Xyloglucan-Cellulose Nanocrystals Mixtures: A Case Study of Nanocolloidal Hydrogels and Levers for Tuning Functional Properties.

The development of fully biobased hydrogels obtained by simple routes and in the absence of toxic or environmentally harmful reagents is a major challenge in meeting new societal demands. In this work, we discuss the development of hydrogels made from cellulose nanocrystals (CNCs) and xyloglucan (XG), two non-toxic, renewable, and biobased components. We present three strategies to fine-tune the functional properties. The first one consists in varying the XG/CNC ratio that leads to the modulation of the mechanical properties of hydrogels as well as a better comprehension of the gel mechanism formation. The second relies on tuning the XG chains' interaction by enzymatic modification to achieve thermoresponsive systems. Finally, the third one is based on the increase in the hydrogel solid content by osmotic concentration. The high-solid-content gels were found to have very high mechanical properties and self-healing properties that can be used for molding materials. Overall, these approaches are a case study of potential modifications and properties offered by biobased nanocolloidal hydrogels.

Action of AA9 lytic polysaccharide monooxygenase enzymes on different cellulose allomorphs.

Lytic polysaccharide monooxygenase (LPMO)-catalyzed oxidative processes play a major role in natural biomass conversion. Despite their oxidative cleavage at the surface of polysaccharides, understanding of their mode of action, and the impact of structural patterns of the cellulose fiber on LPMO activity is still not fully understood. In this work, we investigated the action of two different LPMOs from Podospora anserina on celluloses showing different structural patterns. For this purpose, we prepared cellulose II and cellulose III allomorphs from cellulose I cotton linters, as well as amorphous cellulose. LPMO action was monitored in terms of surface morphology, molar mass changes and monosaccharide profile. Both PaLPMO9E and PaLPMO9H were active on the different cellulose allomorphs (I, II and III), and on amorphous cellulose (PASC) whereas they displayed a different behavior, with a higher molar mass decrease observed for cellulose I. Overall, the pretreatment with LPMO enzymes clearly increased the accessibility of all types of cellulose, which was quantified by the higher carboxylate content after carboxymethylation reaction on LPMO-pretreated celluloses. This work gives more insight into the action of LPMOs as a tool for deconstructing lignocellulosic biomass to obtain new bio-based building blocks.

Preparation of superabsorbent composite(s) based on dialdehyde cellulose extracted from banana fiber waste.

The study focus is the valorization of banana agriculture by products by the extraction and derivatization of cellulose and its incorporation in formulations to produce superabsorbent materials endowed with high water absorption performances. The extracted cellulose (BP) was subjected to a controlled oxidation by sodium periodate to convert it to cellulose dialdehyde (DAC) with controlled aldehyde content. The cellulosic materials were incorporated into a suspension containing acrylic acid (AA) and itaconic acid (IA) to produce composite hybrid hydrogels (SA-BP/SA-DAC) by radical chain polymerization in water, using N,N-methylene-bis-acrylamide (MBA) as a cross-linking agent and potassium persulfate (KPS) as an initiator. The prepared materials were characterized using techniques such as Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and rheological analysis. Additionally, the absorption and re-swelling capacities of the superabsorbent composites (SAPs) were assessed through kinetic studies in water and NaCl solution. Notably, dialdehyde cellulose (DAC), due to its low crystallinity index, hydrophilicity (attributed to aldehyde and hemiacetal functions), and high polarity, holds promise for enhancing the swelling and water retention capacity of the hydrogel. A water absorption capacity as high as 1240±60 g.g-1 was obtained for SA-DAC with a DAC content of 5 %wt. Additionally, the reusability of the SAPs was evidenced.

Rapid alkalinization factor 22 has a structural and signalling role in root hair cell wall assembly.

Pressurized cells with strong walls make up the hydrostatic skeleton of plants. Assembly and expansion of such stressed walls depend on a family of secreted RAPID ALKALINIZATION FACTOR (RALF) peptides, which bind both a membrane receptor complex and wall-localized LEUCINE-RICH REPEAT EXTENSIN (LRXs) in a mutually exclusive way. Here we show that, in root hairs, the RALF22 peptide has a dual structural and signalling role in cell expansion. Together with LRX1, it directs the compaction of charged pectin polymers at the root hair tip into periodic circumferential rings. Free RALF22 induces the formation of a complex with LORELEI-LIKE-GPI-ANCHORED PROTEIN 1 and FERONIA, triggering adaptive cellular responses. These findings show how a peptide simultaneously functions as a structural component organizing cell wall architecture and as a feedback signalling molecule that regulates this process depending on its interaction partners. This mechanism may also underlie wall assembly and expansion in other plant cell types.