A comprehensive study on multi-mycotoxin screening, changes of mycotoxin residues and fungal community analysis from barley germination to malt.

Multi-mycotoxin contamination of barley reduces malt quality and also poses serious health risks to both humans and animals. Among the detected mycotoxins in barley, Fusarium and Alternaria toxins represent severe food safety issues due to their widespread prevalence and strong synergistic toxicity. In this study, the effects of Fusarium and Alternaria fungi and their related toxins were investigated using simulated malting process conditions for contaminated barley samples. The dynamic changes of the fungal community and their associated mycotoxins were analyzed via high-throughput sequencing and UHPLC-q-trap-MS/MS, respectively. The results showed significant differences in the fungal communities between barley grains and their associated malt samples. These differences were noted for the following: fungal community diversity, dominant flora and the fungal structures at phylum, genus, and family level. Additionally, significant changes in the levels of alternariol monomethyl ether, tentoxin, zearalenone, and 15Acetyl-Deoxynivelenone were observed (p < 0.05) during the malting process. These results provide valuable information for strategies aimed at controlling fungal infections and the presence of mycotoxins in malt, so as to ensure food safety and human health.

Metal-Organic Frameworks with Novel Catenane-like Interlocking: Metal-Determined Photoresponse and Uranyl Sensing.

The assembly of two tripyridinium-tricarboxylate ligands and different metal ions leads to seven isostructural MOFs, which show novel 2D→2D supramolecular entanglement featuring catenane-like interlocking of tricyclic cages. The MOFs show tripyridinium-afforded and metal-modulated photoresponsive properties. The MOFs with d10 metal centers (1-Cd, 1-Zn, 2-Cd, 2-Zn) show fast and reversible photochromism and concomitant fluorescence quenching, 1-Ni displays slower photochromism but does not fluoresce, and 1-Co and 2-Co are neither photochromic nor fluorescent. It is shown here that the network entanglement dictates donor-acceptor close contacts, which enable fluorescence originated from interligand charge transfer. The contacts also allow photoinduced electron transfer, which underlies photochromism and concomitant fluorescence response. The metal dependence in fluorescence and photochromism can be related to energy transfer through metal-centered d-d transitions. In addition, 1-Cd is demonstrated to be a potential fluorescence sensor for sensitive and selective detection of UO2 2+ in water.

Positive Cooperative Protonation of a Metal-Organic Framework: pH-Responsive Fluorescence and Proton Conduction.

Positive cooperative binding, a phenomenon prevalent in biological processes, holds great appeal for the design of highly sensitive responsive molecules and materials. It has been demonstrated that metal-organic frameworks (MOFs) can show positive cooperative adsorption to the benefit of gas separation, but potential binding cooperativity is largely ignored in the study of sensory MOFs. Here, we report the first demonstration of positive cooperative protonation of a MOF and the relevant pH response in fluorescence and proton conduction. The MOF is built of Zr-O clusters and bipyridyl-based tetracarboxylate linkers and has excellent hydrolytic stability. It shows a unique pH response that features two synchronous abrupt turn-off and turn-on fluorescent transitions. The abrupt transitions, which afford high sensitivity to small pH fluctuations, are due to cooperative protonation of the pyridyl sites with a Hill coefficient of 1.6. The synchronous dual-emission response, which leads to visual color change, is ascribable to proton-triggered switching between (n, π*) and (π, π*) emissions. The latter emission can be quenched by electron donating anion-dependent through photoinduced electron transfer and ground-state charge transfer. Associated with cooperative protonation, the proton conductivity of the MOF is abruptly enhanced at low pH by two orders, but overhigh acid concentration is adverse because excessive anions can interrupt the conducting networks. Our work shows new perspectives of binding cooperativity in MOFs and should shed new light on the development of responsive fluorescent MOFs and proton conductive materials.

[Domestic and international research progress of edible and medicinal Arecae Semen].

Arecae Semen, as the first place among "Four South Medicines" in China, has great dual-use value of medicine and food. The research of Arecae Semen was mainly focused on the active ingredients and efficacy value, and its potential safety hazards were also concerned. Until now, there is still a lack of clear boundaries between medicine and food, resulting in its safety cannot be guaranteed. Therefore, it is of great significance to establish clear boundaries of medicine and food use and health risk assessment. In this paper, the differences of pretreatment and application methods of Arecae Semen were analyzed, and the research progress of Arecae Semen in chemical composition identification and toxicology research and safety evaluation were reviewed emphatically. Finally, the differences of quality control and safety evaluation of Arecae Semen in pharmacopoeias or standards were analyzed at home and abroad. It was expected to provide reference value for quality control, safety evaluation and international standardization research of Arecae Semen.

Liquid-curtain-based strategy to restrain plume during flushing.

How to prevent the flushing-induced plume without changing people's daily habits? Enlightened by thoughts of redesigning the restroom, this article provides a redesigned toilet using liquid-curtain-based strategy and verifies its advantages from the computational fluid dynamics. Two favorable effects are spotted: (1) the liquid curtain can suppress the upward virus particles (only 1% viruses can be lifted out of the toilet) and (2) the flow distribution caused by the liquid curtain can deliver virus particles into the sewage efficiently.

Distinct and Selective Amine- and Anion-Responsive Behaviors of an Electron-Deficient and Anion-Exchangeable Metal-Organic Framework.

Smart materials that respond to chemical stimuli with color or luminescence changes are highly desirable for daily-life and high-tech applications. Here, we report a novel porous metal-organic framework (MOF) that shows multiple, selective, and discriminative responsive properties owing to the combination of different functional ingredients [tripyridinium chromogen, Eu(III) luminophore, cationic framework, and special porous structure]. The MOF contains two interpenetrated three-dimensional cationic coordination networks built of a tetrahedral [Eu4(µ3-OH)4] cluster and a tripyridinium-tricarboxylate zwitterionic linker. It shows reversible and discriminative chromic response to aliphatic amines and aniline through different host-guest interactions between electron-deficient pyridinium and electron-rich amines. The size- and shape-selective response to aliphatic amines is ascribed to the radical formation through host-guest electron transfer, whereas the response to aniline is ascribed to the formation of sandwich-type acceptor-donor-acceptor complexes. The MOF is capable of reversible anion exchange with various anions and shows selective and discriminative ionochromic response to iodide, bromide, and thiocyanate, which is attributed to charge-transfer complexation. The above chromic behaviors are accompanied by efficient quenching of Eu(III) photoluminescence. The MOF represents a multi-stimuli dual-output responsive system. It can be used for discrimination and identification of anions and amines. The potential use in invisible printing, reusable sensory films, and optical switches was demonstrated by the ink and the membrane made of the MOF and organic polymers.

Photoresponsivity and antibiotic sensing properties of an entangled tris(pyridinium)-based metal-organic framework.

A two-dimensional Cd(ii) metal-organic framework (MOF) was constructed from a tris(pyridinium)-based hexacarboxylate zwitterionic ligand. The MOF shows a novel fashion of 2-fold 2D → 2D parallel entanglement. It is the entanglement that dictates close interlayer contacts between carboxylate (electron donor) and pyridinium (acceptor), which in turn impart the MOF with reversible photochromic properties through photoinduced electron transfer (PET). This is an extension of PET-based photochromism from bipyridinium to multipyridinium compounds. Thanks to the photoresponsive behaviour, the fluorescence of the MOF can be reversibly modulated or switched by photoirradiation. Besides, the fluorescence of the water-stable MOF in aqueous dispersion is very sensitive to nitrofuran antibiotics with high selectivity, and therefore the MOF is a good candidate of efficient and regenerable sensing material for determination of the antibiotics in water media.

Expression of EZH2 and P53 and their correlation in ovarian cancer tissues.

Previous researches have demonstrated that EZH2 expression is increased in many solid tumors and is closely related to the worse progression, transcriptional silence, distal metastasis, and differential inhibition of tumors. P53 can regulate many cells signaling pathways and play an important role in cell cycle, cell apoptosis, and cell senescence. However, there are few reports on the expression of EZH2 and p53 in ovarian cancer and their correlation with the ovarian cancer. The purpose is to elucidate the expression of EZH2 and p53 in ovarian cancer and to study the relationship of EZH2 and p53 with the clinical parameters of ovarian cancer. In this study, both mRNA and protein level of EZH2 in ovarian cancer group was significantly higher than that in borderline, benign, and normal group; while the mRNA and protein level of p53 was significantly lower than that in borderline, benign, and normal group. The expression of EZH2 protein was mainly located in the cytoplasm and nucleus, while mutated p53 protein was mainly located in the nucleus. Furthermore, the expression of EZH2 is closely related to the FIGO stage and histological grade of ovarian cancer. EZH2 and P53 are closely related to the occurrence of ovarian cancer. We speculate that EZH2 may promote the development of ovarian cancer by inhibiting the expression of p53, suggesting that p53 may be the target gene of EZH2.

Selective chemochromic and chemically-induced photochromic response of a metal-organic framework.

The Zn(ii) MOF with a tripyridinium-based hexacarboxylate shows direct color change on exposure to small primary amines and UV-assisted color response on exposure to small alcohols. The reversible, group-specific and size-selective chemochromic/chemophotochromic behaviours are ascribed to spontaneous/photoinduced guest-to-host electron transfer within the unique confined space furnished with electron-deficient sites.

Interpenetration-Enabled Photochromism and Fluorescence Photomodulation in a Metal-Organic Framework with the Thiazolothiazole Extended Viologen Fluorophore.

A novel metal-organic framework (MOF), formulated as [Cd2(TTVTC)Cl2(H2O)3]·2H2O (1), was synthesized from a tetracarboxylate ligand ([TTVTC]2-) functionalized with the thiazolothiazole extended viologen (TTV2+) fluorophore. The MOF features three-dimensional (10,3)-d frameworks with 6-fold interpenetration. The MOF exhibits reversible photochromism, due to photoinduced electron transfer from carboxylate to TTV2+. The photoactivity benefits from the electron donor-acceptor contacts enabled by mutual interpenetration of the frameworks. This is the first demonstration of photochromism in TTV2+ derivatives. In addition, the fluorescence arising from the TTV2+ fluorophore can be reversibly modulated during the photochromic process. The work demonstrates the great potential of extended viologen based ligands in the construction of MOFs with dual photomodulable optical properties, which could find future applications in photoelectronics.