Thyssenfrank0220

Monolithic flow reactors are widely applied in numerous reactions due to its high efficiency and good reusability, but the green and efficient fabrication of monolithic flow catalytic system is still a challenge. Herein, the cellulose monolith prepared using a facile temperature-induced phase separation method was utilized to generate and immobilize the gold nanoparticles by a continuous-flow strategy, in which the cellulose monolith served as both reducing agent and supporting material. This process was conducted at room temperature and avoided the tedious surface modification of cellulose. The obtained cellulose-Au monolith can be directly applied as a green flow reactor in both water and organic solvents, and exhibited superior catalytic efficiency and good stability. This work provides a highly efficient, scalable and sustainable strategy for developing green catalytic system based on environmentally friendly cellulose monolith materials.Cellulose is the world's most abundant natural polymer that displays highly desirable characteristics such as biodegradability and sustainability. Atuzabrutinib Its derivatives and associated structured functional materials have potential in various fields such as surface engineering, energy and storage, water treatment, flexible electronics, construction, physical protection, and optical components. All of these applications demand nanocellulose-based micro/nano structural reconstruction for high performance. Recently, functional materials based on aligned nanocellulose in wood obtained through a top-down strategy have highlighted the importance of structure reconstruction strategies on functional designs. In this review, various cellulose or wood micro/nano materials designed by structure reconstruction were examined to highlight the importance of structure reconstruction strategies for various functionalities.Nanofibrillated cellulose (NFC) is becoming popular in the field of anti-counterfeiting material due to its favorable biocompatibility, renewability, and easy modification properties, which give it great potentials as carrier of carbon quantum dots (CQDs). Herein, we report an effective method to fabricate Yb and Er doped CQDs grafted onto dialdehyde NFC (DANFC). Owning to special rheological properties of NFC, a waterborne fluorescent dual anti-counterfeiting ink was rationally designed and successfully prepared by adding NFC to waterborne ink to form a stable network structure and increase the thixotropy and yield stress. The resulting CQDs exhibited both photoluminescence (PL) and up-conversion luminescence (UCPL), emitting blue and green fluorescence at excitation wavelengths of 370 and 980 nm, respectively. The study provides a novel method to prepare the waterborne fluorescent dual anti-counterfeiting ink based on Yb and Er doped CQDs/DANFC composites, which provides a reference for its application in printing and packaging industry.In this investigation, a variety of innovative temperature/pH-sensitive hydrogels consisting of hemicellulose (extracted from APMP waste liquor) and acrylic acid/acrylamide monomers were synthesized via free radical polymerization for water retention agents and controlled release. The results showed that the hydrogel polymer was chemically cross-linked and entangled to form a three-dimensional network structure, and the monomer successfully grafted on the hemicellulose chain. The content of crosslinkers and monomers had obvious effects on the swelling ratio of hydrogel. The sensitivity of the hydrogel was determined according to the change of the swelling ratio of the hydrogel under different temperature and pH conditions, combined with the chemical structure analysis of the hydrogel, and explain its sensitivity mechanism. Finally, after 6 days at 25 °C and pH 6, the swelled hydrogel still retained 79.46 % of the moisture, which proved that it has high water retention ability.The production of a chitin-like exopolysaccharide (EPS) was optimized through experimental design methods, evaluating the influence of urea, phosphate, and glucose. Under optimized conditions, up to 1.51 g/L was produced and its physicochemical characteristics were evaluated by chromatography, NMR, and FTIR spectroscopy, and rheological techniques. The results showed a homogeneous EPS (Mw 4.9 × 105 g mol-1) composed of chitin, linear polymer of β-(1→4)-linked N-acetyl-d-glucosamine residues. The acetylation degree as determined by 13C CP-MAS NMR spectroscopy was over 90 %. The EPS biological activities, such as antioxidant effect and antitumor properties, were evaluated. To the best of our knowledge, this is the first study on the production of a new alternative of extracellular chitin-like polysaccharide with promising bioactive properties from the filamentous fungus M. alpina.Tumor-associated macrophages (TAMs) with an M2-like phenotype have been linked to immunosuppression and resistance to chemotherapies of cancer, thus targeting TAMs has been an attractive therapeutic strategy to cancer immunotherapy. We have reported that the β-D-(1→6) glucan (AAMP-A70) isolated from Amillariella Mellea could promote macrophage activation. The present study showed that the β-1,6-glucan could promote the transformation of M2-like macrophages to M1-like phenotype and inhibit the viability of colon cancer cells in vitro and in vivo. On a cellular mechanistic level, the β-1,6-glucan reset tumor-promoting M2-like macrophages to tumor-inhibiting M1-like phenotype via increasing the phosphorylation of Akt/NF-κB and MAPK. Further, TLR2 was identified as the receptor of β-1,6-glucan in the transformation effect. In addition, a very similar β-1,6-glucan with side chains of β-Glc or α-Galρ which was purified from Lentinus edodes showed same activities with those from Amillariella Mellea. Our findings shed light on the action mode of β-1,6-glucan in cancer immunotherapy.Enzymatic transformation of xylans into renewable fuels and value-added products is mediated by xylanases. Here we describe the biochemical and X-ray structural characterization of Thermobacillus composti GH10 xylanase (TcXyn10A) at 2.1 Å resolution aiming to unravel details of its recognition of glucurono- and arabinoxylan at a molecular level. TcXyn10A improves the efficiency of pretreated lignocellulosic biomass hydrolysis by a commercial enzyme cocktail causing a 15.35 % increase in xylose release and 4.38 % glucose release after 24 h of reaction. The enzyme releases predominantly xylobiose and xylotriose, as well as MeGlcA3 × 3 (from beechwood glucuronoxylan) and a range of decorated xylooligosaccharides (XOS) from rye arabinoxylan, with Ara2 × 2 being the major product. The enzyme liberates XOS with the yields of 29.09 % for beechwood glucuronoxylan and 16.98 % for rye arabinoxylan. Finally, TcXyn10A has a high thermal stability, halotolerance, and resistance to ethanol, biochemical properties that can be desirable for a number of industrial applications.