Abstract Background Transferring herbicide resistance genes to plant cultivars is one of the most effective methods for managing weed growth in agricultural land. The RePAT gene, previously isolated from the marine bacterium Rhodococcus sp . strain YM12, was found to provide glufosinate resistance to plants. Objective In this study, we further investigated the protein structure and function of RePAT isolated from the marine. Methods The physicochemical properties, two-dimensional structure, three-dimensional structure, and functional domains of the RePAT protein were analyzed and predicted using bioinformatics tools, and RePAT was optimized according to codon bias present in Arabidopsis thaliana . Site-directed mutagenesis of RePAT was performed, and the wild-type ( RePAT ) and mutant ( RePAT V120I ) genes were successfully transferred into A. thaliana . Results Our results showed that RePAT was an unstable hydrophilic protein, and six phosphorylation sites and two N-glycosylation sites were predicted. In addition, conserved domains containing the NAT_SF super family and coenzyme A-binding pocket were predicted in RePAT. Transgenic experiments and glufosinate resistance assays showed that the glufosinate resistance of A. thaliana containing the mutant gene ( RePAT V120I ) was lower than that of plants containing the wild-type gene, indicating that the missense mutation in RePAT V120I had a significant effect on its glufosinate resistance. Conclusions Our study provided improvement result for knowing the transferring herbicide resistance gene RePAT .

Effects of various rare-earth elements (RE: Gd, Nd and Ce) additions on microstructures and mechanical properties of ultra-light dual phase Mg-9Li-0.4Zr alloy were investigated. The results indicated that Mg-9Li-5RE-0.4Zr alloys exhibited α-Mg, β-Li and RE-containing intermetallic compound structures. 5 wt.% Gd, Nd and Ce additions enhanced the strength properties of as-extruded Mg-9Li-0.4Zr alloy, but greatly deteriorated the ductility. The final mechanical properties of Mg-9Li-5RE-0.4Zr alloys were 161MPa∼167MPa in ultimate strength, 141MPa∼156MPa in yield strength and 20.8%∼32.5% in elongation. Heat treatment was hardly able to improve the mechanical properties for Mg-9Li-5RE-0.4Zr alloys.

OBJECTIVES: Our previous study demonstrated that superoxide dismutase levels were higher in tuberculous pleural effusions than in malignant pleural effusions, but that this difference could not be used to discriminate between the two. The objective of the present study was to investigate the levels of superoxide dismutase 2 in pleural effusions and to evaluate the diagnostic significance of pleural effusion superoxide dismutase 2. METHODS: Superoxide dismutase 2 concentrations were determined in pleural effusions from 54 patients with tuberculous pleural effusion and 33 with malignant pleural effusion using an enzyme-linked immunosorbent assay (ELISA) kit. Pleural effusion interferon gamma and tumor necrosis factor alpha levels were also analyzed by ELISA. The Mann-Whitney U test was used to evaluate the significance of differences. Associations between superoxide dismutase 2 concentrations and sex, age and smoking habits were assessed using Spearman's or Pearson's correlation coefficient analysis. Receiver operator characteristic analysis was performed to evaluate the value of superoxide dismutase 2 levels in the discrimination of tuberculous pleural effusion from malignant pleural effusion. RESULTS: Superoxide dismutase 2 levels were significantly higher in patients with tuberculous pleural effusion compared with those with malignant pleural effusion (p<0.05). When superoxide dismutase 2 was used to differentiate between tuberculous pleural effusions and malignant pleural effusions, the area under the receiver operator characteristic curve was 0.909 (95% confidence interval, 0.827-0.960; p<0.01). With a cut-off value of 54.2 ng/mL, the sensitivity, specificity, positive likelihood ratio and negative likelihood ratio were 75.8% (95%CI: 57.7-88.9%), 98.1% (95%CI: 90.1-99.7%), 40.91 and 0.25, respectively. Furthermore, significant correlations between pleural effusion superoxide dismutase 2 and interferon gamma (r = 0.579, p<0.01) and between pleural effusion superoxide dismutase 2 and tumor necrosis factor alpha (r = 0.396, p<0.01) were observed. CONCLUSION: Pleural effusion superoxide dismutase 2 can serve as a biomarker for differentiating between tuberculous pleural effusions and malignant pleural effusions. Because of the high correlations of superoxide dismutase 2 with pleural effusion interferon gamma and tumor necrosis factor alpha levels, this marker may act as an inflammatory factor that plays an important role in the development of tuberculous pleural effusion.