亚硝化细菌的筛选及培养条件的研究

从活性污泥中分离出16株亚硝化细菌,筛选出亚硝酸盐氮积累速率较高的两株菌Y8和Y16,初步鉴定Y8菌株为亚硝化球菌(Nitrosococcns.sp),Y16菌株为亚硝化单胞菌(Nitrosomonas.sp),并对其生长曲线进行了测定。通过氨氮去除率或亚硝酸盐氮的质量浓度来验证亚硝化细菌的活性,考察了生成的亚硝酸盐氮的质量浓度与培养时间的关系、亚硝化细菌的活性与培养温度的关系、亚硝化细菌的活性与培养基pH的关系。Y8和Y16菌株在30℃、培养基pH为7.5、130r/min的条件下振荡培养5d,氨氮去除率分别为81.12%,75.36%。

应用AHP构建城市森林树种综合评价指标体系

阐述了建立城市森林树种综合评价体系的指导思想与基本原则。建立了由7个抗性功能指标、5个生态功能指标5、个美学功能指标组成的城市森林树种综合评价指标体系;应用层次分析法(AHP),利用13位专家对评价指标成对比较的平均值构建了判断矩阵,进而确定了各层指标的权重值,并进行了一致性检验。研究表明,固碳释氧、抗污染、防风固沙、抗旱、滞尘5项指标的权重值最高,这与沈阳地区的基本状况以及城市森林树种选择的基本原则有着高度的一致性,研究在城市树种评价方面做了一次定性与定量、主观与客观相结合的有益尝试。

中国东北植被生态学研究中的焦点问题

中国东北植被经过半个多世纪的系统研究 ,但有关植被生态学一些争论性问题尚未统一 .本文仅就作者近年来研究工作涉及到的内容和关注的问题 ,提出一些看法 :1)中国东北植被地带性分布规律可用Kira的温暖指数 (WI)、寒冷指数 (CI)和作者的湿度指数 (HI)进行定量解释 .2 )大兴安岭北部山地 ,在海拔14 0 0m以上存在冻原植被 ,是作者于 196 3年首次发现的我国第三块冻原植被 ,其WI <15℃·月 .3)大小兴安岭植被分界线是我国植被区划中第一级分区界线 ,其位置在爱辉 -果松沟 -嫩江以南附近 ,WI为 4 5℃·月 .4 )大兴安岭植被地带性分异显著 ,南段、中段为典型草原地带和森林草原地带 ,北段为针叶林地带 ,HI值分别为 3 5～ 5 5、5 5～ 7 5、>7 5mm/℃·月 .大兴安岭东麓阔叶林是森林草原带上的森林植被类型 .5 )东北东部山地岳桦林是山地植被垂直带谱重要组成部分之一 ,是山地森林垂直分布林线 ,WI为 2 0～ 15℃·月为地带性植被类型 ,而WI>2 0℃·月为非地带性植被类型 .6 )内蒙古浑善达克沙地云杉林是陆地上非常罕见的森林生态系统类型 ,但这种云杉林究竟是哪一树种组成 ,在中国植物分类上一直是个争论性问题 ,作者通过核型分析和同工酶实验进一步证明是一个新种即沙地云杉Piceamongolica(H .Q .Wu)W .D .

中国水源保护林生态系统功能评价与营建技术体系

揭示了水源保护林的内涵 ,阐述了我国 7大水源保护林体系的布局及其涵养水源的效应机理 ,分析了水源保护林覆被率、林分结构、空间位置等功能扰动内部因子 ,及人为活动、火灾、气候变化等功能扰动外部因子 ,对我国现阶段水源保护林的现状进行评价 ,在此基础上提出包括 5大营建技术子系统的水源保护林的营建技术体系和提高综合功能和生产力的分类经营管理方式。

SARS控制与预警地理信息系统的研制与应用

针对中国当前非典型肺炎(SARS)疫情防治工作的迫切需求,作者基于其在地理信息科研领域具有大型国产GIS软件平台(SuperMAP)及其在辅助决策空间信息模型工具等方面的科研优势,紧急研制了“国家SARS疫情控制与预警信息系统”。该系统由5个子系统构成,是一个将空间定位、空间信息管理、空间信息分析技术和通信技术进行有机的整合,形成了前后端一体的SARS疫情实时传输、处理、分析和分布完整的信息系统。在SARS疫情的信息采集、管理、分析及其防治与监控措施的发布等方面发挥了重要的作用。

中国两种萤火虫荧光素酶基因的分子克隆表达及其序列分析

本文通过5’-RACE和3’-RACE方法克隆了西双版纳地区的卵黄萤Luciola ovalis和端黑萤Luciola terminalis两种荧光素酶基因。两个荧光素酶基因被连接到pET-15b载体上并在BL21(DE3)菌株中表达。L. ovalis荧光素酶基因的开放阅读框有1635个碱基，编码一个544个氨基酸的蛋白。L. terminalis荧光素酶基因有一个1647bp的开放阅读框，编码一个548个氨基酸的蛋白。它们的氨基酸序列和北美萤火虫(Photinus pyralis)的氨基酸序列分别有65.3%和65.9%的相似性，而彼此之间又有73.5%的相似性。两种在大肠杆菌中表达的荧光素酶均有很高的活性，它们的最大发光波长分别是566 nm和563 nm。同时表达的四种荧光素酶(L. ovalis、L. terminalis、Hotaria parvula和Pyrocoelia miyako)在不同pH下活性变化很大，四种荧光素酶在pH 6.5-7.5之间有比较高的活性，其中L. ovalis和P. miyako两种荧光素酶在pH 7.0时活性最高，而另两种在pH 7.5时活性最高。当pH大于8.0时，这四种荧光素酶的活性都散失很快，可见它们对pH变化非常敏感。序列分析和结构模拟发现，荧光素酶活性位点周围有六个非常保守的结构域，这六个保守区域包含了大多数在催化发光反应中与底物荧光素和ATP结合的氨基酸。L. terminalis萤火虫荧光素酶的三级结构与L. cruciata荧光素酶晶体结构非常相似，而L. ovalis荧光素酶的三级结构在AMP结合位点附近有两个偏离的环。

Gold Nanoparticle-based Colorimetric Sensor for pH Sensing

We present a newly designed colormetric sensor sensitive to pH value based on a gold nanocomposite composed of gold nanoparticles and pH-sensitive polymer{dodecylthioether end functionalized poly[2-(diethlamino) ethyl methacrylate], poly(DEAEMA)-DDT}. We have shown that this design can produce stable GNP precipitate under weakly basic condition(pH=7.5) and this precipitate can be dispersed in acidic solution(pH=4.0), due to the 2-(diethylamino) ethyl methacrylate protonated by H+.

New Organic Sensitizer for Stable Dye-Sensitized Solar Cells with Solvent-Free Ionic Liquid Electrolytes

We report a high molar extinction coefficient metal-free sensitizer composed of a triarylamine donor in combination with the 2-(2,2'-bithiophen-5-yl)acrylonitrile conjugation unit and cyanoacrylic acid as an acceptor. In conjugation with a volatile acetonitrile-based electrolyte or a solvent-free ionic liquid electrolyte, we have fabricated efficient dye-sensitized solar cells showing a corresponding 7.5% or 6.1% efficiency measured under the air mass 1.5 global sunlight. The ionic liquid cell exhibits excellent stability during a 1000 h accelerated test under the light-soaking and thermal dual stress. Intensity-modulated photocurrent and photovolatge spectroscopies were employed along with the transient photoelectrical decay measurements to detail the electron transport in the mesoporous titania films filled with these two electrolytes.

Controllable Synthesis and Luminescence Properties of La(OH)(3) and La(OH)(3):Tb3+ Nanocrystals with Multiform Morphologies

One-dimensional La(OH)(3) nanocrystals with multiform morphologies have been successfully synthesized by a facile bydrothermal process without using any surfactant, catalyst, or template. It can be found that the pH values of the initial solutions and the alkaline sources play a crucial role in controlling the morphologies of the products. The possible formation process of the 1D samples was investigated in detail, Furthermore, the as-prepared Tb3+-doped La(OH)(3) samples show a strong green emission corresponding to D-5(4)-F-7(5) transition of the Tb3+ ions under ultraviolet or low-voltage excitation.

Five supramolecular compounds of water-soluble sulfonylcalix[4]arenetetrasulfonate showing two calixarene conformations

Five new compounds of sulfonylcalix[4]arenetetrasulfonate (SC4AS), [H7Na(H2O)(3)(SC4AS)(phen)(5)](H2O)(11.9) (1), [H6Mn(H2O)(4)(SC4AS)(phen)(5)] (H2O)(12.7) (2), [Cu-4(SC4AS) (phen)(6)] (H2O)(4.5) (3), {[Cu (2)(SC4AS) (bpy)(2)][Cu(bpy)(2)(H2O)](2)} (H2O)(6.6) (4), and {[Zn-2(SC4AS) (phen)(2)][Zn(phen)(2)(H2O)(2)](2)} (H2O)(7) (5) (where phen 1,10-phenanthroline and bpy = 2,2'-bipyridine), were synthesized by a hydrothermal method and structurally determined by single crystal X-ray diffraction. The SC4AS ligand adopts partial cone conformation in compounds 1 and 2 and 1,2-alternate form in compounds 3-5. According to the structural analysis and density functional theory (DFT) calculations, we suggest that the metal can affect the conformation of SC4AS.

In Situ Preparation and Luminescent Properties of CeF3 and CeF3:Tb3+ Nanoparticles and Transparent CeF3:Tb3+/PMMA Nanocomposites in the Visible Spectral Range

CeF3 and CeF3:Tb3+ nanoparticles were prepared by reverse microemulsion with a functional monomer, methyl methacrylate (MMA), as the oil phase, and CeF3:Tb3+/poly (methyl methacrylate) (PMMA) nanocomposites were obtained via polymerization of the MMA monomer. The nanoparticles and nanocomposites have been well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), low- and high-resolution transmission electron microscope (TEM), selected-area electron diffraction (SAED), thermogravimetric analysis (TGA), UV/vis transmission spectra, photoluminescence excitation, and emission spectra and luminescence decays. The well-crystallized CeF3 and CeF3:Tb3+ nanoparticles are spherical with a mean diameter of 15 nm. They show the characteristic emission of Ce3+ 5d-4f (313 nm, D-2-F-2(5/2); 323 nm, D-2-F-2(7/2)) and Tb3+ D-5(4)-F-7(J) (J = 6-3, with D-5(4)-F-7(5) green emission at 541 nm as the strongest one) transitions, respectively.

Growth of highly crystalline CaMoO4 : Tb3+ phosphor layers on spherical SiO2 particles via sol-gel process: Structural characterization and luminescent properties

Highly crystalline CaMoO4:Tb3+ phosphor layers were grown on monodisperse SiO2 particles through a simple sol-gel method, resulting in formation of core-shell structured SiO2@CaMoO4:Tb3+ submicrospheres. The resulting SiO2@CaMoO4: Tb3+ core-shell particles were fully characterized by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL), low-voltage cathodoluminescence (CL), and kinetic decays. The XRD results demonstrate that the CaMoO4:Tb3+ layers begin to crystallize on the SiO2 spheres after annealing at 400 degrees C and the crystallinity increases with raising the annealing temperature. SEM and TEM analysis indicates that the obtained submicrospheres have a uniform size distribution and obvious core-shell structure. SiO2@CaMoO4:Tb3+ submicrospheres show strong green emission under short ultraviolet (260 nm) and low-voltage electron beam (1-3 kV) excitation, and the emission spectra are dominated by a D-5(4) -F-7(5) transition of Tb3+(544 nm, green) from the CaMoO4:Tb3+ shells.

Biofunctionalization of CeF3 : Tb3+ nanoparticles

CeF3: Tb3+ nanoparticles (short pillar-like morphology with an average length and width of 11 and 5 nm, respectively) were successfully prepared by a polyol process using diethyleneglycol (DEG) as solvent. After being functionalized with a SiO2-NH2 layer, these CeF3: Tb3+ nanoparticles can be conjugated with biotin molecules (activated by thionyl chloride) and further with avidin. The as-formed CeF3: Tb3+ nanoparticles, CeF3: Tb3+ nanoparticles functionalized with amino groups, biotin conjugated amino-functionalized CeF3: Tb3+ nanoparticles and biotinylated CeF3: Tb3+ nanoparticles bonded with avidin were characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), UV/vis absorption spectra and luminescence spectra, respectively. The biofunctionalization of the CeF3: Tb3+ nanoparticles has less effect on their luminescence properties, i.e. they still show strong green emission (from Tb3+, with D-5(4) - F-7(5) at 543 nm as the most prominent group), indicative of the great potential for these CeF3: Tb3+ nanoparticles to be used as biological fluorescence probes.

Host-sensitized luminescence of Dy3+, Pr3+, Tb3+ in polycrystalline SrIn2O4 for field emission displays

SrIn2O4:Dy3+/Pr3+/Tb3+ white/red/green phosphors were prepared by the Pechini sol-gel process. X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), diffuse reflectance, photoluminescence, cathodoluminescence spectra, and lifetimes were utilized to characterize the samples. XRD reveal that the samples begin to crystallize at 800 degrees C and pure SrIn2O4 phase can be obtained at 900 degrees C. FE-SEM images indicate that the SrIn2O4:Dy3+, SrIn2O4:Pr3+, and SrIn2O4:Tb3+ samples consist of fine and spherical grains with size around 200-400 nm. Under the excitation of ultraviolet light and low-voltage electron beams (1 - 5 kV), the SrIn2O4:Dy3+, SrIn2O4: Pr3+, and SrIn2O4: Tb3+ phosphors show the characteristic emissions of Dy3+ (F-4(9/2) - H-6(15/2) at 492 nm and 4F(9/2) - 6H(13/2) at 581 nm, near white), Pr3+ (P-3(0) - H-3(4) at 493 nm, D-1(2) - H-3(4) at 606 nm, and P-3(0) - H-3(6) at 617 nm, red) and Tb3+ (D-5(4) - F-7(6,5,4,3) transitions dominated by D-5(4) - F-7(5) at 544 nm, green), respectively. All of the luminescence resulted from an efficient energy transfer from the SrIn2O4 host lattice to the doped Dy3+, Pr3+, and Tb3+ ions, and the luminescence mechanisms have been proposed.

荧光法研究PTB与白蛋白的结合

利用药物对蛋白的荧光猝灭作用,用荧光法研究了N-苯酰甲噻唑溴（PTB）与牛血清白蛋白（BSA）及人血清白蛋白（HSA）的相互作用。测定发现BSA溶液的最大激发波长为280nm,HSA溶液的最大激发波长为290nm。分别向溶液中加入PTB后,原有的最大发射波长处的强度明显减弱。说明PTB对BSA和HAS有荧光猝灭作用。PTB与BSA,HSA有中等强度的结合。测得15℃时PTB与BSA,HSA的结合常数分别为3.66×10^3和3.83×10^3,结合位点数n分别为1.02和1.16;37℃时PTB与BSA,HSA的结合常数分别为3.58×10^3和3.35×10^3,结合位点数分别为0.95和0.87。根据热力学常数确定了PTB与BSA,HSA之间的主要作用力类型均为静电作用力。通过Fster偶级-偶级非辐射能量转移原理,得到BSA,HSA与PTB结合的位置距色氨酸残基的距离分别为7.5和7.9nm。根据白蛋白的结构,可以推测BSA,HSA与PTB结合的位点在ⅡA亚结构域,靠近Try214的区域。