Engineered Penicillium funiculosum produces potent lignocellulolytic enzymes for saccharification of various pretreated biomasses.

• The secretome of Penicillium funiculosum demonstrated potent saccharification. • Saccharification by derepressed P. funiculosum (Pf Mig188) was 2-fold higher. • Optimal saccharification was achieved at pH 4.0 and a temperature range of 45-55°C. • The Pf Mig188 secretome hydrolysed variety of alkali and acid pretreated biomasses. • The secretome demonstrated minimal product inhibition at a 20 % biomass load. PfMig188, a catabolically derepressed engineered strain of the hyper-cellulolytic fungus Penicillium funiculosum NCIM1228, was investigated for the efficacy of its secretome for biomass saccharification. An inexpensive version of media containing microcrystalline cellulose, wheat bran and soya protein was optimized for producing a high-quality secretome from the PfMig188 strain in both shake flasks and in a 20-L bioreactor. The activities of four classes of core cellulolytic enzymes required for saccharification in the PfMig188 secretome, namely, cellobiohydrolase (Avicelase activity), endoglucanase (CMCase activity), β-glucosidase (PNPGase activity) and xylanase (xylanase activity), were found to be 2.29 U/mL, 28.24 U/mL, 150 U/mL and 76 U/mL, respectively. The saccharification potential of the PfMig188 secretome was evaluated on rice straw and sugarcane bagasse pretreated with nitric acid and/or ammonium hydroxide. Saccharification performed using a 15 % (w/v) biomass load and a 3% (w/w) enzyme load released >100 g/L sugar in the hydrolysate, irrespective of the type of biomass and pre-treatment, with >80 % hydrolysis. Furthermore, the presence of lignin in nitric acid-pretreated biomass only marginally affected saccharification. Overall, the results demonstrated that the PfMig188 secretome, having relatively broad substrate specificity, is a viable and efficient substitute for T. reesei -based secretomes for diverse biomass saccharification. [ABSTRACT FROM AUTHOR]