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In order to improve the cathodic protection and wear resistance of cold spraying Zn-based coatings, Zn–Ni/Cu–Al2O3 composite coating was prepared by co-depositing Zn powders, nickel-coated Cu powders, and Al2O3 powders on the steel substrate using the low-pressure cold spraying method. The structure and composition of Zn–Ni/Cu–Al2O3 coatings were analyzed by scanning electron microscopy, energy dispersive spectrum analysis, and X-ray diffraction, respectively. And their wear and corrosion resistance were tested. The results show that the structure of the Zn–Ni/Cu–Al2O3 composite coating is compact and the nickel powder is evenly distributed in the coating. Compared with the Zn–Al2O3 coating and Zn–Cu–Al2O3 coating, the Zn–Ni/Cu–Al2O3 composite coating has better wear resistance in air and stronger corrosion resistance in the 3.5 wt.% NaCl solutions. The Zn–Ni/Cu–Al2O3 coating has the lowest corrosion rate and maximum impedance after the immersion and scratch tests. Due to the promoting effect of Ni, the Zn–Ni/Cu–Al2O3 coating can quickly form a dense protective layer of corrosion products, which makes the Zn–Ni/Cu–Al2O3 composite coating has better cathodic protection and defect self-repair performance. [ABSTRACT FROM AUTHOR]

Polyaniline (PANI) has been widely studied and applied due to its easy‐to‐obtain raw materials, excellent electrochemical performance and high environmental stability. Here, we present a general synthetic strategy for preparing two‐dimensional (2D) fluorescent PANI derivatives. The double bonds are used as a conjugated spacer between benzene rings in PPED and PPBA. The work breaks through the limitation of PANI derivatives are non‐emissive in solutions. The fluorescence quantum yields (Фf) of PPED and PPBA are 2.5% and 1.5%, respectively. PPED and PPBA show highly selective and sensitive detection of iron ion (Fe3+), copper ion (Cu2+) and hydrochloric acid (HCl). It is worth noting that the detection limit of PPED for Fe3+ is 35 nM. In addition, the theoretical study indicates that the introduction of double bonds in PPED and PPBA greatly enhances their conjugation extent. The results demonstrate that we provide a powerful method for the preparation of highly sensitive fluorescent chemosensors based on 2D PANI derivatives. [ABSTRACT FROM AUTHOR]

RNA editing generates genetic diversity in mammals by altering amino acid sequences, miRNA targeting site sequences, influencing the stability of targeted RNAs, and causing changes in gene expression. However, the extent to which RNA editing affect gene expression via modifying miRNA binding site remains unexplored. Here, we first profiled the dynamic A-to-I RNA editome across tissues of Duroc and Luchuan pigs. The RNA editing events at the miRNA binding sites were generated. The biological function of the differentially edited gene in skeletal muscle was further characterized in pig muscle-derived satellite cells. RNA editome analysis revealed a total of 171,909 A-to-I RNA editing sites (RESs), and examination of its features showed that these A-to-I editing sites were mainly located in SINE retrotransposons PRE-1/Pre0_SS element. Analysis of differentially edited sites (DESs) revealed a total of 4,552 DESs across tissues between Duroc and Luchuan pigs, and functional category enrichment analysis of differentially edited gene (DEG) sets highlighted a significant association and enrichment of tissue-developmental pathways including TGF-beta, PI3K-Akt, AMPK, and Wnt signaling pathways. Moreover, we found that RNA editing events at the miRNA binding sites in the 3′-UTR of HSPA12B mRNA could prevent the miRNA-mediated mRNA downregulation of HSPA12B in the muscle-derived satellite (MDS) cell, consistent with the results obtained from the Luchuan skeletal muscle. This study represents the most systematic attempt to characterize the significance of RNA editing in regulating gene expression, particularly in skeletal muscle, constituting a new layer of regulation to understand the genetic mechanisms behind phenotype variance in animals. Abbreviations: A-to-I: Adenosine-to-inosine; ADAR: Adenosine deaminase acting on RNA; RES: RNA editing site; DEG: Differentially edited gene; DES: Differentially edited site; FDR: False discovery rate; GO: Gene Ontology; KEGG: Kyoto Encyclopaedia of Genes and Genomes; MDS cell: musclederived satellite cell; RPKM: Reads per kilobase of exon model in a gene per million mapped reads; UTR: Untranslated coding regions [ABSTRACT FROM AUTHOR]

The Bama Xiang pig (BM) is a unique pig species in Guangxi Province, China. Compared to other breeds of domestic pig, such as the Debao pig (DB), it is smaller in size, better in meat quality, resistant to rough feeding and strong in stress resistance. These unique advantages of Bama Xiang pigs make them of great edible value and scientific research value. However, the differences in muscle metabolites between Bama Xiang pigs (BM) and Debao pigs (DB) are largely unexplored. Here, we identified 214 differential metabolites between these two pig breeds by LC-MS. Forty-one such metabolites are enriched into metabolic pathways, and these metabolites correspond to 11 metabolic pathways with significant differences. In Bama pigs, the abundance of various metabolites such as creatine, citric acid, L-valine and hypoxanthine is significantly higher than in Debao pigs, while the abundance of other metabolites, such as carnosine, is significantly lower. Among these, we propose six differential metabolites: L-proline, citric acid, ribose 1-phosphate, L-valine, creatine, and L-arginine, as well as four potential differential metabolites (without the KEGG pathway), alanyl-histidine, inosine 2′-phosphate, oleoylcarnitine, and histidinyl hydroxyproline, as features for evaluating the meat quality of Bama pigs and for differentiating pork from Bama pigs and Debao pigs. This study provides a proof-of-concept example of distinguishing pork from different pig breeds at the metabolite level and sheds light on elucidating the biological processes underlying meat quality differences. Our pork metabolites data are also of great value to the genomics breeding community in meat quality improvement. [ABSTRACT FROM AUTHOR]