松胞素B对人血淋巴细胞和CHL细胞微核率的影响

研究了不同浓度的松胞素Ｂ对人血淋巴细胞和中国仓鼠肺成纤维细胞（ＣＨＬ）分裂吉周期和微核率的影响。结果表明,松胞素Ｂ浓度增高过高能引起细胞微核率增高。在本研究中,对ＣＨＬ细胞微核率试验以３μｇ／ｍＬ松胞素Ｂ较适合;而对人血淋巴细胞微核试验,松胞素Ｂ浓度以２－４μｇ／ｍＬ为宜,松胞表Ｂ浓度过高会提高微核背景值,降低试验的灵敏度和精确性。     

极端嗜热菌海栖热袍菌木聚糖酶B的克隆和表达

极端嗜热菌海栖热袍菌MSB8(ThermotogamaritimaMSB8)能够利用木聚糖代谢 ,并具有两个产木聚糖酶的基因 .本研究首次克隆和在大肠杆菌中表达海栖热袍菌MSB8的第 2个木聚糖酶基因即xynB基因 .以基因组DNA为模板 ,根据xynB基因的全序列设计了两对引物 ,在合适的PCR反应条件下有效地扩增出了xynB基因片段 .选用pET2 8a(+)表达载体 ,NcoI-HindⅢ酶切位点并编码了羧基端 6×His标签的阳性克隆表达成可溶且具有生物活性的蛋白质 .xynB结构基因由 10 4 4对碱基组成 ,编码 347个氨基酸 .根据已知木聚糖酶蛋白质氨基酸的同源性分析 ,XynB与T .sp.strainFjSS3-B .1的XynA的同源性最大 ,为 85 % ,与T .neapolitana的XynB同源性次之 ,为 82 % ,与其它木聚糖酶的同源性小于 4 3% .另外 ,XynB属于F/ 10族木聚糖酶 ,且含有单一功能区 .表 3图 3参 12     

三种类型油菜(Brassica spp.)和野芥菜(B. juncea var.gracilis Tsen et Lee)杂交亲和性及F1的适合度--潜在基因转移的研究

通过人工去雄授粉，采用荧光显微镜观察了3种类型栽培油菜花粉在两地采集的野芥菜柱头上的萌发生长情况，结合杂交后的结实率，探讨了3种类型油菜和野芥菜杂交的亲和性．结果表明，甘蓝型油菜和芥菜型油菜与野芥菜的亲和性都非常高，亲和性指数达10．0以上，而白菜型油菜和野芥菜的亲和性较低，亲和指数小于0．2．子一代的适合度研究结果表明，芥菜型油菜向野芥菜杂交一代的适合度没有降低，而甘蓝型及白菜型和野芥菜杂交一代的适合度明显下降，表现在花粉活力降低，结实率极低．上述结果表明，白菜型油菜和野芥菜的基因转移可能性最小，甘蓝型居中，而芥菜型极易向野芥菜发生基因转移．     

无机阳离子对TiO2光催化降解染料的影响

考察了6种无机阳离子对P-25 TiO2光催化降解染料的影响，结果发现，Cu^2 ，Mn^2 和Ni^2 对光催化反应有强烈的抑制作用，Ca^2 ，Mg^2 和Al^3 对光催化反应速率无明显的负影响．经X光电能谱(XPS)的分析，确定锰离子以氧化物的形式沉积在氧化钛表面，使催化剂不可逆的中毒．Cu^2 和Ni^2 通过俘获光致电子导致催化活性降低。     

凝胶模板燃烧法制备纳米ZnO及其光催化性能

以硝酸锌为原料,明胶为模板分散剂,采用凝胶模板燃烧法制备纳米ZnO.利用TG-DTA,FT-IR,XRD,TEM和HPLC等手段对制备过程、样品的结构和性能进行了研究,探讨燃料及氧化剂的比例以及热处理温度的变化对产物粒径和光催化活性的影响.结果表明:产物粒子形状为球形,属六方晶系结构且无杂相.以染料罗丹明B溶液为目标降解物,1h的降解率为99.9%,最佳光催化剂的合成条件为:燃料与氧化剂的比例为0.84,400℃热处理3h.     

紫外线B对海洋生态系统的影响

近年来随着臭氧损失现象日益严重，到达地球表面的紫外线B辐射不断加强，海洋生态系统受到了前所未有的威胁。UV-B的增强改变了生物体赖以生存的水体环境，影响了浮游植物对营养盐的吸收同化，抑制了浮游植物的光合作用，从而减少了海洋对CO2的吸收能力，其结果直接增加了温室效应。同时UV-B也直接影响生态系统食物链的各个营养级，伤害海洋病毒、细菌和浮游植物，降低浮游动物和仔稚鱼的成活率，进而影响到整个海洋生态系统的结构和功能。     

苏云金芽胞杆菌苏云金素缺失突变株的筛选及特性研究

利用高温和SDS对苏云金素高产菌株CT-43-1c进行了质粒消除,筛选得到一株不产苏云金素的无晶体突变株BMB0806;并通过SDS-PAGE、高效液相色谱(HPLC)和脉冲电泳(PFGE)分析了野生型菌株CT-43、出发菌株CT-43-1c和突变株BMB0806杀虫晶体蛋白的组成、苏云金素的产量和质粒图谱之间的差异.结果表明,突变株BMB0806与菌株CT-43和CT-43-1c相比,分别缺失了3个和2个大质粒,从而不再产生苏云金素和由cry1B基因编码的分子量为140×103的杀虫晶体蛋白.进一步分析三者质粒图谱后发现,突变株BMB0806中苏云金素的缺失和cry1B基因所在的大质粒A直接相关.图5参12     

Comparative studies of the Fe–UV, H2O2–UV, TiO2–UV/vis systems for the decolorization of a textile dye X-3B in water

The degradation of a common textile dye, Reactive-brilliant red X-3B, by several advanced oxidation technologies was studied in an air-saturated aqueous solution. The dye was resistant to the UV illumination (wavelength λ  320 nm), but was decolorized when one of Fe³⁺, H₂O₂ and TiO₂ components was present. The decolorization rate was observed to be quite different for each system, and the relative order evaluated under comparable conditions followed the order of Fe²⁺–H₂O₂–UV  Fe²⁺–H₂O₂ > Fe³⁺–H₂O₂–UV > Fe³⁺–H₂O₂ > Fe³⁺–TiO₂–UV > TiO₂–UV > Fe³⁺–UV > TiO₂–visible light (λ  450 nm) > H₂O₂–UV > Fe²⁺–UV. The mechanism for each process is discussed, and linked together for understanding the observed differences in reactivity.     

Modelling the environmental degradation of water contaminants. Kinetics and mechanism of the riboflavin-sensitised-photooxidation of phenolic compounds

The aerobic visible-light-photosensitised irradiation of methanolic solutions of either of the phenolic-type contaminants model compounds (ArOH) p-phenylphenol (PP), p-nitrophenol (NP) and phenol (Ph), and for two additional phenolic derivatives, namely p-chlorophenol (ClP) and p-methoxyphenol (MeOP), used in some experiments, was carried out. Employing the natural pigment riboflavin (Rf) as a sensitiser, the degradation of both the ArOH and the very sensitiser was observed. A complex mechanism, common for all the ArOH studied, operates. It involves superoxide radical anion (O₂^√−) and singlet molecular oxygen (O₂(¹Δ_g)) reactions. Maintaining Rf in sensitising concentrations levels (≈0.02 mM), the mechanism is highly dependent on the concentration of the ArOH. Kinetic experiments of oxygen and substrate consumption, static fluorescence, laser flash photolysis and time-resolved phosophorescence detection of O₂(¹Δ_g) demonstrate that at ArOH concentrations in the order of 10 mM, no chemical transformation occurs due to the complete quenching of Rf singlet excited state. When ArOH is present in concentrations in the order of mM or lower, O₂^√− is generated from the corresponding Rf radical anion, which is produced by electron transfer reaction from the ArOH to triplet excited Rf. The determined reaction rate constants for this step show a fairly good correlation with the electron-donor capabilities for Ph, PP, NP, ClP and MeOP. In this context, the main oxidative species is O₂^√−, since O₂(¹Δ_g) is quenched in an exclusive physical fashion by the ArOH. The production of O₂^√− regenerates Rf impeding the total degradation of the sensitiser. This kinetic scheme could partially model the fate of ArOH in aquatic media containing natural photosensitisers, under environmental conditions.     

膨胀珍珠岩负载TiO2光催化脱色性能的研究

以钛酸四丁酯为原料 ,膨胀珍珠岩为载体 ,用溶胶 -凝胶法制备可漂浮于水面的负载型TiO2 。利用该负载型TiO2 对罗丹明B(RB)进行光催化脱色实验 ,结果表明 ,浸渍 3次的负载型TiO2 光催化活性最高 ,催化剂最佳用量为 5 0 0mg/10 0mLRB ,经 5h光照 ,对 10 0mL浓度为 1mg/L和 2 .5mg/LRB脱色率分别为 76 .6 7%和 4 7.2 7% ;该催化剂使用寿命长 ,2 5h后催化剂脱色性能没有减弱 ,可重复使用 ;经 8h光照 ,染料废水脱色效果好。