Influences of Environmental Conditions on the Cracking Tendency of Dry-Mixed Plastering Mortar

Cracking tendency is one of the important performances of dry-mixed plastering mortar (DMPM). Environmental condition is a key factor to affect the cracking tendency of DMPM. For the purpose of evaluating the cracking resistance of DMPM and revealing the influence of environmental conditions on the cracking tendency of DMPM, a series of experiments were performed on restriction-induced cracking behaviors as well as free shrinkage, water loss, and mechanical properties of DMPM. The restricted shrinkage tests were based on ring tests and plate experiments. The results showed that the initial drying age exhibits significant influence on the cracking tendency of DMPM, and there was a stress balance period when the initial drying age was 2 days. But, the phenomena cannot be observed when the initial age was 3 d, 5 d, and 7 d. In order to eliminate the cracking tendency of DMPM, it should avoid water loss from the plaster layer during construction in practical engineering, especially, before initial drying ages

Genome-Wide Identification of the HMA Gene Family and Expression Analysis under Cd Stress in Barley

In recent years, cadmium (Cd) pollution in soil has increased with increasing industrial activities, which has restricted crop growth and agricultural development. The heavy metal ATPase (HMA) gene family contributes to heavy metal stress resistance in plants. In this study, 21 HMA genes (HvHMAs) were identified in barley (Hordeumvulgare L., Hv) using bioinformatics methods. Based on phylogenetic analysis and domain distribution, barley HMA genes were divided into five groups (A–E), and complete analyses were performed in terms of physicochemical properties, structural characteristics, conserved domains, and chromosome localization. The expression pattern analysis showed that most HvHMA genes were expressed in barley and exhibited tissue specificity. According to the fragments per kilobase of exon per million fragments values in shoots from seedlings at the 10 cm shoot stage (LEA) and phylogenetic analysis, five HvHMA genes were selected for expression analysis under Cd stress. Among the five HvHMA genes, three (HvHMA1, HvHMA3, and HvHMA4) were upregulated and two (HvHMA2 and HvHMA6) were downregulated following Cd treatments. This study serves as a foundation for clarifying the functions of HvHMA proteins in the heavy metal stress resistance of barley

Effects of salicylic acid on growth, physiology, and gene expression in rice seedlings under salt and drought stress

Salt and drought stress has been an important factor limiting agricultural production, and SA is an important phenolic involved in stress response, but the function of SA in response to dual salt and drought stress in rice is not clear. In this study, the effects and mechanisms of exogenous SA-triggered in rice adaptation to dual salt and drought stress were investigated by detecting physiological and biochemical indexes and the expression of salt and drought tolerance genes. The results showed that the application of SA could significantly increase the antioxidant enzyme activities of rice seedlings under salt and drought stress, thereby reducing the contents of rice H2O2 and MDA and maintaining the growth of rice seedlings. Moreover, the expression of genes involved in the response of abiotic stress, such as OsDREB2A, OsSAPK8, OsSAPK10 and OsMYB2, were up-regulated under salt and drought treatment, and SA application could further enhance the expression of those genes like OsDREB2A and OsSAPK8, suggesting that SA might regulate antioxidant enzyme activity via inducing the expression of salt and drought tolerance genes and enhancing the salt and drought tolerance of rice. The results will enrich the knowledge of the function of SA and provide a reference for studying the mechanism of SA in the salt and drought resistance of rice, and breeding new rice germplasm with improved salt and drought resistance

Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota

The genus Bifidobacterium widely exists in human gut and has been increasingly used as the adjuvant probiotics for the prevention and treatment of diseases. However, the functional differences of Bifidobacterium genomes from different regions of the world remain unclear. We here describe an extensive study on the genomic characteristics and function annotations of 1512 genomes (clustered to 849 non-redundant genomes) of Bifidobacterium cultured from human gut. The distribution of some carbohydrate-active enzymes varied among different Bifidobacterium species and continents. More than 36% of the genomes of B. pseudocatenulatum harbored biosynthetic gene clusters of lanthipeptide-class-iv. 99.76% of the cultivated genomes of Bifidobacterium harbored genes of bile salt hydrolase. Most genomes of B. adolescentis, and all genomes of B. dentium harbored genes involved in gamma-aminobutyric acid synthesis. B. longum subsp. infantis were characterized harboring most genes related to human milk oligosaccharide utilization. Significant differences between the distribution of antibiotic resistance genes among different species and continents revealed the importance to use antibiotics precisely in the clinical treatment. Phages infecting Bifidobacterium and horizontal gene transfers occurring in genomes of Bifidobacterium were dependent on species and region sources, and might help Bifidobacterium adapt to the environment. In addition, the distribution of Bifidobacterium in human gut was found varied from different regions of the world. This study represents a comprehensive view of characteristics and functions of genomes of cultivated Bifidobacterium from human gut, and enables clinical advances in the future

Table_1_Combined treatment of disulfiram with PARP inhibitors suppresses ovarian cancer.docx

IntroductionDue to the difficulty of early diagnosis, nearly 70% of ovarian cancer patients are first diagnosed at an advanced stage. Thus, improving current treatment strategies is of great significance for ovarian cancer patients. Fast-developing poly (ADP-ribose) polymerases inhibitors (PARPis) have been beneficial in the treatment of ovarian cancer at different stages of the disease, but PARPis have serious side effects and can result in drug resistance. Using PARPis in combination with other drug therapies could improve the efficacy of PRAPis.In this study, we identified Disulfiram as a potential therapeutic candidate through drug screening and tested its use in combination with PARPis.MethodsCytotoxicity tests and colony formation experiments showed that the combination of Disulfiram and PARPis decreased the viability of ovarian cancer cellsResultsThe combination of PARPis with Disulfiram also significantly increased the expression of DNA damage index gH2AX and induced more PARP cleavage. In addition, Disulfiram inhibited the expression of genes associated with the DNA damage repair pathway, indicating that Disulfiram functions through the DNA repair pathway.DiscussionBased on these findings, we propose that Disulfiram reinforces PARPis activity in ovarian cancer cells by improving drug sensitivity. The combined use of Disulfiram and PARPis provides a novel treatment strategy for patients with ovarian cancer.</p

DataSheet_1_Combined treatment of disulfiram with PARP inhibitors suppresses ovarian cancer.docx

IntroductionDue to the difficulty of early diagnosis, nearly 70% of ovarian cancer patients are first diagnosed at an advanced stage. Thus, improving current treatment strategies is of great significance for ovarian cancer patients. Fast-developing poly (ADP-ribose) polymerases inhibitors (PARPis) have been beneficial in the treatment of ovarian cancer at different stages of the disease, but PARPis have serious side effects and can result in drug resistance. Using PARPis in combination with other drug therapies could improve the efficacy of PRAPis.In this study, we identified Disulfiram as a potential therapeutic candidate through drug screening and tested its use in combination with PARPis.MethodsCytotoxicity tests and colony formation experiments showed that the combination of Disulfiram and PARPis decreased the viability of ovarian cancer cellsResultsThe combination of PARPis with Disulfiram also significantly increased the expression of DNA damage index gH2AX and induced more PARP cleavage. In addition, Disulfiram inhibited the expression of genes associated with the DNA damage repair pathway, indicating that Disulfiram functions through the DNA repair pathway.DiscussionBased on these findings, we propose that Disulfiram reinforces PARPis activity in ovarian cancer cells by improving drug sensitivity. The combined use of Disulfiram and PARPis provides a novel treatment strategy for patients with ovarian cancer.</p