Cloning and expression of Neurospora crassa cellobiohydrolase II in Pichia pastoris.

A major cellobiohydrolase of Neurospora crassa CBH2 was successfully expressed in Pichia pastoris. The maximum Avicelase activity in shake flask among seven transformants which selected on 4.0 g/L G418 plates was 0.61 U/mL. The optimal pH and temperature for Avicelase activity of the recombinant CBH2 were determined to be 4.8 and 60 °C, respectively. The new CBH2 maintained 63.5 % Avicelase activity in the range of pH 4.0–10.4, and 60.2 % Avicelase activity in the range of 30–90 °C. After incubation at 70–90 °C for 1 h, the Avicelase activity retained 60.5 % of its initial activity. The presence of Zn2+, Ca2+ or Cd2+ enhanced the Avicelase activity of the CBH2, of which Cd2+ at 10 mM causing the highest increase. The recombinant CBH2 was used to enhance the Avicel hydrolysis by improving the exo-exo-synergism between CBH2 and CBH1 in N.crassa cellulase. The enzymatic hydrolysis yield was increased by 38.1 % by adding recombinant CBH2 and CBH1, and the yield was increased by 215.4 % when the temperature is raised to 70 °C. This work provided a CBH2 with broader pH range and better heat resistance, which is a potential enzyme candidate in food, textile, pulp and paper industries, and other industrial fields. • A cellobiohydrolase of Neurospora crassa CBH2 was expressed in Pichia pastoris. • The recombinant CBH2 maintained 63.5 % Avicelase activity in the range of pH 4.0–10.4. • The recombinant CBH2 maintained 60.5 % Avicelase activity at 70–90 °C for 1 h. • The enzymatic hydrolysis yield was increased by 38.1 % by adding recombinant CBHs. [ABSTRACT FROM AUTHOR]