珠江水体中细菌碱性磷酸酶基因phoD的多样性

碱性磷酸酶(APase)是最主要的有机磷水解酶,在无机磷匮乏的情况下,APase释放的无机磷供藻类利用,致使藻类大量繁殖,因此,对APase基因多样性的研究有利于揭示对水体富营养化有重要影响的微生物类群.基于此,本文以珠江水体为研究对象,构建了珠江广州段穗石、坦尾和南沙3个点细菌的pho D基因克隆文库.限制性酶切片段多态性(RFLP)分析结果表明,上述3个点的pho D基因分别含有15、17、13个操作分类单元(Operational Taxa Unit,OTU),穗石点的多样性(Shannon指数和Simpson指数)均高于其他两个点;pho D基因序列系统发育分析表明,珠江水体中pho D基因主要来源于Plesiocystis、Limnohabitans、Pirellula等属的细菌,而Limnohabitans属的pho D基因在文库中含量最高,占文库的44%~50%.研究表明,珠江水体中细菌的pho D基因具有较高的多样性,这些基因编码的碱性磷酸酶可能在珠江水体的富营养化过程中有重要的作用.     

京津冀PM2.5浓度控制目标可达性分析

雾霾污染已成为京津冀地区最突出的环境问题,国务院颁布了《大气污染防治行动计划》,明确提出了京津冀地区雾霾治理的浓度目标和减排措施。但是这些减排措施能否够实现PM2.5的浓度目标呢?本文基于数据分析方法,量化了2013—2014年京津冀地区PM2.5浓度与污染物排放量的关系,预测了现有减排措施可以达到的PM2.5浓度以及实现既定的PM2.5浓度目标的大气污染物减排要求,对"大气十条"减排政策的有效性进行了科学评估。结果显示,现有的减排措施难以实现PM2.5浓度控制目标,天津和河北的大多数地市需要进一步加大污染物减排力度。河北的部分地市即使实现了PM2.5浓度下降25%的目标,PM2.5浓度仍然过高,应改下降百分比为绝对值目标。北京的污染物减排率过高,减排难度较大,可以考虑一个现实合理的PM2.5浓度目标和污染物减排计划。由于污染物减排行动涉及区域经济和民生保障,PM2.5浓度受到风力等自然因素的影响较大,京津冀地区的雾霾治理应确定现实可行的浓度控制目标,并制定相应的污染物排放量管理目标。     

Impacts of produced water origin on bacterial community structures of activated sludge

The purpose of this study was to reveal how activated sludge communities respond to influent quality and indigenous communities by treating two produced waters from different origins in a batch reactor in succession. The community shift and compositions were investigated using Polymerase Chain Reaction–denaturing gradient gel electrophoresis(PCR–DGGE) and further16 S ribosomal DNA(r DNA) clone library analysis. The abundance of targeted genes for polycyclic aromatic hydrocarbon(PAH) degradation, nah Ac/phn Ac and C12O/C23 O, was tracked to define the metabolic ability of the in situ microbial community by Most Probable Number(MPN) PCR. The biosystem performed almost the same for treatment of both produced waters in terms of removals of chemical oxygen demand(COD) and PAHs. Sludge communities were closely associated with the respective influent bacterial communities(similarity 60%), while one sludge clone library was dominated by the Betaproteobacteria(38%) and Bacteriodetes(30%)and the other was dominated by Gammaproteobacteria(52%). This suggested that different influent and water quality have an effect on sludge community compositions. In addition, the existence of catabolic genes in sludge was consistent with the potential for degradation of PAHs in the treatment of both produced waters.     

Cloning and expression of the first gene for biodegrading microcystin LR by Sphingopyxis sp. USTB-05

Harmful cyanobacterial blooms are a growing environmental problem worldwide in natural waters, the biodegradation is found to be the most efficient method for removing microcystins (MCs) produced by harmful cyanobacteria. Based on the isolation of a promising bacterial strain of Sphingopyxis sp. USTB-05 for biodegrading MCs, we for the first time cloned and expressed a gene USTB-05-A (HM245411) that is responsible for the first step in the biodegradation of microcystin LR (MC-LR) in E. coli DH5αup, with a cloning vector of pGEM-T easy and an expression vector of pGEX-4T-1, respectively. The cell-free extracts (CE) of recombinant E. coli DH5αup containing USTB-05-A had high activity for biodegrading MC-LR. The initial MC-LR concentration of 40 mg/L was completely biodegraded within 1 hr in the presence of CE with a protein concentration of 0.35 mg/mL. Based on an analysis of the liquid chromatogram-mass spectrum (LC-MS), the enzyme encoded by gene USTB-05-A was found to be active in cleaving the target peptide bond between 3-amino-9-methoxy-2,6, 8-trimethyl-10-phenyl-deca-4,6-dienoic acid (Adda) and arginine of MC-LR, and converting cyclic MC-LR to linear MC-LR as a first product that is much less toxic than parent MC-LR, which offered direct evidence for the first step on the pathway of MC-LR biodegradation by Sphingopyxis sp. USTB-05.     

Isolation and characterization of deodorizing bacteria for organic sulfide malodor

Strain JII screened out from different odor origins can efficiently degrade methyl mercaptan and ethanethiol whereas has no ability to remove dimethyl sulfide. The results indicated that the strain JII breaks only the C-SH bond. The optimum temperature and pH of JII are 20-30℃ and 6.0-8.3 respectively. A systematic identificatio nmethod-16S rDNA gene sequence comparison, for deodorizing bacteria was carried out. The 16S rDNA gene sequence analysis of strain JII showed the highest level of 97 % homology to Rape rhizosphere.     

应急场景下矿工脑电成分特征的实验研究

为探究矿工在应急场景下的脑电成分变化规律,研究通过脑电实验的方法对矿工在观看应急与正常作业场景下文字与图片素材的脑电数据进行分析.结果表明:矿工在实验素材的靶刺激下,ERP成分明显,且图片刺激效果强于文字,在200～400 ms时,P200,P300成分峰值最大;矿工大脑α节律不断下降,β节律不断上升,且β节律波幅面积...     

铁矿石和生物炭添加对潜流人工湿地污水处理效果和温室气体排放及微生物群落的影响

人工湿地中基质的种类和填充方式会影响人工湿地中微生物的多样性及丰度,进而影响污水处理效果.通过在温室内构建空白-人工湿地(CW0)、铁矿石-人工湿地(CW1)、生物炭-人工湿地(CW2)和铁矿石+生物炭-人工湿地(CW3)这4组湿地,研究不同填料人工湿地系统的污水处理效果和温室气体排放及微生物群落结构的差异.结果表明,...     

泗顶矿区剖层土固氮微生物群落结构和丰度

以广西柳州泗顶矿区的上游区、下游区和尾矿区12个剖层土(每个区域分为4层)为研究对象,采用高通量测序技术和荧光定量PCR技术,分析了剖层土中固氮微生物的群落结构、丰度和多样性特征.结果表明,变形菌门在各区域剖层土中均为优势菌门,所占比例超过70％;α-变形菌纲在上游区和下游区剖层土中均为优势菌纲.上游区、下游区和尾矿区...     

吸烟与非吸烟肺癌患者中P53基因突变的检测

P53基因定位于人类第17号染色体的短臂,野生型P53基因是肿瘤抑制基因。这一基因正成为研究人类肿瘤DNA的主要目标。作者运用聚合酶链反应－单链构象多态性技术（PCR－SSCP）,研究了45例石蜡包埋的肺癌组织标本中肿瘤抑制基因P53基因突变,结果发现在P53基因的第5～8外显子中共检测到19例P53基因突变的样本,检出率为42.2％,并且发现吸烟的肺癌患者中P53基因突变的检出频率明显高于非吸烟的肺癌患者。     

抓住机遇创新开拓打好天津市环境保护“一控双达标”攻坚战

本文全面回顾了１９９８年天津市环境保护工作,分析了当前形势以及进一步做好工作应把握的几个问题。围绕抓住机遇,打好天津市环境保护“一控双达标”攻坚战,提出了１９９９年的工作目标任务及具体措施。