Resolution of Racemic Acids, Esters and Amines by Candida rugosa Lipase in Slightly Hydrated Organic Media
Andrés R. Alcántara, Pablo Domínguez de María, María Fernández, María José Hernaíz, José María Sánchez-Montero and José Vincente Sinisterra*
Biotransformations group, Department of Organic & Pharmaceutical Chemistry, Faculty of Pharmacy, Universidad Complutense, Plza. Ramón y Cajal s/n, Ciudad Universitaria, E-28040 Madrid, Spain
Article history:
Received: July 19, 2004
Accepted: November 22, 2004
Key words:
lipase, isoenzymes, biocatalysis, purification of lipases, resolution of racemics
Summary:
Commercial crude lipase from Candida rugosa is widely used as a biocatalyst in the resolution of racemic mixtures and in organic synthesis in slightly hydrated organic solvents. In many cases, reproducible results are not obtained when the same crude lipase is used, but from different suppliers of lots, this being due to the presence of different isoenzymes. The current work addresses this problem and strategies to overcome it. The yeast Candida rugosa ATCC 14380 was cultivated in a minimal culture medium, using different substances as inducers and carbon sources. The percentage of inducer that gave the optimum productivity of extracellular lipases was determined. Lyophilized extracellular enzymes were characterized by SDS-PAGE electrophoresis and isoelectric focusing (IEF). Depending on the nature of the carbon source, different isoenzymes were produced in various proportions. These samples were partially purified by different methodologies, including dialysis, adsorption chromatography and precipitation with ammonium sulfate or organic solvents. These characterizations allowed us to explain the relative catalytic activity of different samples, showing that in biocatalysis enzymes should not be treated simply as a »white magic powder« that can solve all the challenges in organic synthesis. Heptyl oleate synthesis, alcoxycarbonylation of amines and hydrolysis of the ester of ketoprofen are excellent reaction tests for the evaluation of lipase samples as biocatalysts.
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