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Journal of Dairy Science Vol. 47 No. 10 1056-1061
© 1964 by American Dairy Science Association ®
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Measurement of Protein Stability in Sterile Concentrated Milk1

S. Nakai2, H. K. Wilson and E. O. Herreid

Department of Food Science, University of Illinois, Urbana

ABSTRACT

Gold sols were used to determine stability of protein to Ca++ by adding 0.5 ml of 0.01 to 0.02% protein solution to 10 ml of gold sol, followed by 1.0 ml of M CaCl2. Optical densities were determined at 535 mµ after 1 hr. Reference protein solutions served as standards.

Stable milk proteins had higher optical densities than the unstable ones. {alpha}-Casein lost its stability to Ca++ and noncasein and nonprotein N increased during storage. Losses of gold sol stabilities of sterile {kappa}-casein at zero time, and at 35 C for 30 days, and at 65 C for 4 and 8 days were 37, 62, 77, and 84%, respectively; whereas, by the CaCl2-centrifugal method they were 31, 55, 78, and 83%, respectively. {kappa}-Casein restored to concentrated milk stability that was decreased by heating.

Concentrated milk coagulated with rennet lost about 60% of its stability to Ca++, whereas about 30% was lost during gelation of concentrated milk at 35 C storage.

Changes in protein structure which affect protection of the gold sol may be detected with 5 M NaCl instead of M CaCl2. The gold sol and CaCl2-centrifugal methods agreed for determining stability of milk proteins.


FOOTNOTES

1 This research was supported by U. S. Public Health Grant EF-141.

2 Research Associate.







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Copyright © 1964 by the American Dairy Science Association ®.