菌源对多环芳烃降解菌的筛选及降解性能的影响

高效降解菌的筛选对利用生物修复技术有效去除环境中的多环芳烃具有重要意义。分别以石油污染土壤和焦化废水活性污泥为菌源,分离出芘降解菌和混合PAHs(菲、荧蒽和芘)降解菌共14株并对其降解性能进行对比研究。结果表明,筛选得到的菌株分别属于9个菌属,其中2种菌源共有的菌属为Mycobacterium sp.、Ralstonia sp.和Shinella sp.。芘和PAHs的高效降解菌(CP16和CM32)均属于分支杆菌属(Mycobacterium),来源于焦化废水活性污泥;菌株CP16对芘(50mg/L)的7 d降解率为74.99%,CM32对PAHs(菲50 mg/L、荧蒽和芘各10 mg/L)的7 d降解率为100%。因此,以焦化废水活性污泥为菌源更有利于获得高效的多环芳烃降解菌。     

固废拆解场污染土壤中多环芳烃降解菌的筛选鉴定与降解特性

以腐植酸(HA)溶液为吸附剂、从受多环芳烃污染的土壤中分离出来的降解菌制成为生物修复剂,以多环芳烃(PAHs)萘、菲、芘、荧蒽、苯并蒽、苯并芘为土壤污染物,对PAHs污染土壤进行修复实验。目的是筛选与分离吸附于HA的PAHs降解菌,研究HA与降解菌的协同效应对PAHs的降解效率的影响。用经过HA吸附的PAHs富集分离培养出1株高效降解菌株,命名为Tzyx3,鉴定其为解脂耶氏酵母菌(Yarrowia lipolytica)。15 d后,土壤中萘、菲、芘、荧蒽、苯并蒽、苯并芘的降解率分别为90.7%、91.0%、74.7%、86.9%、84.7%和74.7%,表明Tzyx3和HA在PAHs污染土壤中存在协作关系,Tzyx3能够直接利用HA对土壤中的多环芳烃进行降解。     

用于青霉素废水处理的高效菌株的分离及特性研究

从某制药厂污水处理站的活性污泥中筛选出两株能以青霉素废水中有机物为惟一碳源和能源的高效降解菌k1和k2。通过形态及生理生化特征分析,初步鉴定2株菌为芽孢菌,其中k2为短小芽孢杆菌（bacillus pumilus）。2株菌的最适pH值分别为8和7,温度均为35℃,当废水含量50%时,菌株k1和k2对青霉素废水的COD去除率分别为79%和81%。单菌株与混合菌株对废水的降解特性试验表明,前48 h混菌对废水的去除率不及单菌株,而48 h后混合菌株去除率高于单菌株,60 h时达到最高为85%。     

樟脑废水高效优势降解菌的选育及降解效果

针对樟脑废水，从活性污泥中筛选出降解樟脑废水的高效优势菌，通过分离纯化，优选出三株适应能力强、生长旺盛的菌株，分别为ZH-1，ZH-2、TZH-2。经初步鉴定分别为动胶菌属、假单胞菌属、短杆菌属。试验测定了单株菌和混合菌对樟脑废水的降解效果，结果表明，混合菌的降解效果最为明显，降解率为75．23％。     

降解菌对堆肥中多环芳烃降解作用的研究

通过在堆肥中加入经过驯化的降解菌这种土壤有机污染生物修复技术 ,对堆肥中多环芳烃的浓度变化进行监测 ,从而了解降解菌对堆肥中多环芳烃的降解作用。实验结果表明 ,降解菌的加入能明显地提高多环芳烃的降解率 ,本次实验中 ,菲、芴的去除率提高了 2 5 %左右 ,芘的去除率提高了约 4 5 %。     

一株荧蒽降解菌的筛选鉴定及降解特性

采用富集培养方法,从多环芳烃污染的土壤中分离筛选到一株能以高分子量的多环芳烃荧蒽为惟一碳源和能源且生长状况良好的菌株DN002。通过形态观察、生理生化指标及16S rRNA同源序列分析比对,结果表明,该菌株为木糖氧化产碱菌(Achromobacter xylosoxidans),最适生长温度为32℃,最适生长pH为7～7.5。该菌株对荧蒽有较强的降解能力,在14 d内对500 mg/L的荧蒽的降解率为92.8%。菌株细胞蛋白SDS-PAGE结果显示,经荧蒽诱导后,在分子量为18～66 kDa范围内有显著的差异蛋白条带。     

一株多环芳烃降解菌的筛选及其降解特性

微生物修复是治理土壤多环芳烃(polycyclic aromatic hydrocarbons, PAHs)污染的主要方法,而高效降解菌筛选是微生物修复技术的重要基础。从北京焦化厂土壤中筛选分离得到一株PAHs降解菌Q3,通过生理生化和16S rDNA等分析手段鉴定其为Rhodococcus rhodochrous。结果表明:该菌株对芘的耐受能力较强,可降解初始浓度为200 mg·L~(-1)的芘;该菌株具有降解广谱性,可利用苯并[a]芘、苯并[b]荧蒽、二苯并[a,h]蒽、苯并[g,h,i]苝等9种PAHs为唯一碳源进行代谢,特别是对苯并[a]芘等高环PAHs具有较好的降解效果;此外,该菌株可有效降解模拟液中的混合PAHs,并且对野外被PAHs长期污染的土壤具有较好的强化修复效果。投加菌株处理后的处理组与对照组相比,土壤PAHs总去除率提高了24%。以上结果表明该菌株对环境中被PAHs污染的土壤具有较好的强化修复潜力,可为PAHs污染土壤的微生物修复技术提供技术参考。     

含油污泥中石油降解菌的分离及其降解特性

从渤海油田含油污泥中分离出3株石油烃降解菌,通过16S rRNA基因序列鉴定RS1、RS2和RS3分别为棒状杆菌、短杆菌和假单胞菌。经单因素实验确定,3株细菌对石油的最适降解条件分别为37℃、盐度3%、pH 8;32℃、盐度1%、pH 8;42℃、盐度1%、pH 6。降解实验结果表明,3株细菌30 d内对含油污泥中总石油烃的降解率分别为39.69%、31.13%和53.29%,而混合菌的降解效果明显高于单一菌株,降解率为58.08%;不同菌株对原油中不同组分的降解能力不同,其中,RS1对饱和烃的降解率最高,达20.74%,RS3对芳香烃的降解率最高,达到8.08%;GC-MS分析表明,混合菌对nC12~n-C34等正构烷烃均有明显降解,且对萘、苊、屈和苯并[b]荧蒽等多环芳烃的降解能力较强。     

一株有机浮选药剂--黄原酸盐降解菌的特性研究

从矿山废水中经富集分离到一株能以黄原酸盐为惟一碳源的黄原酸盐降解菌,初步鉴定为铜绿假单胞菌属.菌株降解黄原酸盐的最佳条件为:pH为8,温度30℃,振荡速率120 r/min.当黄原酸盐浓度达到1500 mg/L时,24 h后浓度降解率为95.7%,COD去除率为84.7%.黄原酸盐浓度越高,COD去除率越高.当加入0.2 g/L的葡萄糖时可大大提高菌对黄原酸盐的降解率.     

甲醛降解菌的筛选及降解特性研究

从采集活性污泥中筛选得到1株具有高效降解甲醛能力的菌株并命名为JQ-1,根据其形态特征,初步判断菌株JQ-1属假单胞菌属。同时对菌株JQ-1的生长特性及降解特性进行了初步研究。实验结果表明,该菌株降解甲醛的最适条件为：甲醛废水浓度为50mg／L,pH值为6,培养温度为25℃,摇床转速为150r／min。在最适条件下,菌株JQ-1具有较强的降解甲醛能力,当甲醛废水浓度为50mg／L时,在24h内甲醛降解率可达87％以上。     

粉末活性炭对三烯丙基异氰脲酸酯的吸附性能简

用静态吸附法考察粉末活性炭对水中三烯丙基异氰脲酸酯（CAIC）的吸附行为,采用单因素分析法对活性炭吸附化工废水中TAIC的工艺条件进行研究。实验结果表明,在TAIC模拟废水中,其TAIC初始浓度为800 mg/L,pH为7,在温度为298 K、转速为150 r/min的条件下,当活性炭的投加量达到4.4 g/L,吸附反应时间为50 min时,TAIC的去除效率最高为96.17%;对于实际废水,其TAIC初始浓度为1 500 mg/L,溶液pH为3,在温度为298 K、转速为150 r/min的条件下,当活性炭投加量达到10 g/L,吸附反应时间为2 h时,TAIC的去除效率最高为46.8%。这也是由于实际废水组分复杂,其他有机物存在一定的吸附竞争机制。     

Polycyclic aromatic hydrocarbon sampling in wastewaters using semipermeable membrane devices: accuracy of time-weighted average concentration estimations of truly dissolved compounds

Semipermeable membrane devices (SPMDs) previously spiked with performance reference compounds were exposed in wastewater. After 6 days of exposure, 13 polycyclic aromatic hydrocarbons (PAHs) were quantified in SPMDs. Exchange rate constants and time-weighted average (TWA) concentrations of SPMD-available PAHs in water were calculated. The bias of using SPMDs to estimate an actual TWA concentration if the concentration in water fluctuates, as can be expected in wastewater, was studied with numerical simulations. The bias increased with the exchange rate constant. However, most exchange rate constants evaluated in SPMDs exposed in wastewater were small enough for SPMDs to estimate a TWA concentration of PAHs even when the water concentration varied. TWA-SPMD-available concentrations were always below total dissolved (operationally defined as 0.7 microm) concentrations, indicating that part of the dissolved PAHs was not available for sampling. In situ partitioning coefficients K(DOC) were computed and found to be slightly higher than data from the literature. This confirms that only truly dissolved PAHs should be sampled by SPMDs in wastewater.     

Treatability studies on wastewater from textile dyeing factories in Bursa, Turkey

The textile industry is one of the most rapidly developing industries in Turkey. It generates a large amount of wastewater, with corresponding concerns about pollution. The main sources of pollution in wastewater are the dyeing and finishing processes. The dyestuffs and polyvinyl alcohol (PVA) are the main refractory organics of concern in terms of meeting more stringent effluent standards of chemical oxygen demand (COD) and colour. In this study, wastewaters from textile dyeing factories in Bursa were characterised, and physical, chemical and biological treatability studies were carried out. In the physical and chemical studies, 60.80% COD, 80% suspended solids (SS) and 10.92% turbidity removal efficiencies were obtained. In the biological studies, 90% COD and 40% SS removal were obtained. The initial soluble inert COD of wastewater was determined by using comparison methods. The initial inert COD of wastewater and the microbial product concentration were determined as 37 mg/l and 13 mg/l, respectively.     

The toxicity and fate of phenolic pollutants in the contaminated soils associated with the oil-shale industry

Phenol, cresols, dimethylphenols and resorcinols are considered major pollutants in the oil-shale semi-coke dump leachates (up to 380 mg phenols/L) that contaminate the surrounding soils and pose a threat to the groundwater in the North-East of Estonia. However, despite high residual concentrations of polyaromatic hydrocarbons (PAHs) and oil products in these soils, the concentration of phenols (especially their water-extractable fraction) was low, not exceeding 0.7 mg/kg dwt. The aim of the current study was to evaluate the role of biodegradation and aging on the decrease of hazard caused by phenolic pollution. The extractability of phenols (phenol, cresols, dimethylphenols and resorcinols) and their biodegradability by the microbial population was studied in the 13 soils sampled from the Estonian oil-shale region, territories of former gas stations, and from presumably non-polluted areas. Phenol, 5-methylresorcinol, p-cresol and resorcinol could be considered easily degradable in the soils as the microbial populations from majority of the soils studied were able to grow on mineral medium supplemented with these phenols as a single source of carbon. 2,3- and 2,4- and 3,4-dimethylphenols could be considered less easily biodegradable.The semi-coke dump leachate polluted soil (containing no dibasic phenols, 43 mg of monobasic phenols, 1348 mg of oil products and 35 mg of PAHs per g dwt) was analyzed chemically (HPLC) and toxicologically (Flash-Assay usingVibrio fischeri) for the leaching of phenols during shaking of soil-water slurries for 24 h. Only 5.8% of the total concentration of phenols was water-extractable, whereas about 50% of the leached amount was biodegraded by the soil microorganisms. Phenol and cresols were biodegraded by 80%, but the concentration of dimethyl-phenols practically did not change. The pollutants (measured as total water-extractable toxicity) were desorbed from the soil particles by the 8^th h of extraction, whereas the toxicity of the aqueous phase continued to increase, probably due to the formation of toxic metabolites. The concentration of water-extractable phenols was too low to explain the toxicity of the extract. Also the impact of PAHs and oil products was excluded. Thus, the relatively low concentration of phenols in the oil-shale region soils is most probably the reflection of both natural attenuation and pollution aging. Therefore, the impact of phenolic compounds to the net bioavailable hazard is probably not so remarkable as it has been considered. The actual pollutants causing the toxicity of the soils from the oil-shale region, however, need to be elucidated.     

酵母菌处理马铃薯淀粉废水研究

马铃薯淀粉废水属高浓度废水,COD达到30 000 mg/L左右,BOD为15 000 mg/L左右,可生化性较好。针对废水中主要含有淀粉、蛋白质和可溶性纤维等成分,筛选分离出能降解这些有机成分的6种酵母。以废水为培养液分别培养这6种酵母及其混合菌,实验结果表明,各酵母菌株对该废水都有较好的降解效果,混合菌的处理效果要好于单个菌株。在连续流废水培养条件下,混合酵母活性和菌体量也较高,MLSS稳定在12 g/L左右,其COD去除率稳定在77%左右。     

Carbon dissipation from surgical cotton production wastewater using macroalgae,microalgae, and activated sludge microbes

Surgical cotton production has drastically been increased in the past few years due to excessive use by medical health professionals especially in countries like India, which is among the top three exporters of cotton worldwide. The effluent generated from surgical cotton industries differ from textile effluents by the conspicuous absence of dyeing chemicals. This wastewater has a high concentration of suspended particles, COD, dissolved ions, organic carbon, and alkaline pH. Several studies have been published on the treatment of textile effluents and the degradation of dyeing chemicals, while the treatment studies on surgical cotton wastewater have been rarely reported in spite of their potential to cause pollution in receiving land/water bodies. Activated sludge microbes have been extensively studied and well documented in the treatment of several industrial effluent but does not match to the production of valuable biomass from algae. The global energy demand has prompted the scientific community to investigate and explore the possibility of using algae for energy production with simultaneous wastewater treatment. To the best of the authors’ knowledge, no research articles have been published which compare the effectiveness of activated sludge microorganisms, microalgae, and macroalgae in removing contaminants from real wastewater. To date, there is a knowledge gap in understanding and selecting the right choice of biological system for effective and economical effluent treatment. In an attempt to minimize this gap, carbon removal by microalgae, macroalgae, and activated sludge microbes were investigated on real effluent from surgical cotton industries. It was observed that the strain of Chlorella vulgaris could dissipate 83% of COD from real wastewater, while consortia of macroalgae (consisting predominantly of Ulvaceae and Chaetomorpha) and activated sludge microbes could remove 81% and 69% of the carbon, respectively. The microalgal growth (in terms of wet weight) increased from 0.15 to 0.3 g, whereas the macroalgal wet weight increased from 1.5 to 3 g in over 7 days of batch experiments conducted in triplicates. This indicated the superlative performance of microalgae over activated sludge microbes in carbon dissipation.

     

废水中难降解性有机污染物的共代谢降解

微生物共代谢是污水中难降解性有机物生物降解的重要方式 ,关键酶的诱导、生长基质与目标污染物之间的竞争抑制、目标污染物及其降解产物对微生物的毒性反应是影响共代谢反应的关键因素。选择合适的生长基质、优化反应条件可以提高微生物共代谢在实际污水处理及地下水污染修复中的应用效果     

新型填料曝气生物滤池处理抗生素类废水

针对抗生素类制药工业废水难处理的特点,将某高效复合微生物菌群负载在以中孔和大孔为主的污泥炭颗粒的表面和孔隙内部,制备得到生物改性污泥炭。采用装填生物改性污泥炭的新型填料曝气生物滤池及向下流、中下部曝气的运行方式对以抗生素类制药废水为主的混合工业废水絮凝沉淀池出水中的主要污染物进行深度处理。结果表明,污泥炭载体在水中发挥2种作用,即吸附功能和载体功能,污泥炭表面及内部孔隙结构非常发达,为不同种类和功能的高效微生物菌群的构建和负载提供了良好的载体;采用粒径为8~10 mm的生物改性污泥炭、HRT 100 min及气水比3∶1,进水COD浓度96~123 mg/L、NH3-N浓度8.8~17.4 mg/L、TP浓度0.390~0.623 mg/L、pH 6~9,新型填料曝气生物滤池对混合工业废水中的COD、NH3-N和TP的平均去除率分别为47.2%、49.2%和35.6%,相比污水厂常规陶料填料生物滤池分别提高了27.9、21.6和12.8个百分点,该工艺处理效果稳定,运营管理简单,为极难生物降解的抗生素类废水为主的混合工业废水的深度处理提供了新思路。     

Photo-oxidation of biodegraded crude oil and toxicity of the photo-oxidized products

We investigated the physicochemical changes resulting from irradiation by sunlight of biodegraded crude oil. An Arabian light crude oil sample was first subjected to microbial degradation. n-Alkanes and aromatic compounds such as naphthalenes, fluorenes, dibenzothiophenes and phenanthrenes possessing short, alkyl side chain(s) were almost completely degraded, while the contents of the saturated and aromatic fractions were reduced by 70% and 40%, respectively. This biodegraded oil was then suspended in seawater and exposed to sunlight irradiation for several weeks. The most remarkable change caused by the irradiation was a substantial decline in the aromatic fraction with a concomitant increase in the resin and asphaltene fractions. A 13C-nuclear magnetic resonance (NMR) spectroscopic analysis showed that the aromaticity of the biodegraded oil was significantly lower in the irradiated sample. A field desorption-mass spectrometric (FD-MS) analysis showed that sunlight irradiation reduced the average molecular weight of the oil components and formed oxygenated compounds. Consistent with this observation is that the oxygen content in the oil increased as the irradiation was prolonged. The bioavailability of the biodegraded oil was increased by the photo-oxidation: the growth of seawater microbes was minimal when the non-irradiated biodegraded oil was used as the source of carbon and energy; however, growth was significant when irradiated biodegraded oil was used. The concentration of dissolved organic carbon (DOC) increased linearly during the sunlight irradiation of the biodegraded oil, and this increase was matched by an increase in ultraviolet-absorptive materials in the seawater. The photochemically formed, water-soluble fraction (WSF) showed acute toxicity against the halophilic crustacean, Artemia.