Chicken egg white proteins were fractionated by high-speed counter-current
chromatography (HSCCC) using a cross-axis coil planet centrifuge (X-axis CP
C). The separation was performed with an aqueous polymer two-phase system c
omposed of 16% polyethylene glycol (PEG) 1000 and 12.5% potassium phosphate
buffer at different pH of 6.8, 8.0, and 9.2. From 20 g of the crude egg wh
ite solution, the best separation was achieved with a polymer phase system
at pH 8.0 by eluting the lower phase at 1.0 mL/min. After the sequential el
ution of ovotransferrin, ovalbumin, and lysozyme from the column, ovomucin
still retained in the column was eluted in the reverse direction with upper
PEG-rich phase. All four proteins in the CCC fractions were identified by
SDS gel electrophoresis with Coomassie brilliant blue staining.