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Kinetic properties and characterization of purified proteases from Pacific whiting (Merluccius productus)

Kinetic properties of the two proteases, causing textural degradation of Pacific
whiting (Merluccius productus) during heating, were compared and characterized with the
synthetic substrate, Z-Phe-Arg-NMec. Pacific whiting P-I and P-II showed the highest
specificity on Z-Phe-Arg-NMec, specific substrate for cathepsin L. The K [subscript m] of
preactivated P-I and P-II were 62.98 and 76.02 (μM), and k [subscript cat], 2.38 and 1.34 (s⁻¹)
against Z-Phe-Arg-NMec at pH 7.0 and 30°C, respectively. Optimum pH stability for
preactivated P-I and P-II is between 4.5 and 5.5. Both enzymes showed similar pH-induced
preactivation profiles at 30°C. The maximal activity for both enzymes was
obtained by preactivating the enzyme at a range of pH 5.5 to 7.5. The highest activation
rate for both enzymes was determined at pH 7.5. At pH 5.5, the rate to reach the
maximal activity was the slowest, but the activity was stable up to 1 hr. P-I and P-II shared similar temperature profiles at pH 5.5 and pH 7.0 studied. Optimum temperatures
at pH 5.5 and 7.0 for both proteases on the same substrate were 55°C. Significant
thermal inactivation for both enzymes was shown at 75°C. Preactivated P-I and P-II
displayed a similar first order thermal inactivation profile at pH 7.0. At 30 and 90°C, half
lives, t [subscript 1/2], for Pacific whiting P-I were 49.50 and 0.20 min and for P-II, 32.54 and 0.18
min, respectively. The rate constant of inactivation for both proteases increased about
200-fold between two limits, 30 and 90°C. Half lives at 55°C, optimum temperature, for
P-I and P-II were also determined to be 5.29 and 6.75 min. The increase in thermal
inactivation rate constants independent of substrates corresponded to an activation energy
for heat denaturation of 21.18 kcal/mol for P-I and 19.97 kcal/mol for P-II by Arrhenius
plot. These similar kinetic properties, i.e., kinetic parameters, pH profile and thermal
inactivation rate constant, suggested that Pacific whiting P-I and P-II are the same
enzyme. / Graduation date: 1994

Identiferoai:union.ndltd.org:ORGSU/oai:ir.library.oregonstate.edu:1957/27168
Date10 March 1994
CreatorsWu, JuWen
ContributorsAn, Haejung
Source SetsOregon State University
Languageen_US
Detected LanguageEnglish
TypeThesis/Dissertation

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