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130 2 Enzymes

In order to better understand the form of the

enzyme involved in catalysis, a hypothetical

enzyme-substrate system will be assayed and

interpreted. We will start from the assumption

that data are available for v 0 (initial velocity)

as a function of substrate concentration at

several pH’s, e. g., for the Lineweaver and

Burk. The values for K m and V are obtained

from the family of straight lines (Fig. 2.32) and

plotted against pH. The diagram of K −1

m = f(pH)

depicted in Fig. 2.33a corresponds to Fig. 2.31c

which implies that neutral (E n ) and positively

charged (E n+1 ) enzyme forms are active in

binding the substrate.

Figure 2.33b: V is dependent on one prototropic

group, the pK value of which is below neutrality.

Therefore, of the two enzyme-substrate complexes,

E n+1 AandE n A, present in the equilibrium

state, only the latter complex is involved in

the conversion of A to the product.

In the example given above, the overall effect of

pH on enzyme catalysis can be illustrated as follows:

(2.79)

This schematic presentation is also in agreement

with the diagram of V/K m = f(pH) (Fig. 2.33c)

Fig. 2.33. Evaluation of K m and V versus pH for a hypothetical

case

which reveals that, overall, two prototropic

groups are involved in the enzymecatalyzed

reaction.

An accurate determination of the pK values of

prototropic groups involved in enzyme-catalyzed

reactions is possible using other assays (cf. J.R.

Whitaker, 1972). However, identification of these

groups solely on the basis of pK values is not

possible since the pK value is often strongly influenced

by surrounding groups. Pertinent to this

claim is our recollection that the pH of acetic acid

in water is 4.75, whereas in 80% acetone it is

about 7. Therefore, the enzyme activity data as

related to pH have to be considered only as preliminary

data which must be supported and verified

by supplementary investigations.

2.5.4 Influence of Temperature

Fig. 2.32. Determination of V and K m at different pH

values

Thermal processes are important factors in the

processing and storage of food because they allow

the control of chemical, enzymatic and microbial

changes. Undesired changes can be delayed

or stopped by refrigerated storage. Heat

treatment may either accelerate desirable chemical

or enzymatic reactions or inhibit undesirable

changes by inactivation of enzymes or microorganisms.

Table 2.12 informs about quality dete-

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