Journal
BIOTECHNOLOGY FOR BIOFUELS
Volume 14, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s13068-021-01927-9
Keywords
Fusarium solani species complex; Fusarium metavorans; Genome analysis; Secretome; Mass spectrometry; Proteomics; CAZyme analysis; Cellulose degradation; Residual biomass treatment
Funding
- Projekt DEAL
- German federal ministry BMBF [03A0150B]
- International Center for the Chemical and Biological Sciences, University of Karachi
- Fundacao Faculdade de Medicina (FFM, Sao Paulo/Brazil)
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Efficient cellulose degraders were identified through screening fungi, with a high-performance cellulase-producing strain from Vietnam showing promising results on untreated sugarcane bagasse and maize leaves. The enzyme cocktail released reduced sugars without process disadvantages or loss of carbohydrates, making it a potential alternative for degrading agro-industrial lignocellulosic materials.
Background The transition to a biobased economy involving the depolymerization and fermentation of renewable agro-industrial sources is a challenge that can only be met by achieving the efficient hydrolysis of biomass to monosaccharides. In nature, lignocellulosic biomass is mainly decomposed by fungi. We recently identified six efficient cellulose degraders by screening fungi from Vietnam. Results We characterized a high-performance cellulase-producing strain, with an activity of 0.06 U/mg, which was identified as a member of the Fusarium solani species complex linkage 6 (Fusarium metavorans), isolated from mangrove wood (FW16.1, deposited as DSM105788). The genome, representing nine potential chromosomes, was sequenced using PacBio and Illumina technology. In-depth secretome analysis using six different synthetic and artificial cellulose substrates and two agro-industrial waste products identified 500 proteins, including 135 enzymes assigned to five different carbohydrate-active enzyme (CAZyme) classes. The F. metavorans enzyme cocktail was tested for saccharification activity on pre-treated sugarcane bagasse, as well as untreated sugarcane bagasse and maize leaves, where it was complemented with the commercial enzyme mixture Accellerase 1500. In the untreated sugarcane bagasse and maize leaves, initial cell wall degradation was observed in the presence of at least 196 mu g/mL of the in-house cocktail. Increasing the dose to 336 mu g/mL facilitated the saccharification of untreated sugarcane biomass, but had no further effect on the pre-treated biomass. Conclusion Our results show that F. metavorans DSM105788 is a promising alternative pre-treatment for the degradation of agro-industrial lignocellulosic materials. The enzyme cocktail promotes the debranching of biopolymers surrounding the cellulose fibers and releases reduced sugars without process disadvantages or loss of carbohydrates.
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