Evaluation of the Enzymatic Arsenal Secreted by Myceliophthora thermophila During Growth on Sugarcane Bagasse With a Focus on LPMOs

• Published in: Frontiers in bioengineering and biotechnology 2020-08, Vol.8, p.1028-1028
• Main Authors: Grieco, Maria Angela B., Haon, Mireille, Grisel, Sacha, de Oliveira-Carvalho, Ana Lucia, Magalhães, Augusto Vieira, Zingali, Russolina B., Pereira, Nei, Berrin, Jean-Guy
• Format: Article
• Language: English
• Subjects: Bioengineering and Biotechnology; biofuels; biomass; biorefinery; enzyme; filamentous fungi; Life Sciences; LPMO
• ISSN: 2296-4185; 2296-4185
• DOI: 10.3389/fbioe.2020.01028

The high demand for energy and the increase of the greenhouse effect propel the necessity to develop new technologies to efficiently deconstruct the lignocellulosic materials into sugars monomers. Sugarcane bagasse is a rich polysaccharide residue from sugar and alcohol industries. The thermophilic fungusMyceliophthora thermophila(syn.Sporotrichum thermophilum) is an interesting model to study the enzymatic degradation of biomass. The genome ofM. thermophilaencodes an extensive repertoire of cellulolytic enzymes including 23 lytic polysaccharide monooxygenases (LPMOs) from the Auxiliary Activity family 9 (AA9), which are known to oxidatively cleave the beta-1,4 bonds and boost the cellulose conversion in a biorefinery context. To achieve a deeper understanding of the enzymatic capabilities ofM. thermophilaon sugarcane bagasse, we pretreated this lignocellulosic residue with different methods leading to solids with various cellulose/hemicellulose/lignin proportions and grewM. thermophilaon these substrates. The secreted proteins were analyzed using proteomics taking advantage of two mass spectrometry methodologies. This approach unraveled the secretion of many CAZymes belonging to the Glycosyl Hydrolase (GH) and AA classes including several LPMOs that may contribute to the biomass degradation observed during fungal growth. Two AA9 LPMOs, calledMtLPMO9B andMtLPMO9H, were selected from secretomic data and enzymatically characterized. AlthoughMtLPMO9B andMtLPMO9H were both active on cellulose, they differed in terms of optimum temperatures and regioselectivity releasing either C1 or C1-C4 oxidized oligosaccharides, respectively. LPMO activities were also measured on sugarcane bagasse substrates with different levels of complexity. The boosting effect of these LPMOs on bagasse sugarcane saccharification by aTrichoderma reeseicommercial cocktail was also observed. The partially delignified bagasse was the best substrate considering the oxidized oligosaccharides released and the acid treated bagasse was the best one in terms of saccharification boost.