Abstract
The racemization half-lives (i.e., the time required to reach a D/L = 0.33) at pH 6.8 for aspartic acid and phenylalanine in the sweetener aspartame (L-aspartyl-L-phenylalanine methyl ester) were determined to be 13 and 23 hours, respectively, at 100 degrees C. Racemization at this pH does not occur in aspartame but rather in its diketopiperazine decomposition product. Our results indicate that the use of aspartame to sweeten neutral pH foods and beverages that are then heated at elevated temperature could generate D-aspartic acid and D-phenylalanine. The nutritive consequences of these D-amino acids in the human diet are not well established, and thus aspartame should probably not be used as a sweetener when the exposure of neutral pH foods and beverages to elevated temperatures is required. At pH 4, a typical pH of most foods and beverages that might be sweetened with aspartame, the half-lives are 47 hours for aspartic acid and 1200 hours for phenylalanine at 100 degrees C. Racemization at pH 4 takes place in aspartame itself. Although the racemization rates at pH 4 are slow and no appreciable racemization of aspartic acid and phenylalanine should occur during the normal use of aspartame, some food and beverage components could conceivably act as catalysts. Additional studies are required to evaluate whether the use of aspartame as a sugar substitute might not in turn result in an increased human consumption of D-aspartic acid and D-phenylalanine.
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Selected References
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- Bada J. L. In vivo racemization in mammalian proteins. Methods Enzymol. 1984;106:98–115. doi: 10.1016/0076-6879(84)06011-0. [DOI] [PubMed] [Google Scholar]
- Beardsley T. Sour welcome for aspartame. Nature. 1983 Sep 15;305(5931):175–175. doi: 10.1038/305175b0. [DOI] [PubMed] [Google Scholar]
- Furda I., Malizia P. D., Kolor M. G., Vernieri P. J. Decomposition products of L-aspartyl-L-phenylalanine methyl ester and their identification by gas-liquid chromatography. J Agric Food Chem. 1975 Mar-Apr;23(2):340–343. doi: 10.1021/jf60198a034. [DOI] [PubMed] [Google Scholar]
- Horwitz D. L., Bauer-Nehrling J. K. Can aspartame meet our expectations? J Am Diet Assoc. 1983 Aug;83(2):142–146. [PubMed] [Google Scholar]
- Hurrell R. F., Finot P. A. Food processing and storage as a determinant of protein and amino acid availability. Experientia Suppl. 1983;44:135–156. doi: 10.1007/978-3-0348-6540-1_9. [DOI] [PubMed] [Google Scholar]
- Manning J. M., Moore S. Determination of D- and L-amino acids by ion exchange chromatography as L-D and L-L dipeptides. J Biol Chem. 1968 Nov 10;243(21):5591–5597. [PubMed] [Google Scholar]
- Mazur R. H. Aspartame--a sweet surprise. J Toxicol Environ Health. 1976 Sep;2(1):243–249. doi: 10.1080/15287397609529429. [DOI] [PubMed] [Google Scholar]
- Ott H., Frey A. J., Hofmann A. The stereospecific cyclolization of n-(alpha-hydroxyacyl)-phenylalanyl-proline lactams. Tetrahedron. 1963 Nov;19(11):1675–1684. doi: 10.1016/s0040-4020(01)99240-3. [DOI] [PubMed] [Google Scholar]
- Smith R. J. Aspartame approved despite risks. Science. 1981 Aug 28;213(4511):986–987. doi: 10.1126/science.7268411. [DOI] [PubMed] [Google Scholar]
- Steinberg S., Bada J. L. Diketopiperazine formation during investigations of amino Acid racemization in dipeptides. Science. 1981 Jul 31;213(4507):544–545. doi: 10.1126/science.213.4507.544. [DOI] [PubMed] [Google Scholar]
