Pea protein hydrolysate was obtained by enzymatic hydrolysis with trypsin.
The degree of hydrolysis (DH) was controlled by using the pH-stat method. S
olubility of the trypsin-treated hydrolysate was tested at nine different p
H values starting from 2 up to 10. Protein determinations were carried out
using Kjeldahl, Lowry and modified Lowry methods. The results revealed that
samples analysed with either the Kjeldahl or Lowry method gave similar val
ues. However, systematic consistent differences existed for those results o
btained by the Kjeldahl and the modified Lowry as well as between those res
ults obtained by the Lowry and the modified Lowry.