土壤微生物群落结构对生活源和工业源再生水灌溉的差异化响应

为研究不同来源再生水灌溉对土壤微生物群落结构的影响,以地下水灌溉土壤为对照,采用Illumina MiSeq高通量测序技术对长期利用生活源和工业源再生水灌溉的土壤微生物群落结构进行分析,进一步探究土壤环境因子及其相互作用对微生物群落结构的影响.结果表明,与地下水灌溉相比,长期生活源再生水灌溉可显著提高土壤中TOC、 DOC、 Eh、 NH~+_4-N和TP的含量,长期工业源再生水灌溉导致Cd、 Cr、 Cu、 Pb和Zn在表层土壤大量累积.再生水灌溉显著增加了土壤中Acidobacteria和Planctomycetes的相对丰度,降低了Firmicutes和Tectomicrobia的相对丰度,且不同来源再生水对土壤中功能微生物的影响不同,生活源再生水灌溉可显著增加Chloroflexi和Nitrospirae的相对丰度,而工业源再生水灌溉对Actinobacteria具有显著的抑制作用.db-RDA分析结果表明,生活源再生水灌溉土壤菌群主要受TN、 TP、 DOC和Eh影响(P0.05),工业源再生水灌溉土壤菌群主要受重金属影响(P0.05).长期再生水灌溉可改变土壤环境因子间的相互作用,进而影响微生物群落结构,生活源再生水灌溉土壤中微生物主要受DOC、 TN和TP等营养物质含量的增加和氧化还原条件的改变控制,工业源再生水灌溉土壤中微生物与重金属的积累显著相关.     

不同基质生物炭对厌氧处理餐厨垃圾效能及微生态的影响

探究了剩余污泥（SS）、餐厨垃圾（FW）、玉米芯（CC）、甘蔗渣（BG）4种不同基质生物炭对厌氧生物处理餐厨垃圾效能的影响,对厌氧污泥的关键酶活性、微生物群落分布以及代谢途径等微生态进行了分析.结果表明,厌氧反应器分别加入4种生物炭后,COD平均去除率分别提高了29.49%、23.16%、29.42%、40.32%;傅里叶红外分析表明,投加SS生物炭组出水中羟基、酰胺基以及C-O-C伸缩振动峰减弱.4个厌氧反应器中厌氧污泥的乙酸激酶活性分别为0.40,0.42,0.96,0.98 μmol/g,表明投加CC与BG生物炭促进了餐厨垃圾的厌氧水解酸化过程;厌氧污泥胞外聚合物的蛋白质/多糖之比分别为0.415、0.56、1.89、2.8,投加CC、BG生物炭提高了污泥的稳定性.4个厌氧反应器中拟杆菌门、变形菌门、厚壁菌门为主要菌群,投加BG生物炭促进了变形菌门与厚壁菌门的生长;对于古细菌而言,甲烷杆菌属与甲烷丝菌属为优势种群,SS组的甲烷杆菌属丰度最高（53.48%）,而BG组中甲烷丝菌属丰度最高（42.72%）.KEGG功能分析表明古菌及细菌均以碳水化合物代谢、氨基酸代谢为主;而投加BG与SS生物炭后,微生物膜运输水平得到了提高.     

构树修复对重金属污染土壤环境质量的影响

通过温室盆栽试验,研究构树（Broussonetia papyrifera）生长对重金属污染土壤酶活性和微生物群落结构的影响.结果表明,构树修复污染土壤中酶活性和微生物多样性明显提高.经270d培养后,构树生长土壤中蔗糖酶和酸性磷酸酶活性与种植土壤相比分别显著（P<0.05）提高3.12倍和2.29倍;土壤脱氢酶与有效态As、Cd、Pb、Zn和Cu含量,蔗糖酶与有效态Cd含量,以及磷酸酶与有效态Cd和Cu含量之间呈显著负相关（P<0.05）.根据16S和18S rDNA PCR-DGGE分析表明,构树修复可提高污染土壤中细菌和丛枝菌根真菌多样性.上述结果表明,构树修复可有效改善重金属污染土壤的环境质量.然而,污染土壤中重金属有效态含量下降不明显,必须辅助物理和化学措施来强化构树对重金属污染土壤的生态修复潜力.     

水稻土中五氯酚的降解转化动态及其对微生物群落的影响

采用室内培养实验,研究厌氧条件下水稻土中五氯酚(Pentachlorophenol,PCP)的还原转化与微生物群落组成变化。结果表明,室内培养实验条件下,PCP在水稻土样品中降解比较迅速,在反应17 d时,实验添加的PCP能够完全被还原转化。高通量测序结果显示PCP的添加明显改变了水稻土壤的微生物群落结构,其微生物多样性显著下降,在PCP降解完之后逐渐恢复。原始土壤以及添加PCP的土壤样品中其优势微生物主要分布在变形菌门(Proteobacteria)。PCP添加刺激了水稻土中伯克氏菌科(Burkholderiaceae)、丛毛单胞菌科(Comamonadaceae)、地杆菌科(Geobacteraceae)、红环菌科(Rhodocyclaceae)和假单胞菌科(Pseudomonadaceae)等脱氯相关的微生物菌群繁殖,成为PCP降解过程中的优势菌群,有利于PCP还原降解。本研究结果可为水稻土中有机氯农药污染物的微生物降解脱毒提供理论依据。     

Microbiological characteristics in a zero-valent iron reactive barrier

Zero-valent iron (Fe⁰)-based permeable reactive barriertreatment has been generating great interest for passivegroundwater remediation, yet few studies have paid particularattention to the microbial activity and characteristics withinand in the vicinity of the Fe⁰-barrier matrix. The presentstudy was undertaken to evaluate the microbial population andcommunity composition in the reducing zone of influence byFe⁰ corrosion in the barrier at the Oak Ridge Y-12 Plantsite. Both phospholipid fatty acids and DNA analyses were usedto determine the total microbial population and microbialfunctional groups, including sulfate-reducing bacteria,denitrifying bacteria, and methanogens, in groundwater andsoil/iron core samples. A diverse microbial community wasidentified in the strongly reducing Fe⁰ environment despitea relatively high pH condition within the Fe⁰ barrier (up topH 10). In comparison with those found in the backgroundsoil/groundwater samples, the enhanced microbial populationranged from 1 to 3 orders of magnitude and appeared to increase from upgradient of the barrier to downgradient soil. Inaddition, microbial community composition appeared to change overtime, and the bacterial types of microorganismsincreased consistently as the barrier aged. DNA analysisindicated the presence of sulfate-reducing and denitrifyingbacteria in the barrier and its surrounding soil. However, theactivity of methanogens was found to be relatively low,presumably as a result of the competition by sulfate/metal-reducing bacteria and denitrifying bacteria because of the unlimited availability of sulfate and nitrate in the site groundwater. Results of this study provide evidenceof a diverse microbial population within and in the vicinity ofthe iron barrier, although the important roles of microbial activity, either beneficially or detrimentally, on the longevityand enduring efficiency of the Fe⁰ barriers are yet to be evaluated.     

Time dependent influx and efflux of phenol by immobilized microbial consortium

Phenol, like many other organic solvents, is toxic to micro-organisms even at low concentrations. However, some micro-organisms can withstand this toxicity to a certain concentration. To observe the uptake mechanism of phenol, bacteria were isolatedfrom a petroleum refinery effluent and identified. Study was carried out to understand the effect of varying sub-lethal concentrations of phenol, on all the isolated individual bacterial cultures. Out of the bacteria isolated, Serratia liquefaciens was found to tolerate phenol concentration up to 1500 mg l^-1. A microbial consortium of the isolated bacteriawas formulated and immobilized. Individual cultures were also immobilized and uptake of phenol by the immobilized micro-organisms was observed in a nutrient-rich and nutrient-stressed medium containing phenol as a sole source of carbon. A time-dependent uptake of phenol was exhibited by the micro-organismsin nutrient-stressed medium, after which a sudden increase in phenol concentration occurred in the extracellular medium, till it reached back to the initial concentration. This was attributedto an active efflux mechanism adopted by the micro-organisms to withstand the toxic shock.     

Characterization of microbial communities from coastal waters using microarrays

Molecular methods, including DNA probes, were used to identify and enumerate pathogenic Vibrio species in the Chesapeake Bay; our data indicated that Vibrio vulnificus exhibits seasonal fluctuations in number. Our work included a characterization of total microbial communities from the Bay; development of microarrays that identify and quantify the diversity of those communities; and observation of temporal changes in those communities. To identify members of the microbial community, we amplified the 16S rDNA gene from community DNA isolated from a biofilm sample collected from the Chesapeake Bay in February, 2000. The resultant 75 sequences were 95% or more similar to 7 species including two recently described Shewanella species, baltica and frigidimarina, that have not been previously isolated from the Chesapeake. When the genera of bacteria from biofilm after culturing are compared to those detected by subcloning amplified 16S fragments from community DNA, the cultured sample exhibited a strong bias. In oysters collected in February, the most common bacteria were previously unknown. Based on our 16S findings, we are developing microarrays to detect these and other microbial species in these estuarine communities. The microarrays will detect each species using four distinct loci, with the multiple loci serving as an internal control. The accuracy of the microarray will be measured using sentinel species such as Aeromonas species, Escherichia coli, and Vibrio vulnificus. Using microarrays, it should be possible to determine the annual fluctuations of bacterial species (culturable and non-culturable, pathogenic and non-pathogenic). The data may be applied to understanding patterns of environmental change; assessing the health of the Bay; and evaluating the risk of human illness associated with exposure to and ingestion of water and shellfish.     

生物质气化洗焦废水的预处理和微生物降解

为了对生物质气化洗焦废水进行深度处理,达到废水排放标准,采用物理过滤和微生物降解相结合的方法,对洗焦废水的原液进行处理。实验结果表明,用木屑、颗粒活性碳、微生物降解的连续步骤处理生物质气化洗焦废水,可达到理想的生物质气化洗焦废水COD的去除效果。     

Influence of chlorsulfuron herbicide on size of microbial biomass in the soil

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