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One-dimensional negative thermal expansion material has important applications in thermal expansion control and fiber toughened composite. Orthorhombic Al1.6Sc0.4Mo3O12 nanofibers have been prepared by electrospinning. The phase composition, microstructure, morphology, and thermal expansion performance of the samples prepared at various temperatures were investigated. Results show that as-prepared Al1.6Sc0.4Mo3O12 nanofibers are smooth and homogeneous with a fiber diameter of about 370.00 nm, but they show an amorphous structure. Orthorhombic Al1.6Sc0.4Mo3O12 nanofibers can be obtained at 550 ℃ with a diameter of around 140.00 nm. With the increase of post-annealing temperatures, the crystallization of the samples was improved. However, higher post-annealing temperatures will destroy the nanofiber structure of the samples. HTXRD reveals that orthorhombic Al1.6Sc0.4Mo3O12 nanofibers show anisotropic NTE in 25–700 °C. The expansion coefficients αa, αb, and αc of Al1.6Sc0.4Mo3O12 nanofibers are −5.05 × 10–6 °C−1, 4.41 × 10–6 °C−1, and −3.18 × 10–6 °C−1, respectively. The αv is −3.83 × 10–6 °C−1, and the corresponding αl is −1.28 × 10–6 °C−1. [ABSTRACT FROM AUTHOR]

This study investigates the effects of ground tire rubber (GTR) on the cracking resistance of asphalt mortar from different analysis scales. Furthermore, the effectiveness of different fracture test methods was compared for GTR-modified asphalt mortar, including the indirect tensile cracking test (IDEAL-CT), disk-shaped compact tension test (DCT) and Illinois flexibility index test (I-FIT). To achieve this, a mesoscopic fracture test based on the SEM-Servo Plus device was proposed firstly to obtain the micro-parameters of constitutive models in discrete-element modelling (DEM). A unified fracture modelling procedure that can avoid any interference factors was carried out for comparative fracture analysis. Results from the tests and simulations show that rubber filler plays a positive role in enhancing the fracture properties of the asphalt mortar. The fracture energy measured by IDEAL-CT is almost 5–6 times of the DC(T) test and 1.5–2 times of the I-FIT test. It is not an inherent attribute of material and can only be regarded as a relative index for fracture resistance evaluation. The FI and CTindex obtained from the I-FIT and IDEAL-CT test show a weak correlation of fracture resistance, especially when comparatively evaluating the GTR-modified asphalt mortar with minor difference in filler content. [ABSTRACT FROM AUTHOR]

Smart aggregate (SA) is a multi-module integrated embedded monitoring sensor that has been employed in the construction, operation and maintenance of civil infrastructure. However, the differences in the shape and Yong's modulus of the SA and the host matrix lead to the matching errors between the SA sensor readings and the actual in-situ stress values. A systematic analysis of how the modulus ratio of the SA to the host matrix (E p/ E m), the length-to-height ratio of the sensor (L / H), and the non-homogeneity of the particle media interfere with the sensor monitoring data has been conducted in this paper using the finite element method and the discrete element method. In addition, the differences of the stress response from SA sensor under different load contact areas have been further investigated. Simultaneously, the numerical analysis has been validated by means of both theoretical derivations and laboratory tests. The analysis results show that E p/ E m and L / H are the two key factors affecting the matching error. In particular, when E p/ E m > 1, the matching error is positive and vice versa, while the L / H of the sensor is negatively correlated with the matching error. It is also noteworthy that the errors in the SA sensor monitoring data due to media inhomogeneity can only be negligible when the sensor diameter is larger than 20 times of the largest particle size in the host matrix. This study provides a theoretical guidance for optimizing the design of SA sensors and improving the accuracy of their measurement results. [ABSTRACT FROM AUTHOR]

The work aims to reveal relationship between solution temperature, microstructure, and mechanical properties of Ti–5Al5Mo5V3Cr1Zr (Ti‐55 531) alloy. The alloys are prepared via solution processing in a temperature ranging from Tβ − 100 °C (where Tβ is β‐transus temperature) to Tβ + 100 °C for 2 h; and then air cooled, aged at 600 °C for 6 h, and air cooled again. Results indicate that solution temperature range (from Tβ − 100 °C to Tβ + 100 °C) can be divided into following five ranges according to performance of Ti‐55 531 alloy. The alloy presents excellent mechanical performance combining high strength and good ductility for solution temperatures ranging from Tβ − 50 °C to Tβ − 30 °C and from Tβ + 10 °C to Tβ + 30 °C. Interestingly, the Ti‐55 531 alloy exhibits a dramatically enhanced strength, while ductility drops rapidly as solution temperature exceeds Tβ + 70 °C. The enhanced strength's main reason is that grain boundary α phase changes from continuous to discontinuous with increasing solution temperature; nevertheless, the increased size of β grains results in a reduction in ductility. Thus, continuity of grain boundary α phase has a dramatical influence on performance of Ti‐55 531 alloy. [ABSTRACT FROM AUTHOR]

Microcystins (MCs) are extremely hazardous to the ecological environment and public health. How to control and remove MCs is an unsolved problem all over the world. Some microbes and their enzymes are thought to be effective in degrading MCs. Microcystinase can linearize microcystin-leucine-arginine (MC-LR) via a specific locus. However, linearized MC-LR is also very toxic and needs to be removed. How linearized MC-LR was metabolized by linearized-microcystinase, especially how linearized-microcystinase binds to linearized MC-LR, has not been defined. A combination of in vitro experiments and computer simulation was applied to explore the characterization and molecular mechanisms for linearized MC-LR degraded by linearized-microcystinase. The purified linearized-microcystinase was obtained by recombinant Escherichia coli overexpressing. The concentration of linearized MC-LR was detected by high-performance liquid chromatography, and linearized MC-LR degradation products were analyzed by the mass spectrometer. Homology modeling was used to predict the structure of the linearized-microcystinase. Molecular docking techniques on the computer were used to simulate the binding sites of linearized-microcystinase and linearized MC-LR. The purified linearized-microcystinase was obtained successfully. The linearized-microcystinase degraded linearized MC-LR to tetrapeptide efficiently. The second structure of linearized-microcystinase consisted of many alpha-helices, beta-strands, and colis. Linearized-microcystinase interacted the linearized MC-LR with hydrogen bond, hydrophobic interaction, electrostatic forces, and the Van der Waals force. This study firstly reveals the characterization and specific enzymatic mechanism of linearized-microcystinase for catalyzing linearized MC-LR. These findings encourage the application of MC-degrading engineering bacteria and build a great technique for MC-LR biodegradation in environmental engineering. [ABSTRACT FROM AUTHOR]

Members of genus Sphingopyxis are frequently found in diverse eco-environments worldwide and have been traditionally considered to play vital roles in the degradation of aromatic compounds. Over recent decades, many aromatic-degrading Sphingopyxis strains have been isolated and recorded, but little is known about their genetic nature related to aromatic compounds biodegradation. In this study, bacterial genomes of 19 Sphingopyxis strains were used for comparative analyses. Phylogeny showed an ambiguous relatedness between bacterial strains and their habitat specificity, while clustering based on Cluster of Orthologous Groups suggested the potential link of functional profile with substrate-specific traits. Pan-genome analysis revealed that 19 individuals were predicted to share 1,066 orthologous genes, indicating a high genetic homogeneity among Sphingopyxis strains. Notably, KEGG Automatic Annotation Server results suggested that most genes pertaining aromatic compounds biodegradation were predicted to be involved in benzoate, phenylalanine, and aminobenzoate metabolism. Among them, β-ketoadipate biodegradation might be the main pathway in Sphingopyxis strains. Further inspection showed that a number of mobile genetic elements varied in Sphingopyxis genomes, and plasmid-mediated gene transfer coupled with prophage- and transposon-mediated rearrangements might play prominent roles in the evolution of bacterial genomes. Collectively, our findings presented that Sphingopyxis isolates might be the promising candidates for biodegradation of aromatic compounds in pollution sites. [ABSTRACT FROM AUTHOR]

The aromatic compound phenylacetic acid (PAA) is present in the environment, and released in the catabolism of phenylalanine, 2-phenylethylamine, or environmental contaminants such as ethylbenzene and styrene. PAA was also proposed to be involved in human chronic kidney disease development. Several bacteria and fungi utilize these aromatic acids as sole carbon source either during aerobic or anaerobic conditions. The aromatic structure of PAA makes this compound resistant toward oxidation or reduction, because the stabilizing resonance energy of the aromatic ring system is difficult to overcome. In the case of bacteria that utilize aromatic compounds as growth substrates, the aromatic ring system limits survival due to a lack of carbon source. Sphingopyxis sp. YF1 isolated from Lake Taihu was found to be beneficial in bioremediation of aromatic compounds. This study thus aimed to examine the influence of environmental factors such as temperature, PAA concentration, and pH on the effectiveness of Sphingopyxis sp. YF1 to degrade aromatic compounds using PAA as model compound. Data showed the highest PAA-degrading rate of strain Sphingopyxis sp. YF1 was 7.6 mg/L·h under the condition of 20°C, pH 9 with a 1000 μg/ml concentration of PAA. Evidence indicates that PAA-degrading ability of strain Sphingopyxis sp. YF1 appears to be primarily influenced by the concentration of PAA, followed by temperature and pH. PAA-degrading gene PAAase was identified in this strain using polymerase chain reaction (PCR) method. These results illustrate that the bacteria Sphingopyxis sp. YF1 removes PAA effectively at certain environmental conditions and this proves beneficial in bioremediation of aromatic compounds. [ABSTRACT FROM AUTHOR]

The presence of cyanobacteria in drinking water, aquatic foods and bathing water has created a significant major problem to global public health as these toxins induce damage in various organ including liver, cardiovascular, intestinal and central nervous systems. Although the morphologic, phylogenetic and toxicogenetic characteristics of cyanobacteria were identified in several lakes in China, many freshwater sources such as Dong Ting Lake, Hunan Province, China remain to be determined. Since the presence of these cyanobacteria may potentially affect human health, the aim of this study was to isolate, identify and characterize the most frequent occurring bloom-forming cyanobacteria in Dong Ting Lake, Hunan Province, China, which can provide information on the safety of utilization of this water source for drinking water, agriculture and recreation. Samples collected from the surface water of Dong Ting Lake were subjected to serial dilution in the lab for morphological analysis. Data demonstrated the morphological features were 2–5 µm diameters with rounded shapes and green color resembling Microcystis sp. The isolated cyanobacterial strain obtained from surface water samples in Dong Ting Lake was termed Microcystis sp. YFM2. The MC concentration was detected by enzyme-linked immunosorbent assay (ELISA) and found to be 92.88 µg/107 cells in Microcystis sp. YFM2. By polymerase chain reaction (PCR) results indicated that Microcystis sp. YFM2 isolated from Dong Ting Lake contained synthetase genes (mcyA-C). Our findings indicated that the dominant cyanobacteria Microcystis sp. YFM2 isolated from the freshwater Dong Ting Lake demonstrated morphologic, phylogenetic and toxicogenetic properties resembling a toxin generating cyanobacterium. Based upon this knowledge, it is essential to monitor the use of this Lake for future domestic, agricultural and recreational purposes. [ABSTRACT FROM AUTHOR]

Microcystin-LR (MC-LR), a known hepatotoxin present in drinking water, and contaminated food and algal dietary supplements poses a threat to environmental and public health and thus needs to be removed. Previously microbial aerobic degradation was considered the predominant catabolic process for MC-LR inactivation, but the potential role of anaerobic microbes still needs to be determined. In our study an anaerobic MC-degrading bacterium Enterobacter sp. YF3 was isolated and identified that was capable of degrading MC-LR. Under optimal conditions the anaerobic Enterobacter sp. YF3 displayed a MC-degrading rate of 0.34 µg/ml/day. This process was dependent on temperature, pH and MC-LR concentration. Further the extracellular secretion of metabolites of anaerobic bacterium degraded MC-LR at 0.22 µg/ml/day. The parent MC-LR as well as two MC-degrading products was identified by high performance liquid chromatography (HPLC). The anaerobic MC-degrading Enterobacter sp. bacterium metabolized MC-LR independent of MC-degrading genes mlrABCD. Data indicate that anaerobic Enterobacter sp. YF3 produces MC-degrading products via a pathway that acts independently of mlrABCD genes which may add to the arsenal of bacteria to degrade microcystins. [ABSTRACT FROM AUTHOR]

Harmful Microcystis aeruginosa blooms occurred frequently in many eutrophic lakes and rivers with resultant serious global environmental consequences. Algicidal bacteria may play an important role in inhibiting the growth of Microcystis aeruginosa and are considered as an effective method for preventing the appearance of blooms. In order to counteract the harmful effects of Microcystis aeruginosa, a critical step is to identify, isolate and characterize indigenous algicidal bacteria. This study aimed to isolate a novel indigenous algicidal bacterium identified as Chryseobacterium species based upon its 16S rDNA sequence analysis, and determine whether this bacterium was effective in lysing Microcystis aeruginosa FACHB 905. The influence of environmental factors including temperature, pH, quantity of Chryseobacterium species as well as Microcystis aeruginosa concentration were examined with respect to algae-lysing properties of this bacterial strain. Data demonstrated that the highest algae-lysing activity of 80% against Microcystis aeruginosa FACHB 905 occurred within 72 hr. In addition, the algae-lysing activities of Chryseobacterium species cells were significantly higher than those of cell-free supernatant. In conclusion, data showed the algicidal bacterium Chryseobacterium species exhibited potent Microcystis aeruginosa-lysing activities and attacked Microcystis aeruginosa directly suggesting this algicidal bacterium may be potentially useful for reducing the number of harmful Microcystis aeruginosa blooms. [ABSTRACT FROM AUTHOR]

Microcystins (MCs) are the most common and toxic cyanotoxins that are hazardous to human health and ecosystems. Microcystinase is the enzyme in charge of the initial step in the biodegradation of MCs. The characterization, application conditions, and detoxification mechanisms of microcystinase from an indigenous bacterium Sphingopyxis sp. YF1 towards MC-LR were investigated in the current study. The microcystinase gene of strain YF1 was most similar to Sphingomonas sp. USTB-05 and contained a CAAX-family conversed abortive Infection (ABI) domain. The microcystinase was successful obtained and purified by overexpression in Escherichia coli. The highest degradation rate of MC-LR was 1.0 μg/mL/min under the optimal condition of 30 ℃, pH 7, 20 μg/mL MC-LR, and 400 μg/mL microcystinase. The MC-degrading product was identified as linearized MC-LR, which possessed a much lower inhibitory activity against protein phosphatase 2A than MC-LR. Microcystinase interacted with MC-LR via amino acid residues involved in through the formation of conventional Hydrogen Bond, Pi-Pi T-shapes, Van der Waals force, and so on. The optimal MC-degrading condition of pure microcystinase and its detoxification mechanisms against MC-LR were revealed. The toxicity of purified linearized MC-LR was explored for the first time. These findings suggest that pure microcystinase may efficiently detoxify MCs and it is promising in the bioremediation of MC-polluted environments. [Display omitted] • The purified microcystinase of Sphingopyxis sp. YF1 was obtained successfully. • The highest MC-LR degradation rate of microcystinase was 1.0 μg/mL/min. • Purified linearized MC-LR possessed much lower toxicity than that of MC-LR. • The detoxification mechanisms of microcystinase against MC-LR was elucidated. [ABSTRACT FROM AUTHOR]

In this paper, we investigate a magnetic diffusion field (MDF) within a guided wave wire, and analyze a one-to-one mapping between the MDF and the signal of a magnetostrictive position sensor (MPS). In order to control the MDF, two approaches—a magnetism absorption strap (MAS) and a magnetized MAS—are proposed. On the operation mechanisms of the two approaches, the similarity between the two methods is to establish a branch for the magnetic energy of the MDF. However, the difference between them is that the MAS relies on magnetic energy to be leaked and the magnetized MAS relies on the magnetic energy to be absorbed. The feasibility of the proposed concept and approaches has been verified by simulation and experiments. This work contributes to the theory of MPS by enriching the signal mechanism. Finally, it is suggested that the proposed approaches can be applied to develop new sensors for measurement of the micro-distance and the magnetic permittivity. [ABSTRACT FROM AUTHOR]

Microcystis blooms and their secondary metabolites microcystins (MCs) occurred all over the world, which have damaged aquatic ecosystems and threatened public health. Techniques to reduce the Microcystis blooms and MCs are urgently needed. This study aimed to investigate the algicidal and inhibitory mechanisms of a red pigment prodigiosin (PG) against the growth and MC-producing abilities of Microcystis aeruginosa (M. aeruginosa). The numbers of Microcystis cells were counted under microscope. The expression of microcystin synthase B gene (mcyB) and concentrations of MCs were determined by quantitative real-time polymerase chain reaction (qRT-PCR) and enzyme linked immunosorbent assay (ELISA) methods, respectively. The inhibitory effects of PG against M. aeruginosa strain FACHB 905 with 50% algicidal concentration (LC 50) at 120 h was 0.12 μg/mL. When M. aeruginosa cells exposed to 0.08 μg/mL, 0.16 μg/mL, 0.32 μg/mL PG, the expression of mcyB of M. aeruginosa was down-regulated 4.36, 8.16 and 18.51 times lower than that of the control at 120 h. The concentrations of total MC (TMC) also were 1.66, 1.72 and 5.75 times lower than that of the control at 120 h. PG had high algicidal effects against M. aeruginosa , with the activities of superoxide dismutase (SOD) initially increased and then decreased after 72 h, the contents of malondialdehyde (MDA) increase, the expression of mcyB gene down-regulation, and MCs synthesis inhibition. This study was first to report the PG can simultaneously lyse Microcystis cells, down-regulate of mcyB expression and inhibit MCs production effectively probably due to oxidative stress, which indicated PG poses a great potential for regulating Microcystis blooms and MCs pollution in the environment. Image 1 • PG has high algicidal effects against Microcystis aeruginosa. • PG down-regulates mcyB expression and reduces MCs production effectively. • The algicidal and inhibitory mechanisms of PG against Microcystis sp. are related to oxidative stress. PG poses a great potential for regulating Microcystis blooms and MCs pollution by simultaneously lysing M. aeruginosa and inhibiting the synthesis of MCs. [ABSTRACT FROM AUTHOR]

The increasing cyanobacterial blooms have recently been considered a severe environmental problem. Microcystin-leucine arginine (MC-LR) is one of the secondary products of cyanobacteria metabolism and most harmful cyanotoxins found in water bodies. Studies show MC-LR negatively affects various human organs when exposed to it. The phenotype of the jejunal chronic toxicity induced by MC-LR has not been well described. The aim of this paper was to investigate the effects of MC-LR on the jejunal microstructure and expression level of inflammatory-related factors in jejunum. Mice were treated with different doses (1, 30, 60, 90 and 120 μg/L) of MC-LR for six months. The microstructure and mRNA expression levels of inflammation-related factors in jejunum were analyzed. Results showed that the microstructure of the jejunum was destroyed and expression levels of inflammation-related factors interleukin (IL)-1β, interleukin (IL)-8, tumor necrosis factor alpha, transforming growth factor-β1 and interleukin (IL)-10 were altered at different MC-LR concentrations. To the best of our knowledge, this is the first study that mice were exposed to a high dose of MC-LR for six months. Our data demonstrated MC-LR had the potential to cause intestinal toxicity by destroying the microstructure of the jejunum and inducing an inflammatory response in mice, which provided new insight into understanding the prevention and diagnosis of the intestinal diseases caused by MC-LR. [ABSTRACT FROM AUTHOR]

Microcystin-LR (MC-LR) is the most toxic and frequently detected monocyclic heptapeptide hepatotoxin produced by cyanobacteria, which poses a great threat to the natural ecosystem and public health. It is very important to seek environment-friendly and cost-efficient methods to remove MC-LR in water. In this study, the MC-degrading capacities of a novel indigenous bacterial community designated as YFMCD4 and the influence of environmental factors including various temperatures, MC concentrations and pH on the MC-degrading activities were investigated utilizing high-performance liquid chromatography (HPLC). In addition, the MC-degrading mechanism of YFMCD4 was also studied using HPLC coupled with a mass spectrometry equipped with electrospray ionization interface (HPLC-ESI-MS). The data showed MC-LR was completely removed at the maximum rate of 0.5 µg/(mL·h) under the optimal condition by YFMCD4. Two pure bacterial strains Alcaligenes faecalis and Stenotrophomonas acidaminiohila were isolated from YFMCD4 degraded MC-LR at a slower rate. The MC-degrading rates of YFMCD4 were significantly affected by different temperatures, pH and MC-LR concentrations. Two intermediates of a tetrapeptide and Adda appeared in the degradation process. These results illustrate that the novel YFMCD4 is one of the highest effective MC-degrading bacterial community, which can completely remove MC-LR and possesses a significant potential to treat water bodies contaminated by MC-LR. [ABSTRACT FROM AUTHOR]

Ethnopharmacological relevance Kai-Xin-San, an ancient formula composed of Ginseng Radix et Rhizoma, Polygalae Radix, Acori Tatarinowii Rhizoma and Poria, was frequently applied for major depression disorders for thousands of years. However, its molecular mechanism has not clearly been investigated. Aim of the study We aimed to reveal the action mechanism of KXS on anti-depression on inducing neuronal differentiation on PC12 cells. Materials and methods A chemically standardized water extract of KXS was applied onto cultured PC12 cells in determining its effect on neurotransmitter regulation enzymes and neurite outgrowth. Results Single KXS treatment showed obvious changes in the expression of neurofilament and neurotransmitter regulation enzymes, which in parallel to treatment of nerve growth factor (NGF). Although KXS by itself did not show significant inductive effect on neurite outgrowth of PC12 cells, KXS could potentiate the NGF induced neurite outgrowth. Among the three ratios, K-652 showed the most powerful effect and cAMP-dependent pathway might play the major role. Conclusions KXS might exert the anti-depressant-like action of be inducing neuronal differentiation, which supported the clinically usage of this decoction. [ABSTRACT FROM AUTHOR]

The increasing production of microcystin-LR (MC-LR) causing animal and human health issues is found in eutrophic water bodies, marine habitats and desert environments. The health threat posed by MC-LR has led to the establishment of World Health Organization's water guideline value of 1 μg/mL. Combating this has increased the search for cost-effective approach to degrade MC-LR. The study aimed to optimize the MC-degrading environmental factors of bacterial community YFMCD4. Response surface methodology (RSM) was employed to evaluate the influence of varying temperatures, pH and initial MC-LR concentration on the biodegradation efficiency of MC-LR by bacterial community YFMCD4. The optimal MC-LR biodegradation environmental factors were found to be 30 °C, pH 7 and 2 μg/mL initial MC-LR. The biodegradation rate reached 100% after 10 h. YFMCD4 mainly consisted of genera Alacligenes , Sphingobacterium and Pseudomonas using High-throughput pyrosequencing technology. The mlrA gene encoding MlrA enzyme considered most important for MC-LR biodegradation was obtained from YFMCD4. Data demonstrated that the bacterial structure and biodegradation efficiency of YFMCD4 varied with the change of environmental factors including temperature, pH and MC-LR concentrations. RSM is considered a good method to examine the optimal biodegradation environmental conditions for MC-LR. To date, RSM and High-throughput pyrosequencing technology are employed to optimize the biodegradation conditions (30 °C, pH 7 and 2 μg/mL initial MC-LR) and analyze the structure of bacterial community for the first time. • RSM was used to optimize MC-LR biodegradation conditions by YFMCD4 for the first time. • Varying temperatures, pH and MC-LR concentrations influenced MC-LR biodegradation. • Structure of YFMCD4 was analyzed by high-throughput pyrosequencing technology. • mlrA and mlrD homologues genes were amplified from YFMCD4. [ABSTRACT FROM AUTHOR]