4 mL of an iodine solution containing 3% (w/v) KI, 0.3% (w/v) I2 diluted to 4% (v/v) and its optical density was read at 620 nm using a spectrophotometer (Secoman). A standard curve for optical density as a function of starch concentration

was used to determine starch concentration. One unit of α-amylase activity PARP inhibitor (U) was defined as the amount of enzyme able to hydrolyze 1 g of soluble starch in 60 min under the experimental conditions. All the values presented are means of three replicates. The optimization of α-amylase in mixed culture was focused on three important independent variables, the initial yeast to bacteria ratio (R0), the temperature (T) and the pH. A Box–Behnken design with five replicates at the central point resulting in 17 experiments generated by Design Expert 8.0 software was used [5]. Each independent variable was studied at three different levels (low, medium, and high, coded as −1, 0, and +1, respectively). The coded variables are shown in Table 1 and the experimental design is shown in Table 2. All the experiments were done in triplicate and the average

of α-amylase ABT-199 nmr production obtained was taken as the dependent variable or response (Yi). The second order polynomial coefficients were calculated and analyzed using the Design Expert 8.0 software. The general form of the second order polynomial equation is: equation(4) Yi=α0+∑αiXi+∑αiiXi2+∑αiiXiXjWhere Yi is the predicted response, XiXj are input variables which influence the response variable Y; α0 is the offset term; αi is the ith linear coefficient; αii the ith quadratic coefficient and αij is the ijth interaction coefficient. In order to confirm effective interaction between studied microbial strains, the ANOVA of growth parameters μmax and Nmax when passing from pure to mixed culture was performed. This analysis included the Fisher’s F-test and its associated probability p(F). All these statistical analyses were carried out using a computer’s program Design Expert 8.0. The microbial strains propagated in culture broth according to a usual profile including lag, exponential and stationary phases. The maximum specific growth rate (μmax) and lag

time of each strain in starch broth at 30 °C in mono and mixed cultures were derived by the curve fitting procedure Carnitine palmitoyltransferase II of Baranyi and Robert [3]. The values of μmax and lag time were 0.142 h−1; 3.302 h, 0.163 h−1; 5.574 h, 0.105 h−1; 6.445 h (average of three replications) respectively for B. amyloliquefaciens 04BBA5, L. fermentum 04BBA19 and S. cerevisiae. These kinetics parameters, their standard deviations and the ANOVA are summarized in Table 3 and Table 4. The first mixed culture (mixed culture I) involved B. amyloliquefaciens 04BBA15 and S. cerevisiae. The comparison of the profile of growth for pure and mixed cultures ( Fig. 1a and b) showed that when B. amyloliquefaciens 04BBA15 was growing together with S. cerevisiae, the growth curve of S.