The degradation of biopolymers induced by the action of specific enzymes is a natural process that is nowadays employed as pre-treatment for plant biomass valorization, with the aim of producing fuels and bioplastics in a sustainable transition towards renewable sources [1]. Despite the current applications, the mechanisms of diffusion of decomposers ni the complex matrices they degrade, e.g. viscous polymer solutions or gels, are still poorly understood [2, 3]. We investigate the directional enzymatic hydrolyzation of lignocellulosic biopolymers by means of an original optical setup (Fig. 1) which combines Fluorescence Microscopy and Photon Correlation Imaging (PCI), a multispeckle Dynamic Light Scattering technique allowing one to probe the spatio-temporal heterogeneous dynamics of arrested systems [4]. We measure simultaneously the evolution of the spatial distribution of the fluorescently-labelled enzymatic decomposers and the microscopic dynamics of the polymer matrix undergoing degradation. Surprisingly, we find that the degradation kinetics of lignocellulosic gels follows a linear evolution ni time, rather than the diffusive propagation that one might have expected.Figure 1 : Left: Scheme of the Fluorescence-PCI setup. The light scattered from the polymer in the sample volume indicatedby the dashed blue region si detected by camera 1, while camera 2 measures the fluorescent intensity emitted by the enzymes. Right: Dynamic Activity Map (DAM) of a degrading polymer gel obtained by PCI measurements, showing the spatially heterogeneous dynamics of the gel matrix, 300 s after depositing an enzyme solution on top of the gel. Thedynamic activity si evaluated by the 'correlation index' c, [4] at a fixed lag-time t = 1,s which si close to one (dark shades) for the slow dynamics of the pristine gel and close to zero (bright shades) in the fluidized regions where the enzyme has[1] Kumar, M., Vivekanand, D., & Pareek N. (2021). Chapter 8 - Enzymatic degradation lignocellulosic waste: bioremediation and industrial implementation, Bioremediation for Environmental Sustanaibility, 163-191.[2] Cai L.-H., Paniukov, S., & Rubinstein, M. (2011). Macromolecules, 44(19), 7853-7863.[3] Sridar, R. L., & Verveney, F. (2018). Physical Review Applied, 9(3), 031001.[4] Duri, A., Sessoms, D. A., Trappe, V., & Cipelletti L.(2009). Physical Review Letters, 102(8), 085702.

To enhance the viscoelastic properties of Feruloylated Water Extractable ArabinoXylan (F-WEAX) gels, F-WEAX were covalently linked by a laccase in the presence of cellulose nanocrystals (CNC). The CNC/ F-WEAX weight ratios varied from 0 to 1.5 at a constant F-WEAX concentration of 1 % (w/v). The resulting CNC/ F-WEAX gels became stiffer with increasing CNC content with the elastic modulus scaling as [CNC]3. CNC also altered the relaxation spectrum of the CNC/ F-WEAX gels: the loss factor increased at low frequencies while remaining constant at high frequencies. The strong affinity between F-WEAX and CNC was demonstrated by in situ QCM-D analysis which showed that F-WEAX adsorb spontaneously and irreversibly onto CNC. Following laccase oxidative gelation, the rate of recovered ferulic acid (FA) in di-and trimer forms was twice as high when oxidation occurred in the presence of CNC. Due their higher covalent cross-link density, the swelling capacity of F-WEAX-CNC gels slightly decreased. The increased elasticity of the F-WEAX-CNC gels can thus be attributed to 3 factors: a higher volume fraction of CNC leading to increased entanglement, a greater number of di- or tri-ferulic acid covalent cross-links between F-WEAX chains, and the formation of multiarm physical junctions between F-WEAX and CNC.

Nous présentons dans cette étude une expérience de microscopie holographique numérique en ligne pour le suivi de bactéries en milieu confiné. Cette technique, simple de mise en œuvre, nous permet de caractériser la dynamique d'une suspension bactérienne dans un capillaire d'une centaine de micromètres. Nous présentons également le logiciel holotracker en libre accès qui permet de propager des hologrammes par la méthode du spectre angulaire et également d'utiliser différentes fonction de focus puis de tracking.

A double septin ring accompanies cytokinesis in yeasts and mammalian cells. In budding yeast, reorganisation of the septin collar at the bud neck into a dynamic double ring is essential for actomyosin ring constriction and cytokinesis. Septin reorganisation requires the Mitotic Exit Network (MEN), a kinase cascade essential for cytokinesis. However, the effectors of MEN in this process are unknown. Here we identify the F-BAR protein Hof1 as a critical target of MEN in septin remodelling. Phospho-mimicking HOF1 mutant alleles overcome the inability of MEN mutants to undergo septin reorganisation by decreasing Hof1 binding to septins and facilitating its translocation to the actomyosin ring. Hof1-mediated septin rearrangement requires its F-BAR domain, suggesting that it may involve a local membrane remodelling that leads to septin reorganisation. In vitro Hof1 can induce the formation of intertwined septin bundles, while a phosphomimetic Hof1 protein has impaired septin-bundling activity. Altogether, our data indicate that Hof1 modulates septin architecture in distinct ways depending on its phosphorylation status.

Hyper-Raman scattering is used to study the temperature dependence of the longitudinal optic (LO) modes of three prototypical ferroelectric relaxors in a broad temperature range from 20 to 800 K. The three LO bands observed in all spectra of the three materials are linked to the three transverse optic (TO) modes in cubic relaxors where LOi is linked to TOi , with i = 1 to 3. The Last, Slater, and Axe eigenvector pictures of the TO modes are consistent with our observations on LO1, LO2, and LO3, respectively. Within this framework, the splitting of LO2 would mostly be linked to a structural disorder on the B site while the strength of an anomaly of LO1 near the freezing temperature Tf relies on the ability of the material to develop a long-range ordering. Moreover, the more pronounced the splitting, the more important the structural disorder and the lower the value of the dielectric constant.