The formation of casein micelles reconstituted with Ca+2 and added inorganic phosphate is influenced by the non-phosphorylated form of human β-casein

Satish M. Sood, Grant Erickson, Charles W. Slattery

Research output: Contribution to journalArticlepeer-review

Abstract

The β-casein (CN) human milk fraction is comprised of a single protein phosphorylated at levels from 0 to 5. Component interactions are dependent on the phosphorylation level. Here, 3 mg/ml of β-CN-0P, β-CN-2P, β-CN-4P, a 2P/4P 1:1 (wt:wt) mixture, or a mixture of all six forms in the ratio in human milk, were mixed with bovine κ-CN at a κ/β molar ratio of 0.33. Measurements were with 0, 5 and 10 mM Ca+2 and 4 and 8 mM added inorganic phosphate (Pi). The turbidity (OD 400 nm) and a lack of precipitation as T increased from 4 to 37°C was an index of micelle formation. The results indicate: (1) while micelles will form with Ca+2 alone, added Pi has a significant enhancing effect on micelle formation; (2) the patterns of micelle formation as a function of T are influenced by the β-CN-0P and β-CN-1P forms of β-CN to an unexpected extent.

Original languageEnglish
Pages (from-to)227-232
Number of pages6
JournalProtein Journal
Volume24
Issue number4
DOIs
StatePublished - May 2005

ASJC Scopus Subject Areas

  • Analytical Chemistry
  • Bioengineering
  • Biochemistry
  • Organic Chemistry

Keywords

  • Colloidal calcium phosphate
  • Human β-casein
  • Protein phosphorylation level
  • Reconstituted milk micelle formation

Cite this