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Hu, Hong Bo,Yao, Shan Jing,Zhu, Zi Qiang,Hur, Byung Ki 한국화학공학회 2001 Korean Journal of Chemical Engineering Vol.18 No.3
The static and kinetic adsorption characteristics of Streamline DEAF and DEAF-Sepharose FF were studied under various operating conditions. The adsorption isotherms for the two types of adsorbents were obtained and found to fit well to a Langmuir-type expression. The adsorption kinetics of Streamline DEAF at different concentrations, temperatures, and viscosities were studied and a mathematical model including particle size distribution was developed to describe the adsorption performance of Streamline DEAE. Comparing the uptake curves of Streamline DEAF with DEAF-Sepharose FF, it could be concluded that Streamline DEAF achieves equilibrium faster to get equilibrium than DEAE-Sepharose FF, indicating that Streamline DEAF could be used in higher flow rate systems.
Bo Feng,Qian Zhang,Jianfang Wang,Hong Dong,Xiang Mu,Ge Hu,Tao Zhang 한국분자세포생물학회 2018 Molecules and cells Vol.41 No.4
IFIT1 (also known as ISG56) is a member of the interferoninducible protein with tetratricopeptide repeats (IFITs) family. IFITs are strongly induced by type I interferon (IFN), doublestranded RNA and virus infection. Here, we investigated IFIT1 expression in human umbilical vein endothelial cells (HUVECs) and in human bronchus epithelial cells (BEAS-2Bs) induced by the H9N2 virus and inactivated viral particle at different time points. We also investigated the effect of H9N2 virus and viral particle infection on IFN-α/β production, and assessed whether hemagglutinin or neuraminidase protein induced IFIT1 expression. Results showed that both H9N2 virus infection and viral particle inoculation induced the expression of IFIT1 at mRNA and protein levels in the two cell lines. Hemagglutinin or neuraminidase protein binding alone is not sufficient to induce IFIT1 expression. Surprisingly, the expression patterns of IFIT1 in response to H9N2 virus and viral particles in the two cell lines were opposite, and production kinetics of IFN-α/β also differed. An additional finding was that induction of IFIT1 in response to H9N2 virus infection or viral particle inoculation was more sensitive in HUVECs than in BEAS-2Bs. Our data offers new insight into the innate immune response of endothelial cells to H9N2 virus infection.
( Bo Wen Liu ),( Shang Feng Liu ),( Shan He ),( Ying Zhao ),( Hong Xia Hu ),( Zhao Wang ) 생화학분자생물학회 2005 BMB Reports Vol.38 No.2
Gonadogenesis is a complicated process which involves multi-gene interactions. A rainbow trout (Oncorhynchus mykiss) gene spermatogenesis associated 4 (SPATA4) was cloned and characterized from adult rainbow trout testis. The cDNA sequence of rainbow trout SPATA4 contains an open reading frame of 1, 081 nucleatides encoding a putative protein of 259 amino acids. The putative protein from rainbow trout shares a 76.8% homology with zebrafish SPATA4. No trans-membrane regions or signal peptide were detected using bioinformatics methods. Subcellular localization analysis revealed that rainbow trout SPATA4 was a nuclear protein with highest possibility (39.1%). Multi-tissue reverse transcriptase PCR (RT-PCR) was performed to examine the distribution of rainbow trout SPATA4 in eleven organs of adult rainbow trout. The result demonstrated that this gene express specifically in testis and slight amount of expression was detected in ovary. Further analysis of SPATA4 characterization and function in rainbow trout may provide insight into the understanding of gonadogenesis process.
Hu, Yue,Makogon, Taras Y.,Karanjkar, Prasad,Lee, Kun-Hong,Lee, Bo Ram,Sum, Amadeu K. Elsevier 2018 The Journal of chemical thermodynamics Vol.117 No.-
<P><B>Abstract</B></P> <P>Gas hydrates phase equilibria for structure I and II hydrates with chloride salts (NaCl, CaCl<SUB>2</SUB>, KCl and MgCl<SUB>2</SUB>) were measured at high salt concentrations and up to 200MPa. The measured equilibrium data represent three-phase (Solution – Hydrate – Vapor) or four-phase (Solution – Hydrate – Salt precipitated – Vapor) equilibrium depending on the salt concentration. The hydrate phase boundary with salts was shifted to lower temperatures and higher pressures when the experimental system was below the salt saturation concentration, while the boundaries were unchanged at salt concentrations above saturation, corresponding to quadruple points. The experimental data were compared with hydrate equilibrium predictions calculated by commonly used predictive tools to assess the reliability of these tools for the brines and conditions considered. The comparison demonstrates that predictive tools exhibit large deviation to the measured data, especially at high pressures and high salinity conditions.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Gas hydrates phase equilibria with chloride salts were measured up to 200MPa. </LI> <LI> Predictions deviate from measured data at high salt concentration and high pressure. </LI> <LI> Measured data are valuable to test and improve hydrate predictive tools. </LI> </UL> </P>
Hu, Bo,Liang, Minjian,Hong, Guoqiang,Li, Zhaoxia,Zhu, Zhenyu,Li, Lin Korean Society for Biochemistry and Molecular Biol 2005 Journal of biochemistry and molecular biology Vol.38 No.6
Antibody to hepatitis B surface antigen (HBsAb) is the important serological marker of the hepatitis B virus (HBV) infection. Conventionally, the hepatitis B surface antigen (HBsAg) obtained from the plasma of HBV carriers is used as the diagnostic antigen for detection of HBsAb. This blood-origin antigen has some disadvantages involved in high cost, over-elaborate preparation, risk of infection, et al. In an attempt to explore the suitable recombinant HBsAg for the diagnostic purpose, the HBV S gene was expressed in Pichia pastoris and the product was applied for detection of HBsAb. Hepatitis B virus S gene was inserted into the yeast vector and the expressed product was analyzed by sodium dodecyl sulphate polyacrolamide gel electrophoresis (SDS-PAGE), immunoblot, electronic microscope and enzyme linked immunosorbent assay (ELISA). The preparations of synthesized S protein were applied to detect HBsAb by sandwich ELISA. The S gene encoding the 226 amino acid of HBsAg carrying ahexa-histidine tag at C terminus was successfully expressed in Pichia pastoris. The His-Tagged S protein in this strain was expressed at a level of about 14.5% of total cell protein. Immunoblot showed the recombinant HBsAg recognized by monoclonal HBsAb and there was no cross reaction between all proteins from the host and normal sera. HBsAb detection indicated that the sensitivity reached 10 mIu (micro international unit)/ml and the specificity was 100% with HBsAb standard of National Center for Clinical Laboratories. A total of 293 random sera were assayed using recombinant S protein and a commercial HBsAb ELISA kit (produced by blood-origin HBsAg), 35 HBsAb positive sera and 258 HBsAb negative sera were examined. The same results were obtained with two different reagents and there was no significant difference in the value of S/CO between the two reagents. The recombinant HBV S protein with good immunoreactivity and specificity was successfully expressed in Pichia pastoris. The reagent for HBsAb detection prepared by Pichia pastoris-derived S protein showed high sensitivity and specificity for detection of HBsAb standard. And a good correlation was obtained between the reagent produced by recombinant S protein and commercial kit produced by blood-origin HBsAg in random samples.
Bo Li,Meng-Fei Luo,Geng-Shen Hu,Ling-Yun Jin,Xiao Hong,Ji-Qing Lu 한국공업화학회 2013 Journal of Industrial and Engineering Chemistry Vol.19 No.1
Ru catalysts supported on ZnO with different Ru contents were prepared by an impregnation method and were applied to the vapor-phase selective hydrogenation of crotonaldehyde. The catalysts were characterized by X-ray powder diffraction (XRD), NH3 temperature-programmed desorption (NH3-TPD),transmission electron microscopy (TEM) and temperature-programmed oxidation (TPO). It was found that with increasing Ru contents in the Ru/ZnO catalysts, the activity (TOF), surface acidity amount and deactivation rate increased and the selectivity to crotyl alcohol increased first and then decreased. The 3Ru/ZnO catalyst showed the highest selectivity to crotyl alcohol (up to 88.0%) for the hydrogenation of crotonaldehyde. The initial TOF values of the catalysts depended on the strength of surface acidity and the Ru particle sizes. The more Lewis acid sites made catalysts deactivate more easily. It was assumed that the deactivation was due to the formation of organic compounds deposition and poison effect of CO strongly adsorbed on the Ru atoms.