Cryomilling-assisted high purity ß-chitin extraction from Uroteuthis edulis pens.

We report on the extraction of ß-chitin from pens (or Gladius) of Uroteuthis edulis, a squid species prevalent in the Pacific coastal regions of East Asia. In particular, we employ cryogenic mechanical grinding (or cryomilling) as a pre-treatment process for the raw squid pens. We show that the cryomilling step enables an effective pulverization of the raw materials, which facilitates the removal of protein residues allowing the extraction of high-purity ß-chitin with a high acetylation degree (∼97 %) and crystallinity (∼82 %). We also demonstrate that the Uroteuthis edulis extract ß-chitin affords a free-standing film with excellent optical transmittance and mechanical properties.

Transparent nanocellulose paper-based biodegradable colorimetric nerve agent detectors.

Transparent cellulose nanofiber (t-CNF) films were prepared by succinylation and an aqueous collision counter system treatment, and used for the colorimetric detection of diethyl chlorophosphate (DCP), a nerve agent mimic in the vapor phase. DCP receptor with an oxime residue was anchored on the surface of succinylated CNF films, resulting in the target probe (CNF-Azo films). CNF-Azo films exhibited selective detection behavior toward DCP in the vapor phase. The oxime groups of CNF-Azo film reacted with DCP upon exposure to DCP vapor, which was accompanied by a color change from yellow to purple. Significantly, the film's transparency was preserved throughout the detection process, allowing it to identify objects behind the film during DCP detection. This property could apply to any detection system in which the color change caused by detection does not interfere with the film's transparency. The CNF-based film sensor was biodegradable, allowing it to be disposable after use.

Transparent, water-stable, cellulose nanofiber-based packaging film with a low oxygen permeability.

Herein, we report on a transparent, water-stable, high oxygen barrier packaging film made from a combination of cellulose nanofiber (CNF) and a fluoropolymer (FP) coating. Nanofibrillation of the hardwood kraft pulp was carried out using succinic anhydride pretreatment and aqueous counter collision (ACC) technique to obtain ultrafine (5-7 nm) succinylated cellulose nanofibers (SCNF), which was readily fabricated into a thin coating (on PET film) as well as a self-standing film. Introducing the FP topcoat on SCNF enabled a synergistic enhancement of both oxygen barrier performance and stability against water-swelling.

Tailored Poly(vinylidene fluoride-co-trifluoroethylene) Crystal Orientation for a Triboelectric Nanogenerator through Epitaxial Growth on a Chitin Nanofiber Film.

Tailoring the crystal orientation of poly(vinylidene fluoride-co-trifluoroethylene) (PVDF-TrFE) has attracted widespread interest because of its effects on the ferroelectric properties required for various electronic devices. In this study, we investigated the epitaxial growth of PVDF-TrFE on a chitin film for developing triboelectric nanogenerators (TENGs). The crystallographic match between the chitin and PVDF-TrFE enables the development of the intended crystal orientation, with the PVDF-TrFE polarization axis aligned perpendicular to the substrate. In addition, the epitaxially grown PVDF-TrFE on chitin not only enhances the performance of the TENG but also increases the stability of the hygroscopic chitin film against water. The corresponding TENG exhibits a significantly higher output current compared to that of a nonepitaxial PVDF-TrFE/chitin film. Furthermore, the triboelectric sensors based on epitaxial PVDF-TrFE/chitin films allow the monitoring of subtle pressures, suggesting that tailoring the crystal orientation of PVDF-TrFE is a promising approach for developing high-performance TENGs.

Hierarchical Chitin Fibers with Aligned Nanofibrillar Architectures: A Nonwoven-Mat Separator for Lithium Metal Batteries.

Here, we introduce regenerated fibers of chitin (Chiber), the second most abundant biopolymer after cellulose, and propose its utility as a nonwoven fiber separator for lithium metal batteries (LMBs) that exhibits an excellent electrolyte-uptaking capability and Li-dendrite-mitigating performance. Chiber is produced by a centrifugal jet-spinning technique, which allows a simple and fast production of Chibers consisting of hierarchically aligned self-assembled chitin nanofibers. Following the scrutinization on the Chiber-Li-ion interaction via computational methods, we demonstrate the potential of Chiber as a nonwoven mat-type separator by monitoring it in Li-O2 and Na-O2 cells.

The changed immunoreactivity of StarD6 after pilocarpine-induced epilepsy.

This study was designed whether StarD6 is also affected by neurodegenerative stimuli, as other START proteins may be one of the delivery proteins in cholesterol metabolism of neurosteroid synthesis. Increased immunoreactivity of StarD6 was observed in all zones of the hippocampus by the administration of pilocarpine (350 mg/kg, intraperitoneally). More intense StarD6 immunolocalization was seen in the strata radiatum and lacunosum-moleculare, particularly in CA1-2 areas until 12 h after pilocarpine-induced epilepsy. StarD6 protein level was transiently increased at 3 h after pilocarpine-treated rat hippocampus comparing with normal rat. This raises the possibility that StarD6 might have nuclear roles and contribute to subsequent formation of neuroprotective steroids after excitotoxic brain injury.

Retardation of the unfolding process by single N-glycosylation of ribonuclease A based on molecular dynamics simulations.

The conformational characteristics of glycosylated- and unglycosylated bovine pancreatic ribonuclease A (RNaseA) were traced with unfolding molecular dynamics simulations using CHARMM program at 470 K. The glycosylated RNase (Glc_RNase) possesses nearly identical protein structure with RNaseA, differing only by presence of a single acetylglucosamine residue N-linked to Asn34 in the RNaseA. Attaching of monomeric N-acetylglucosamine residue to the Asn34 in RNaseA resulted in a change of denaturing process of Glc_RNase. Simulations showed that the unfolding of RNaseA involved significant weakening of nonlocal interactions whereas the glycosylation led Glc_RNase to preserve the nonlocal interactions even in its denatured form. Even in simulations over 8 ns at 470 K, Glc_RNase remained relatively stable as a less denatured conformation. However, conformation of RNaseA was changed to a fully unfolded state before 3 ns of the simulations at 470 K. This difference was due to fact that formation of hydrogen bond bridges and nonlocal contacts induced by the attached N-acetylglucosamine of Glc_RNase showing in the unfolding simulations. These high-temperature unfolding MD simulations provided a theoretical basis for the previous experimental work in which Glc_RNase showed slower unfolding kinetics compared with unglycosylated RNaseA, suggesting that single N-glycosylation induced retardation of unfolding process of the ribonuclease protein.