Peer-Reviewed Journal Details
Mandatory Fields
Considine, T,Healy, A,Kelly, AL,McSweeney, PLH;
2004
February
International Dairy Journal
Hydrolysis of bovine caseins by cathepsin B, a cysteine proteinase indigenous to milk
Validated
()
Optional Fields
cathepsin B beta-casein alpha(s1)-casein specificity somatic cells LACTIS SUBSP CREMORIS ENVELOPE-LOCATED PROTEINASE SOMATIC-CELL COUNT BETA-CASEIN PROTEOLYTIC SPECIFICITY CHEDDAR CHEESE PIII-TYPE PROTEASE ALPHA-S1-CASEIN SUBSTRATE
14
117
124
The presence of the lysosomal cysteine proteinase cathepsin B in milk has been demonstrated recently. The potential significance of this enzyme to proteolysis in milk and dairy products was evaluated by the study of its proteolytic specificity towards the caseins. Bovine cathepsin B (1.4 units mL(-1)) was added separately to beta-casein or alpha(s1)-casein (5 mg mL(-1), in 100 mm Na acetate buffer, pH 6.0, containing 1.5 mm dithiothreitol). Samples were taken over a 24 h period and analysed by urea polyacrylamide gel electrophoresis and RP-HPLC; peptides were identified by N-terminal sequencing and mass spectrometry. Cathepsin B cleaved beta-casein at 32 sites and alpha(s1)-casein at 35 sites, extensively hydrolysing both proteins. Thus, cathepsin B has a very broad specificity against the caseins, with an apparent preference for bonds incorporating the amino acids Leu, Val, Gln, Pro and Ser. Cathepsin B cleaved some bonds in common with chymosin (including the Phe(23)-Phe(24) bond of alpha(s1)-casein), plasmin and the cell envelope-associated protemases of Lactococcus, suggesting that it could be involved in proteolysis in dairy products, particularly if manufactured from high somatic cell count milk. (C) 2003 Elsevier Ltd. All rights reserved.
DOI 10.1016/S0958-6946(03)00171-7
Grant Details