Electrically conducting films prepared from graphite and lignin in pure water.

In this study, we present electrically conducting self-standing graphite films consisting of lignin derivatives extracted by simultaneous enzymatic saccharification and comminution (SESC). Sonication of graphite powder in the presence of SESC lignin and pure water allows dispersion of the SESC-lignin-attached graphite without addition of other chemicals. The SESC-lignin-attached graphite having a diameter of several micrometers can be used as a surface electroconductive coating and molded into self-standing films by drying.

Nonflammable UV protective films consisting of clay and lignin with tunable light/gas transparency.

In this paper, we present nonflammable UV protective films consisting of clay minerals and lignin derivatives. The nonflammable transparent films were produced by mixing clay with a lignin derivative extracted from plants by simultaneous enzymatic saccharification and comminution. The preparation procedure did not require hazardous chemicals.

Spontaneous Alignment of Microtubules Via Tubulin Polymerization in a Narrow Space Under a Temperature Gradient.

In this chapter, protocols for spontaneous alignment of microtubules (MTs), such as helices and spherulites, via tubulin polymerization in a narrow space and under a temperature gradient are presented for tubulin solutions and tubulin-polymer mixtures. These protocols provide an easy route for hierarchical MT assembly and may extend our current understanding of cytoskeletal protein self-assembly under dissipative conditions.

Correction: Enhanced ionic conduction in composite polymer electrolytes filled with plant biomass "lignin".

Correction for 'Enhanced ionic conduction in composite polymer electrolytes filled with plant biomass "lignin"' by Zitong Liu , , 2022, DOI: 10.1039/d1cc07148c.

Enhanced ionic conduction in composite polymer electrolytes filled with plant biomass "lignin".

The addition of a small amount of plant biomass-based lignin causes a large improvement in the ionic conductivity of composite polymer electrolytes at room temperature, which can be fabricated easily in a low carbon way for use in future all-solid-state battery applications.

Radial alignment of microtubules through tubulin polymerization in an evaporating droplet.

We report the formation of spherulites from droplets of highly concentrated tubulin solution via nucleation and subsequent polymerization to microtubules (MTs) under water evaporation by heating. Radial alignment of MTs in the spherulites was confirmed by the optical properties of the spherulites observed using polarized optical microscopy and fluorescence microscopy. Temperature and concentration of tubulins were found as important parameters to control the spherulite pattern formation of MTs where evaporation plays a significant role.

Solvent-Free Fabrication of an Elastomeric Epoxy Resin Using Glycol Lignin from Japanese Cedar.

In this study, a simple formulation of softwood-derived glycol lignin (GL)-based epoxy resin with a high GL content of greater than 50 wt % was demonstrated by direct mixing with poly(ethylene glycol) diglycidyl ether (PEGDGE), an aliphatic epoxide, without using any solvent. Because the GL powder produced from poly(ethylene glycol) (PEG400) solvolysis of Japanese cedar softwood meal was a PEG400-modified lignin (GL400), a strong affinity between PEG counterparts facilitates the uniform mixing of GL400 with PEGDGE, and one component uncured GL400/PEGDGE epoxy resin was prepared at a relatively lower temperature (100 °C) than the curing temperature (130 °C). The epoxy curing reaction was monitored by H NMR and Fourier transform infrared spectroscopies.

Liquid Crystalline Colloidal Mixture of Nanosheets and Rods with Dynamically Variable Length.

Here, we demonstrate the novel double-component liquid crystalline colloids composed of mesogenic inorganic nanosheets and the rods with dynamically variable length controlled by temperature. As the length-controllable rod, stiff biopolymer microtubule is used, which was successfully polymerized/depolymerized from tubulin proteins through a biochemical process even in the presence of the nanosheets. The mesoscopic structure of the liquid crystal phase was reversibly modifiable as caused by the change of the rod length.

Simultaneous enzymatic saccharification and comminution for the valorization of lignocellulosic biomass toward natural products.

Background: Large-scale processing of lignocellulosics for glucose production generally relies on high temperature and acidic or alkaline conditions. However, extreme conditions produce chemical contaminants that complicate downstream processing. A method that mainly rely on mechanical and enzymatic reaction completely averts such problem and generates unmodified lignin.

Tuneable shape-memory properties of composites based on nanoparticulated plant biomass, lignin, and poly(ethylene carbonate).

In this article, we propose a thermally responsive shape-memory polymer (SMP) consisting of poly(ethylene carbonate) and non-deteriorated lignin nanoparticles. This SMP was obtained readily by thermal kneading and melt molding without requiring any chemical reaction. The shape-recovering properties of the SMP can be tuned by changing the feed ratio of the components.

Plant-Based Antioxidant Nanoparticles without Biological Toxicity.

Here, we present a function to derive non-deteriorated nanoparticulated lignin as an antioxidant without biological toxicity that is supplied through the simultaneous enzymatic saccharification and comminution of plants. The lignin exhibits an oxygen radical absorption capacity, even in its macromolecular nature. The non-deteriorated lignin nanoparticles never inhibit the biological activity of living things, despite their antioxidant nature.

Utilization of Lignocellulosic Biomass via Novel Sustainable Process.

In this review, we show novel methods for utilizing lignocellulosic biomass, polysaccharides, and lignin. Firstly, the simultaneous enzymatic saccharification and comminution (SESC) of plant materials is described as an extraction method for lignocellulosic biomass that does not require toxic reagents or organic solvents. Secondly, we demonstrate the material utilization of non-deteriorated lignocellulosic biomass extracted by SESC, such as for sugar and ethanol synthesis, and as a heatproof filler.

Application of microalgae hydrolysate as a fermentation medium for microbial production of 2-pyrone 4,6-dicarboxylic acid.

Actual biomass of microalgae was tested as a fermentation substrate for microbial production of 2-pyrone 4,6-dicarboxylic acid (PDC). Acid-hydrolyzed green microalgae Chlorella emersonii (algae hydrolysate) was diluted to adjust the glucose concentration to 2 g/L and supplemented with the nutrients of Luria-Bertani (LB) medium (tryptone 10 g/L and yeast extract 5 g/L). When the algae hydrolysate was used as a fermentation source for recombinant Escherichia coli producing PDC, 0.

Chiral-Linkage-Induced Hierarchical Ordering of Colloidal Achiral Nanotubes in their Thixotropic Gel.

Macroscopic continuous hierarchical ordering of achiral nanotube "imogolite" was achieved by thixotropic gelation of imogolite with chiral hydroxy acid and their flow-orienting/subsequent standing for uniaxial alignments of imogolite. The chirality change of the hydroxy acids resulted in an inversion of the helical ordering. The study presented here first exhibits the millimeter-scale supramolecular chirality induced by angstrom-scale molecular handedness in the architecture of nanotubes.

Helical alignment inversion of microtubules in accordance with a structural change in their lattice.

Giant helical (oriented chiral nematic) alignments of microtubules of nanometer to centimeter lengths are known to form over a temperature gradient during anisotropic spiral propagation via tubulin dimer addition in a capillary cell. Such helical alignments may be modified by the addition of either paclitaxel or dimethyl sulfoxide, which induces a lattice (helical) structural change in the microtubule itself. In this study, we found that the lattice structural change of microtubules brings about inversion of microtubule alignments in the helical ordering.

Preparation of a sulfo-group-containing rod-like polysilsesquioxane with a hexagonally stacked structure and its proton conductivity.

A sulfo-group-containing rod-like polysilsesquioxane with a hexagonally stacked structure (PSQ-SO3H) was successfully prepared by oxidation and hydrolytic polycondensation of 3-mercaptopropyltrimethoxysilane (MPTMS) in a mixed aqueous solution of NaOH and H2O2. The X-ray diffraction pattern of the PSQ-SO3H film exhibited three diffraction peaks with a d-value ratio of 1:1/√3:1/2, indicating the formation of a hexagonally stacked structure. In addition, the transmission electron microscopy image of PSQ-SO3H exhibited a striped pattern, indicating that the rod-like PSQs were stacked in a parallel fashion.

Direct evidence for structural transition promoting shear thinning in cylindrical colloid assemblies.

In this paper, we describe stimuli-responsive hydrogels prepared from a rigid rod-like polyelectrolyte 'imogolite' and a dicarboxylic acid. The hydrogel exhibited thixotropy in response to mechanical shock within the order of seconds or sub-seconds. Here, using the latest structural/rheological characterisation techniques, the relationship between the structural transition processes and the shear thinning was estimated.

Thermoresponsive synthetic polymer-microtubule hybrids.

Thermoresponsive hybrids consisting of synthetic polymers and microtubules (MTs), i.e., assemblies of tubulins, were prepared by bonding MTs covalently to a few reactive units in a macromolecular strand.

Structural and mechanical properties of Laponite-PEG hybrid films.

Inorganic/organic hybrids were obtained by the sol-gel type organic modification reaction of Laponite sidewalls with poly(ethylene glycol) (PEG) bearing alkoxysiloxy terminal functionality. By casting an aqueous dispersion of the hybrid, the flexible and transparent hybrid films were obtained. Regardless of the inorganic/organic component ratio, the hybrid film had the ordered structure of Laponite in-plane flat arrays.

Controlled clockwise-counterclockwise motion of the ring-shaped microtubules assembly.

The microtubule (MT)-kinesin system has been proposed as the building block of biomolecular motor based artificial biomachines. Considerable efforts have been devoted to integrate this system that produced a variety of ordered structures including the ring-shaped MT assembly which is being considered as a promising candidate for the further development of the biomachines. However, lack of proper knowledge that might help tune the direction of motion of ring-shaped microtubule assembly from counterclockwise to clockwise direction, and vice versa, significantly restricted their potential applications.

Flexible, transparent nanocomposite film with a large clay component and ordered structure obtained by a simple solution-casting method.

A flexible, transparent nanocomposite (NC) film with 57 wt % inorganic components was obtained by the simple casting of a solution of Laponite and modified organic molecules through a sol-gel reaction. The NC film has solvent resistance and a disco-nematic liquid-crystalline-like structure of Laponite that originates from the cross linking of Laponite by silanol agents and the large amount of Laponite in the film.

Integration of motor proteins - towards an ATP fueled soft actuator.

We present a soft bio-machine constructed from biological motors (actin/myosin). We have found that chemically cross-linked polymer-actin complex gel filaments can move on myosin coated surfaces with a velocity as high as that of native F-actin, by coupling to ATP hydrolysis. Additionally, it is shown that the velocity of polymer-actin complex gel depends on the species of polycations binding to the F-actins.

Mechanism on polarity sorting of actin bundles formed with polycations.

In this paper we explored factors that determine the polarity of an Actin bundle formed with polycation through electrostatic interaction. We found that the polarity decreases with an increase in the polycation concentration while it hardly depends on the KCl salt concentration. Additionally, the polarity of the Actin bundle increases with an increase in the degree of polymerization of the polycation at a constant polymer concentration.

Morphogenesis of liposomes caused by polycation-induced actin assembly formation.

We investigated the effects of polycation-mediated actin assembly on the morphological transformation of the lipid vesicle membrane by spatiotemporally controlling actin assembly. By triggering the radical polymerization of the cationic monomer using UV irradiation, we achieved a varied photoinduced assembly of actin in bulk solution. Furthermore, we designed liposomes containing actin and cationic monomers.