Euglena gracilis as a model for the study of Cu and Zn toxicity and accumulation in eukaryotic cells

We have observed the effect of copper and zinc on the biology of Euglena gracilis. The cells displayed different sensitivities to these metals, as the apparent LC₅₀ for Cu²⁺ was 0.22 mM, and for Zn²⁺ it was 0.88 mM. While Zn²⁺ was able to increase cell proliferation even at 0.1 mM, the minimal CuCl₂ concentration tested (0.02 mM) was sufficient to impair cell division. Higher concentrations of these metals not only inhibited cell division in a concentration-dependent manner, but also interfered with the metabolism of E. gracilis. A higher accumulation of proteins and lipids per cell was observed at the DI₅₀ concentration for metal-treated cells. These results suggest that the test concentration of both metals leads to a failure in completing cell division. Ultrastructural analysis indicated a chloroplast disorganization in copper-treated cells, as well as the presence of electron dense granules with different shapes and sizes inside vacuoles. Microanalysis of these granules indicated an accumulation of copper, thus suggesting a detoxification role played by the vacuoles. These results indicate that E. gracilis is an efficient biological model for the study of metal poisoning in eukaryotic cells. They also indicate that copper and zinc (copper being more poisonous) had an overall toxic effect on E. gracilis and that part of the effect can be ascribed to defects in the structure of chloroplast membranes.     

Two-site kinetic modeling of bacteriophages transport through columns of saturated dune sand

Breakthrough curves, on a semi-log scale, from tests in porous media with block-input of viruses, bacteria, protozoa and colloidal particles often exhibit a typical skewness: a rather slowly rising limb and a smooth transition of a declining limb to a very long tail. One-site kinetic models fail to fit the rising and declining limbs together with the tail satisfactorily. Inclusion of an equilibrium adsorption site does not seem to improve simulation results. This was encountered in the simulation of breakthrough curves from a recent field study on the removal of bacteriophages MS2 and PRD1 by passage through dune sand. In the present study, results of laboratory experiments for the study of this issue are presented. Breakthrough curves of salt and bacteriophages MS2, PRDI, and phiX174 in 1 D column experiments have been measured. One- and two-site kinetic models have been applied to fit and predict breakthrough curves from column experiments. The two-site model fitted all breakthrough curves very satisfactorily, accounting for the skewness of the rising limb as well as for the smooth transition of the declining limb to the tail of the breakthrough curve. The one-site model does not follow the curvature of the breakthrough tail, leading to an overestimation of the inactivation rate coefficient for attached viruses. Interaction with kinetic site 1 is characterized by relatively fast attachment and slow detachment, whereas attachment to and detachment from kinetic site 2 is fast. Inactivation of viruses and interaction with kinetic site 2 provide only a minor contribution to removal. Virus removal is mainly determined by the attachment to site 1. Bacteriophage phiX174 attached more than MS2 and PRD1, which can be explained by the greater electrostatic repulsion that MS2 and PRD1 experience compared to the less negatively charged phiX174.     

附载型复合光催化剂TiO2·SiO2/beads降解有机磷农药

研究以四异丙醇钛 [Ti( iso- O C3 H7) 4]、硅酸乙酯为原料 ,以空心玻璃微球为载体 ,用溶胶—凝胶法制备可漂浮附载型复合光催化剂 Ti O2 · Si O2 / beads的过程 ,利用附载型复合光催化剂降解有机磷农药。结果表明 ,复合型光催化剂 Ti O2 · Si O2 摩尔比存在最佳值 ,n ( Ti O2 ) / m ( Si O2 ) =30 / 70时 ,光催化剂活性最高 ,其活性是同样降解条件下、同样含量 Degussa P- 2 5Ti O2 的 2倍左右。该光催化剂比表面大 ,吸附性强。并用 XRD和 SEM对附载型复合光催化剂进行表征     

Untersuchungskonzept zur Charakterisierung toxischer Stoffe in belastetem Wasser

Zusammenfassung  Zur ?kotoxikologischen Beurteilung von belastetem Wasser werden h?ufig einfache Biotests eingesetzt. Nicht selten werden dabei toxische Effekte festgestellt. Es stellt sich dann die Frage nach den verantwortlichen Wasserinhalts-stoffen. Durch Festphasenextraktion (SPE) werden diese angereichert, gewonnen und dünnschichtchromatographisch unter Verwendung der automatisierten Mehrfachentwicklung aufgetrennt. Von der DC-Platte wird ein Streifen abgetrennt und darauf direkt die biologische Detektion mit Mikroorganismen (Bacillus subtilis, Leuchtbakterien) durchgeführt. Dadurch k?nnen toxische Banden erkannt werden, Auf dem DC-Plattenrest wird von der toxischen Bande mit einem DC-scanner ein UV-Spektrum aufgenommen, die entsprechende Bande herausgekratzt, der toxische Stoff eluiert und infrarotspektroskopisch untersucht. Durch Spektrenvergleich gelingt es meistens, den Stoff zu charakterisieren. In der vorliegenden Arbeit wird am Beispiel eines Zitzengummieluates das Analysenkonzept vorgestelit. Es zeigte sich, dass dieser Gummiartikel einen Vulkanisationsbeschleuniger (2-Mercaptobenzothiazol) freisetzt. Online-Publikation am: 21.12.1999     

Formation of polychlorobiphenyls in silicone rubber

In silicone rubber crosslinked with bis(2,4-dichlorobenzoyl) peroxide (DCBP) as initiator about 0.1% of DCBP is converted into polychlorobiphenyls (PCBs). The PCB content in silicone rubber determined by high resolution gas chromatography (HRGC) after its destruction by HF is around 10 mg/kg. 29 PCB congeners were detected. Instead of the expected PCB-47, lower chlorinated congeners are predominant. Some possible pathways of their origin are presented.     

Chemische Reaktionen von chlorvinylarsinverbindungen (Lewisite)

Zusammenfassung  2-Chlorvinylarsindichlorid (Lewisit I) und 2,2′-Dichlordivinylarsinchlorid (Lewisit II) reagieren bei Raumtemperatur in einer Substitutionsreaktion schnell und quantitativ mit Dithiolen. Die Derivate wurden massenspetrometrisch identifiziert. Sie sind mit GC/ECD detektierbar. Diese Reaktionen k?nnen zur gaschromatographischen Bestimmung von Lewisiten in Wasser-und Bodenproben eingesetzt werden.      

L-半胱氨酸改性甲壳素处理含铅、镉工业废水

研究了L 半胱氨酸改性甲壳素作为吸附剂对Pb2 + 、Cd2 + 的动态吸附性能 ,同时考察了流速、溶液中离子的含量、吸附剂的相对用量等因素对吸附效果的影响 ,以及洗脱液的种类和酸度、洗脱速度、洗脱液体积等因素对解吸率的影响。结果表明 ,用该吸附剂填装的吸附柱对含Pb2 + 、Cd2 + 工业废水直接进行处理 ,处理后的水达到了排放标准。     

Isomer distribution of nitrotriphenylenes in airborne particles, diesel exhaust particles, and the products of gas-phase radical-initiated nitration of triphenylene

The formation of mutagenic nitro-polycyclic aromatic hydrocarbons (NPAHs) 1- and 2-nitrotriphenylene (1- and 2-NTP) via gas-phase OH or NO₃ radical-initiated reactions of triphenylene was demonstrated for the first time using a flow reaction system. In contrast with the results of conventional electrophilic nitration, 2-NTP was formed in larger yield than 1-NTP, but this is consistent with the mechanism proposed for gas-phase radical-initiated nitration of PAH. In diesel exhaust particle (DEP) samples, both 1- and 2-NTP were identified and their concentrations determined, as well as 1-nitropyrene (1-NP), which is a representative combustion-derived NPAH: the mean concentrations of 1-NTP, 2-NTP, and 1-NP were 4.7, 1.9, and 32 pmol mg_DEP^–1, respectively. The mean 2-NTP/1-NTP, 1-NTP/1-NP, and 2-NTP/1-NP ratios in samples of airborne particles collected in a residential area in Osaka, Japan, were>1.55,<0.25, and 0.37, respectively; these values are much higher than those of the DEP samples. This finding indicates that there is another source for airborne NTPs, especially 2-NTP, apart from diesel exhaust. These results strongly suggest that airborne NTPs originate from atmospheric processes such as radical-initiated reactions of triphenylene, and this has a significant influence on the atmospheric occurrence of NTPs.     

有机污染物的光催化降解过程中的分析技术进展

本文对有机物的光催化降解动力学研究 ,降解产物的鉴定、定量检测等过程中所使用的一些分析技术和手段 ,尤其是在有机物的光降解机理研究中羟自由基的检测技术和方法进行了综述     

微波加热对活性炭表面基团及其对SO2吸附性能的影响

采用了微波加热技术,通过在不同微波功率和辐射时间条件下对不同粒径活性炭进行改性,研究了改性前后活性炭的表面化学基团、元素组成的变化,以及对SO2吸附性能的影响.结果表明,经过微波改性后活性炭的SO2吸附性能大为提高,微波功率是影响改性活性炭脱硫性能的主要因素.活性炭经微波热处理后,酸性基团发生分解,表面含氧量减少,碱性特征增强,是吸附性能增加的主要原因之一.