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Food Lipids: Chemistry, Nutrition, and Biotechnology

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VII. CONCLUSIONS<br />

Despite the benefits of using lipase-catalyzed interesterification, it is unlikely that it<br />

will replace chemical interesterification in the future. This is due to the higher cost<br />

associated with enzymatic interesterification <strong>and</strong> the low cost of products, such as<br />

margarines <strong>and</strong> shortenings, that are currently being produced using chemical interesterification.<br />

The main attraction of lipase-catalyzed interesterification reactions is<br />

in the specificities of individual lipases <strong>and</strong> their application to the development of<br />

novel fats <strong>and</strong> oils that cannot be produced by chemical means. Future applications<br />

will involve continued development of reduced-calorie products, enriched lipids, <strong>and</strong><br />

structured lipids. In addition, research will continue in the area of the characterization<br />

of fatty acid specificities of new lipases particularly in the identification of 2-specific<br />

lipases. In order for any of these new applications to be useful in the food industry,<br />

scale-up studies simulating industrial processes are necessary.<br />

REFERENCES<br />

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Cauwenbergh, <strong>and</strong> P. P. Tobback. Lipase-catalyzed ester exchange reactions in organic<br />

media with controlled humidity. Biotechnol. Bioeng. 30:258–266 (1987).<br />

2. R. W. Stevenson, F. E. Luddy, <strong>and</strong> H. L. Rothbart. Enzymatic acyl exchange to vary<br />

saturation in diglycerides <strong>and</strong> triglycerides. J. Am. Oil Chem. Soc. 56:676–680 (1979).<br />

3. W. W. Nawar. <strong>Chemistry</strong>. In: Bailey’s Industrial Oil <strong>and</strong> Fat Products, Vol. 1, Edible<br />

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8. A. R. Macrae. Interesterification of fats <strong>and</strong> oils. In: Biocatalysts in Organic Syntheses<br />

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9. A. R. Macrae. Lipase-catalyzed interesterification of oils <strong>and</strong> fats. J. Am. Oil Chem.<br />

Soc. 60(2):291–294 (1983).<br />

10. F. D. Gunstone. Chemical properties. In: The Lipid H<strong>and</strong>book, 2nd ed. (F. D. Gunstone,<br />

J. L. Harwood, <strong>and</strong> F. D. Padley, eds.). Chapman <strong>and</strong> Hall, London, 1994, pp. 594–<br />

595.<br />

11. P. Desnuelle. The lipases. In: The Enzymes, Vol. 7, 3rd ed. (P. D. Boyer, ed.). Academic<br />

Press, New York, 1972, pp. 575–616.<br />

12. K.-E. Jaeger, S. Ransac, B. W. Dijkstra, C. Colson, M. van Heuvel, <strong>and</strong> O. Misset.<br />

Bacterial lipases. FEMS Microbiol. Rev. 15:29–63 (1994).<br />

13. P. Kalo, P. Parviainen, K. Vaara, S. Ali-Yrrkö, <strong>and</strong> M. Antila. Changes in the triglyceride<br />

composition of butter fat induced by lipase <strong>and</strong> sodium methoxide catalysed<br />

interesterification reactions. Milchwiss. 41(2):82–85 (1986).<br />

Copyright 2002 by Marcel Dekker, Inc. All Rights Reserved.

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