分枝杆菌TZh51菌株的分离鉴定及其生物修复污染土壤的特性

[目的]为获得降解芘的微生物菌株,并用其生物修复被多环芳烃污染的土壤.[方法]芘降解菌的分离采用平板升华法.根据表型观察、生理生化特性和16S rDNA的序列同源性分析,对菌株进行分类学鉴定.通过活菌计数、HPLC测定多环芳烃的残留量,研究菌株在固体、液体无机盐培养基以及在污染土壤中降解多环芳烃(polycyclic aromatic hydrocarbons,PAHs)的能力.[结果]分离到4株能降解芘的菌株TZh51、TZh52、TG42和TG52.实验结果表明,TZh51降解PAHs的能力强于其余3株菌.TZh51被鉴定为分枝杆菌属(Mycobacterium sp.),但与已发表的分枝杆菌菌株M11为不同的种.TZh51接种在芘膜的固体无机盐培养基上,测定获得最大芘降解量的条件是培养温度为3512和芘膜厚度为130 ng/mm2.在芘浓度为50、100 mg/L的液体无机盐培养基中培养,6天时TZh51的芘降解率分别达到91.9%、71.8%,10天时菌体数量分别达到最大值为2.0、6.0×108cfu/mL;TZh51降解芘的效果强于M11.在种植作物的处理中,到第6周时TZh51的菌体数量达到每克干土含7.2×108个菌落数,到第8周时菲、荧蒽和芘的降解率分别达到91.4%、86.9%和85.8%;[结论]TZh51具有很强降解PAHs的能力;另外,TZh51与作物联合生物修复污染土壤的效果明显.     

The polycyclic aromatic hydrocarbon phenanthrene causes oxidative stress and alters polyamine metabolism in the aquatic liverwort Riccia fluitans L

The polycyclic aromatic hydrocarbon (PAH) phenanthrene (PHEN) is a highly toxic pollutant, commonly found in aquatic environments, the effects of which on aquatic plants have not been studied in depth. As PAHs are known to induce oxidative stress and recent studies have shown that polyamines (PAs) participate in the defence reactions protecting plants against environmental stresses, PA metabolism and oxidative damage were investigated in the aquatic form of the liverwort Riccia fluitans L. exposed to PHEN. Exposure of Riccia fluitans plants to PHEN at concentrations of 0.5 microm or less induced oxidative stress, but at a level from which plants could recover. Despite increased levels of enzymatic and non-enzymatic antioxidants, recovery appeared, at least in part, due to increased synthesis of PAs, achieved via increased activities of the enzymes arginine decarboxylase (ADC) and S-adenosylmethionine decarboxylase (SAMDC). Chemical inhibition of these enzymes inhibited plant recovery, while treatment with PAs aided recovery. Finally, as chloroplasts and the plasma membrane appeared to be key targets for PHEN-induced damage, the potential roles of PAs in protecting these cellular components were considered. How PAs could protect plant cells from serious environmental pollutants such as PHEN and could prevent oxidative stress is discussed.     

Optimization and modeling of phenanthrene degradation by <Emphasis Type="Italic">Mycobacterium</Emphasis> sp. 6PY1 in a biphasic medium using response-surface methodology

In the present paper, the degradation of phenanthrene, a model polycyclic aromatic hydrocarbon compound, by the Mycobacterium strain 6PY1 was optimized in a biphasic culture medium. The optimization and modeling were performed using the design of experiments methodology. The temperature, the silicone oil/mineral salts medium volume ratio, and the initial cell concentration, were used as the central composite design parameters. In all experiments, the phenanthrene was degraded to undetectable levels. Response surface methodology was successfully employed to derive an empirical model describing the rate and time of degradation and to deduce the optimal degradation conditions. As a result of the optimization processes, the optimal responses for the degradation rate, the volumetric degradation rate, and the 90% degradation time were estimated to be 0.172 mg h⁻¹, 22 mg l⁻¹ h⁻¹, and 18 h, respectively.     

好氧细菌对多环芳烃降解机制的研究进展

多环芳烃(PAHs)是指两个或两个以上的苯环以线性排列、弯接或簇聚方式构成的一类碳氢化合物.这类化合物广泛分布于环境中,具有潜在的致畸性、致癌性和遗传毒性.在自然环境中,好氧细菌对PAHs的生物降解是一种很重要的方式,凸显其在清除环境PAHs污染物中具有广阔的应用前景.在过去二十多年中,科学家们已经从基因水平上对好氧细菌降解PAHs的机制进行了深入的研究,其中包括PAHs降解基因的多样性、与PAHs降解有关的基因以及细菌群体PAHs遗传适应机制等.在此,就好氧细菌对多环芳烃降解机制的研究进展进行了综述和讨论.     

The crystal structure of the C-terminal DAP5/p97 domain sheds light on the molecular basis for its processing by caspase cleavage

DAP5/p97 (death-associated protein 5) is a member of the eukaryotic translation initiation factor 4G family. It functions as a scaffold protein promoting cap-independent translation of proteins. During apoptosis, DAP5/p97 is cleaved by caspases at position 792, yielding an 86-kDa C-terminal truncated isoform (DAP5/p86) that promotes translation of several mRNAs mediated by an internal ribosome entry site. In this study, we report the crystal structure of the C-terminal region of DAP5/p97 extending between amino acids 730 and 897. This structure consists of four HEAT-Repeats and is homologous to the C-terminal domain of eIF4GI, eIF5, and eIF2Bε. Unlike the other proteins, DAP5/p97 lacks electron density in the loop connecting α3 and α4, which harbors the caspase cleavage site. Moreover, we observe fewer interactions between these two helices. Thus, previous mapping of this site by mutation analysis is confirmed here by the resolved structure of the DAP5/p97 C-terminus. In addition, we identified the position of two conserved aromatic and acidic boxes in the structure of the DAP5/p97 C-terminus. The acidic residues in the two aromatic and acidic boxes form a continuous negatively charged patch, which is suggested to make specific interactions with other proteins such as eIF2β. The caspase cleavage of DAP5/p97 removes the subdomain carrying acidic residues in the AA-box motif, which may result in exposure of a hydrophobic surface. These intriguing structural differences between the two DAP5 isoforms suggest that they have different interaction partners and, subsequently, different functions.     

Heterogeneous Catalytic Oxidation of Phenanthrene by Hydrogen Peroxide in Soil Slurry: Kinetics,Mechanism, and Implication

The degradation of phenanthrene sorbed on soil has been carried out using a H₂O₂/goethite heterogeneous catalytic oxidation process. The effect of operating variables, such as the goethite concentration, pH, H₂O₂ concentration, soil organic matter, and bicarbonate ions has been investigated. The reaction followed pseudo-first order kinetics. The rate constants were evaluated and varied between 2.0×10^?4 and 1.1×10^?3?min^?1 depending on the H₂O₂ concentration. The highest rate of degradation of phenanthrene was observed at a H₂O₂ concentration of 5?M and 134.0?g/kg goethite. The intermediate product formed during the degradation of phenanthrene was identified to be salicylic acid that finally degraded to CO₂ and H₂O. H₂O₂ consumption continued as the OH radical attacked the salicylic acid. More than 80% consumption of the 5?M H₂O₂ took place within 30?min, and the degradation was almost complete after 3?h of reaction. Neutral pH was found to be effective in the removal of phenanthrene. Both soil organic matter (SOM) and bicarbonate ions in the soil inhibited the oxidation rate of phenanthrene.     

Characterization of PAH Sources in Sediments of the Thea Foss/Wheeler Osgood Waterways,Tacoma, Washington

The character of polycyclic aromatic hydrocarbons (PAH) in sediments of the Thea Foss and Wheeler-Osgood Waterways in Tacoma, Washington, were investigated with the objective of determining the general source(s) of these compounds to the waterways. In this study, 42 near-surface sediment samples from the Waterways were collected and analyzed for their (1) concentration of 43 individual or groups of PAH, (2) total extractable hydrocarbon “fingerprint” and concentration, (3) grain size and (4) total organic carbon content. Analysis of the sediment data, including comparisons to standard reference materials, indicates that all but two samples contained PAH derived from a pyrogenic source(s), i.e., a non-petroleum source(s). The high concentrations and characteristic distributions of PAH in some sediment samples were consistent with the occurrence of manufactured gas plant (MGP) derived tar(s) or tar distillate(s), particularly in some sediments proximal to a historic MGP and tar distillate storage operation near the head of the Thea Foss Waterway. Most other sediment samples throughout the Waterways contained PAH distributions and concentration indicating (at least) a greater proportion of PAH are derived from urban runoff/fallout.     

微生物降解多环芳烃(PAHs)的研究进展

从多环芳烃(PAHs)的降解菌株的筛选、降解机制以及PAHs污染的生物修复等方面介绍了微生物降解PAHs的最新研究进展。     

大肠杆菌ppsA和tktA基因的串联表达

ppsA和tktA是芳香族氨基酸生物合成中心途径的两个关键酶基因,在大肠杆菌中,ppsA基因编码磷酸烯醇式丙酮酸合成酶A(PpsA),该酶催化丙酮酸合成磷酸烯醇式丙酮酸;tktA基因编码转酮酶A,该酶在磷酸戊糖途径中生成4-磷酸赤藓糖起主要作用。采用PCR方法从大肠杆菌K-12株中扩增到ppsA和tktA,并实现了两基因的高效表达,其中ppsA活性提高了10．8倍,tktA活性提高了3．9倍,当这两个基因串联在一个质粒上导入大肠杆菌进行表达时,PpsA的活性变化较大(2．1～9．1倍),TktA的活性相对稳定(3．9～4．5倍),且这两个基因单独表达和串联表达都能使芳香族氨基酸生物合成共同途径中关键中间产物DAHP的产量提高,且串联表达比单独表达较高。     

Influence of the initial composition of algal-bacterial microcosms on the degradation of salicylate in a fed-batch culture

The influence of the initial composition of an algal-bacterial microcosm constituted of Chlorella sorokiniana and Ralstonia basilensis was tested for the fed-batch degradation of salicylate at 5 mM. Salicylate degradation was always limited by the O₂ generation rate, which was initially proportional to the algal density, but rapidly became limited by the availability of light once the algae started to grow. The decrease of the salicylate removal rate observed at high algal densities was likely caused by mutual shading within the algal population and the increase of O₂ consumption due to algal dark respiration. With repeated salicylate amendments, all systems converged towards the same characteristics, reaching an optimum rate of salicylate degradation at 1 mmol l^–1 day.