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Chemical control of fungal spoilage of postharvest cereal grains is an important strategy for the management of grain storage. Here, the potential antifungal activity of 1-nonanol, a main component of cereal volatiles, against Aspergillus flavus was studied. The growth of A. flavus was completely inhibited by 0.11 and 0.20 μL/mL 1-nonanol at vapor and liquid contact phases, respectively. Metabolomic analysis identified 135 metabolites whose expression was significantly different between 1-nonanol-treated and untreated A. flavus. These metabolites were involved in the tricarboxylic acid cycle, amino acid biosynthesis, protein degradation and absorption, aminoacyl-tRNA biosynthesis, mineral absorption, and in interactions with ABC transporters. Biochemical validation confirmed the disruptive effect of 1-nonanol on A. flavus growth, as indicated by the leakage of intracellular electrolytes, decreased succinate dehydrogenase, mitochondrial dehydrogenase, and ATPase activity, and the accumulation of reactive oxygen species. We speculated that 1-nonanol could disrupt cell membrane integrity and mitochondrial function and might induce apoptosis of A. flavus mycelia. Simulated grain storage experiments showed that 1-nonanol vapor, at a concentration of 264 μL/L, completely inhibited A. flavus growth in wheat, corn, and paddy grain with an 18% moisture content. This study provides new insights into the antifungal mechanism of 1-nonanol against A. flavus, indicating that it has a promising potential as a bio-preservative to prevent fungal spoilage of postharvest grains. KEY POINTS: • 1-Nonanol showed higher antifungal activity against A. flavus. • The antifungal mechanisms of 1-nonanol against A. flavus were revealed. • 1-Nonanol could damage cell membrane integrity and mitochondrial function.

Hexanal, a natural volatile organic compound, exerts antifungal activity against Aspergillus flavus; however, the mechanisms underlying these effects are unclear. In this study, we found that the growth of A. flavus mycelium was completely inhibited following exposure to 0.4 μL/mL hexanal (minimal inhibitory concentration). A detailed metabolomics survey was performed to identify changes in metabolite production by A. flavus cells after exposure to 1/2 the minimal inhibitory concentration of hexanal for 6 h, which revealed significant differences in 70 metabolites, including 20 upregulated and 50 downregulated metabolites. Among them, levels of L-malic acid, α-linolenic acid, phosphatidylcholine, D-ribose, riboflavin, D-mannitol, D-sorbitol, and deoxyinosine were significantly reduced. The metabolomics results suggest that the metabolites are mainly involved in the tricarboxylic acid cycle (TCA), ABC transport system, and membrane synthesis in A. flavus cells. Hexanal treatment reduced succinate dehydrogenase and mitochondrial dehydrogenase activity and stimulated superoxide anion and hydrogen peroxide accumulation in A. flavus mycelia. Increases in the electric conductivity and A260nm of the culture supernatant indicated cell membrane leakage. Therefore, hexanal appears to disrupt cell membrane synthesis, induce mitochondrial dysfunction, and increase oxidative stress in A. flavus mycelia. KEY POINTS: • Metabolite changes of A. flavus mycelia were identified after hexanal treatment. • Most differential metabolites were downregulated in hexanal-treated A. flavus. • An antifungal model of hexanal against A. flavus was proposed.

Swelling deformation tests of GaoMiaoZi (GMZ01) bentonite were performed at 25, 40 60, and 90 °C in distilled water. Experimental results suggested that the maximum swelling strain of GMZ01 bentonite increased with temperature, due to the osmotic swelling dominated the swelling. The em − σv relation for compacted bentonite at a same temperature can be expressed as e m = K σ v D - 3 (em is montmorillonite void ratio, σv is vertical stress). The fractal dimension, D, of GMZ01 bentonite was unaffected by the temperature according to the results of N2 adsorption tests. Calculated by the diffuse double layer (DDL) model under the condition of osmotic swelling, a linearly relation was found between the montmorillonite swelling coefficient K and temperature Tc. Combing the fractal em − σv relation and linear K − Tc relation, a simple method for evaluating the swelling of GMZ01 bentonite affected by temperature was proposed.

Endo-1,4-β-mannosidases catalyze the cleavage of the β-d-1,4-mannopyranosyl linkage in mannan and have potential biotechnological applications in biofuel production, manno-oligosaccharide production, cleansing, and food and feed industries. In this study, an endo-1,4-β-mannosidase gene (TaMan3A) from wheat (Triticum aestivum) was successfully expressed in Pichia pastoris, and the antifungal effectiveness and manno-oligosaccharide production of the enzyme were evaluated. The purified TaMan3A exhibited a molecular weight of approximately 43 kDa, and its highest enzyme activity at pH 4.0 and 40 °C. Comparisons with other β-mannanases showed that TaMan3A had a conserved mannan-binding V-shaped groove, catalytic acid/base residue (E179), and nucleophilic residue (E297). Antifungal assays for TaMan3A against seven fungi commonly associated with wheat kernels showed that this enzyme had higher inhibitory effects on hyphal growth of the field fungi Fusarium graminearum and Alternaria sp. in comparison with that of storage fungi. TaMan3A could hydrolyze mannan polymers of galactomannan and Konjac glucomannan to mannobiose, mannotriose, and mannotetraose as the main products. Overall, these results showed the potential of TaMan3A for enhancing host resistance against fungal pathogens in wheat and manno-oligosaccharide production in the feed and food industries.

Repairing damage in the craniofacial skeleton is challenging. Craniofacial bones require intramembranous ossification to generate tissue-engineered bone grafts via angiogenesis and osteogenesis. Here, we designed a mineralized collagen delivery system for BMP-2 and vascular endothelial growth factor (VEGF) for implantation into animal models of mandibular defects. BMP-2/VEGF were mixed with mineralized collagen which was implanted into the rabbit mandibular. Animals were divided into (i) controls with no growth factors; (ii) BMP-2 alone; or (iii) BMP-2 and VEGF combined. CT and hisomputed tomography and histological staining were performed to assess bone repair. New bone formation was higher in BMP-2 and BMP-2-VEGF groups in which angiogenesis and osteogenesis were enhanced. This highlights the use of mineralized collagen with BMP-2/VEGF as an effective alternative for bone regeneration.

Aspergillus flavus infection is a major issue for safe food storage. In this study, we constructed an efficient prokaryotic expression system for puroindoline B (PINB) protein to detect its antifungal activity. The Puroindoline b gene was cloned into pET-28a (+) vector and expressed in Escherichia coli. Treatment with fusion PINB revealed that it inhibits mycelial growth of A. flavus, a common grain mold. Moreover, fusion PINB-treated A. flavus mycelium withered and exhibited a sunken spore head. As fusion PINB concentration increased, electrical conductivity in mycelium also increased, indicative of cell membrane damage. Furthermore, intracellular malate dehydrogenase and succinate dehydrogenase activity decreased, revealing a disruption in the tricarboxylic acid cycle. Moreover, the dampened activity of the ion pump Na+K+-ATPase negatively affected the intracellular regulation of both ions. Catalase and superoxide dismutase activity decreased, thus reducing antioxidant capacity, a result confirmed with an increase in malondialdehyde content. Changes to the GSH/GSSG ratio indicated a shift to an intracellular oxidative state. At the same time, laser scanning confocal microscopy assay showed the accumulation of reactive oxygen species and nuclear damage. Therefore, the PINB fusion protein may have the potential to control A. flavus in grain storage and food preservation.

In a high-level radioactive waste repository, bentonite may react with the alkaline solution produced by cement degradation. In this study, bentonite was mixed with alkaline solution in a closed system and reacted for 3–24 months. Furthermore, swelling tests were conducted on the alkaline-dissolved bentonite immersed in distilled water. The swelling deformation decreased significantly with increases in the concentration of NaOH solution and reaction time, and this was mainly due to montmorillonite dissolution. The fractal e–p relationship (e is the void ratio and p is the vertical pressure) with two calculation coefficients (the swelling coefficient and the fractal dimension) was employed to determine the swelling of alkaline-dissolved bentonite. The fractal dimension increased slightly with increasing reaction time or concentration of NaOH solution, as the dissolution traces caused by the alkaline solution favoured an increase in the irregularity and fractality of the bentonite surface. The swelling coefficient decreased linearly with decreasing montmorillonite content. In addition, the swelling coefficient and the fractal dimension were related exponentially to the reaction time in alkaline solution. A relationship between the swelling of alkaline-dissolved samples and the reaction time was proposed, which might be used to assess the swelling properties of bentonite barriers that would be affected by long-term dissolution of the alkaline solution in a closed repository.

Surfactin is a promising microbial lipopeptide with wide applications in food, environmental, agricultural, and pharmaceutical fields. However, its high cost caused by low productivity largely limits the commercial application. In this study, genome shuffling was employed to improve surfactin production in Bacillus velezensis strain LM3403 via recursive protoplast fusion. RT-qPCR analysis was employed to evaluate the transcriptional variance of surfactin synthase genes and surfactin efflux gene to insight into the variance underlying the recombinant strain. After three rounds of genome shuffling, a high-yield and genetic stable recombinant F34 was obtained, exhibiting dramatic improvement in surfactin production (from 229.60 ± 7.10 mg/L to 908.15 ± 5.65 mg/L) with high proportion of long carbon chain homologues. Scale-up fermentation confirmed that F34 had good growth performance and reached the yield of 917.05 ± 10.25 mg/L in a 30 L fermenter, which was 3.99-fold that of the initial strain. RT-qPCR analysis showed that the transcriptional levels of surfactin synthase genes srfAA and sfp, and surfactin efflux gene swrC in F34 were 8.12-fold, 9.27-fold, and 8.45-fold higher than those of LM3403, respectively. The upregulation of genes were consistent with the high surfactin yield in F34, indicating the increased capability of surfactin biosynthesis and transmember efflux in F34. To our knowledge, this is the first attempt to employ genome shuffling to breeding a B. velezensis strain to improve surfactin yield. The research helps us to understand the mechanisms underlying surfactin overproduction and provide references for further rational strain improvement.

Aspergillus flavus is a notorious saprophytic fungus that compromises the quantity and quality of postharvest grains and produces carcinogenic aflatoxins. The natural compound hexanal disrupts cell membrane synthesis and mitochondrial function and induces apoptosis in A. flavus; here, we investigated the molecular mechanisms underlying these effects. The minimum inhibition and fungicidal concentration (MIC and MFC) of hexanal against A. flavus spores were 3.2 and 9.6 μL/mL, respectively. Hexanal exposure resulted in abnormal spore morphology and early spore apoptosis. These changes were accompanied by increased reactive oxygen species production, reduced mitochondrial membrane potential, and DNA fragmentation. Transcriptomic analysis revealed that hexanal treatment greatly altered the metabolism of A. flavus spores, including membrane permeability, mitochondrial function, energy metabolism, DNA replication, oxidative stress, and autophagy. This study provides novel insights into the mechanism underlying the antifungal activity of hexanal, suggesting that hexanal can be used an anti-A. flavus agent for agricultural applications. • Hexanal exposure resulted in abnormal spore morphology. • The apoptotic characteristics of A. flavus were induced after hexanal treatment. • Hexanal could change the expression of key A. flavus growth-related genes.

Retinoblastoma (RB) is the most common intraocular malignancy in infants and children. S-phase kinase-associated protein 2 (SKP2) has been unmasked as an oncogene in a great many of carcinomas. The biologic function and the detailed molecular mechanism of SKP2 in RB need to be better understood. In this study, real-time quantitative polymerase chain reaction and Western blot showed the ectopic expression of SKP2 in RB tissues and cell lines. Loss of function assays showed the attenuated cell proliferation in RB as a result of SKP2 knockdown. In addition, bioinformatics analysis predicted the interaction between SKP2 and miR-422a. Luciferase reporter assay and Pearson's correlation analysis validated the negative correlation between miR-422a and SKP2. MiR-422a overexpression led to a decline of SKP2 expression and cell growth in RB. The binding capacity between miR-422a and circ_ODC1 was also predicted by bioinformatics analysis. Pearson's correlation analysis and luciferase reporter assay confirmed that circ_ODC1 is negatively correlated with miR-422a. Silencing circ_ODC1 resulted in a rise in miR-422a expression and RB cell growth. Moreover, reduced cell growth was restored by SKP2 overexpression. In a word, SKP2, induced by circ_ODC1 and miR-422a, promotes RB proliferation. Our new findings in this research might expedite the discovery of novel prognostic markers and therapeutic targets of RB.

The quality of wheat deteriorates naturally during long-term storage. In this study, to evaluate the quality changes of stored wheat, an artificial aging treatment was applied to accelerate the deterioration of wheat grain. The germination rate, free fatty acid content, malondialdehyde (MDA) content, and embryo and endosperm microstructures were examined in the wheat cultivars Zhengmai-103 and Zhengmai-379. In both wheat cultivars, seed germination almost completely ceased during storage for 10 months, whereas the contents of free fatty acids and MDA increased significantly. The variance analysis results showed that the accelerated deterioration process had significant effects on the free fatty acid, MDA, and superoxide radical contents. Further, the storage time was well correlated with the germination rate, free fatty acid content, and MDA content, and there was significant correlation between the free fatty acid and MDA contents (p

In Aspergillus flavus, laeA affects cell morphology and contributes to the production of secondary metabolites (SMs) production including aflatoxin, cyclopiazonic acid, and aflatrem. Here, we investigated the function of this transcription factor by performing proteomics analysis of the wild-type (WT) and ΔlaeA mutant growing on corn. Notably, our proteomics profile confirmed the functions of extracellular hydrolases, conidial hydrophobin, and response to oxidative stress during the induction of aflatoxin biosynthesis regulated by laeA. Unexpectedly, deletion of laeA resulted in the significant upregulation of the NAD+-dependent histone deacetylase sirA involved in silencing SM clusters via chromatin remodeling. Accompanying the chromatin modification, enzymes participating in SM, including aflatoxin and cyclopiazonic acid biosynthesis, were drastically decreased. Another unexpected finding was that enzymes in the recently identified ustiloxin B biosynthesis pathway might be regulated by laeA. These data provided novel insights into the complex regulation of laeA and suggested a potential link between laeA deletion, NAD+-dependent histone deacetylation, and SM production in A. flavus.

Human corneal fibroblasts (HCFs) are implicated in corneal neovascularization (CRNV). The mechanisms underlying the inflammatory response in HCFs and the development of CRNV were explored in this study. Alkali burns were applied to the corneas of rats to establish a CRNV model. The expression of long noncoding RNA (lncRNA) nuclear enriched abundant transcript 1 (NEAT1) and mRNA and protein levels of nuclear factor kappa B (NF-κB)- activating protein (NKAP) were examined by quantitative real-time (qRT-PCR) and Western blot methods, respectively. Lipopolysaccharide (LPS) is used to stimulate HCFs for inflammatory response. The level of inflammation factors in HCF supernatant was detected using an enzyme-linked immunosorbent assay (ELISA). Binding and interactions between NEAT1 and miRNA 1246 (miR-1246) were determined by RNA immunoprecipitation (RIP) and RNA pull-down assays in HCFs. Compared with the control group (n = 6), NEAT1 was upregulated in the corneas of the CRNV rat model (n = 6). The expression of NEAT1 in HCFs was upregulated by LPS. Downregulation of NEAT1 suppressed the secretion of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6). NEAT1 could bind and interact with miR-1246. LPS regulated the expression of NKAP and NF-κB signaling via the NEAT1/miR-1246 pathway. Downregulation of NEAT1in vivoinhibited CRNV progression in the CRNV rat model. The lncRNA NEAT1 induced secretion of inflammatory factors, mediated by NF-κB, by targeting miR-1246, thereby promoting CRNV progression.

Volatile organic compounds (VOCs) are hazardous to the environment and human health. Thus, tremendous effort has gone into developing effective/efficient techniques for VOCs separation from their aqueous mixtures. In this work, a simple and versatile strategy was proposed to fabricate a new material for hydrophobic volatile organic compounds (VOCs) separation, in which a self-assembling hydrogel consisting of TEMPO-oxidized cellulose nanofibers (TOCN) and cationic guar gum (CGG) was used. Specifically, TOCN and CGG were deposited onto a filter paper via a layer-by-layer procedure, resulting in a TOCN/CGG hydrogel-coated filtering material, in which no crosslinking agent was used. The hydrogel is spontaneously formed by electrostatic interactions and hydrogen bonding. The as-prepared filtering material exhibits oil-repellence and underwater oleophobicity resulting from the formation of hydration layer on hydrogel, thus demonstrating good VOCs separation performance. One-layer of TOCN/CGG hydrogel coating (dried mass of 0.032 g·m-2) was proved to realize the VOCs separation (separation efficiency of around 99% and water flux of as high as 905.14 L·m-2·h-1). Further increase of the hydrogel layers has negligible influence on the separation efficiency although it decreases the water flux. This filtering material also exhibits good stability during recycling. Consequently, this TOCN/CGG self-assembling hydrogel-coated filtering material has great potential in VOCs-contaminated wastewater treatment.

Based on the all-atomic molecular dynamics simulation method, the tensile creep behavior of epoxy-based polymer was discussed. The physical and mechanical properties of the model were characterized, such as glass transition temperature and yield strength. The simulation results are very close to the previous simulation and experimental results, and the correctness of the model is verified. On this basis, the tensile creep behavior and free volume evolution of polymer epoxy resin at different temperatures and stress levels were studied. The model fully predicted the three classical stages of epoxy resin creep (the primary, secondary and tertiary) and the dependent behavior of epoxy resin creep on temperature and stress level at the molecular level, and the creep rate increases with the increase of temperature and stress level. It was found that with the progress of the creep process, the proportion of free volume increases gradually under high stress levels, indicating that the effect of creep behavior on the structure of epoxy resin is that the interaction between atoms becomes weaker and weaker by increasing the distance between atoms, which finally induces creep failure in the material.

Based on the piezoresistive effect, the piezoresistive constitutive relation of a carbon fiber mat under orthogonal strain was deduced. Considering the Poisson effect, the piezoresistive responses and measurement of the sensitivity factor of a polymer-matrix carbon fiber mat under bidirectional strain were studied by a two-times uniaxial tension loading method in different directions, which was pasted in the center area of a cruciform aluminum substrate. The relations between the resistance change rate and the orthogonal strains were established, the reasonability of which was confirmed by comparison with the experimental results. The results show that the longitudinal piezoresistive sensitivity factor C11 is 21.55, and the lateral piezoresistive sensitivity factor C12 is 24.15. Using these factors, the resistance change rate of another polymer-matrix carbon mat was predicted, which was made by the same technique, and the error between the predicted and the experimental results was 1.3% in the longitudinal direction and 6.1% in the lateral direction.

Repairing damage in the craniofacial skeleton is challenging. Craniofacial bones require intramembranous ossification to generate tissue-engineered bone grafts via angiogenesis and osteogenesis. Here, we designed a mineralized collagen delivery system for BMP-2 and vascular endothelial growth factor (VEGF) for implantation into animal models of mandibular defects. BMP-2/VEGF were mixed with mineralized collagen which was implanted into the rabbit mandibular. Animals were divided into (i) controls with no growth factors; (ii) BMP-2 alone; or (iii) BMP-2 and VEGF combined. CT and hisomputed tomography and histological staining were performed to assess bone repair. New bone formation was higher in BMP-2 and BMP-2-VEGF groups in which angiogenesis and osteogenesis were enhanced. This highlights the use of mineralized collagen with BMP-2/VEGF as an effective alternative for bone regeneration.

The present study was aimed to develop a novel combination therapeutic strategy of gene therapy and immunotherapy for efficiently treatment of colorectal cancer (CRC). To achieve that goal, the polyethylene glycol-modified poly (2-(N,N-dimethylamino) ethyl methacrylate) (PEG-PDMAEMA)-based nanoparticles loaded with protein tyrosine phosphatase non-receptor type 6 (PTPN6) (NP-PTPN6) was developed first followed by conjugation with anti-PD-L1 monoclonal antibodies (aPD-L1) atezolizumab (aPD-L1NP-PTPN6). Importantly, the aPD-L1 was conjugated on the surface of NP-PTPN6 by the matrix metalloproteinases (MMPs)-cleavable linkage PLGLAG. Therefore, the aPD-L1 would be completely released once the aPD-L1NP-PTPN6 was entrapped into tumour tissues as demonstrated by the release assay. Tumour targeting assay demonstrated the aPD-L1NP-PTPN6 have high affinity to CRC cells and resulted in excellent tumour targeting drug delivery efficacy. Additionally, anti-tumour effect evaluation revealed that the aPD-L1NP-PTPN6 has greater ability to inhibit the growth, invasion and migration of CRC cells and finally led to longer survival time of tumour-bearing mice than other treatments. Further mechanisms studies demonstrated that treatment of CRC cells with aPD-L1NP-PTPN6 contributed to significant suppression of the MAPK/ERK signalling pathway. Besides, it was further demonstrated that treating CRC with aPD-L1NP-PTPN6 resulted in up-regulation of NK cells and T cells percentage within the tumour tissues.

Background Aspergillus flavus, a saprophytic fungus, is regularly detected in oil-enriched seeds. During colonization, this organism releases aflatoxins that pose a serious risk to food safety and human health. Therefore, an eco-friendly biological approach to inhibit the pathogen is desirable. Results Experimental results indicated that A. flavus spores could not germinate in potato dextrose broth culture medium, when the concentration of Sub3 exceeded 0.15 g L-1 . Morphological evaluation performed by flow cytometry and scanning electron microscopy indicated that spores were shrunken and pitted following Sub3 exposure. Physiological assessment using propidium iodide, 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolocarbocyanine iodide, 2,7-dichlorodihydrofluorescein diacetate and 4',6-diamidino-2-phenylindole staining revealed damaged cell membranes, decreased mitochondrial membrane potential, increased intracellular reactive oxygen species levels, and elevated large nuclear condensation and DNA fragmentation. Moreover, mitochondrial dehydrogenase activity was reduced by 29.42% and 45.48% after treatment with 0.1 and 0.15 g L-1 Sub3, respectively. Additionally, colonization capacity in peanut was significantly decreased, and the number of spores on seeds treated with Sub3 was decreased by 26.86% (0.1 g L-1 ) and 77.74% (0.15 g L-1 ) compared with the control group. Conclusion Sub3 likely inhibits A. flavus by crossing the cell wall and targeting the cell membrane, disrupting mitochondrial energy metabolism, and inducing DNA damage, leading to spore death. Thus, Sub3 may provide a useful biocontrol strategy to control A. flavus growth in peanuts. © 2020 Society of Chemical Industry.

Fungal contamination poses a threat to agriculture, food production and human health, and a safe and effective method to limit fungal contamination is still needed. In this study, the inhibitory potency of heptanal, a natural volatile chemical, against Aspergillus flavus growth was evaluated, and its mechanism of action was explored. The minimum inhibitory concentrations (MICs) of heptanal vapor fumigation and liquid contact culture were 0.085 and 0.8 μL/mL, respectively. A total of 79 significant differentially abundant metabolites, including 37 upregulated and 42 downregulated ones, were identified in A. flavus mycelia after exposure to 0.8 μL/mL heptanal for 6 h. Metabolomics analysis revealed that heptanal had destructive effects on plasma integrity and mitochondrial function in mycelia. Biochemical analysis confirmed that heptanal caused intracellular substance leakage and resulted in reduced intracellular ATP content, reactive oxygen species (ROS) accumulation, and lower mitochondrial dehydrogenase and ATPase activities. Evaluation of the control efficacy of heptanal fumigation on wheat grain under simulated storage conditions revealed that 225.0 μL/L heptanal vapor could inhibit A. flavus growth under 19% moisture. These results provide insights into the antifungal mechanism of heptanal against A. flavus growth as a promising bio-preservative.

Sulfamethoxazole (SMX) is a commonly used antibiotic for both human and animals. The frequent detection of SMX in natural water bodies and sediment has become an issue of great environmental concern due to its potential risk to induce antibiotic resistance in pathogenic bacteria. In the present work, the catalytic wet peroxide oxidation (CWPO) was investigated to remove SMX with sludge-derived carbon (SC) as a cheap alternative catalyst. Different acids were used to modify SC. It was found that SC modified with sulphuric acid (SC-H2SO4) demonstrated the best catalytic activity. The removal efficiency of SMX and TOC was 97.7% and 65.7%, respectively, after 260 min, at pH 5 with a dosage of 220 mg/L H2O2. The effects of temperature, initial pH and H2O2 dosage were also investigated. The study demonstrated that the increase of temperature could significantly improve the degradation of SMX from 10.0% at 20°C to 94.7% at 60°C.

Paper-based packaging generally has poor performances in the gas/oil barriers. This work reports a paper-based packaging material prepared via the modification of conventional papers with TEMPO-oxidized cellulose nanofibers (TOCN)/cationic guar gum (CGG) hydrogel film. Specifically, the hydrogel film modification was realized through a layer-by-layer deposition on paper. The hydrogel film modification significantly improved the mechanical and barrier properties of the paper. Specifically, the 4-layer hydrogel film modified paper showed a tensile strength of 34.03 MPa and a burst strength of 510 kPa, respectively. In contrast, the unmodified paper exhibited a tensile strength of 26.78 MPa and a bursting strength of 388 kPa. The packaging performance of this TOCN/CGG hydrogel film modified paper was demonstrated via the fresh mooncake packaging test. Such hydrogel film not only provided the oil resistance, but also maintained the mooncake's freshness. This material can serve as a green and sustainable food packaging.

This study aims to investigate the creep evolution and related performance degradation of epoxy resin polymers in marine environment using molecular simulation. Based on the all-atomic models of epoxy resin, the effect of different moisture absorption rate and different salt solution concentrations on the mechanical properties and creep evolution is studied at several different tensile levels from the micro scale. The present simulation results show that higher moisture absorption rate or salt solution concentration is more likely to lead to creep failure of epoxy system. There is a threshold stress in the creep failure process of epoxy system, and the threshold stress in salt solution environment is lower than that in water environment. The microscopic analysis reveals the movement ability of epoxy resin fragments in the marine environment is stronger than that in the water environment. In the process of creep failure accompanied by energy change, the bond energy of epoxy system remains unchanged, while the non-bond energy increases gradually. These changes of microstructure and energy together determine the macroscopic creep failure of epoxy resin system in marine environment. The results of this study are expected to be a meaningful reference for the practical application of epoxy polymers in marine environment and the further study of creep mechanism.

Aspergillus flavus contamination is of great concern to food safety. Our previous studies demonstrated that recombinant Puroindoline B protein (rPINB) has an inhibitory effect on A. flavus mycelium development. However, fungal contamination often begins with spore germination within food shelf life. Here, rPINB was evaluated for its antifungal properties against A. flavus spores in vivo and in vitro. The results showed that rPINB could inhibit spore formation and aflatoxin B1 of A. flavus on maize. In vitro analysis revealed its dose-dependent antifungal effect on spore germination and germ tube growth of A. flavus. Scanning electron microscopy revealed that rPINB exposure altered spore morphology, indicating it damaged the cell wall. Transmission electron microscopy and the inhibition of ergosterol synthesis further revealed that rPINB exposure significantly damaged the cell membrane. The mitochondrial membrane potential decreased, and DNA fragments were scattered in the cytoplasm as detected using 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolocarbocyanine iodide and 4′,6-diamidino-2-phenylindole staining. The direct antifungal activity of rPINB observed both in vivo and in vitro suggests that rPINB may be used to prevent fungal contamination of stored foods and agricultural products in the future.

Aspergillus flavus is the main cause of postharvest agricultural commodity loss. In this study, puroindoline A (PINA) protein was expressed in Escherichia coli, purified, and its antifungal properties against A. flavus were characterized. Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed that the molecular weight of the recombinant PINA protein was approximately 44 kDa. PINA exerted a powerful antifungal effect against A. flavus at 42.42 μg/mL on potato dextrose agar culture medium. Flow cytometry and scanning electron microscopy revealed that the spore morphology was damaged by PINA exposure; spores were depressed and broken, suggesting that the cell wall was impaired. Transmission electron microscopy and propidium iodide staining illustrated significant changes in intracellular spore structure, indicating cell membrane damage. 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolocarbocyanine iodide staining indicated decreased mitochondrial membrane potential. Large nuclear condensation and DNA fragmentation were detected by 4′,6-diamidino-2-phenylindole staining. The expression of genes related to the cell wall, cell membrane, and spore germination significantly changed in PINA-treated cells; this illustrated the probable mode of PINA action on A. flavus through cell wall destruction and triggered cell membrane, mitochondrial, and DNA damage leading to cell death. The antifungal mechanism of wheat PINA protein on A. flavus has been demonstrated in this study, and has potential application in preventing postharvest loss in the agricultural industry.

Shuai Wang, Shanshan Du, Yong Lv, Fengyan Zhang, Wenzhan WangDepartment of Ophthalmology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, People’s Republic of ChinaPurpose: Previous studies have revealed that microRNA-665 (miR-665) is dysregulated in a variety of human cancers. However, little is known regarding its expression profiles and functions in retinoblastoma (RB). Therefore, the aims of our study were to evaluate miR-665 expression in RB and determine the precise roles of miR-665 in the progression of RB.Patients and methods: Herein, RT-qPCR was used to determine miR-665 expression levels in RB tissues and cell lines, and a series of functional experiments were performed to explore the influence of miR-665 on RB cell proliferation, colony formation, apoptosis, migration, and invasion as well as tumor growth. The molecular mechanisms underlying the tumor-suppressive action of miR-665 in RB were also explored.Results: We found that miR-665 was markedly reduced in RB tissues and cell lines and that lower miR-665 expression was strongly associated with tumor size, TNM stage, and differentiation in patients with RB. Exogenous expression of miR-665 suppressed cell proliferation, colony formation, migration, and invasion, and induced cell apoptosis in RB cells, while silencing miR-665 expression had the opposite effects. In addition, upregulation of miR-665 decreased the tumor growth of RB cells in vivo. High-mobility group box 1 (HMGB1) was identified as a direct target of miR-665 in RB cells, and decreasing the expression of HMGB1 simulated the regulatory effects of miR-665 overexpression in RB cells, while knockdown of HMGB1 expression counteracted the miR-665-mediated antitumor effects in RB cells. Moreover, miR-665 was shown to regulate the Wnt/β-catenin signaling pathway by targeting HMGB1 in vitro and in vivo.Conclusion: Taken together, our in vitro and in vivo results suggest that miR-665 acts as a tumor-suppressive miRNA in RB by directly targeting HMGB1 and inactivating the Wnt/β-catenin pathway. Hence, this miRNA is a candidate prognostic biomarker and therapeutic target in patients with RB.Keywords: microRNA-665, retinoblastoma, high-mobility group box 1, Wnt/β-catenin pathway, oncogenicity

Acute liver failure (ALF) is a serious life-threatening condition. Mesenchymal stem cells (MSCs) may be an effective treatment for this condition and a good alternative to liver transplantation. Icaritin (ICT) is an active ingredient of the genus Epimedium, a traditional Chinese medicine, with the potential to enhance the proliferation of MSCs. The purpose of this study was to explore whether ICT increased the therapeutic effects of MSCs and explore its underlying mechanisms. For in vivo experiments, a rat ALF model was established by intraperitoneal injection of D(+)-galactosamine/ lipopolysaccharide. MSCs cocultured with ICT were used to treat ALF rats and the protective effects assessed as survival rate, levels of serum AST and ALT, and histological changes in liver tissue. For in vitro experiments, MSCs were treated in serum-free culture for 72 h to simulate the disruption of intrahepatic microcirculation. MSCs apoptosis was examined to determine whether ICT rescued impaired MSCs. The role of the hepatocyte growth factor (HGF)/c-Met pathway in MSCs was assessed by constructing genetically modified MSCs overexpressing c-Met and by using the c-Met receptor inhibitor (crizotinib). The results showed that MSCs increased the survival rate of ALF rats and reduced liver damage. MSCs cocultured with ICT exerted a greater therapeutic effect than MSCs alone. Further, the HGF/c-Met pathway played a key role in the antiapoptotic activity of MSCs, which was associated with the optimized efficacy of ICT. In conclusion, this study demonstrated that ICT enhances the therapeutic effect of MSCs in a model of ALF, improving the antiapoptotic potential of MSCs by upregulation of the HGF/c-Met pathway. The combination of stem cell therapy with traditional herbal extracts may improve MSC-based clinical applications.

To improve the green environmental performance and barrier property of the food packaging paper materials, the dialdehyde chitosan (D-CTS) was prepared from the selective oxidation of chitosan by sodium periodate. A surface sizing agent was obtained through complexes of D-CTS and cationic starch (CS). The barrier properties for water vapor of paper-sheet coated by the complex sizing agent of D-CTS/CS were measured. Attenuated total reflectance-fourier transform infrared spectroscopy (ATR-FTIR) was used to explain the mechanism of the improved barrier properties. The results indicate: while the oxidation degree and concentration of D-CTS is 32.3% and 0.3 wt%, the optimum barrier property for water vapor was obtained. While the coating weight increased from 0 to 3.5 g/m2, the barrier property for water vapor (WVP) was reduced from 2.73 × 10−11g cm−1 s−1 Pa−1 to 0.81 × 10−11g cm−1 s−1 Pa−1, reduced by 70.33%. Analyzed by ATR-FTIR, the degree of cross linking between D-CTS, CS and fibers increased. A smooth film formed on the surface can improve the WVP significantly.

Nd[Formula: see text]/Yb[Formula: see text] co-doped lutetium-based glass sample and glass ceramic sample were prepared with the molar ratios of 52SiO2-8Na2CO3-16Al2O3-33NaF-3LuF3-0.15Yb2O3-0.03Nd2O3 by the high temperature melting method in 1400∘C. Under the excitation of 980[Formula: see text]nm diode laser, up-conversion luminescence spectrum of glass sample and glass ceramic sample was measured and three stronger up-conversion luminescence peaks at the wavelength of 552[Formula: see text]nm, 656[Formula: see text]nm and 668[Formula: see text]nm were observed, and up-conversion luminescence strengths of glass ceramic sample are higher than those of glass sample. The two-photon absorption of three emission peaks was determined by the fitting curve graph of up-conversion emission power and LD wording current. Absorption spectrum of glass ceramic sample was obtained and spectral strength parameters were computed as [Formula: see text][Formula: see text]cm2, [Formula: see text][Formula: see text]cm2, [Formula: see text][Formula: see text]cm2 by adopting Judd–Ofelt theory, and the root mean square deviation between the theoretical oscillator strength and the experimental oscillator strength were calculated as [Formula: see text]. Transition probability, branching ratio of 4F[Formula: see text] to its lower level and lifetime of 4F[Formula: see text] level of Nd[Formula: see text] ions were calculated, and the results indicate that the prepared Nd[Formula: see text]/Yb[Formula: see text] co-doped glass ceramic sample is a kind of good up-conversion material.

The Puroindoline A (PINA) from soft wheat endosperm is a broad-spectrum antimicrobial protein. Herein, we investigated the action of the PINA protein on Aspergillus flavus mycelia growth, conidia and sclerotia development, and its ability to control pathogenicity in infected crop seeds. The PINA protein strongly inhibited spore germination, mycelia growth, and conidia and sclerotia formation at 128 μg/mL. Furthermore, scanning electron microscopy revealed altered mycelia morphology, mycelia were dented, shrivelled and holes were observed, suggesting that the cell wall and membrane were damaged, and this was confirmed by calcofluor white fluorescent probe assays and propidium iodide staining. Additionally, there were significant changes in mycelia intramembranous structure based on 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolocarbocyanine iodide and 4′,6-diamidino-2-phenylindole staining, which indicates decreased mitochondrial membrane potential, excessive nuclear condensation, and DNA fragmentation. These results demonstrated that the defects of A. flavus pathogenicity in peanut and corn appeared to be related to cell wall and membrane destruction, which may trigger mitochondrial and DNA damage, leading to cell death. These findings provide visual evidence that the PINA protein inhibits A. flavus pathogenicity, and may assist food preservation applications in future.

β-1,3-glucanases, the plant PR-2 family of pathogenesis-related (PR) proteins, can be constitutively expressed and induced in wheat crop to enhance its anti-fungal pathogen defense. This study aimed to investigate the inhibitory effect of wheat β-1,3-glucanase on fungi most commonly associated with wheat kernel. A β-1,3-glucanase from wheat was successfully expressed in Pichia pastoris X-33 and its biochemical and antifungal properties were characterized herein. The molecular weight of recombinant β-1,3-glucanase is approximately 33 kDa. β-1,3-glucanase displays optimal activity at pH 6.5, remaining relatively high at pH 5.5–8.0. The optimal reaction temperature of β-1,3-glucanase is 50 °C, retaining approximately 84.0% residual activity after heat-treated at 50 °C for 1 h. The steady-state kinetic parameters of β-1,3-glucanase against laminarin was determined and the Km and Vmax were 1.32 ± 0.20 mg/ml and 96.4 ± 4.4 U mg−1 protein, respectively. The inhibitory effect of purified β-1,3-glucanase against the seven fungi commonly associated with wheat kernel was assessed in vitro. β-1,3-glucanase exerted differential inhibitory effects on hyphal growth of Fusarium graminearum, Alternaria sp., A. glaucus, A. flavus, A. niger, and Penicillium sp. Spore formation and mycelial morphology of Alternaria sp., A. flavus, and A. niger were significantly affected by β-1,3-glucanase (1U). The present results would help elucidate the mechanism underlying the inhibition of wheat β-1,3-glucanases on pathogens.

Compelling evidence has suggested the relevance of miRNAs in resistance to chemotherapeutic agents in HCC. miR-505 was reported to be downregulated and function as a tumor suppressor in HCC cells by binding to high-mobility group box 1 (HMGB1). Whether miR-505/HMGB1 axis was involved in ADM cytotoxicity in HCC remains to be addressed. The aim of this study was to explore the effect of miR-505/HMGB1 axis on ADM cytotoxicity in HCC cells. MTT, flow cytometry analysis, and caspase-3 activity assays were conducted to assess ADM-induced cytotoxicity. The protein level of phosphorylation of histone H2 AX at Ser139 (γH2AX) was detected to evaluate DNA damage. The effects of miR-505 and HMGB1 on the protein kinase B (Akt) pathway were determined by examining the protein levels of phosphorylated Akt (p-Akt), Akt, phosphorylated glycogen synthase kinase-3β (p-GSK-3β), and GSK-3β. We found that HMGB1 knockdown and miR-505 overexpression exacerbated ADM-induced cell viability inhibition, enhanced ADM-induced apoptosis, and increased caspase-3 activity in ADM-treated HCC cells. However, HMGB1 overexpression reversed the effects of miR-505 on ADM-induced cytotoxicity in HCC cells. HMGB1 knockdown and miR-505 overexpression promoted ADM-induced DNA damage in HCC cells, which was abated by HMGB1 overexpression. On a molecular mechanism level, HMGB1 silencing and miR-505 overexpression inactivated the Akt pathway in HCC cells, while exogenous HMGB1 resisted miR-505-induced Akt pathway inactivation. In conclusion, miR-505 overexpression enhanced ADM-induced cytotoxicity in HCC cells, at least partly by targeting HMGB1 and inactivating the Akt pathway.

The law of influenced material of liner is researched by numerical simulation.Multiple explosively formed projectiles (MEFP) forming process is numerically simulated with different liner material,such as copper, aluminum, iron and so on.The law that the formation parameters of MEFP such as velocity, length-diameter ratio and radial dispersion angle,influenced by the density and ductility of liner material is educed.It reaches the conclusion that the velocity and radial dispersion angle of projectiles decreases 58% and 56% with the increasing density of the liner material; the length-diameter ratio of central projectile increases276%with the increasing ductility of the liner material, so in order to acquire good formation of MEFP parameters, the appropriate density and higher ductility should be chosen.

The reaction stability is a challenge in the 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation of cellulose. Carbonate buffer solution (Na2CO3/NaHCO3) was used to study pH effects on stability of the oxidation reaction in this work. The structure and morphology of cellulose fibers were characterized by XRD and SEM techniques, respectively. It was found that the carboxyl content of oxidized cellulose was changed with different composition ratio of buffer solutions. The highest carboxyl content was obtained at the molar ratio of 7:3. The NaClO addition, as well as reaction temperature, affected the process of the oxidation reaction. The carboxylate content of the oxidized cellulose was increased as the temperature and NaClO consumption increased. However, both temperature and NaClO consumption have negative effect on yield. SEM results showed that the morphology of oxidized cellulose fibers was significantly changed at high reaction temperature. XRD showed that the oxidized cellulose fibers maintained the crystal structure of cellulose I. However, the crystallinity was decreased from 56.4 to 40.8 % with increasing oxidation temperature from 25 to 40 °C.

Protein lysine acetylation is a prevalent post-translational modification that plays pivotal roles in various biological processes in both prokaryotes and eukaryotes. Aspergillus flavus, as an aflatoxin-producing fungus, has attracted tremendous attention due to its health impact on agricultural commodities. Here, we performed the first lysine-acetylome mapping in this filamentous fungus using immune-affinity-based purification integrated with high-resolution mass spectrometry. Overall, we identified 1383 lysine-acetylation sites in 652 acetylated proteins, which account for 5.18% of the total proteins in A. flavus. According to bioinformatics analysis, the acetylated proteins are involved in various cellular processes involving the ribosome, carbon metabolism, antibiotic biosynthesis, secondary metabolites, and the citrate cycle and are distributed in diverse subcellular locations. Additionally, we demonstrated for the first time the acetylation of fatty acid synthase α and β encoded by aflA and aflB involved in the aflatoxin-biosynthesis pathway (cluster 54), as well as backbone enzymes from secondary metabolite clusters 20 and 21 encoded by AFLA_062860 and AFLA_064240, suggesting important roles for acetylation associated with these processes. Our findings illustrating abundant lysine acetylation in A. flavus expand our understanding of the fungal acetylome and provided insight into the regulatory roles of acetylation in secondary metabolism.

For producing RGB tricolor luminescence, three kinds of components of rare-earth ions is chosen, which are Er3+doping, Er3+-Yb3+co-doping and Tm3+-Yb3+co-doping, respectively. Three kinds of rare-earth doped up-conversion fluoride material are prepared based on high temperature solid-state method. Under being excited by 980nm laser, three materials emit red, green and blue light, whose peak wavelengths are 660nm, 550nm and 480nm, respectively. Through analysis of luminescence process, it can be concluded that red and green luminescence are belong to two-photon absorption transversion, and blue luminescence is three-photon absorption transversion.

The degradation behavior of oxytetracycline (OTC) in aqueous solution using sludge derived carbon (SC) was investigated in this paper. SC treated with different kinds of acids were characterized by BET and thermogravimetric analysis. The results showed that SC-H2SO4 exhibited higher catalytic activity than SC-HCl and SC. The maximum removal of OTC and total organic carbon (TOC) after catalytic oxidation process at 60 °C was 92.6% and 70.2%, respectively. The safety of antibiotics after advanced oxidation processes (AOPs) has attracted much attention due to the possibility of toxicity increasing. Seven intermediate products were identified by GC–MS and four pathways were proposed. Furthermore, the toxicity of OTC degradation was investigated by zebrafish embryos for the first time. Zebrafish incubated with OTC solution (TE2) had haemagglutination, pericardial edema and showed significant changes in heartbeat, body length, and roaming frequency compared with the normal nutrient solution (TE1). Moreover, all zebrafish embryos had condensation phenomenon and did not hatch out in the treated OTC solution (TE3). In contrast, the zebrafish could hatch out without abnormality cultured with the treated OTC solution adjusted to the neutral pH (TE4). Results indicated that the treated OTC solution after catalytic oxidation process should be adjusted to the neutral pH to reduce the toxicity to the ecology.

Previous research demonstrated that soft wheat cultivars have better post-harvest storage tolerance than harder cultivars during accelerated ageing. To better understand this phenomenon, a tandem mass tag-based quantitative proteomic analysis of soft wheat seeds was performed at different storage times during accelerated ageing (germination ratios of 97%, 45%, 28%, and 6%). A total of 1,010 proteins were differentially regulated, of which 519 and 491 were up- and downregulated, respectively. Most of the differentially expressed proteins were predicted to be involved in nutrient reservoir, enzyme activity and regulation, energy and metabolism, and response to stimulus functions, consistent with processes occurring in hard wheat during artificial ageing. Notably, defense-associated proteins including wheatwin-2, pathogenesis-related proteins protecting against fungal invasion, and glutathione S-transferase and glutathione synthetase participating in reactive oxygen species (ROS) detoxification, were upregulated compared to levels in hard wheat during accelerated ageing. These upregulated proteins might be responsible for the superior post-harvest storage-tolerance of soft wheat cultivars during accelerated ageing compared with hard wheat. Although accelerated ageing could not fully mimic natural ageing, our findings provided novel dynamic proteomic insight into soft wheat seeds during seed deterioration.

Nano-PLLA/chitosan scaffolds were prepared through thermally induced phase separation(TIPS). With incorporation of chitosan fibers, composites not only improved the mechanical properties of nano scaffolds, but also reduced the degradation rate of mechanical properties which deepen the applications of scaffolds better.

Wheat (Triticum aestivum L.) is an important crop worldwide. The physiological deterioration of seeds during storage and seed priming is closely associated with germination, and thus contributes to plant growth and subsequent grain yields. In this study, wheat seeds during different stages of artificial ageing (45°C; 50% relative humidity; 98%, 50%, 20%, and 1% Germination rates) and priming (hydro-priming treatment) were subjected to proteomics analysis through a proteomic approach based on the isobaric tandem mass tag labeling. A total of 162 differentially expressed proteins (DEPs) mainly involved in metabolism, energy supply, and defense/stress responses, were identified during artificial ageing and thus validated previous physiological and biochemical studies. These DEPs indicated that the inability to protect against ageing leads to the incremental decomposition of the stored substance, impairment of metabolism and energy supply, and ultimately resulted in seed deterioration. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that the up-regulated proteins involved in seed ageing were mainly enriched in ribosome, whereas the down-regulated proteins were mainly accumulated in energy supply (starch and sucrose metabolism) and stress defense (ascorbate and aldarate metabolism). Proteins, including hemoglobin 1, oleosin, agglutinin, and non-specific lipid-transfer proteins, were first identified in aged seeds and might be regarded as new markers of seed deterioration. Of the identified proteins, 531 DEPs were recognized during seed priming compared with unprimed seeds. In contrast to the up-regulated DEPs in seed ageing, several up-regulated DEPs in priming were involved in energy supply (tricarboxylic acid cycle, glycolysis, and fatty acid oxidation), anabolism (amino acids, and fatty acid synthesis), and cell growth/division. KEGG and protein-protein interaction analysis indicated that the up-regulated proteins in seed priming were mainly enriched in amino acid synthesis, stress defense (plant-pathogen interactions, and ascorbate and aldarate metabolism), and energy supply (oxidative phosphorylation and carbon metabolism). Therefore, DEPs associated with seed ageing and priming can be used to characterize seed vigor and optimize germination enhancement treatments. This work reveals new proteomic insights into protein changes that occur during seed deterioration and priming.