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PROTEOLYTIC ACTIVITY OF CRUDE ENZYME EXTRACTS OF SQUID ILLEX ARGENTINUS LIVER
Author(s) -
KOŁODZIEJSKA ILONA,
SZYC ELŻBIETA,
KARAMAĆ MAGDALENA,
SIKORSKI ZDZISŁZAW E.
Publication year - 1994
Publication title -
journal of food biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.507
H-Index - 47
eISSN - 1745-4514
pISSN - 0145-8884
DOI - 10.1111/j.1745-4514.1994.tb00488.x
Subject(s) - iodoacetamide , chemistry , dithiothreitol , pepstatin , myofibril , chromatography , acetone , biochemistry , proteolytic enzymes , esterase , hydrolysis , enzyme , substrate (aquarium) , cysteine , protease , biology , ecology
The extract obtained from the acetone powder of frozen stored squid liver had optimum proteolytic activity against hemoglobin at pH 2.6 to 4.0. About 90% of the activity at pH 3.0 was inhibited by pepstatin and about 15% was inhibited by phenylmethanesulfonyl fluoride or iodoacetamide. The activity was increased by dithiothreitol and cysteine by about 55 and 40%, respectively. At pH 3 the enzyme extract had a temperature optimum of 45 to 50C; at 5C the activity was about 15% of that at 45 to 50C. At pH 7 the optimum activity was at about 45C. Heating of the extract without substrate at pH 3 and 7 caused a rapid decrease in proteolytic activity above 35 and 30C, respectively. A water extract of the liver was used to treat isolated bovine myofibrils at pH 5.5 and 0C. After 20 h a fragment of slightly lower m.w. than that of the myosin heavy chain was detected. After treatment at pH 7 and 0C, little degradation of the myofibrillar proteins was evident. At 20C the myofibrils were hydrolyzed to several products.