Insights from semi-oriented EPR spectroscopy studies into the interaction of lytic polysaccharide monooxygenases with cellulose

Semi-orientated EPR spectroscopy reveals that lytic polysaccharide monooxygenases interact with their natural cellulose substrate in a specific way, where the copper active site is positioned adjacent to the edge of a crystalline cellulose fibril.

Determination of Surface Accessibility of the Cellulose Substrate According to Enzyme Sorption

As a heterogeneous process, enzymatic hydrolysis depends on the contact area between enzymes and the cellulose substrate. The surface area of a substrate is typically evaluated through the sorption of gases (nitrogen, argon, or water vapor) or sorption of high-molecular-weight pigments or proteins. However, lignocellulosic biomass uninvolved in the reaction because of inefficient binding or even the complete inhibition of the enzymes on the surface consisting of lignin or inorganic compounds is erroneously taken into account under these conditions. The initial rate of enzymatic hydrolysis will directly depend on the number of enzymes efficiently sorbed onto cellulose. In this study, the sorption of cellulolytic enzymes was used to evaluate the surface accessibility of the cellulose substrate and its changes during mechanical pretreatment. It was demonstrated that for pure cellulose, mechanical activation did not alter the chemical composition of the surface and the initial rate of hydrolysis increased, which was inconsistent with the data on the thermal desorption of nitrogen. New active cellulose sorption sites were shown to be formed upon. the mechanical activation of plant biomass (wheat straw), and the ultimate initial rate of hydrolysis corresponding to saturation of the accessible surface area with enzyme molecules was determined.

Facile fabrication of photoinduced superhydrophobic–superhydrophilic surfaces on cellulose substrate without strength loss

A novel strategy was reported on the design and fabrication of functional photosensitive hybrid sols (FPHSs) by non-alcoholic emulsification in the presence of a TiO2 nanoparticle and photoinitiator via a sol-gel process using tetraethylorthosilicate, γ-methacryloxypropyltrimethoxysilane (MPS) and hydrophobic silane coupling agents as precursors. Smart cellulose substrates with alterable superhydrophobic–superhydrophilic conversion were fabricated using FPHS via the ultraviolet (UV) curing process. The liquid FPHS was photocured into solid gel during UV irradiation for 40 s with MPSs in FPHS, which was verified via Fourier transform infrared spectra. The cellulose substrates were modified with FPHSs, and the water contact angles of the modified cellulose substrates were more than 150°. The superhydrophobicity was improved by the gathering of hydrophobic chains and particle deposition of hybrid gel on the fiber surface. Nevertheless, the water contact angles of the modified cellulose substrates were receded with UV irradiation from 158° to 0° in 200 min, due to TiO2 photoinduction. The irradiated cellulose substrates were placed in the dark, and the water contact angles were recovered to about 130°, gradually. What is more, the reversible process can be repeated more than eight times. The modified cellulose substrate presented excellent washing fastness, even suffering 10 times washing processing. The mechanical properties, including breaking strength and elongation rate, were improved after the coating and UV curing process, which considerably remedied the defects of the heating curing process on the mechanical properties.