微囊藻毒素-LR对雄性黑斑蛙精巢中CYP46A1,CYP2H2和CYP2G1 mRNA表达的影响

微囊藻毒素-LR(microcystin-LR,MC-LR)是分布最广泛和毒性最强的一种微囊藻毒素,对水生动物造成潜在的健康威胁。大量科学研究证实,动物体中的细胞色素P450酶(CYP)参与内源性物质及外源毒性物质的代谢过程。为探究两栖动物生殖器官中的CYP酶对低剂量MC-LR生殖毒效应的调节作用,选择雄性黑斑蛙(Rana nigromaculata)为受试动物,采用静态置换法和体内暴露方法,分别暴露于0、0.1、1和10μg·L~(-1)MC-LR溶液0、7和14 d;用实时荧光定量PCR方法检测精巢中CYP46A1、CYP2H2和CYP2G1的mRNA表达水平。结果表明,暴露于0.1、1和10μg·L~(-1)MC-LR 14 d后,CYP46A1在mRNA水平分别上调了1.86、1.65和1.22倍,CYP2H2在mRNA水平分别上调了4.62、1.80和1.04倍,CYP2G1的mRNA水平分别上调了2.63、2.16和1.56倍。MC-LR在1μg·L~(-1)剂量下暴露7 d后,CYP46A1、CYP2H2和CYP2G1 mRNA水平均出现显著上调。上述研究表明,微囊藻毒素对黑斑蛙精巢3种CYP基因在mRNA水平上都存在低剂量刺激效应。低剂量MC-LR能诱导黑斑蛙精巢中CYP46A1转录水平变化,促进胆固醇转化为24S-羟化胆固醇,潜在破坏雄性黑斑蛙精巢中胆固醇水平的平衡; MC-LR也能够诱导精巢中CYP2H2和CYP2G1转录水平的变化,潜在调节CYP2H2和CYP2G1转录水平,进而影响MC-LR的代谢作用。     

Research progress in microbial cytochrome P450 and xenobiotic metabolism北大核心CSCD

Cytochrome P450 (CYP450s) is a type of heme-mercaptide protein superfamily, which is distributed widely in animals, plants, and microorganisms. CYP450s can oxidize and degrade many exogenous compounds such as drugs, herbicides, pesticides, some persistent organic pollutants, and so on. Based on recent researches, this paper reviews the nomenclature, classification, structure, and catalytic mechanism of P450 enzymes, and summarizes the research progresses in the metabolism and biodegradation of xenobiotics using P450 enzymes from microorganisms. The nomenclature and classification of the P450 gene superfamily mainly rely on the similarities of amino acid sequences. Although the structures of P450 are conserved, their recognition sites towards to the substrates are variable. This is also the structural basis for the catalytic diversities of P450 enzymes. Few P450 enzymes from bacteria and fungi can metabolize and degrade xenobiotics such as polycyclic aromatic hydrocarbons, herbicides, and so on. However, these P450 enzymes are less likely be used in practical applications because of their low catalytic activities. In the future, more P450 enzymes with high degradable efficiencies towards xenobiotics are needed to be obtained using multiple omics tools or modifying the existing P450 enzymes, to achieve the bioremediation of the environment. © 2018 Science Press. All rights reserved.     

基于SWAT模型的流域面源污染模拟影响分析

针对流域面源污染模型往往忽略或简化河道内污染物变化过程的缺陷,探讨了河道水质模型对流域面源污染模拟的影响.以太湖流域浙西区的西苕溪流域为研究对象,选取具有一定物理机制的分布式面源污染模型SWAT模型,分别以激活和不激活其嵌套的河道水质模型QUAL2E,即SWAT模型与QUAL2E模型紧密耦合和松散耦合两种情况进行模拟,并比较了对TN及TP的模拟效果.结果表明,丰水期与平水期的模拟结果并没有显著差别;但在枯水期,由于水量较小,河道内污染物变化过程对模拟结果影响较大.同时引入QUAL2K模型,分析认为改进河道水质模型对提高SWAT模型模拟精度有一定的效果.     

漂浮负载型光催化剂制备及降解草甘膦研究

以漂珠(FP)为载体,采用溶胶-凝胶-浸渍法制备了漂浮负载型CdS/TiO2/FP复合膜光催化剂,通过SEM、XRD对其结构进行了表征.以甘草膦农药的光催化降解为模型反应,使用不同光源研究了CdS/TiO2/FP的光催化性能,探讨了影响催化剂活性的因素及采用太阳光做光源处理草甘膦的可行性.结果表明,经4层镀膜500℃热处理的20%(w/w)CdS/TiO2/FP光催化剂具有良好的光催化性能,最佳降解条件为:催化剂加入量3 g/L,初始pH 7～9,Fe2 浓度为2.0×10-3 mol/L.通气量200 mL/min.在最佳条件下,对135 mg/L草甘膦溶液降解率可以分别达到96.3%(125 W高压汞灯,60 min)和82.4%(太阳光,180 min).     

二氧化铅电极的制备、表征及其电催化性能研究

以电沉积法制备了Ti/PbO2和Ti/MnO2/PbO22种电极.采用SEM、XRD和XPS等分析方法表征了电极的形貌、元素组成及元素化学态,并以罗丹明B为目标有机物,考察了所制备电极的析氧极化曲线和电催化活性以及Ti/MnO2/PbO2电极的循环伏安曲线.研究结果表明,Ti/MnO2/PbO2电极的稳定性、使用寿命、析氧电位和电催化活性较Ti/PbO2电极都有所提高,并且罗丹明B在Ti/MnO2/PbO2电极上的反应主要发生在析氧反应区,且反应不可逆.     

溶胶凝胶法制备磷钨酸掺杂TiO2薄膜及其光催化性能

以钛酸四丁酯为前驱物,采用溶胶凝胶法制备了磷钨酸掺杂的二氧化钛薄膜。通过XRD、FT-TR对该薄膜进行了表征,研究了薄膜在对氯苯酚光降解中的催化活性。结果表明,当磷钨酸与二氧化钛摩尔比为0.01∶1、薄膜烧结温度600℃、对氯苯酚溶液浓度30 mg/L（pH＝5）、光催化8 h的条件下,对氯苯酚的降解率超过90%,且薄膜可以重复使用。磷钨酸对二氧化钛的光催化活性具有明显的促进作用。     

超临界CO2回收线路板工艺研究

采用正交试验设计进行了超临界CO₂回收废弃印刷线路板的实验。以温度、压强、时间和夹带剂为实验因素,通过对实验前后样本在重量、厚度、弯曲强度和断裂强度四方面变化的分析考察了各实验因素对实验效果的影响。实验结果表明,影响超临界CO₂法回收印刷线路板的最主要因素为温度、时间和夹带剂,超临界CO₂法回收废弃印刷线路板的最佳工艺条件：温度270℃,压强大于7.38 MPa,时间3 h,夹带剂(水)160 mL。实验进一步验证了压强对实验结果的非显著性影响。     

Mixing-controlled biodegradation in a toluene plume--results from two-dimensional laboratory experiments

Various abiotic and biotic processes such as sorption, dilution, and degradation are known to affect the fate of organic contaminants, such as petroleum hydrocarbons in saturated porous media. Reactive transport modeling of such plumes indicates that the biodegradation of organic pollutants is, in many cases, controlled by mixing and therefore occurs locally at the plume's fringes, where electron donors and electron-acceptors mix. Herein, we aim to test whether this hypothesis can be verified by experimental results obtained from aerobic and anaerobic degradation experiments in two-dimensional sediment microcosms. Toluene was selected as a model compound for oxidizable contaminants. The two-dimensional microcosm was filled with quartz sand and operated under controlled flow conditions simulating a contaminant plume in otherwise uncontaminated groundwater. Aerobic degradation of toluene by Pseudomonas putida mt-2 reduced a continuous 8.7 mg L(-1) toluene concentration by 35% over a transport distance of 78 cm in 15.5 h. In comparison, under similar conditions Aromatoleum aromaticum strain EbN1 degraded 98% of the toluene infiltrated using nitrate (68.5+/-6.2 mg L(-1)) as electron acceptor. A major part of the biodegradation activity was located at the plume fringes and the slope of the electron-acceptor gradient was steeper during periods of active biodegradation. The distribution of toluene and the significant overlap of nitrate at the plume's fringe indicate that biokinetic and/or microscale transport processes may constitute additional limiting factors. Experimental data is corroborated with results from a reactive transport model using double Monod kinetics. The outcome of the study shows that in order to simulate degradation in contaminant plumes, detailed data sets are required to test the applicability of models. These will have to deal with the incorporation of existing parameters coding for substrate conversion kinetics and microbial growth.     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

湖州市埭溪镇污水处理厂的工程设计

湖州市埭溪镇污水处理厂的设计规模,近期为2万m^2／d,远期为3万m^2／d,其污水处理工艺采用改良式A^2／O工艺,污泥处理工艺采用带式浓缩脱水一体机。文中着重介绍了工程设计参数、处理工艺流程及其设计特点。