Food Safety Incidents, Collateral Damage and Trade Policy Responses: China-Canada Agri-Food Trade

As markets become globalized, food safety policy and international trade policy are increasingly intertwined. Globalization also means that food safety incidents are widely reported internationally. One result is that food safety incidents can negatively impact products where no food safety issue exists as consumers lose trust in both foreign and domestic food safety institutions. While the policy framework for dealing with directly effected imported foods is well understood, how to deal with the market failure associated with indirectly affected products within the existing trade policy rules has not been explored. Using the example of China’s 2007 problems with a spate of products safety incidents, a theoretical framework is developed and the response of both the Chinese and Canadian governments analyzed. A cooperative approach to the issues appears to have a number of advantages and does not contravene trade policy commitments.Canada, China, cooperation, food safety, market failure, trade policy, Agricultural and Food Policy, International Development, International Relations/Trade,

Two helices from one chiral centre – self organization of disc shaped chiral nanoparticles

Gold nanoparticles (AuNPs) have been prepared and surfacefunctionalizedwith a mixture of 1-hexanethiol co-ligands and chiraldiscogen ligands separated from a disulfide function via a flexiblespacer. Polarized optical microscopy together with differentialscanning calorimetry showed that the organic corona of thenanocomposite forms a stable chiral discotic nematic (ND*) phasewith a wide thermal range. Synchrotron X-ray diffraction showedthat gold NPs form a superlattice with p2 plane symmetry. Analysisindicated that the corona takes up the shape of a flexiblemacrodisk. Synchrotron radiation-based circular dichroism signalsof thin films are significantly enhanced on the isotropic-LCtransition in line with the formation of a chiral nematic phase of theorganic corona. At lower temperatures the appearance of CDsignals associated with the NPs is indicative of the formation of asecond helical structure. The decreased volume required and thechiral environment of the disc ligands drives the nanoparticles intocolumns that arrange helically parallel to the shortest axis of thetwo dimensional lattice

Intrinsic Lithiophilicity of Li–Garnet Electrolytes Enabling High‐Rate Lithium Cycling

Solid‐state lithium batteries are widely considered as next‐generation lithium‐ion battery technology due to the potential advantages in safety and performance. Among the various solid electrolyte materials, Li–garnet electrolytes are promising due to their high ionic conductivity and good chemical and electrochemical stabilities. However, the high electrode/electrolyte interfacial impedance is one of the major challenges. Moreover, short circuiting caused by lithium dendrite formation is reported when using Li–garnet electrolytes. Here, it is demonstrated that Li–garnet electrolytes wet well with lithium metal by removing the intrinsic impurity layer on the surface of the lithium metal. The Li/garnet interfacial impedance is determined to be 6.95 Ω cm2 at room temperature. Lithium symmetric cells based on the Li–garnet electrolytes are cycled at room temperature for 950 h and current density as high as 13.3 mA cm−2 without showing signs of short circuiting. Experimental and computational results reveal that it is the surface oxide layer on the lithium metal together with the garnet surface that majorly determines the Li/garnet interfacial property. These findings suggest that removing the superficial impurity layer on the lithium metal can enhance the wettability, which may impact the manufacturing process of future high energy density garnet‐based solid‐state lithium batteries.By removing the impurity layer on the surface of the lithium metal, Li–garnet electrolytes are demonstrated to well wet the lithium metal, rendering a Li/garnet interfacial impedance of 6.95 Ω cm2, stable galvanostatic cycling for 950 h, and a current density as high as 13.3 mA cm−2 without showing any sign of short circuiting at room temperature.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/154451/1/adfm201906189-sup-0001-SuppMat.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/154451/2/adfm201906189.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/154451/3/adfm201906189_am.pd

Chirality enhancement in macro-chiral liquid crystal nanoparticles

The amplification of molecular chirality by metal nanoparticles (NPs) is an important and rapidly evolving field in nanomaterial research with wide applications in smart materials, catalysis, and solvent-solute interactions. Here we present the results of the synthesis of gold nanoparticles (AuNPs) functionalized both with chiral ligands based on the binaphthol motif and with nematogenic groups (ChirAuLC). The materials were characterized chemically and the ratios between chiral groups and LC groups was determined. Synchrotron radiation circular dichroism (SRCD) and synchrotron based X-ray diffraction (XRD) studies show that the AuNPs favoured by the LC state arrange themselves into ordered columns and a helical superstructure appears in the mesophase of collective NPs. A specific focus has been the investigation of the chiral induction of ChirAuLC composites in two different nematic LC hosts. For a number of selected mixtures, the helical twisting power (HTP) of these NPs in systems was calculated from systematic optical observations based on optical polarizing microscopy (OPM). The experimental data show that the HTP of the investigated ChirAuLC composite is significantly larger than that of free "small molecule"chiral groups when dispersed in the same LC host and the chiral transfer efficiency of ChirAuLC is higher than NPs functionalized only with chiral groups (ChirAuNP). This is new and can be explained by a combination of a surface chirality and the domino effect of bound mesogens interacting with the bulk. This journal i

Machine learning-guided co-optimization of fitness and diversity facilitates combinatorial library design in enzyme engineering

The effective design of combinatorial libraries to balance fitness and diversity facilitates the engineering of useful enzyme functions, particularly those that are poorly characterized or unknown in biology. We introduce MODIFY, a machine learning (ML) algorithm that learns from natural protein sequences to infer evolutionarily plausible mutations and predict enzyme fitness. MODIFY co-optimizes predicted fitness and sequence diversity of starting libraries, prioritizing high-fitness variants while ensuring broad sequence coverage. In silico evaluation shows that MODIFY outperforms state-of-the-art unsupervised methods in zero-shot fitness prediction and enables ML-guided directed evolution with enhanced efficiency. Using MODIFY, we engineer generalist biocatalysts derived from a thermostable cytochrome c to achieve enantioselective C-B and C-Si bond formation via a new-to-nature carbene transfer mechanism, leading to biocatalysts six mutations away from previously developed enzymes while exhibiting superior or comparable activities. These results demonstrate MODIFY's potential in solving challenging enzyme engineering problems beyond the reach of classic directed evolution

Research Progress on the Formation Mechanism of Protein/Essential Oil-based Composite Films and Application in Food Preservation

It has great significance to maintain the natural state of food and reduce the environmental pollution that use of bio-based packaging materials to research and development food packaging, because it has been unable to meet the demand of consumers for green, environmental protection and high-efficiency, for traditional food packaging. Edible films are attracting great attentions in food packaging due to their safety and zero waste property, among which, the protein often used in the preparation of edible films because of good mechanical properties and nutritional value. Essential oils extracted from aromatic plants, the broad-spectrum antibacterial and antioxidant properties give it great potential in food packaging. Incorporation of essential oils into edible protein-based films can effectively improve their properties, and cover the strong sensory properties of essential oils, meanwhile, the release rate of essential oils is controlled. This review covers the recent developments in protein/essential oils-based composite films, the formation mechanism of protein/essential oils-based composite films is discussed, the two composite methods of single essential oil and complex essential oil with protein-based composite films is introduced. Meanwhile, the application of protein/essential oils-based composite films in food is summarized. This study can provide some reference for the future development of protein/essential oils-based composite films

Isolation of Mycobacterium tuberculosis complex (MTBC) from dairy cows in China

Eleven thousand five hundred and eighty non-blood samples from dairy cows were subjected to mycobacterium culture and genotyping. As a result, a total of 142 isolates of Mycobacterium tuberculosis complex (MBTC) were identified. Among them, 65 were Mycobacterium tuberculosis, while 77 Mycobacterium bovis. The genotype of M. tuberculosis strains was mainly Beijing family. In addition, the isolation rates of MTBC were 33.89% for lung lymph nodes, 2.81% for nasal swabs, and 3.95% for pharyngeal swabs from cattle positive to tuberculin skin test, respectively. This evidence implied that M. tuberculosis infection in cattle is a new risk to public health and should be paid more attention.Key words: Mycobacterium tuberculosis complex, cows, tuberculosis, zoonosis

Enzyme-Catalytic Self-Triggered Release of Drugs from a Nanosystem for Efficient Delivery to Nuclei of Tumor Cells.

Stimulus-responsive drug delivery nanosystems (DDSs) are of great significance in improving cancer therapy for intelligent control over drug release. However, among them, many DDSs are unable to realize rapid and sufficient drug release because most internal stimulants might be consumed during the release process. To address the plight, an abundant supply of stimulants is highly desirable. Herein, a core crosslinked pullulan-di-(4,1-hydroxybenzylene)diselenide nanosystem, which could generate abundant exogenous-stimulant reactive oxygen species (ROS) via tumor-specific NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, was constructed by the encapsulation of β-lapachone. The enzyme-catalytic-generated ROS induced self-triggered cascade amplification release of loaded doxorubicin (DOX) in the tumor cells, thus achieving efficient delivery of DOX to the nuclei of tumor cells by breaking the diselenide bond of the nanosystem. As a result, the antitumor effect of this nanosystem was significantly improved in the HepG2 xenograft model. In general, this study offers a new paradigm for utilizing the interaction between the loaded agent and carrier in the tumor cells to obtain self-triggered drug release in the design of DDSs for enhanced cancer therapy

ASFV infection induces macrophage necroptosis and releases proinflammatory cytokine by ZBP1-RIPK3-MLKL necrosome activation

African swine fever (ASF) is an infectious disease characterized by hemorrhagic fever, which is highly pathogenic and causes severe mortality in domestic pigs. It is caused by the African swine fever virus (ASFV). ASFV is a large DNA virus and primarily infects porcine monocyte macrophages. The interaction between ASFV and host macrophages is the major reason for gross pathological lesions caused by ASFV. Necroptosis is an inflammatory programmed cell death and plays an important immune role during virus infection. However, whether and how ASFV induces macrophage necroptosis and the effect of necroptosis signaling on host immunity and ASFV infection remains unknown. This study uncovered that ASFV infection activates the necroptosis signaling in vivo and macrophage necroptosis in vitro. Further evidence showed that ASFV infection upregulates the expression of ZBP1 and RIPK3 to consist of the ZBP1-RIPK3-MLKL necrosome and further activates macrophage necroptosis. Subsequently, multiple Z-DNA sequences were predicted to be present in the ASFV genome. The Z-DNA signals were further confirmed to be present and colocalized with ZBP1 in the cytoplasm and nucleus of ASFV-infected cells. Moreover, ZBP1-mediated macrophage necroptosis provoked the extracellular release of proinflammatory cytokines, including TNF-α and IL-1β induced by ASFV infection. Finally, we demonstrated that ZBP1-mediated necroptosis signaling inhibits ASFV replication in host macrophages. Our findings uncovered a novel mechanism by which ASFV induces macrophage necroptosis by facilitating Z-DNA accumulation and ZBP1 necrosome assembly, providing significant insights into the pathogenesis of ASFV infection