Summary

[http://www.sigmaaldrich.com/catalog/product/sigma/51639?lang=de&region=DE TVEL0] was characterized in terms of its activity to establish activity test protocols and to create a standard which can be used as a reference.

TVEL0 Activity Tests

Initial Activity Test

Figure 1:Activity of TVEL0 laccase using 0.1 mM ABTS in 100 mM sodium actetate buffer (pH 5) measured at 25°C over a time period of 5 minutes. Saturation takes place after 3 minutes with 80% ABTS oxidized.

To standardize activity test methods used for this project a [http://www.sigmaaldrich.com/catalog/product/sigma/51639?lang=de&region=DE laccase from Trametes versicolor] (TVEL0) was used. The optimal composition for activity measurements contains 140 µL of 0.03 mg mL^-1 concentrated TVEL0 laccase solution, 100 mM sodium acetate buffer, 0.1 mM ABTS, ad 200 µL H₂O. With this approach activity in oxidizing ABTS of TVEL0 was measured over a time period of 5 minutes at 25°C. The saturation of the reaction was reached after 3 minutes when ~80% ABTS got oxidized (see figure 1). This result proofed the activity measurement method and can therefor be used as a positive control.

Optimal pH of TVEL0

Figure 2: Activity of TVEL0 laccase using 0.1 mM ABTS in 100 mM sodium actetate buffer testing a pH range from pH 1 to pH 9. Measurements were done at 25°C over a time period of 5 minutes. Only at pH 5 a saturation takes place after 3 minutes with 80% ABTS oxidized.

To determine the activity of TVEL0 in regard of optimal pH conditions different sodium acetate buffer pHs were under consideration for activity tests. Ranging from pH 1 to pH 9 the standardized activity setup of 100 mM sodium acetate, 140 µL of 0.03 mg mL^-1 concentrated TVEL0 laccase solution, 0.1 mM ABTS, ad 200 µL deionized H₂O was used. Only at pH 5 a saturation in ABTS_ox can be reached (see figure 2). As in the initial activity test above the maximal amount of ABTS_ox accounts ~80%. In summary the optimal pH for TVEL activity in oxidizing ABTS is ph 5.

TVEL0 activity depending on different ABTS concentrations

TVEL0 laccase were tested using different amounts of ABTS to calculate K_M and K_cat values. Instead of using 140 µL of a 0.03 mg mL^-1 TVEL0 protein solution, the amount was quartered to 35 µL of this solution. Reducing the enzyme concentration was necessary to detect the change in OD₄₂₀ at the beginning of the reaction. The standardized measurement setup as described above was used only with different amounts of ABTS. As expected, the amount of oxidized ABTS increased in dependence of the amount of ABTS used (Figure x).

Figure 3: Activity test of 35 µL of 0.03 mg mL^-1 concentrated TVEL0 laccase solution, 100 mM sodium acetate buffer, ad 200 µL deionized H₂O and different amounts of ABTS ranging from 0.5 µL to 16 µL ABTS.

Impact of MeOH and acteonitrile on TVEL0

For substrate analysis the usage of MeOH and acetonitrile is necessary to dissolve the substrates. To make sure TVEL0 laccase activity is not affected by these solvents activity tests using different amounts of MeOH and acetonitrile were done. An increase in MeOH or acetonitrile amount affects the activity of TVEL0, but leads to a saturation curve in most cases. Regarding tests with MeOH an addition of 14 µL of MeOH or more causes a loss of saturation (see figure 4). Under the usage of 12 µL acetonitrile or more the saturation curves get disordered (see figure 5). Still activity is detectable in all cases leading to the result that the usage of MeOH and acetonitrile for substrate analysis is possible.

Figure 4: Activity test of 140 µL of 0.03 mg mL^-1 concentrated TVEL0 laccase solution, 100 mM sodium acetate buffer, 0.1 mM ABTS, ad 200 µL deionized H₂O and different amounts of MeOH.

Figure 5: Activity test of 140 µL of 0.03 mg mL^-1 concentrated TVEL0 laccase solution, 100 mM sodium acetate buffer, 0.1 mM ABTS, ad 200 µL deionized H₂O and different amounts of acetonitrile.