Back to Search
Start Over
Production of a high-efficiency cellulase complex via β-glucosidase engineering in Penicillium oxalicum
- Source :
- Biotechnology for Biofuels
- Publisher :
- Springer Nature
-
Abstract
- Background Trichoderma reesei is a widely used model cellulolytic fungus, supplying a highly effective cellulase production system. Recently, the biofuel industry discovered filamentous fungi from the Penicillium genus as a promising alternative to T. reesei. Results In our study, we present a systematic over-expression analysis of nine β-glucosidase encoding genes in the wild-type strain 114-2 of Penicillium oxalicum. We found that the over-expression of BGL1, BGL4, or BGL5 significantly enhanced both β-glucosidase activity and hydrolysis efficiency of the enzyme system on filter paper. We utilised two strategies to over-express β-glucosidase in the strain RE-10 that—although over-producing cellulase, does so at the cost of the cellulase mixture deficiency. The constitutive promoter of gene pde_02864 encoding 40S ribosomal protein S8 was used to over-express three β-glucosidases: BGL1, BGL4, and BGL5. We found that all mutants show significantly enhanced levels of β-glucosidase at transcriptional, protein, and activity levels. Furthermore, the inducible promoter from bgl2 was used to conditionally over-express the β-glucosidases BGL1 and BGL4. Surprisingly, this induced expression strategy enables significantly improved expression efficiency. The BGL1 over-expressing mutant I1-13 particularly improved the β-glucosidase activity at a factor of 65-folds, resulting in levels of up to 150 U/ml. All our BGL over-expression mutants displayed significant enhancement of cellulolytic ability on both microcrystalline cellulose and filter paper. In addition, they substantially reduced the enzyme loads in the saccharification of a natural lignocellulose material delignified corncob residue (DCCR). The mutant I4-32 with over-expression of BGL4 achieved the highest glucose yield in the saccharification of DCCR at only 25 % enzyme load compared to the parental strain RE-10. Conclusions In summary, genetically engineering P. oxalicum to significantly improve β-glucosidase activity is a potent strategy to substantially boost the hydrolytic efficiency of the cellulase cocktail, which will ultimately lead to a considerable reduction of cost for biomass-based biofuel. Electronic supplementary material The online version of this article (doi:10.1186/s13068-016-0491-4) contains supplementary material, which is available to authorized users.
- Subjects :
- 0106 biological sciences
0301 basic medicine
Mutant
Cellulase
Management, Monitoring, Policy and Law
01 natural sciences
Applied Microbiology and Biotechnology
Microbiology
03 medical and health sciences
Hydrolysis
chemistry.chemical_compound
Biofuel
010608 biotechnology
Cellulose
Trichoderma reesei
biology
Renewable Energy, Sustainability and the Environment
Beta-glucosidase
Research
Penicillium oxalicum
biology.organism_classification
Enzyme assay
030104 developmental biology
General Energy
Biochemistry
chemistry
β-glucosidase
Genetic engineering
Penicillium
biology.protein
Biotechnology
Subjects
Details
- Language :
- English
- ISSN :
- 17546834
- Volume :
- 9
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Biotechnology for Biofuels
- Accession number :
- edsair.doi.dedup.....e1ada621e638137493f0a91c64ec08ee
- Full Text :
- https://doi.org/10.1186/s13068-016-0491-4