Phenol degradation on novel nickel-antimony doped tin dioxide electrode.

Nickel and antimony doped tin dioxide is a novel anodic material for its good performance of electrochemical ozone generation and direct electro-catalytic oxidation. Electro-catalytic oxidation of phenol on this novel nickel-antimony doped tin dioxide electrode is presented here. The morphology and composition of the electrode are characterized. The effects of applied current densities on phenol degradation rate, energy consumption and coulomb efficiency are discussed. In 0.1 M sulfuric acid, after 4 h electrolysis with current density of 25 mA cm(-1), 90% phenol is removed. And with current density of 20 mA cm(-1), the highest energy efficiency of 6.85 g kWh(-1) and the highest coulomb efficiency of 6.87 µg C(-1) are obtained. The effect of current densities on TOC removal is also discussed.

[Prokaryotic expression, purification, and polyclonal antibody generation of beta subunit of human F1F0-ATP synthase].

AIM: To express and purify the beta subunit of human F1F0-ATP synthase (hATP5B) in prokaryotic system, and generate its polyclonal antibody in rabbits. METHODS: The coding sequence of hATP5B mature peptide was amplified by RT-PCR from human umbilical vein endothelial cells (HUVEC) and then cloned into prokaryotic expression vector pET28a(+). The plasmid was transformed into E.coli BL21(DE3) to express hATP5B in reponse to IPTG induction. Expressed protein was purified by Ni(2+) metal-chelating chromatograph, and refolded by dialysis. The products were analyzed by SDS-PAGE and Western blot. Refolded protein was injected into rabbits to generate polyclonal antibody. The titer of the polyclonal antibody was determined by indirect ELISA. The specificity and the binding ability were detected by Western blot and cell immunofluorescence analysis. RESULTS: DNA sequencing confirmed that the coding sequence of hATP5B mature peptide was completely concordant with the original sequence (NM_001686, hATP5B's GenBank accession number). SDS-PAGE showed that the relative molecular masses (M(r)) of the expressed, purified, and refolded products were about relative molecular masses M(r) 55,000, which was in accordance with the predicted. Grayscale scanning showed that the expressed recombinant hATP5B (rhATP5B) accounted for 36.8% of the total bacteria protein, and the purity of purified product was 98.3%, of refolded 99.1%. The result of Western blot is positive. The titer of the polyclonal antibody was 1:640,000, and it specifically recognized the native antigen in HUVEC. CONCLUSION: hATP5B expressed in prokaryotic system has strong immunogenicity, and the polyclonal antibody with high titer and specificity was obtained from immunization of rabbits. The high level prokaryotic expression of hATP5B and the preparation of its antibody lay the foundation for further function research of hATP5B.