Changes in TcpA gene frequency explain 2,4,6-trichlorophenol degradation in mesocosms

Soils are often polluted by chlorophenols in timber production areas in the northern hemisphere. The tcpA gene encodes the first step of 2,4,6-trichlorophenol (246-TCP) degradation. We tested tcpA gene frequency in three natural pristine soils with different 246-TCP degradation capacity. Gene tcpA frequency increased more in spiked than non-spiked 10-L pails containing coniferous humus soil with high degradation capacity, in contrast to soils where degradation was slower. As the soil in each mesocosm originated from a spatially separate field plot, changes in tcpA gene frequency affected 246-TCP degradation over a range of soil origins. This indicates that the abundance of and changes in tcpA gene frequency could be utilized in estimating the efficacy of natural attenuation and biostimulation treatments in controlled conditions.     

Telomere length in workers was effected by omethoate exposure and interaction between smoking and p21 polymorphisms

Abstract

Omethoate is an organophosphorus pesticide that poses a major health hazard, especially DNA damage. The purpose of this study was to investigate the factors affecting telomere length in workers exposed to omethoate by analyzing the interaction between cell cycle gene polymorphism and environmental factors. The exposure group consisted of 118 workers exposed to omethoate for 8–10?years, the control group comprised 115 healthy people without occupational toxicant exposure history. The telomere length of genomic DNA from peripheral blood leucocyte was determined with real-time PCR. Polymerase chain reaction and restriction fragment length polymorphism was used to detect the polymorphisms in p53, p21 and MDM2 gene. The telomere length in the (CA?+?AA) genotypes for p21 rs1801270 polymorphism was longer than that in the CC genotype in control group (P?=?0.015). The generalized linear model analysis indicated the interaction of the p21 rs1801270 polymorphic (CA?+?AA) genotypes and smoking has a significant effect on telomere length (β = ?0.258, P?=?0.085). The prolongation of telomere length in omethoate-exposed workers was associated with genotypes (CA?+?AA) of p21 rs1801270, and interactions of (CA?+?AA) genotypes and smoking factor.     

超强静磁场对染料脱色菌Escheriehia coli的acpD基因的影响

将大肠杆菌E.coli ATCC8739置于12.0 T超强静磁场(ultra-strong static magnetic field,SMF)中进行处理,获得了磁场处理0.5、1、2、4和8 h的菌株E.coli-SMFn(n=0.5、1、2、4、8)。在37℃、pH 7、静置的条件下,菌株对偶氮染料AR14(I.C.Acid Red 14)的脱色结果指出,当反应进行到4、6和8 h时,E.coli-SMF8的脱色效率分别为18%、55%和96%,远高于E.coli ATCC8739的3%、19%和50%,表明SMF作用显著地增强了菌株的脱色效率。基因组DNA提取、PCR扩增、分子克隆以及基因测序的实验结果进一步表明,全部6例E.coli ATCC8739菌株的偶氮还原酶基因(acpD)序列均与GenBank中报道的完全一致;而E.coli-SMF8菌株的acpD-SMF8核酸序列中缺失了第99位的胞嘧啶。该缺失突变不仅使acpD-SMF8的核酸序列与acpD的存在显著不同,同时得到了具新活性中心的偶氮还原酶AzoR-SMF8。这个新的活性中心具有更强的黄素(FMN)结合能力,因此使该酶与偶氮染料的亲和力大大增加,促进了脱色效率的提高。     

复合型絮凝剂处理景观水体

利用以生物絮凝剂(1 g/L MBF-28)与化学絮凝剂(5 g/L PAC)复配后的复合絮凝剂CBF28C处理景观水体,考虑了复配比、投加量、pH和投加顺序对处理景观水的影响。实验结果表明:对于反应体系为100 mL景观水体,当MBF-28与PAC溶液复配体积比为3∶1,反应体系pH为7.0,1 mL 1%CaCl2作助凝剂,1.5 mL CBF28C时,其絮凝效果最好,其COD,色度,TN,TP的去除率分别为90.7%,54.1%、46.6%和51.5%。最佳水力条件为:快速320 r/min,快搅时间45 s,慢速80 r/min,慢搅时间100 s。并且得出了前10 min内絮凝率的反应关系方程式。     

基于GIS的景观生态功能指标分析

针对当前我国规划及战略环评指标体系中缺乏直接反映生态功能指标的问题,提出可通过系统研究区域景观生态结构与景观功能变化间的关系,由斑块面积指数计算生物生产力、由景观香农多样性指数和景观香农均匀度指数反映生态质量,以此表征景观生态功能。以地理信息系统（GIS）为平台,提出了利用基于斑块面积而得到的景观要素转移矩阵及基于年鉴统计而得到的景观单位面积生物生产力的转移矩阵来计算生物生产力的方法,并在统计若干研究流域景观格局异质性指数文献的基础上发掘了景观多样性指数、景观均匀度指数与生态质量间的关系。最后,以江苏省沿江地区2000、2004年的数据开展了实例分析,结果表明,提出的生物生产力和生态质量这两个指标确实能反映区域景观功能的变化,在今后的规划和战略环评中具有一定的应用前景.     

基于复合生态系统理论的长沙湘江滨水区景观资源评价与优化

近年来,随着我国经济的飞速发展、社会经济的转型,以及人们环境意识的提高,滨水区开发已成为我国城市开发建设的热点。城市滨水区景观规划设计研究对于合理、充分利用城市滨水区景观资源,塑造特色鲜明的城市形象,提高城市生态环境质量,促进城市滨水区开发有着重要意义。从复合生态系统理论的角度,在湘江滨水区景观资源调查、景观资源分类的基础上,运用灰色聚类法对湘江滨水区景观资源进行定量评价,提出景观资源优化思路,探讨滨水区景观规划设计的途径。认为现代城市大规模滨水区更新改造和开发大背景下的城市滨水区景观规划设计,应尊重城市地域性特点、文化内涵和风土人情,并与传统的滨水活动有机结合,保护和突出城市历史格局和风貌特色。     

Salmonella Enterica Serovar Typhimurium HilA-LacZY Fusion Gene Response to Iron Chelation or Supplementation in Rich and Minimal Media

Abstract

Virulence expression of Salmonella enterica serovar Typhimurium under iron limited condition was measured by β-galactosidase (β-gal) assay using a hilA-lacZY fusion strain and calculated as Miller units. hilA-lacZY β-galactosidase assays were performed in brain heart infusion (BHI) and minimal media (M9), after iron chelation with 2, 2-dipridyl and iron-supplementation respectively. Before performing virulence assays, concentrations of iron in the media were estimated using ferrozine. Iron content was found to be more in BHI (42.6 µg dL^?1) as compared to M9 (10.03 µg dL^?1). β-gal activity of Salmonella Typhimurium in BHI was generally less than that observed in M9. After exposure to various combinations of iron chelator in BHI, hilA-lacZY activity only increased at the highest concentration of chelator (200 µM) but decreased in M9 media for all iron concentrations when compared to controls with no iron amendment. These results indicate that iron availability may influence S. Typhimurium hilA expression.     

碳源及反硝化芽孢杆菌强化低C/N比景观水体的生物脱氮

实验探讨了添加碳源及投加反硝化细菌对低碳氮比景观水体生物脱氮的影响。结果表明,有机碳源及B.subtilis FS05均能显著促进实验水体的生物脱氮作用,实验水体在28℃静置72 h后,乙醇添加组的TN、氨氮、硝酸盐及亚硝酸盐的去除率分别达到了62.7%、67.0%、69.8%和29.4%,而同样条件下,B.subtilis FS05投加组的去除率分别达到了66.9%、73.4%、66.0%和82.2%。从水质变化趋势可以看出,投加B.subtilis FS05能在更短时间内完成生物脱氮过程,其中,硝酸盐和亚硝酸盐去除速率最快,分别仅需要18 h和12 h。     

Use of reporter-gene based bacteria to quantify phenanthrene biodegradation and toxicity in soil

A phenanthrene-degrading bacterium, Sphingomonas paucimobilis EPA505 was used to construct two fluorescence-based reporter strains. Strain D harboring gfp gene was constructed to generate green fluorescence when the strain started to biodegrade phenanthrene. Strain S possessing gef gene was designed to die once phenanthrene biodegradation was initiated and thus to lose green fluorescence when visualized by a live/dead cell staining. Confocal laser scanning microscopic observation followed by image analysis demonstrates that the fluorescence intensity generated by strain D increased and the intensity by strain S decreased linearly at the phenanthrene concentration of up to 200 mg/L. Such quantitative increase and decrease of fluorescence intensity in strain D (i.e., from 1 to 11.90 ± 0.72) and strain S (from 1 to 0.40 ± 0.07) were also evident in the presence of Ottawa sand spiked with the phenanthrene up to 1000 mg/kg. The potential use of the reporter strains in quantitatively determining biodegradable or toxic phenanthrene was discussed.