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Enzyme activity, variations

In order to achieve satisfactory accuracy, it is essential to avoid errors. However, distinction should be made between experimental errors and mistakes. Mistakes are the type of errors ( blunders ) which necessitate the repetition of the test, whereas experimental errors are inherent to the test and may result from random error, from bias or from both. Random errors may be due to slight fluctuations in measuring enzyme activity, variations in temperature, ionic composition of the sample, etc., and can be minimized by the use of standards. Bias is a systematic error (storage effects, improper... [Pg.6]

In the following years some more studies appeared in the literature concerning trypsin activity in reverse micelles in relation to various characteristics of the reaction medium. Fadnavis et al. studied the pH dependence of hydrolytic activity of trypsin in CTAB reverse micelles toward a positively charged model ester substrate [74]. It was found that enzyme activity variations as a function of w are pH dependent. In 2005, Dasgupta and coworkers related the catalytic activity of trypsin in reverse micelles formulated with cationic surfactants with the concentration of the water-pool components and the aggregate size to delineate the independent role of both parameters [75]. Finally, in 2006, the influence of ethylene glycol on the thermostability of trypsin in AOT reverse micelles was examined and was found to exhibit a positive effect [76]. [Pg.358]

The diagram in Fig. 18 shows direct comparisons with the corresponding results for the floccular system. The particle diameters dpv and dp and the relative enzyme activity a/a in Fig. 18 show similar patterns of variation as with the specific impeller power P/V. It is therefore appropriate to represent these results by means of the correlation function obtained for the floccular system according to Eq. (20). As in Fig. 9, a clear correlation of the results is found for both systems (see Figs. 19 and 20). It is thus clear that particle disintegration in a stirred tank with baffles follows a similar pattern for other particle systems. [Pg.67]

Chromatin remodeling, transcription factor modification by various enzyme activities, and the communication between the nuclear receptors and the basal transcription apparatus are accomplished by protein-protein interactions with one or more of a class of coregulator molecules. The number of these coregulator molecules now exceeds 100, not counting species variations and splice variants. The first of these to be described was the CREB-binding protein, CBP. CBP, through an amino terminal domain, binds to phosphorylated serine 137 of CREB and mediates transactivation in response to cAMP. It thus is described as a coactivator. CBP and... [Pg.471]

Many more papers deal with rhizosphere phosphatase activity (63-83) in the presence of a number of different plant species this will partly be due to the simplicity of the enzyme activity assay (85,86) and the generally reported, well-correlated variation trends among organic and inorganic phosphorus content and phosphatase activity. More precisely, closer to the roots, the inorganic P depletion zone in comparison with bulk soil is more pronounced in addition, organic and inorganic P contents are inversely correlated, and the mineralization rate of or-... [Pg.172]

Ethic variations in medication responses include differences in therapeutic responses and susceptibility to adverse effects. Such differences are attributable mostly to two aspects, the variation of enzyme activities for the metabolism of medications, and variations of the drugs interactions with target binding sites. [Pg.90]

Figure 2. Temporal profile of DDC enzyme activity during Drosophila development. Note the major peaks of DDC induction during late embryo-genesis, at pupariation, and at the time of eclosion of the adult from the pupal case. At these developmental times when there is extensive synthesis and hardening of cuticle, the induced DDC in the hypoderm is involved in this process. Levels of DDC in the CNS show much less developmental variation (Hirsh, 1986). Figure adapted from Hirsh, 1986. Figure 2. Temporal profile of DDC enzyme activity during Drosophila development. Note the major peaks of DDC induction during late embryo-genesis, at pupariation, and at the time of eclosion of the adult from the pupal case. At these developmental times when there is extensive synthesis and hardening of cuticle, the induced DDC in the hypoderm is involved in this process. Levels of DDC in the CNS show much less developmental variation (Hirsh, 1986). Figure adapted from Hirsh, 1986.
Approximation refers to the bringing together of the substrate molecules and reactive functionalities of the enzyme active site into the required proximity and orientation for rapid reaction. Consider the reaction of two molecules, A and B, to form a covalent product A-B. For this reaction to occur in solution, the two molecules would need to encounter each other through diffusion-controlled collisions. The rate of collision is dependent on the temperature of the solution and molar concentrations of reactants. The physiological conditions that support human life, however, do not allow for significant variations in temperature or molarity of substrates. For a collision to lead to bond formation, the two molecules would need to encounter one another in a precise orientation to effect the molecular orbitial distortions necessary for transition state attainment. The chemical reaction would also require... [Pg.27]

Fig. 4. Anaerobic titration of xanthine oxidase with xanthine at pH 8.2 with a reaction time of 2 min. at about 20°. The integrated intensity of the Rapid molybdenum EPR signals (in arbitrary units) is plotted against the number of moles of xanthine added per mole of active enzyme. Activity/A4jo for the enzyme samples used was 112 corresponding to an active enzyme content of 57%. Thus the molar ratios of xanthine/total xanthine oxidase have been multiplied by 1.76 to refer to the active form only. Some of the EPR spectra (recorded at about — 130° and 9.3 GHz) are reproduced to show the changes in signal type as the amount of xanthine is increased. (Data re-calculated from ref. 88, with intensities corrected for variations in tube diameter and enzyme concentration calculated in terms of active enzyme.)... Fig. 4. Anaerobic titration of xanthine oxidase with xanthine at pH 8.2 with a reaction time of 2 min. at about 20°. The integrated intensity of the Rapid molybdenum EPR signals (in arbitrary units) is plotted against the number of moles of xanthine added per mole of active enzyme. Activity/A4jo for the enzyme samples used was 112 corresponding to an active enzyme content of 57%. Thus the molar ratios of xanthine/total xanthine oxidase have been multiplied by 1.76 to refer to the active form only. Some of the EPR spectra (recorded at about — 130° and 9.3 GHz) are reproduced to show the changes in signal type as the amount of xanthine is increased. (Data re-calculated from ref. 88, with intensities corrected for variations in tube diameter and enzyme concentration calculated in terms of active enzyme.)...
Enzymes of the hepatic microsomes of most marine organisms, with the notable exception of certain molluscs, metabolize xeno-biotic substrates however, as much as 600-fold variations in enzyme activities have been noted between different species of marine teleosts (40). The hepatic enzyme activities of aquatic species are generally lower, with most substrates tested, than the hepatic enzymes of mammals (40). The mixed function oxidase enzymes in marine organisms are inducible by hydrocarbons, such as 3-methylcholanthrene or benzo[a]pyrene. Moreover, it is known... [Pg.64]

Some of the main types of cellular regulation associated with rhythmic behavior are listed in Table III. Regulation of ion channels gives rise to the periodic variation of the membrane potential in nerve and cardiac cells [27, 28 for a recent review of neural rhythms see, for example, Ref. 29]. Regulation of enzyme activity is associated with metabolic oscillations, such as those that occur in glycolysis in yeast and muscle cells. Calcium oscillations originate... [Pg.257]


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