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Wax ester-synthesizing activity of lipases
T Tsujita1, M Sumiyoshi, H Okuda
1Central Research Laboratory, School of Medicine, Ehime University, Onsen-gun, Japan. tsujita@m.ehime-u.ac.jp
Lipids
|December 22, 1999
Summary
Lipases can synthesize wax esters from fatty acids or triacylglycerols in water. Equilibrium favors ester formation at neutral pH, influenced by alcohol chain length.
Area of Science:
- Biochemistry
- Enzymology
Background:
- Wax esters are important lipids with diverse biological functions.
- Lipases are enzymes known for hydrolyzing ester bonds, but their synthetic capabilities are also of interest.
Purpose of the Study:
- To investigate the synthesis and hydrolysis of wax esters in an aqueous solution using various lipases.
- To determine the optimal conditions for lipase-catalyzed wax ester synthesis.
Main Methods:
- Utilized purified rat pancreatic lipase, porcine pancreatic carboxylester lipase, and Pseudomonas fluorescens lipase.
- Studied reactions in aqueous solutions using free fatty acids or triacylglycerols as acyl donors and long-chain alcohols as acyl acceptors.
- Measured synthesis and hydrolysis kinetics and apparent equilibrium ratios.
Main Results:
- Lipases catalyzed wax ester synthesis from free fatty acids and long-chain alcohols, and also hydrolysis of pre-formed wax esters.
- Apparent equilibrium favored ester formation (ratio ~0.9/0.1) at neutral pH.
- Synthesis occurred in a dose- and time-dependent manner, influenced by pH and fatty alcohol chain length.
- Wax esters were synthesized from triacylglycerols and fatty alcohols.
Conclusions:
- Lipases can effectively catalyze wax ester synthesis in aqueous media.
- The equilibrium of wax ester synthesis/hydrolysis is pH-dependent and favors ester formation at neutral pH.
- These findings highlight the dual role of lipases in both ester hydrolysis and synthesis.