercetin (QCT) is a plant-produced polyphenolic compound well-known for its antioxidant activities and beneficial health effects. Its solubility, stability, bioavailability and biological activities may be improved by a selective acylation of its hydroxyl groups. This work aims at studying the possibility of QCT enzymatic acetylation by Candida antarctica lipase B (CALB), the most industrially exploited lipase for regio- and enantioselective esterifications. In prospect of the rational enzyme design, a molecular modeling approach was implemented to understand the interactions that govern the substrate positioning and orientation in the lipase's active site. In a first experimental part, the absence of CALB acetylation activity towards quercetin in excess of vinyl acetate was confirmed. In a second part, this inactivity of CALB was explained by means of docking and molecular dynamics simulations. This results from an inappropriate positioning of the acyl donor linked to the catalytic serine and from an insufficient proximity of QCT hydroxyls vis-à-vis catalytic residues. The distance of QCT from the catalytic triad is due to its rigidity and to the narrow active site as well as to hydrophobic and electrostatic interactions between the substrate and the cavity residues. On the contrary, this molecular simulation approach predicts an appropriate positioning of both substrates in the active site of Pseudomonas cepacia lipase (PCL), which can perform QCT acetylation. In a third part, the impact of mutations of two residues implicated in the stabilization of QCT by hydrophobic interactions in CALB was investigated through simulations. The substitution of isoleucines by alanines and valines led to an increase in the catalytic pocket volume which intensified the mobility of QCT. However, these mutations are insufficient to allow an appropriate positioning of acetate and QCT in relation to the catalytic triad. The last part of this work focuses on the electrostatic interactions between QCT and CALB's active site. The substrate orientation in the cavity following methylation or acetylation of QCT's hydroxyl groups was clarified
Document type :
Theses
Complete list of metadatas

https://hal.univ-lorraine.fr/tel-01749457
Contributor : Thèses Ul <>
Submitted on : Thursday, March 29, 2018 - 12:16:47 PM
Last modification on : Wednesday, April 11, 2018 - 1:28:00 AM
Long-term archiving on : Friday, September 14, 2018 - 10:39:17 AM

File

DDOC_T_2012_0263_BIDOUIL.pdf
Files produced by the author(s)

Identifiers

  • HAL Id : tel-01749457, version 1

Collections

Citation

Christelle Bidouil. Modélisation moléculaire de l'acétylation de la quercétine par des lipases : étude des interactions enzyme-substrat. Alimentation et Nutrition. Université de Lorraine, 2012. Français. ⟨NNT : 2012LORR0263⟩. ⟨tel-01749457⟩

Share

Metrics

Record views

51

Files downloads

103