Some studies indicated that enzyme activity
and microbial biomass can vary high both seasonal and interannual (Sardans et al.
Change in enzyme activity
was measured by incubating crude enzyme at temperatures 30degC-90degC for 25 min.
01) on holo, total and apo enzyme activity
The enzyme activity
was maximum at 40[degrees]C for protease and 30[degrees]C for Xylanase (Table 4).
After incubation enzyme activity
was measured as described above, using MUGS for rhHex-A, and MUG for rhHex-B and rhHex-S.
However, the traditional optimization method in which the level of one parameter is varied at a time over a certain range, while keeping the other variables constant, is generally time consuming, requiring a large number of tests (Sen & Swaminathan, 1997), and does not reflect the interaction effects among the variables and, consequently, does not depict the net effect of the various factors on the enzyme activity
(Dagbagli & Goksungur, 2008).
Thus, the purpose of the present study was to compare the effects of moderate and low training moderate volume on mitochondrial enzyme activity
and oxidative stress on skeletal muscle.
Apparent enzyme activity
(AEA) was determined at each wavelength using the following equation:
Effects of treatment with ARTEA330EC on changes in enzyme activity
Most investigations regarding quantification of soil enzyme activity
are conducted directly by measuring its activity (Dick, 1997).
After 48 hours incubation, enzyme activity
of cell free supernatant of each isolate was determined.
(Cellulase) was determined by using DNS method/13) as follows; 1ml enzyme solution was mixed with 1ml DNS reagent and boil the mixture for five minutes, then cooled.