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Eel aquaculture, though thriving nowadays, is totally dependent on the successful capture of wild eel fry and glass eels for its seedlings. The declination of eel resources in recent years has resulted in an urgent need for technology development in artificial seedlings production on an aquaculture basis, in order to protect natural resources and to stabilize the eel supply in the farming industry. Since the life history of the eel holds many mysteries, artificial hatching and rearing of larvae has long been regarded as an extremely difficult task. However, in recent years, the spawning ground of the Japanese eel has finally been located after continuous effort with intensive marine surveys, in which wild parental eels were captured, followed by the collection of fertilized eggs and the harvest of newly hatched preleptocephali. Meanwhile, through the collaborative efforts of many researchers, progress has also been made in improving technologies for artificial maturation of parental eels, which do not mature naturally in captivity, as well as in the technology for artificial hatching. Moreover, a technology for producing feed-rearing eel hatchlings, the most challenging process of all, has advanced rapidly after suitable feed was developed in the 1990s. Then, in 2002, for the first time in the world, larvae were successfully reared up to the glass eel stage, and second generation artificial hatchlings were born in 2010. In this way, eel farming technology that is not reliant on natural resources has been developed. There are strong hopes now for a technology for stable mass production of glass eels to be developed in the near future.

Establishing new energy-saving systems for gas separation using porous materials is indispensable for ensuring a sustainable future. Herein, we show that ELM-11 ([Cu(BF 4 ) 2 (4,4′-bipyridine) 2 ] n ), a member of flexible metal–organic frameworks (MOFs), exhibits rapid responsiveness to a gas feed and an ‘intrinsic thermal management’ capability originating from a structural deformation upon gas adsorption (gate-opening). These two characteristics are suitable for developing a pressure vacuum swing adsorption (PVSA) system with rapid operations. A combined experimental and theoretical study reveals that ELM-11 enables the high-throughput separation of CO 2 from a CO 2 /CH 4 gas mixture through adiabatic operations, which are extreme conditions in rapid pressure vacuum swing adsorption. We also propose an operational solution to the ‘slipping-off’ problem, which is that the flexible MOFs cannot adsorb target molecules when the partial pressure of the target gas decreases below the gate-opening pressure. Furthermore, the superiority of our proposed system over conventional systems is demonstrated. Separation processes in industry use substantial energy and energy-efficient purification systems should be developed for sustainability. Here the authors report a flexible metal–organic framework for high-throughput separation of CO 2 from a CO 2 /CH 4 gas mixture in a pressure vacuum swing adsorption system.

A phase diagram of water in single-walled carbon nanotubes at atmospheric pressure is proposed, which summarizes ice structures and their melting points as a function of the tube diameter up to 1.7 nm. The investigation is based on extensive molecular dynamics simulations over numerous thermodynamic states on the temperature-diameter plane. Spontaneous freezing of water in the simulations and the analysis of ice structures at 0 K suggest that there exist at least nine ice phases in the cylindrical space, including those reported by x-ray diffraction studies and those unreported by simulation or experiment. Each ice has a structure that maximizes the number of hydrogen bonds under the cylindrical confinement. The results show that the melting curve has many local maxima, each corresponding to the highest melting point for each ice form. The global maximum in the melting curve is located at [almost equal to]11 Å, where water freezes in a square ice nanotube.

Water-containing layered materials have found various applications such as water purification and energy storage. The highly structured water molecules around ions under the confinement between the layers determine the ion storage ability. Yet, the relationship between the configuration of interlayer ions and water structure in high ion storage layered materials is elusive. Herein, using layered double hydroxides, we demonstrate that the water structure is sensitive to the filling density of ions in the interlayer space and governs the ion storage. For ion storage of dilute nitrate ions, a 24% decrease in the filling density increases the nitrate storage capacity by 300%. Quartz crystal microbalance with dissipation monitoring studies, combined with multimodal ex situ experiments and theoretical calculations, reveal that the decreasing filling density effectively facilitates the 2D hydrogen-bond networking structure in water around interlayer nitrate ions along with minimal change in the layered structure, leading to the high storage capacity. Structured water is ubiquitous but not fully understood in confinement. Here authors show that the structure of water is sensitive to the configuration of ions in the nanoconfinement and governs ion storage in layered materials.

The drug efficacy evaluation of tumor-selective photosensitive substances was expected to be enabled by imaging the fluorescence intensity in the tumor area. However, fluorescence observation is difficult during treatments that are performed during gastrointestinal endoscopy because of the challenges associated with including the fluorescence filter in the camera part. To address this issue, this study developed a device that integrates a narrow camera and a laser diffuser to enable fluorescence imaging through a forceps port. This device was employed to demonstrate that a laser diffuser with an NIR fluorescence imaging sensor could be delivered through a 3.2 mm diameter port. In addition, fluorescence images of Cetuximab-IR700 were successfully observed in two mice, and the fluorescence intensity confirmed that the fluorescence decayed within 330 s. This device is expected to have practical application as a tool to identify the optimal irradiation dose for tumor-selective photosensitive substances under endoscopy.

Tup1-Cyc8 (also known as Tup1-Ssn6) is a general transcriptional corepressor. D-Mannitol (mannitol) and D-sorbitol (sorbitol) are the major polyols in nature. Budding yeast Saccharomyces cerevisiae is unable to assimilate mannitol or sorbitol, but acquires the ability to assimilate mannitol due to a spontaneous mutation in TUP1 or CYC8 . In this study, we found that spontaneous mutation of TUP1 or CYC8 also permitted assimilation of sorbitol. Some spontaneous nonsense mutations of CYC8 produced a truncated Cyc8 with a C-terminal polyglutamine. The effects were guanidine hydrochloride-sensitive and were dependent on Hsp104, but were complemented by introduction of CYC8 , ruling out involvement of a prion. Assimilation of mannitol and sorbitol conferred by other mutations of TUP1 or CYC8 was guanidine hydrochloride-tolerant. It is physiologically reasonable that S . cerevisiae carries this mechanism to acquire the ability to assimilate major polyols in nature.

Graphene oxide (GO) is the one of the most promising family of materials as atomically thin membranes for water-related molecular separation technologies due to its amphipathic nature and layered structure. Here, we show important aspects of GO on water adsorption from molecular dynamics (MD) simulations, in-situ X-ray diffraction (XRD) measurements, and ex-situ nuclear magnetic resonance (NMR) measurements. Although the MD simulations for GO and the reduced GO models revealed that the flexibility of the interlayer spacing could be attributed to the oxygen-functional groups of GO, the ultra-large GO model cannot well explain the observed swelling of GO from XRD experiments. Our MD simulations propose a realistic GO interlayer structure constructed by staggered stacking of flexible GO sheets, which can explain very well the swelling nature upon water adsorption. The transmission electron microscopic (TEM) observation also supports the non-regular staggered stacking structure of GO. Furthermore, we demonstrate the existence of the two distinct types of adsorbed water molecules in the staggered stacking: water bonded with hydrophilic functional groups and “free” mobile water. Finally, we show that the staggered stacking of GO plays a crucial role in H/D isotopic recognition in water adsorption, as well as the high mobility of water molecules. Graphene oxide is a promising material for molecular separation technologies. Here, the authors propose a realistic staggered stacking structure that plays a crucial role in H/D recognition in water adsorption, as well as high mobilities of water.

Nano-confined spaces in nanoporous materials enable anomalous physicochemical phenomena. While most nanoporous materials including metal-organic frameworks are mechanically hard, graphene-based nanoporous materials possess significant elasticity and behave as nanosponges that enable the force-driven liquid–gas phase transition of guest molecules. In this work, we demonstrate force-driven liquid–gas phase transition mediated by nanosponges, which may be suitable in high-efficiency heat management. Compression and free-expansion of the nanosponge afford cooling upon evaporation and heating upon condensation, respectively, which are opposite to the force-driven solid–solid phase transition in shape-memory metals. The present mechanism can be applied to green refrigerants such as H 2 O and alcohols, and the available latent heat is at least as high as 192 kJ kg −1 . Cooling systems using such nanosponges can potentially achieve high coefficients of performance by decreasing the Young’s modulus of the nanosponge. Conventional cooling systems rely on environmentally harmful halocarbons, while alternatives based on solid–solid transitions do not reach the required performance. Here the authors demonstrate using water and alcohol as refrigerants, through their confinement in nanosponges and their release by mechanical pressure.

The thermal transitions of confined polymers are important for the application of polymers in molecular scale devices and advanced nanotechnology. However, thermal transitions of ultrathin polymer assemblies confined in subnanometre spaces are poorly understood. In this study, we show that incorporation of polyethylene glycol (PEG) into nanochannels of porous coordination polymers (PCPs) enabled observation of thermal transitions of the chain assemblies by differential scanning calorimetry. The pore size and surface functionality of PCPs can be tailored to study the transition behaviour of confined polymers. The transition temperature of PEG in PCPs was determined by manipulating the pore size and the pore–polymer interactions. It is also striking that the transition temperature of the confined PEG decreased as the molecular weight of PEG increased. Understanding the thermal transitions of confined polymers is important for the design of molecular scale devices. In this study, unusual thermal transitions are observed in polyethylene glycol chains incorporated in nanochannels of porous coordination polymers.

Periodontitis is an inflammatory condition that causes the destruction of the supporting tissues of teeth and is a major public health problem affecting more than half of the adult population worldwide. Recently, members of the herpes virus family, such as the Epstein–Barr virus (EBV), have been suggested to be involved in the etiology of periodontitis because bacterial activity alone does not adequately explain the clinical characteristics of periodontitis. However, the role of EBV in the etiology of periodontitis is unknown. This study aimed to examine the effect of inactivated EBV on the expression of inflammatory cytokines in human gingival fibroblasts (HGFs) and the induction of osteoclast differentiation. We found that extremely high levels of interleukin (IL)-6 and IL-8 were induced by inactivated EBV in a copy-dependent manner in HGFs. The levels of IL-6 and IL-8 in HGFs were higher when the cells were treated with EBV than when treated with lipopolysaccharide and lipoteichoic acid. EBV induced IκBα degradation, NF-κB transcription, and RAW264.7 cell differentiation into osteoclast-like cells. These findings suggest that even without infecting the cells, EBV contributes to inflammatory cytokine production and osteoclast differentiation by contact with oral cells or macrophage lineage, resulting in periodontitis onset and progression.