Optimization of inulinase production by Kluyveromyces marxianus using factorial design
Applied biochemistry and biotechnology, 2001•Springer
Factorial design and response surface techniques were used to optimize the culture medium
for the production of inulinase by Kluyveromyces marxianus. Sucrose was used as the
carbon source instead of inulin. Initially, a fractional factorial design (2 5–1) was used in
order to determine the most relevant variables for enzyme production. Five parameters were
studied (sucrose, peptone, yeast extract, pH, and K 2 HPO 4), and all were shown to be
significant. Sucrose concentration and pH had negative effects on inulinase production …
for the production of inulinase by Kluyveromyces marxianus. Sucrose was used as the
carbon source instead of inulin. Initially, a fractional factorial design (2 5–1) was used in
order to determine the most relevant variables for enzyme production. Five parameters were
studied (sucrose, peptone, yeast extract, pH, and K 2 HPO 4), and all were shown to be
significant. Sucrose concentration and pH had negative effects on inulinase production …
Abstract
Factorial design and response surface techniques were used to optimize the culture medium for the production of inulinase by Kluyveromyces marxianus. Sucrose was used as the carbon source instead of inulin. Initially, a fractional factorial design (25–1) was used in order to determine the most relevant variables for enzyme production. Five parameters were studied (sucrose, peptone, yeast extract, pH, and K2HPO4), and all were shown to be significant. Sucrose concentration and pH had negative effects on inulinase production, whereas peptone, yeast extract, and K2HPO4 had positive ones. The pH was shown to be the most significant variable and should be preferentially maintained at 3.5. According to the results from the first factorial design, sucrose, peptone, and yeast extract concentrations were selected to be utilized in a full factorial design. The optimum conditions for a higher enzymatic activity were then determined: 14 g/L of sucrose, 10 g/L of yeast extract, 20 g/L of peptone, 1 g/L of K2HPO4. The enzymatic activity in the culture conditions was 127 U/mL, about six times higher than before the optimization.
Springer
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