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The ability of Methylobacterium extorquensto grow on methanol as the sole carbon and energy source has been the object of intense research activity. Unquestionably, the bacterial cell envelope serves as a defensive barrier against such an environmental stressor, with a decisive role played by the membrane lipidome, which is crucial for stress resistance. However, the chemistry and the function of the main constituent of the M. extorquensouter membrane, the lipopolysaccharide (LPS), is still undefined. Here, we show that M. extorquensproduces a rough-type LPS with an uncommon, non-phosphorylated, and extensively O-methylated core oligosaccharide, densely substituted with negatively charged residues in the inner region, including novel monosaccharide derivatives such as O-methylated Kdo/Ko units. Lipid A is composed of a non-phosphorylated trisaccharide backbone with a distinctive, low acylation pattern; indeed, the sugar skeleton was decorated with three acyl moieties and a secondary very long chain fatty acid, in turn substituted by a 3-O-acetyl-butyrate residue. Spectroscopic, conformational, and biophysical analyses on M. extorquensLPS highlighted how structural and tridimensional features impact the molecular organization of the outer membrane. Furthermore, these chemical features also impacted and improved membrane resistance in the presence of methanol, thus regulating membrane ordering and dynamics.

β-Glucosidase (BG) catalyzes the hydrolysis of cellobiose to glucose, a substrate for fermentation to produce the carbon-neutral fuel bioethanol. Enzyme thermal stability and reusability can be improved through immobilization onto insoluble supports. Moreover, nanoscaled matrixes allow for preserving high reaction rates. In this work, BG was physically immobilized onto wrinkled SiO2nanoparticles (WSNs). The adsorption procedure was tuned by varying the BG:WSNs weight ratio to achieve the maximum controllability and maximize the yield of immobilization, while different times of immobilization were monitored. Results show that a BG:WSNs ratio equal to 1:6 wt/wt provides for the highest colloidal stability, whereas an immobilization time of 24 h results in the highest enzyme loading (135 mg/g of support) corresponding to 80% yield of immobilization. An enzyme corona is formed in 2 h, which gradually disappears as the protein diffuses within the pores. The adsorption into the silica structure causes little change in the protein secondary structure. Furthermore, supported enzyme exhibits a remarkable gain in thermal stability, retaining complete folding up to 90 °C. Catalytic tests assessed that immobilized BG achieves 100% cellobiose conversion. The improved adsorption protocol provides simultaneously high glucose production, enhanced yield of immobilization, and good reusability, resulting in considerable reduction of enzyme waste in the immobilization stage.

Ibuprofen is one the most used non-steroidal anti-inflammatory drug, which is considered an emerging pollutant that may contaminate surface and underground water. Photodegradation using nanomaterials is one of the most sustainable and cheap technologies that can be used in water purification. In this study, the photodegradation efficiency of in-house prepared ceria (CeO2) nanostructured materials towards ibuprofen was assessed under UV irradiation. CeO2nanoparticles (NPs) were prepared through wet-chemical synthesis and characterized by several techniques. The photodegradation activity of the synthesized CeO2-NPs was compared to the commercial Aeroxide TiO2-P25. Small crystalline CeO2-NPs were obtained with about 15nm particle size, band-gap of 3.1eV with irregular morphology. The surface area of CeO2-NPs was estimated to be 76 ± 5 m2/g. Dynamic light scattering analysis revealed that these nanoparticles have a strong tendency to self-aggregate and to form clusters in aqueous suspension. The results showed a slightly better performance of Aeroxide TiO2-P25 compared to CeO2-NPs. On the other hand, five reusability tests confirmed the stability of CeO2-NPs in the reaction conditions, without any significant effect on their photodegradation activity. The goodness of the kinetic modeling of the experimental data was proven through the estimated kinetic parameters, together with the statistical information. The temperature effect confirmed that the higher the temperature, the greater the dissociation rate. Thus, there is a direct relationship between temperature, reaction rate, and the activation energy for each reaction. Furthermore, the thermodynamic parameters, namely: changes in Gibbs free energy (∆G°), enthalpy (∆H°), and entropy (∆S°) have been reported revealing the efficient photodegradation performance of CeO2-NPs.