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Glycomacropeptide Hydrolysed from Bovine K-Casein ; II. Chromatographic Changes of k-Casein Macropetide as Related to Trichloroacetic Acid Concentration  

Moon Yong-Il (Division of Pet & Herb Science, Woosuk University)
Lee Wonjae (Department of Food Science, University of Wisconsin-Madison)
Oh Sejong (Department of Animal Science, Institute of Agricultural Science & Technology, Chonnam National University)
Publication Information
Food Science of Animal Resources / v.25, no.4, 2005 , pp. 478-482 More about this Journal
Abstract
Bovine k-casein macropeptide was prepared by adding TCA (3, 6, and $12\%$) treatment after chymosin reaction. Each TCA soluble macropeptide was fractionated into five peak by ion exchange column chromatography. In proportiion to TCA concentrations, the ratio of peak area showed different the elution pattern. At the 6 and $12\%$ TCA concentration, area ratio of P-I which did not content carbohydrates was decreased to 19.9 and $17.0\%$ of total peak area respectively. The area of P-III was changed from $10.2\%\;to\;26.2\;and\;13.2\%$ when the TCA concentration was increased from 3 to 6 and $12\%$ Cholera toxin binding activity of k-casein macropeptide eluted at $0.17\~0.18M$ NaCl gradient was not inhibited by 6 and $12\%$ TCA treatments. The use of $6\%$ TCA as extraction buffer was feasible and led to an effective separation of the peak III.
Keywords
k-casein macropeptide; glycomacropeptide; cholera toxin;
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1 El-Salam, M. H. A., El-Shibiny, S., and Buchheim, W. (1996) Characteristics and potential uses of the casein macropeptide. Int. Dairy Journal 6, 327-341   DOI   ScienceOn
2 Walker, J. M. and Gaastra, W. (1988) Detection of protein blots using enzyme-linked second antibodies or Protein A. In: Methods in Molecular Biology Vol 3 : New protein techniques. Walker, J. M. (ed), Humana Press, Clifton, New Jersey, pp.427-440
3 Kim, Y. K., Yaguchi, M., and Rose, D. (1968) Isolation and amino acid composition of para-kappa-casein. J. Dairy Sci. 52, 316-320
4 Oh, S., Worobo, R. W., Kim, B. C., Rheem, S., and Kim, S. Detection of cholera-toxin-binding activity of macropeptide from bovine ${\kappa}$-casein and optimization of its production by use of response surface methodology. Biosci. Biotech. Biochem. 64, 516-522   DOI   ScienceOn
5 Eigel, W. N., Butler, J. E., Ernstrom, C. A., Farrell, Jr. H. M., Harwalkar, V. R., Jenness, R. and Whitney, R. McL. (1984) Nomenclature of proteins of cow's milk: Fifth revision. J. Dairy Sci. 67, 1599-1631   DOI
6 Oh, S. I., Kim, S. H., Jeon, W. M., Kim B. C., and Kim, Y. K. (1997) Glycomacropeptide hydrolysed from bovine ${\kappa}$-casein; I. The fractionation of glycomaropeptide. Korean J. Food Sci. Ani. Resour. 17, 51-57
7 Slattery, C. W. (1976) Casein micelle structure: A examination of models. J. Dairy Sci. 59, 547
8 Doi, H., Ibuki, F., and Kanamori, M. Heterogeneity of reduced bovine ${\kappa}$-casein. J. Dairy Sci. 62, 195 (1979)
9 Kim, Y. K. (1971) Fractionation of ${\kappa}$-casein macropeptide. Korean J. Ani. Sci. 13, 82-86
10 Yvon, M., Chabanet, C., and Pelissier, J. P. (1989) Solubility of peptides in trichloroacetic acid (TCA) solutions: Hypothesis on the precipitation mechanism. Int. J. Peptide Protein Res., 34, 166-176   DOI
11 Pohl, T. (1993) Concentration of proteins and removal of solutes. In: Method in enzymology vol. 182. Guide to protein purification. Deutscher, M. P. (ed), Academic Press. London, pp.68-83
12 Chang, Y. C. (1992) Efficient precipitation and accurate quantitation of detergent-solublized membrane proteins. Anal. Biochem., 205, 22-26   DOI   PUBMED   ScienceOn
13 Kim, Y. K. (1993) Structure and some properties of bovine casein micelles. Natural Resources Research 1, 138-152
14 McKenzie, H. A. (1971) Milk proteins II, chemistry and molecular biology. Academic Press, New York
15 Lieske, B. and Konrad, G. (1996) A new method to estimate caseinomacropeptide and glycomacropeptide from trichloroacetic acid filtrates. Michwissenschaft. 51, 431-434