苯酚降解菌CN-6的分离及其生长特性

从台湾某纺织厂污泥中分离得到一株能够将苯酚作为唯一碳源和能源生长的细菌。根据其形态和生理生化反应结合16S rDNA测定分析,该菌被鉴定为假单胞杆菌(Pseudomonas sp.)。降解特性研究表明,该菌降解苯酚的最适pH和温度分别为8.5和30℃,在此条件下,浓度高达500mg/L的苯酚能被该菌在17 h内将完全降解。在动力学研究中,由于高浓度苯酚对CN-6菌株的降解过程存在底物抑制现象,故采用Haldane非竞争性底物抑制模型,计算确定了模型参数μmax、KS和KI分别为0.452 h-12、8.617 mg/L7、82.4 mg/L,该动力学方程对实验数据能很好拟合。     

Removal of phenolic compounds from raw industrial wastewater by Achromobacter sp. isolated from a hydrocarbon‐contaminated area

The discharge of raw industrial wastewaters, specifically coking wastewater, represents a severe environmental problem. In this work, a phenol‐degrading aerobic strain isolated from a hydrocarbon contaminated site, Achromobacter sp. C‐1, was tested for degrading raw coking wastewater to explore its potential for use in biological treatment. Initially, phenol degradation was reached after 24 h of inoculation in synthetic wastewater [600 mg/L of phenol]. The maximum specific degradation rate was 0.436 h^–1 found in the concentration 300 mg/L. In a raw industrial wastewater containing a mixture of phenols as carbon source [phenol 370 mg/L, m‐cresol 100 mg/L and o‐cresol 60 mg/L], 90% biodegradation of a mixture of phenols was achieved after 80 h of inoculation. Following the biodegradation process to remove the colour from the wastewater, polishing was performed by activated carbon adsorption, resulting in a clear wastewater (without colour and contaminants) ready for industrial reuse purposes. These results provided useful information about use of the phenol‐degrading bacteria for bioaugmentation in industrial wastewater treatment improving the quality of final wastewater. The quality of the resulting wastewater was confirmed by mass spectrometry analysis. This work shows the biodegradation process could be a cost‐effective and promising solution for the treatment and reuse of phenolic wastewater.      

Treatment of wastewater in sewer by Spirogyra sp. green algae: effects of light and carbon sources

The aim of this study is to evaluate the use of Spirogyra sp. green algae for wastewater treatment process in sewer. The effects of light and carbon sources were investigated on growth of the algae Spirogyra sp, removal of nitrate, nitrite, phosphate, chemical oxygen demand (COD) and pH changes. Samples 1 & 4 were grown in autotroph form, while samples 2 & 5 and 3 & 6 were grown in media containing 100 and 200 mg/L of glucose, respectively. Samples 1 up to 3 were grown in cycling light but samples 4 up to 6 were grown in continuous light. Results indicated that algal growth, levels of nitrites and pH and removal of nitrate and phosphate were increased in continuous illumination and carbon sources availability (100 and 200 mg/L of glucose). It can be recommended to apply Spirogyra sp. for wastewater treatment proces s in sewer collection system.     

Biodegradation of low density polyethylene (LDPE) by certain indigenous bacteria and fungi

Low-density polyethylene (LDPE) is an environmental problem because it is discarded randomly, and because in dumpsites, it does not readily degrade. This study reports evidence of successful biodegradation by two fungal species (Aspergillus flavus MCP₅ and Aspergillus flavus MMP₁₀) and eight bacterial species (Acinetobacter sp. MGP₁, Bacillus sp. MGP₁, Pseudomonas sp. MMP₁, Bacillus sp. MMP₅, Staphylococcus sp. MMP₁₀, Bacillus sp. MGP₁, Micrococcus sp. MMP₅ and Bacillus sp. MMP₁₀). These were demonstrated to have used LDPE as both nitrogen and carbon source. LDPE-users were then characterised and identified using standard microbiological procedures. Biodegradation study was done using selected bacterial and fungal isolates, singly and in consortia, to degrade heat-sterilised ground LDPE in media devoid of carbon source, and carbon and nitrogen source. Biodegradation was monitored using gravimetric methods and Fourier transform infrared spectroscopy. This study revealed some microorganisms can use LDPE as both nitrogen and carbon source in the absence of additives.     

Biodegradation of 2-methylisoborneol by single bacterium in culture media and river water environment

2-Methylisoborneol (2-MIB) is a typical odorant in water sources. It is difficult for conventional water treatment to remove it. In this study, three strains capable of removing 2-MIB were isolated from activated carbon of sand filter. They were identified to be Shinella zoogloeoides, Bacillus idriensis and Chitinophagaceae bacterium based on 16S rRNA gene sequence analysis. The biodegradation of 2-MIB was improved with the presence of external carbon (glycerol, glucose, etc.). In the period of 20 days, Bacillus idriensis can remove 2 mg L^?1 2-MIB to 368.2 and 315.4 μg L^?1 in mineral salts medium without and with glycerol. Chitinophagaceae bacterium can remove it to 265.6 and 185.4 μg L^?1 without and with glucose. The enzymatic activity of B. Idriensis was lower when external carbon coexisted with 2-MIB. This indicated that a carbon source can inhibit the use of 2-MIB, but it can provide rich nutrients for the growth of bacteria.     

Biodegradation of chlorpyrifos and 3, 5, 6‐trichloro‐2‐pyridinol by a novel rhizobial strain Mesorhizobium sp. HN3

A chlorpyrifos (CP) and 3,5,6‐trichloro‐2‐pyridinol (TCP) degrading bacterial strain, Mesorhizobium sp. HN3, was isolated and characterized. Mesorhizobium sp. HN3 degraded CP efficiently up to 400 mg/L initial concentration at wide range of temperatures (30–40°C) and pH (6.0–8.0). However, optimal degradation of CP was achieved at 37°C and neutral pH (7.0) at an initial inoculum density 2 × 10⁷ colony forming unit/mL of culture medium. Kinetic parameters for CP degradation by Mesorhizobium sp. HN3 were estimated at different initial concentrations. Cultures exhibited significant variation (P ≤ 0.05) in the specific growth rate (μ), cell mass formation rate (Q_X) and the substrate uptake rate (Q_S) during degradation of CP. The values of kinetic parameters increased up to 100 mg/L CP and decreased at higher concentration. Investigation of degradation metabolites indicated that CP is converted to diethylthiophosphate and TCP that leads to the formation of 3,5,6‐trichloro‐2‐methoxypyridine.     

NaClO与KMnO4氧化对针杆藻灭活特性研究

以针杆藻（Synedra sp 。）为研究对象，考察了 NaClO 与 KMnO4在不同投量和不同 pH 条件下对针杆藻的灭活特点以及对光合活性的影响。结果表明，在0～5 mg／L 投加范围内，NaClO对针杆藻的灭活效果随剂量的增大而提高，投加量为3 mg／L 是抑制藻活性的最佳投量，并且在酸性条件下 NaClO 能更好的发挥其氧化降解的作用；KMnO4对针杆藻的降解效果不明显，说明投加KMnO4（≤5 mg／L）对针杆藻没有很好的灭活效果。氯化对针杆藻灭活效果好，但是会造成细胞解体，引起藻内有机物的释放，危及饮用水安全。     

A novel bioflocculant produced by Klebsiella sp. and its application to sludge dewatering

A bioflocculant‐producing bacterium, named N‐10, was isolated from activated sludge and was identified as Klebsiella sp. The bioflocculant (named MBF10) produced by Klebsiella sp. had a good flocculating capability and could achieve a flocculating rate of 86.5% to kaolin suspension at the dosage of 0.034 g/L. Compared with chemical flocculants, such as Al₂(SO₄)₃, polyaluminum chloride (PAC) and cationic polyacrylamide (PAM) at their optimal dosages, MBF10 showed a similar performance for sludge dewatering. After preconditioning, dry solids (DS) and specific resistance to filtration (SRF) of the sludge were 17.5% and 3.36 × 10¹² m/kg, respectively. The combined use of MBF10 and Al₂(SO₄)₃ resulted in optimum sludge dewatering properties, SRF reduced from 10.87 × 10¹² m/kg to 1.72 × 10¹² m/kg, and DS increased from 13.1% to 21.3%. Charge neutralisation and interparticle bridging were proposed as the reasons for the enhanced performance based upon the experimental observations.     

Bioremediation of phenol,sulfate sodium,and polycyclic aromatic hydrocarbons by Rhodococcus sp. first time isolated and molecular characterized from aquatic and terrestrial ecosystems

Environmental pollutions are the most significant problem worldwide. Rhodococcus sp. has a high potential for the production of secondary metabolites and degradation activity. This study aims to screen and characterize biodegradable Rhodococcus from Iranian ecosystems. The Rhodococcus isolates were recovered from 90 environmental samples and identified using conventional and molecular methods. The growth rate in the presence of pollutants and chromatography (high-performance liquid chromatography [HPLC]) was used to determine their biodegradation capability. A total of 13 Rhodococcus isolates were characterized from the cultured samples (14.5%) that belonged to seven species. The prevalent species were R. erythropolis (4 isolates; 30.8%), R. atherivorans (3 isolates; 23%), R. ruber (2 isolates; 15.4), and R. zopfii, R. phenolicus, R. equi and R. rhodochrous 1 isolate each. The result showed that these isolates could degrade and consume phenol, polycyclic aromatic hydrocarbon (PAH) and sulfate sodium. Our results showed that the Rhodococcus species have significant potential for bioremediation of diverse types of pollutants. Therefore, more studies are recommended for the biodegradation activity of Rhodococcus.     

Influence of feed concentration on the kinetics of biodegradation of phenol in a continuous stirred reactor

The rate of phenol degradation by activated sludge was studied in a completely mixed continuous-flow reactor with sludge recycle, operated at steady-state conditions at 20°C. Monod kinetics was followed when the influent concentration (C_s°) was kept constant. When using different C_s° levels, the phenol removal rate was found to have an inverse dependence on C_s°. It is suggested that this kinetic anomaly is due to inhibition of the biooxidation by some secondary reaction product(s). A kinetic model based on this concept is able to interpret experimental facts.     

Fenton氧化处理炼化废水中苯酚的实验研究

通过单因素实验探索了Fenton氧化炼化废水中苯酚的最佳工艺条件。实验结果表明,Fenton试剂处理苯酚废水时,最佳氧化反应条件为:pH=3.5,反应温度为20℃,H2O2投加量为12mL·L-1,反应时间为30min,FeSO4·7H2O投加量为600mg·L-1。因此用Fenton氧化法处理含苯酚废水是一种非常有效的方法。     

Biodegradation pathway of o-cresol by heterogeneous culture Phenol acclimated activated sludge

The biodegradation process of o-cresol by heterogeneous culture is presented in this paper. Metabolic intermediates of o-cresol by phenol acclimated activated sludge were analyzed by GC-MS. o-Cresol was first transformed to three dihydroxytoluenes; 3-methylcatechol, 4-methylresorcinol and methylhydroquinone. Three dihydroxytoluene biodegradation experiments with 3-methylcatechol, 4-methylresorcinol and methylhydroquinone revealed that 3-methylcatechol was the main route, and 3-methylcatechol was further degraded through at least two meta cleavage pathways. Various hydroxylated toluenes, namely trihydroxytoluenes and tetrahydroxytoluene were also found among the metabolites from 3-methylcatechol, 4-methylresorcinol and methylhydroquinone. These results indicated that various metabolism with main and side pathways coexisted in the biodegradation process by the heterogeneous culture.     

Dynamics of microcystin production and quantification of potentially toxigenic Microcystis sp. using real-time PCR

Cyanobacterial blooms in eutrophied water body are generally composed of various genotypes with or without microcystin-producing genes (mcy gene cluster). Thus there is a need for quantification of potent toxin producing strains. The present study aimed at identifying microcystin variants and its producer strains in Durgakund pond, Varanasi, India, based on quantification of cpcBA-IGS and mcyA (condensation domain) genes using real-time PCR and LC-MS. Increase in microcystin concentrations was correlated with increase in mcyA copy number and the level of pigments (chlorophyll a, phycocyanin and carotenoids). Also, selected environmental factors (water temperature, light irradiance, rainfall, pH, N and P) and the concentration of microcystin variants (MC-LR, -RR and -YR) were also assessed in samples during May 2010 to April 2011 to establish the possible correlation among these parameters. Nutrients favored cyanobacterial bloom but it could not be correlated with the levels of microcystin variants and seemed to be geographically specific. Microcystis sp. dominant in the pond comprised potentially toxigenic cells. The ratio of potentially toxigenic Microcystis sp. to that of total Microcystis sp. ranged from 0% to 14%. Such studies paved the way to identify and quantify the most potent microcystin producer in the tropical aquatic body.     

A study of external mass transfer effect on biodegradation of phenol using low‐density polyethylene immobilized Bacillus flexus GS1 IIT (BHU) in a packed bed bioreactor

The impact of external mass transport on the biodegradation rate of phenol in a packed bed bioreactor (PBBR) was studied. A potential bacterial species, Bacillus flexus GS1 IIT (BHU), was isolated from the petroleum‐contaminated soil. Low‐density polyethylene (LDPE) immobilized with the B. flexus GS1 IIT (BHU) was used as packing material in the PBBR. The PBBR was operated by varying the inlet feed flow rate from 4 to 10 mL/min, and the corresponding degradation rate coefficients were found to be in the range of 0.119–0.157 L/g h. In addition, the highest removal rate of phenol was obtained to be 1.305 mg/g h at an inlet feed rate of 10 mL/min. The external mass transfer was studied using the model . A new empirical correlation for the biodegradation of phenol in the PBBR was developed after the evaluation at various values of K and n.     

Biodegradation of polycyclic aromatic hydrocarbons by Sphingomonas sp. enhanced by water-extractable organic matter from manure compost

The effectiveness of in-situ bioremediation of polycyclic aromatic hydrocarbons (PAHs) may be inhibited by their low aqueous solubility and strong absorption to soil constituents. The aim of this research was to evaluate the effect of water-extractable organic matter (WEOM) from manure compost on the biodegradation of various PAHs. The aqueous solubilities of PAHs including phenanthrene, pyrene and benzo[a]pyrene under different concentrations of WEOM from cow manure compost were initially evaluated. The contribution of WEOM on the degradation of PAHs by Sphingomonas sp. was then investigated. Dissolution results confirmed the ability of WEOM to increase the apparent solubility of the 3PAHs. Time course of biodegradation also revealed its positive contribution to their removal. For example, the degradation of pyrene was 118% higher in the presence of 1000 mg-C L^− 1 WEOM as compared to the mineral salt medium (MSM) alone after 48 h incubation. In addition, degradation was 12% higher with WEOM than with Glucose-Ammonium nitrate despite the more than 6 times higher cell concentration in the latter. WEOM from other manure composts such as chicken and pig were found to have the same effect. Finally, additional tests confirmed that high molecular weight WEOM (> 1000 Da) contributed mainly to solubility and biodegradation enhancements. On the basis of these results, the increase in apparent solubility of PAHs in WEOM solutions may have a significant impact on their biodegradation. It is postulated that the application of WEOM-rich manure composts may be extended in the in-situ bioremediation of PAHs-polluted soil.     

Biodegradation of the cyanobacterial toxin microcystin LR in natural water and biologically active slow sand filters

A bacterium (MJ-PV) previously demonstrated to degrade the cyanobacterial toxin microcystin LR, was investigated for bioremediation applications in natural water microcosms and biologically active slow sand filters. Enhanced degradation of microcystin LR was observed with inoculated (1 x 10(6) cell/mL) treatments of river water dosed with microcystin LR (>80% degradation within 2 days) compared to uninoculated controls. Inoculation of MJ-PV at lower concentrations (1 x 10(2)-1 x 10(5) cells/mL) also demonstrated enhanced microcystin LR degradation over control treatments. Polymerase chain reactions (PCR) specifically targeting amplification of 16S rDNA of MJ-PV and the gene responsible for initial degradation of microcystin LR (mlrA) were successfully applied to monitor the presence of the bacterium in experimental trials. No amplified products indicative of an endemic MJ-PV population were observed in uninoculated treatments indicating other bacterial strains were active in degradation of microcystin LR. Pilot scale biologically active slow sand filters demonstrated degradation of microcystin LR irrespective of MJ-PV bacterial inoculation. PCR analysis detected the MJ-PV population at all locations within the sand filters where microcystin degradation was measured. Despite not observing enhanced degradation of microcystin LR in inoculated columns compared to uninoculated column, these studies demonstrate the effectiveness of a low-technology water treatment system like biologically active slow sand filters for removal of microcystins from reticulated water supplies.     

Optimization of phenol removal from wastewater by activation of persulfate and ultrasonic waves in the presence of biochar catalyst modified by lanthanum chloride

In this paper, the effects of phenol concentration, pH, catalyst dose, persulfate concentration, temperature and contact time on the phenol removal from wastewater by activation of persulfate (S₂O₈^?2) in the presence of biochar modified by lanthanum chloride and ultrasonic waves (US) are optimized. Experimental design and optimization were carried out by response surface methodology. The optimum conditions for the maximum phenol removal were obtained pH of 4, phenol concentration of 86 mg/L, catalyst dose of 43 mg/L, persulfate concentration of 86 mg/L, temperature of 41 °C and contact time of 63 min. The optimum phenol removal from synthetic wastewater was attained 97.68%. Phenol removal by the mentioned system was fitted with the first‐order kinetic model. The combination of the ingredients of ‘S₂O₈^?2/US/Biochar‐LaCl₃’ system had a synergistic effect on the phenol removal.     

Batch and continuous biooxidation of sulphide by Thiomicrospira sp. CVO: reaction kinetics and stoichiometry

Aqueous phase biooxidation of sulphide by the novel sulphide-oxidizing bacterium Thiomicrospira sp. CVO was studied in batch and continuous systems. CVO was able to oxidize sulphide at concentrations as high as 19 mM. Sulphide biooxidation occurred in two distinct phases, one resulting in the formation of sulphur and possibly other dissolved sulphur compounds rather than sulphate, followed by sulphate formation. The specific growth rate of CVO in the first and second phases were 0.17-0.27 and 0.04-0.05 h(-1), respectively. Nitrite accumulated in the culture during the first phase and was consumed during the second phase. The composition of end-products was influenced by the ratio of sulphide to nitrate initial concentrations. At a ratio of 0.28, sulphate represented 93% of the reaction products, while with a ratio of 1.6 the conversion of sulphide to sulphate was only 9.3%. In the continuous bioreactor, complete removal of sulphide was observed at sulphide volumetric loading rates as high as 1.6mM/h (residence time of 10h). Overall sulphide removal efficiency decreased continuously upon further increases in volumetric loading rate. However, the volumetric removal rate increased until a maximum value of 2.4mM/h was obtained at a loading rate of 3.2mM/h. The corresponding sulphide conversion and residence time were 76% and 5.6h, respectively. As expected from the high ratio of sulphide to nitrate loading rates (1.7-1.9 mM/h), no sulphate was formed in the continuous reactor. Using the experimental data the value of maximum specific growth rate, saturation constant, decay coefficient, maintenance coefficient and yield were determined to be 0.36 h(-1), 1.99 mM sulphide, 0.0014 h(-1), 0.078 mmol sulphide/mg ATPh and 0.018 mg ATP/mmol sulphide, respectively.     

Improvement of metal adsorption onto chitosan/Sargassum sp. composite sorbent by an innovative ion-imprint technology

Technology for immobilization of biomass has attracted a great interest due to the high sorption capacity of biomass for sequestration of toxic metals from industrial effluents. However, the currently practiced immobilization methods normally reduce the metal sorption capacities. In this study, an innovative ion-imprint technology was developed to overcome the drawback. Copper ion was first imprinted onto the functional groups of chitosan that formed a pellet-typed sorbent through the granulation with Sargassum sp.; the imprinted copper ion was chemically detached from the sorbent, leading to the formation of a novel copper ion-imprinted chitosan/Sargassum sp. (CICS) composite adsorbent. The copper sorption on CICS was found to be highly pH-dependent and the maximum uptake capacity was achieved at pH 4.7-5.5. The adsorption isotherm study showed the maximum sorption capacity of CICS of 1.08 mmol/g, much higher than the non-imprinted chitosan/Sargassum sp. sorbent (NICS) (0.49 mmol/g). The used sorbent was reusable after being regenerated through desorption. The FTIR and XPS studies revealed that the greater sorption of heavy metal was attributed to the large number of primary amine groups available on the surfaces of the ion-imprinted chitosan and the abundant carboxyl groups on Sargassum sp. Finally, an intraparticle surface diffusion controlled model well described the sorption history of the sorbents.     

Detection of viable antibiotic‐resistant/sensitive Acinetobacter baumannii in indoor air by propidium monoazide quantitative polymerase chain reaction

Acinetobacter baumannii represents a significant cause of nosocomial infections. Therefore, we combined real‐time quantitative polymerase chain reaction (PCR) with the propidium monoazide (PMA‐qPCR) to assess the feasibility of detecting viable, airborne A. baumannii. The biological collection efficiencies of three samplers for collecting airborne A. baumannii were evaluated by PMA‐qPCR in a chamber study. After sampling, the effects of storage in collection fluid on A. baumannii were evaluated. The results showed that the culturable ratio of A. baumannii measured using the culture method was significantly correlated with the viable ratio measured using PMA‐qPCR, but was not significantly correlated with the qPCR results. It was indicated that the AGI‐30 impinger and the BioSampler were much more effective than the Nuclepore filter sampler for collecting airborne A. baumannii. The storage temperature was critical for aerosol samples, as the loss of viable A. baumannii was minimized when the PMA‐bound DNA was stored at ?20°C or if the collected cells were stored at 4°C and subsequently processed by PMA‐qPCR within 1 month. The PMA‐qPCR method was also to distinguish between colistin‐sensitive and colistin‐resistant A. baumannii, and no colistin‐sensitive A. baumannii was detected by PMA‐qPCR upon treatment of the BioSampler collection medium with 2 μg/ml colistin for 5 min.