Reversed enantiopreference of Candida rugosa lipase supports different modes of binding enantiomers of a chiral acyl donor

• Molecular modelling identifies two different productive modes of binding the enantiomers of a 2-methyldecanoic acid ester to the active site of Candida rugosa lipase (CRL). The fast reacting S-enantiomer occupies the previously identified acyl-binding tunnel of the enzyme, whereas the R- enantiomer leaves the tunnel empty. The modelling suggested that if both enantiomers were forced to bind to the active site leaving the tunnel empty, the enzyme would reverse its enantiopreference to become R-enantioselective. To test this hypothesis, we designed a structural analogue to 2- methyldecanoic acid, 2-methyl-6-(2-thienyl)hexanoic acid, which was expected to be too bulky to fit its acyl moiety into the acyl-binding tunnel. The CRL- catalysed hydrolysis of the ethyl ester of this substrate resulted in the preferential conversion of the R-enantiomer as predicted by molecular modelling. This represents the first kinetic evidence supporting the existence of two different modes of binding the enantiomers of a 2- methyldecanoic acid ester to the active site of CRL. We have shown that a rational 3D based approach in combination with substrate engineering can be used to predict and control the stereochemical outcome of a lipase catalysed reaction.

Ämnesord

TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Biokatalys och enzymteknik (hsv//swe)

ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Biocatalysis and Enzyme Technology (hsv//eng)

Nyckelord

2-Methylalkanoic acid

Candida rugosa lipase

Chiral recognition

Enantiopreference

Enantioselective inhibition

Kinetic resolution

Reversed enantioselectivity

alkanoic acid

carboxylic acid derivative

decanoic acid derivative

ester

fungal protein

triacylglycerol lipase

candida

candida rugosa

catalysis

chirality

conference paper

enantiomer

enzyme activity

enzyme kinetics

enzyme substrate

nonhuman

stereochemistry

Publikations- och innehållstyp

ref (ämneskategori)

art (ämneskategori)