共表达分子伴侣蛋白提高III型普鲁兰水解酶在短小芽孢杆菌中的分泌表达及发酵优化

本研究旨在通过共表达分子伴侣蛋白以及优化发酵条件来提高III型普鲁兰水解酶(TK-PUL)在短小芽孢杆菌中的分泌表达水平。通过构建共表达TK-PUL和分子伴侣蛋白的多种重组短小芽孢杆菌,并以胞外酶活为指标对其进行筛选,确定最有利于TK-PUL分泌表达的分子伴侣蛋白及对应的重组短小芽孢杆菌。在此基础上采用单因素实验和响应面法优化重组短小芽孢杆菌的发酵条件。结果表明,共表达分子伴侣蛋白PrsA^(Ba)的重组短小芽孢杆菌的胞外酶活达到98.79 U/mL,提高了0.31倍。该重组短小芽孢杆菌的最佳培养基包括19.65 g/L葡萄糖、21.46 g/L酵母提取物、12.01 g/L MgCl_(2)·6H_(2)O、9.02 g/L脯氨酸、0.01 g/L FeSO4·7H_(2)O、0.01 g/L MnSO4·4H_(2)O、0.001 g/L ZnSO4·7H_(2)O。在发酵温度为35℃、起始发酵pH为7.0的条件下,该重组短小芽孢杆菌于最佳培养基中培养66 h时,其胞外酶活达到192.68 U/mL,提高了1.56倍。本研究通过共表达分子伴侣蛋白和发酵优化实现了TK-PUL在短小芽孢杆菌的高效分泌表达,为TK-PUL的应用提供了基础。

混合牙列期骨性III类错合与骨性I类错合基骨及牙弓对比研究

目的:通过测量混合牙列期骨性III类错合患者与骨性I类错合患者的锥形束计算机断层扫描(Cone beam computed tomography, CBCT),对比分析上下颌牙弓、基骨弓长度与宽度差异及协调性,以期为替牙期骨性III类错合畸形治疗提供参考依据。方法:选择替牙列期骨性III类错合与骨性I类错合各30例,通过Dolphin软件处理收集到的DICOM (Digital Imaging and Communications in Medicine)医学图像数据,行三维重建并测量上下颌牙弓、基骨弓的长度与宽度,计算同一牙段牙弓宽度与基骨弓宽度之间的差值,比较骨性III类与骨性I类错牙合畸形牙弓与基骨弓宽度差值的差异。结果:1) 骨性III类错合组上颌牙弓及基骨弓长度均小于骨性I类错合组,下颌基骨弓长度大于骨性I类错合组,且差异有统计学意义(P 0.05)。2) 骨性III类错合组下颌前段及中段基骨弓宽度大于骨性I类错合组,差异有统计学意义(P 0.05)。3) 骨性III类错合组上颌牙弓与基骨弓宽度的差值均大于骨性I类错合组,下颌牙弓与基骨弓宽度的差值均小于骨性I类错合组,其中上颌后段牙弓宽度与基骨弓宽度差值差异有统计学意义(P < 0.05)。结论:混合牙列期骨性III类错合存在牙弓、基骨弓不调,上颌可扩大基骨弓,下颌可扩大牙弓,以期改善牙弓与基骨弓的协调性。

基于NSGA-III算法求解柔性作业车间调度问题

针对多目标柔性作业车间调度问题,提出一种改进NSGA-Ⅲ算法,以完工时间、机器总负荷、瓶颈机器负荷为目标建立调度模型。首先,为提高种群的多样性,提出一种基于惩罚的边界相交距离定义关联操作中种群个体与参考向量之间的距离;其次,为提高环境选择的计算效率,利用基于惩罚的边界相交距离消除机制来保护个体,降低了个体保护策略的计算成本;最后,为避免种群陷入局部最优,在遗传算子中采用一种改进的变异策略。运用两个评价指标与NSGA-Ⅲ算法进行比较,其收敛性与多样性均由于NSGA-Ⅲ算法。同时在4个Kacem算例上进行测试得出改进NSGA-Ⅲ算法解的质量较高,最后通过实际的生产实例证明改进的NSGA-Ⅲ算法优于或等同于现存在的方法,也证明了该方法在解决多目标柔性作业车间调度难题上的可操作性。

Study on Effect of Gd (III) Speciation on Ca (II) Speciationin Human Blood Plasma by Computer Simulation

Ca (II) speciation and effect of Gd (III) speciation on Ca (II) speciation in human blood plasma were studied by computer simulation. [CaHCO3](-) is a predominant compound species of Ca (II). Gd (III) can compete with Ca (II) for biological molecules. The presence of Gd (III) results in a increase of concentration of free Ca (II) and a decrease of concentration of Ca (II) compounds.

Adsorptive Removal of Antimony (III) Using Modified Montmorillonite: A Study on Sorption Kinetics

The adsorptive removal of antimony (III) has been successfully obtained on montmorillonite (MMT) and modified MMT from synthetic solution. The adsorption behavior of the modified and unmodified MMT has been investigated as a function of initial concentration of metal ion in the solution, pH of the solution and contact time using a batch extraction process. The optimized process can be applied for the adsorption, detection and estimation of antimony from 0.006 μg/ml (6.0 ppb) to 100.00 μg/ml (100.0 ppm) in aqueous solution. It has been observed that almost 99% of antimony (III) can be successfully extracted from a solution containing 100 μg/ml of the metal ion at pH 6.0 at 25?C ± 2?C. The investigation of the kinetics of sorption of antimony (III) on MMT/modified MMTshows intraparticle diffusion to be the rate limiting step during the initial stages of adsorption followed by chemisorption.

Experimental study on the inhibition of biological reduction of Fe(III)EDTA in NO_x absorption solution

Scrubbing of NOx from the gas phase with Fe(II)EDTA has been shown to be highly effective. A new biological method can be used to convert NO to N2 and regenerate the chelating agent Fe(II)EDTA for continuous NO absorption. The core of this biological regeneration is how to effectively simultaneous reduce Fe(III)EDTA and Fe(II)EDTA-NO, two mainly products in the ferrous chelate absorption solution. The biological reduction rate of Fe(III)EDTA plays a main role for the NOx removal efficiency. In this paper, a bacterial strain identified as Klebsiella Trevisan sp. was used to demonstrate an inhibition of Fe(III)EDTA reduction in the presence of Fe(II)EDTA-NO. The competitive inhibition experiments indicted that Fe(II)EDTA-NO inhibited not only the growth rate of the iron-reduction bacterial strain but also the Fe(III)EDTA reduction rate. Cell growth rate and Fe(III)EDTA reduction rate decreased with increasing Fe(II)EDTA-NO concentration in the solution.

Solubility measurement and thermodynamic modeling of carbamazepine(form III)in five pure solvents at various temperatures

In this work,the solubilities of carbamazepine(CBZ)(form III)in ethyl acetate,methyl acetate,ethylene glycol,chloroform and cyclohexylamine were determined by laser monitoring techniques at pressure above sea level,and the solubility data of CBZ(form III)in different pure solvents were fitted by the Modified Apelblat model andλh model.The result shows that the solubility of CBZ(form III)in five solvents increases as temperature rises,and the solubility in chloroform was the largest.The experimental solubility values of CBZ(form III)in ethyl acetate,methyl acetate,chloroform and cyclohexylamine were in better agreement with the simulated fitting values of theλh model.For ethylene glycol,the r value was much larger than the other four solvents,and it can be seen from theλh model that ethylene glycol was closer to the ideal solution system than the other four solvents.

Study on Speciation of Pr(III) in Human Blood Plasma by Computer Simulation

Speciation of Pr(III) in human blood plasma has been investigated by computer simulation. The speciation and distribution of Pr(III) has been obtained. It has been found that most of Pr(III) is bound to phosphate and to form precipitate. The results obtained-are in accord with experimental observations.

High Performance Affinity Chromatography of Antithrombin III Based on Monodisperse Poly (glycidyl methacrylate) Beads

A new approach for the separation of antithrombin III with high performance affinity chromatography (HPAC) was described. A novel monodisperse, non-porous, cross-linked poly (glycidyl methacrylate) beads (PGMA) were used as the affinity support. With the water-soluble carbodiimide, heparin was linked covalently to amino-PGMA-beads, which was prepared by amination of PGMA. The adsorbent obtained exhibits high binding activity to antithrombin III (ATIII), good resolution and excellent mechanical properties and can be used under high flow rate.

Molecular Simulation study of Alkyl Monolayers on Si(III) Surface

The structure of eight-carbon monolayers on the H-terminated Si(III) surface was investigated by molecular simulation method. The best substitution percent 50% for octene or octyne-derived monolayer can be obtained using molecular mechanics calculation. And the densely packed, well-ordered monolayer on Si(III) surface can be shown through energy minimization in the suitable-size simulation cell.

Mechanistic Study of Ruthenium(III) Catalyzed Oxidation of Cyclohexanone by Acidic Bromate

In this work, kinetics and mechanism of Ru(III) catalyzed oxidation of cyclohexanone by acidified solution of potassium bromate has been studied. Present study employ mercuric acetate Hg (OAc)2 as a scavenger for Br&#175;?ion to prevent parallel oxidation by bromine. The kinetics and mechanism have also been studied in the temperature range of 30°C - 45°C. The reaction exhibits first order kinetics with respect to Ru (III), while zero order kinetics with respect to KBrO3 and HClO4. The influence of Hg(OAc)2 and ionic strength on the rate of reaction was found to be insignificant. Positive effect in the reaction mixture was also observed upon addition of chloride ion;while as the negative effect was revealed with acetic acid. A suitable mechanism in conformity with the kinetic observations has been proposed and the rate law is derived on the basis of obtained data. The various activation parameters such as energy of activation (ΔE*), Arrhenius factor (A), entropy of activation (ΔS*) were calculated from the rate measurements at 30°C, 35°C - 40°C and 45°C.

Gd_(2)MgTiO_(6):Dy^(3+)荧光粉的制备与发光性能研究

采用高温固相法制备出一系列Dy^(3+)掺杂双钙钛矿Gd_(2)MgTiO_(6)白色荧光粉样品,通过X射线衍射仪和荧光光谱仪对荧光粉样品的晶体结构及荧光性能进行分析和表征。结果表明:在355 nm近紫外光激发下,样品发出极强的蓝光(484 nm)和黄光(575 nm)。通过调节Dy^(3+)的浓度可以使样品发光颜色向白光区移动,因此Gd_(2)MgTiO_(6):Dy^(3+)是一种可调荧光粉。当Dy^(3+)掺杂浓度为3%时可以发出色坐标为(0.3598,0.3946)的白光。Gd_(2)MgTiO_(6)合成方法简便、组份易调控,是一种具有潜在应用价值荧光材料。

Valence electronic engineering of superhydrophilic Dy-evoked Ni-MOF outperforming RuO_(2) for highly efficient electrocatalytic oxygen evolution

Tackling the problem of poor conductivity and catalytic stability of pristine metal-organic frameworks(MOFs) is crucial to improve their oxygen evolution reaction(OER) performance.Herein,we introduce a novel strategy of dysprosium(Dy) doping,using the unique 4f orbitals of this rare earth element to enhance electrocatalytic activity of MOFs.Our method involves constructing Dy-doped Ni-MOF(Dy@Ni-MOF) nanoneedles on carbon cloth via a Dy-induced valence electronic perturbation approach.Experiments and density functional theory(DFT) calculations reveal that Dy doping can effectively modify the electronic structure of the Ni active centers and foster a strong electronic interaction between Ni and Dy.The resulting benefits include a reduced work function and a closer proximity of the d-band center to the Fermi level,which is conducive to improving electrical conductivity and promoting the adsorption of oxygen-containing intermediates.Furthermore,the Dy@Ni-MOF achieves superhydrophilicity,ensuring effective electrolyte contact and thus accelerating reaction kinetics,Ex-situ and in-situ analysis results manifest Dy_(2)O_(3)/NiOOH as the actual active species.Therefore,Dy@Ni-MOF shows impressive OER performance,significantly surpassing Ni-MOF.Besides,the overall water splitting device with Dy@NiMOF as an anode delivers a low cell voltage of 1.51 V at 10 mA cm^(-2) and demonstrates long-term stability for 100 h,positioning it as a promising substitute for precious metal catalysts.

Myxopapillary Ependymoma of the III Ventricle: Example of a Histological Variant of Ependymoma with Exceptional Localization

We present morphological findings observed from the study of a myxopapillary ependymoma located in the III ventricle. This tumor, which is a rare occurrence at this level, was observed in a 73-year-old woman with no relevant medical history who presented with obstructive hydrocephalus due to compression and blockage of the foramen of Monro. The good delineation of the lesion allowed its surgical excision, and histological examination of the material obtained after excisional biopsy revealed a glial neoplasm with a low degree of cytological malignancy that was strongly positive for glial fibrillary acidic protein (GFAP) as well as a myxopapillary architecture analogous to that observed in ependymomas of the filum terminale. Subsequent radiological examination allowed us to rule out a metastatic nature of the tumor, confirming its primary origin. We briefly discuss the case and review the main characteristics of this neoplasia, which is quite rare at the site identified in our patient.

STUDY ON BINUCLEAR COPPER(I)COMPLEXES III.SYNTHESIS,CHARACTERIZATION AND ELECTROCHEMISTRY OF DICHLORO-TRIS(4-VINYLPYRIDINE)-DICOPPER(I)COMPLEX

Recent years,many novel complexes have been prepared by using hetero-bidentate ligands.However,complexes with such ligands as 4-vinylpyridine which has two different coordinating sites have not been reported,and only a few complexes of Cu(I)have been published^(1-3).The title complex Cu_2(C_5H_4N·CH=CH_2)_3Cl was prepared and characterized by elemental analyses,ICP,IR,and electronic spectra.Its conductivity,oxidation potential and reduction potential were measured.

Synthesis and Crystal Structure of N-(2-Pyridylmethyl)-L-Alanine) Isothiocyanate Cobalt(III)

The title compound, [N-(2-pyridylmethyl)-(L)-alanine]Co(III) thiocyanate (1) was obtained from the reaction of Co(OOCH3)2·H2O with the tridentate reduced Schiff base ligand, N-(2-pyridylmethyl)-(L)-alanine (L) and NH4SCN and characterized by elemental analysis, IR, UV-visible, TGA and single- crystal X-ray diffraction. Structural and spectroscopic analyses reveal [Co(L)2)]SCN to be monomeric with Cobalt(III) adopting a pseudo-octahedral geometry, coordinating to two reduce Schiff base ligands. In the crystal lattice, the thiocyanate anion forms an intermolecular SCN···HNamine hydrogen bond, while adjacent monomers are linked by intermolecular Ocarboxyl···HNamine···H-bonds to form a supramolecular network. This work is therefore undertaken in an attempt to construct coordination framework structures of varying properties using the mixed-ligand strategy involving reduced Schiff bases and the thiocyanate ion.

合成染料与染料脱色过氧化物酶Il-DyP4相互作用的光谱分析

利用紫外-可见吸收光谱法和荧光光谱法,分析蒽醌类染料(reactive blue 19(RB19),reactive blue 4(RB4))、偶氮类染料(reactive violet 5(RV5),reactive black 5(RB5))及底物2,2′-联氮-双(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS)与染料脱色过氧化物酶Il-DyP4之间的相互作用.紫外-可见吸收光谱法结果表明,Il-DyP4和上述底物之间均形成了复合物;荧光光谱法结果表明,上述底物均使Il-DyP4产生了荧光淬灭效应,且淬灭类型为静态淬灭,符合紫外-可见吸收光谱的结果.根据双对数方程■,计算出RB19,RB4,RV5,RB5,ABTS与Il-DyP4相互作用的表观结合常数(Ka)分别为:9.386 2×10^(4)L·mol^(-1)(298 K),5.615 7×10^(6) L·mol^(-1)(298 K),1.926 2×10^(6) L·mol^(-1)(288 K),5.277 8×10^(5) L·mol^(-1)(298 K),2.234 6×10^(5) L·mol^(-1)(298 K).热力学参数分析结果表明,上述底物与Il-DyP4的结合依赖于疏水相互作用,是自发的吸热过程.

STUDY ON THE DETERMINATION OF TRACE BISMUTH(III) BY THIN-LAYER RESIN PHASE SPECTROPHOTOMETRY

In this paper, a new thin-layer ion-exchange resin phase analytical method is introduced. It is based on that, the bismuthous cation can associate with iodic anions, so as to formed an anion complex [BiI4-] in a strong acidic environments. This anion complex can also exchanges with a weaker anions on the surface active site of anion exchange resin, so that a [R+] [BiI4-] solid phase binary associational system is produced. Owing to the solid system is a great many dispersive particulates, it can be pressed to a thin-layer by press tools of the so called 搕hin-layer resin phase?or 搑esin phase? and using this solid association system spectrophotometry for the determination of trace metals. So it can increase the analytical sensitivity. This association system exhibits maximum absorbance at 460nm, and obeys Beer抯 law over the concentration range 0.01ug/ml^1.20ug/ml of bismuthous(III). It has a molar absorptivity of 7.1×105 [L/mol穋m]. It indicated the resin phase spectrophotometry is a sensitive analytical method for trace bismuthous. It is 18 times higher than routine aqueous spectrophotometry. The relative standard deviations is 1.82% (n=6) for the measurements of 0.5ug/ml Bi(III). The detection limit of Bismuthous(III) is 1.4×10-8mol/L. The method has applied to the analysis Bi(III) in environmental water samples.

Archives of Animal Center of Ur-III Dynasty in Drehem: AACUD Project in IHAC (2005-2010)

Principal Investigator and Supervisor of Project: Wu Yuhong 1. QI Bing, MA Thesis, June, 2005 Reconstruction of the Early Archive of Naram-ili, Storage Official (sukkal, ì-du8) of the Animal Center of the Ur-III

Prevalence of metabolic syndrome in type 2 diabetic patients: A comparative study using WHO, NCEP ATP III, IDF and Harmonized definitions

To determine the prevalence of metabolic syndrome (MetS) in Malaysian type 2 diabetic patients using WHO, NCEP ATP III, IDF and the new Harmonized definitions, and the concordance between these definitions. This study involved 313 patients diagnosed with type 2 diabetes mellitus (T2DM) at two Malaysian tertiary hospitals. Socio-demographic data were assessed using a pre-tested interviewer-administered structured questionnaire. Anthropometric measurements were carried out according to standard protocols. Clinical and laboratory characteristics were examined. Kappa (k) statistics were used for the agreement between the four MetS definitions. The overall prevalence rates of MetS (95% CI) were 95.8% (93.6-98.1), 96.1% (94.0-98.3), 84.8% (80.8-88.9) and 97.7% (96.1-99.4) according to the WHO, NCEP ATP III, IDF and the Harmonized definitions, respectively. The Kappa statistics demonstrated a slight to substantial agreement between the definitions (k = 0.179-0.875, p k = 0.875, p hest specificity (100%) in identifying MetS. In conclusion, the new Harmonized criteria established the highest prevalence of MetS among the four definitions applied. There was a very good concordance between the WHO and NCEP ATP III criteria. The extremely high prevalence of MetS observed in type 2 diabetic patients indicates an impending pandemic of CVD risk in Malaysia. Aggressive treatment of MetS components is required to reduce cardiovascular risk in T2DM.