Table 3. Effects of temperature, pH, and co-solvents on recombinant laccases.
IC50d (v/v %) | ||||||||
Laccase | Tm a (°C) | t1/2,50C b (min.) | Stable pHc | pH optimum | ACE | ACN | EtOH | MeOH |
Lcc4A | 49 | 28 | 2–8 | 2.5 | 42 | 30 | 34 | 28 |
Lcc5 | 33 | <15 | 3–6.5 | 2.5 | 20 | 18 | 18 | 22 |
Lcc7 | 57 | >120 | 3.5–5 | 3 | 25 | 17 | 22 | 24 |
Lcc1A | 47 | <15 | 2–8 | 2 | 30 | 36 | 30 | 28 |
Lcc1B | 47 | <15 | 2–8 | 2 | 30 | 36 | 30 | 26 |
Tm was defined as the temperature that 30-minute incubation led to 50% loss of enzyme activity. Assays were performed in 1×McIlvanie buffer (pH 4) by using 1 mM ABTS at 30°C (Fig. S3).
t1/2,50C was defined as the incubation time at 50°C that caused 50% loss of enzyme activity. Assays were performed in 1×McIlvanie buffer (pH 4) by using 1 mM ABTS at 30°C (Fig. S3).
Defined by residual activity ≥80%. Assays were performed in 1×McIlvanie buffer (pH 2–8) by using 1 mM ABTS at 30°C (Fig. S6).
Half maximal inhibitory concentration (IC50) was defined as the concentration of co-solvent that caused 50% loss of enzyme activity. Assays were performed in 1×McIlvanie buffer (pH 4) by using 1 mM ABTS at 30°C in the presence of respective solvent (Fig. S4).