Glyphosate degradation by immobilized bacteria: field studies with industrial wastewater effluent.

Immobilized bacteria have been shown in the laboratory to effectively remove glyphosate from wastewater effluent discharged from an activated sludge treatment system. Bacterial consortia in lab columns maintained a 99% glyphosate-degrading activity (GDA) at a hydraulic residence time of less than 20 min. In this study, a pilot plant (capacity, 45 liters/min) was used for a field demonstration. Initially, activated sludge was enriched for microbes with GDA during a 3-week biocarrier activation period. Wastewater effluent was then spiked with glyphosate and NH4Cl and recycled through the pilot plant column during start-up. Microbes with GDA were enhanced by maintaining the pH at less than 8 and adding yeast extract (less than 10 mg/liter). Once the consortia were stabilized, the column capacity for glyphosate removal was determined in a 60-day continuous-flow study. Waste containing 50 mg of glyphosate per liter was pumped at increasing flow rates until a steady state was reached. A microbial GDA of greater than 90% was achieved at a 10-min hydraulic residence time (144 hydraulic turnovers per day). Additional studies showed that microbes with GDA were recoverable within (i) 5 days of an acid shock and (ii) 3 days after a 21-day dormancy (low-flow, low-maintenance) mode. These results suggest that full-scale use of immobilized bacteria can be a cost-effective and dependable technique for the biotreatment of industrial wastewater.     

Glyphosate degradation by immobilized bacteria: field studies with industrial wastewater effluent.

Immobilized bacteria have been shown in the laboratory to effectively remove glyphosate from wastewater effluent discharged from an activated sludge treatment system. Bacterial consortia in lab columns maintained a 99% glyphosate-degrading activity (GDA) at a hydraulic residence time of less than 20 min. In this study, a pilot plant (capacity, 45 liters/min) was used for a field demonstration. Initially, activated sludge was enriched for microbes with GDA during a 3-week biocarrier activation period. Wastewater effluent was then spiked with glyphosate and NH4Cl and recycled through the pilot plant column during start-up. Microbes with GDA were enhanced by maintaining the pH at less than 8 and adding yeast extract (less than 10 mg/liter). Once the consortia were stabilized, the column capacity for glyphosate removal was determined in a 60-day continuous-flow study. Waste containing 50 mg of glyphosate per liter was pumped at increasing flow rates until a steady state was reached. A microbial GDA of greater than 90% was achieved at a 10-min hydraulic residence time (144 hydraulic turnovers per day). Additional studies showed that microbes with GDA were recoverable within (i) 5 days of an acid shock and (ii) 3 days after a 21-day dormancy (low-flow, low-maintenance) mode. These results suggest that full-scale use of immobilized bacteria can be a cost-effective and dependable technique for the biotreatment of industrial wastewater.     

以圆币草发酵液为碳源时硫酸盐还原菌处理重金属废水

【目的】探索以圆币草(Hydrocotyle verticillata)发酵液作为碳源时硫酸盐还原菌处理重金属废水的效果,以便于高效去除废水中的重金属离子。【方法】以厌氧污泥为硫酸盐还原菌接种菌群,添加大型水生植物圆币草发酵液,并以乙醇、乳酸钠、葡萄糖、蔗糖和乙酸钠为对照,测定不同碳源下硫酸盐还原效率,分析其对废水中重金属离子(Pb2+,Cd2+,Cu2+,Ni2+)的去除能力。【结果】硫酸盐还原菌能有效利用圆币草发酵液中有机物,在COD/SO42-为1.2、5.0和7.0时硫酸盐最大还原率分别为24.4%、43.6%和60.0%。以发酵液为碳源时硫酸盐还原效率高于葡萄糖、蔗糖和乙酸钠,但低于乙醇和乳酸钠。在添加圆币草发酵液的批次试验反应器中,对低浓度4种重金属离子混合废水具有良好的处理效果,Cd2+、Cu2+、Pb2+和Ni2+的去除率分别为95.2%、98.7%、93.0%和89.6%。当Cd2+、Cu2+、Pb2+和Ni2+浓度为10 mg/L时,以圆币草发酵液为碳源的批次反应器对4种重金属离子仍具有良好的处理效果,去除率均超过90%,且硫酸盐还原菌的活性没有受到抑制。【结论】大型水生植物发酵液作为硫酸盐还原菌的碳源,不仅能有效进行重金属废水的生物深度处理,而且可以实现大型水生植物的资源化。     

含酚废水处理高效菌株的筛选

酚类化合物属于持久性有机污染物,含酚废水在我国水污染控制中被列为需要重点解决的有害废水之一。本文通过对本钢焦化厂含酚分废水处理工艺中曝气池内活性污泥所含未知菌株进行分离纯化,并经过对酚的耐受性实验和降解率实验,得到处理酚的高效菌株。通过对筛选出的菌株进行细胞个体形态和菌群形态特征观察及一系列生理生化实验,确定筛选出来的7株能高效降解盼的菌株为假单胞菌。本文的实验结果将有利于今后对含酚废水的处理。     

Use of immobilized algicidal bacteria to control natural freshwater diatom blooms

The purpose of this investigation was to assess the possible use of algicidal bacteria in conjunction with an immobilization technique for efficient termination of natural blooms of Stephanodiscus concomitant with minimization of adverse effects caused by a single application of bacteria. The performance of Pseudomonas fluorescens cells immobilized on cellulose sponges (CIS) was compared with that of freely suspended cells (FSC) of the organism at low water temperature (WT) of <10°C in co-cultures and natural microcosms. In the co-cultures, CIS resulted in more effective lysis of Stephanodiscus, irrespective of similar bacterivore (Spumella sp.) density, and significantly reduced the concentrations of nitrate and soluble reactive phosphorus (SRP), but not that of silicate, compared with FSC. In the microcosms containing natural freshwater, CIS reduced the densities of Stephanodiscus spp. and Aulacoseira spp. but had no effect on other phytoplankton. Compared with FSC, removal of nutrients by the CIS prevented secondary blooms caused by other phytoplankton. Our results indicate that the CIS affords effective protection of P. fluorescens from low WT and heterotrophs, and restrained regeneration of both SRP and nitrate. Thus, it was demonstrated that the CIS may be an attractive alternative to FSC for control of natural blooms.     

Solid fermentation by fixed dominant bacteria for industrial wastewater

为实现优势菌种的工程应用,由焦化废水处理站污泥筛选优势好氧菌A和兼性厌氧菌F,使用谷壳g、豆皮d为载体,采用固体发酵法进行固定化产品制备.初步研究表明固体发酵法固定菌种具有可行性,主要调控因素有温度、初始含水率、工业废水比例、pH、通风量和发酵时间.以pH 8.0、温度好氧菌30℃(兼性厌氧菌35℃)、接种量1mL菌液/g固定化液体,初始含水量80％,固体发酵时间5d,低于60℃鼓风干燥,制备固定化产品.保存三个月,谷壳固定化产品好氧菌Ag的硝化能力和兼性厌氧菌Fg的反硝化能力不随保存时间的延长而改变;豆皮固定化产品Ad、Fd降解能力随保存时间延长下降12％左右.以实验室A2/O工艺系统验证固定化产品处理焦化废水效果,缺氧池中无NO3 - -N积累,反硝化作用明显.Ad和Ag对氰化物的去除率均达99％以上;对苯酚的去除效果Ag(98.84％)优于Ad(79.6％);但对NH4+ -N的去除率Ad (75.46％)优于Ag (62.55％).     

固体发酵法固定工业废水处理优势菌的研究

为实现优势菌种的工程应用,由焦化废水处理站污泥筛选优势好氧菌A和兼性厌氧菌F,使用谷壳g、豆皮d为载体,采用固体发酵法进行固定化产品制备。初步研究表明固体发酵法固定菌种具有可行性,主要调控因素有温度、初始含水率、工业废水比例、pH、通风量和发酵时间。以pH8．0、温度好氧菌30℃（兼性厌氧菌35℃）、接种量1mL茴液儋田定化载体,初始含水量80％,固体发酵时间5d,低于60℃鼓风干燥,制备固定化产品。保存三个月,谷壳固定化产品好氧菌八的硝化能力和兼性厌氧菌R的反硝化能力不随保存时间的延长而改变;豆皮固定化产品氏、Fd降解能力随保存时问延长下降12％左右。以实验室岔／O工艺系统验证固定化产品处理焦化废水效果,缺氧池中无NO3-N积累,反硝化作用明显。氐和气对氰化物的去除率均达99％以上;对苯酚的去除效果气（98．84％）优于氏（79．6％）;但对NH4＋-N的去除率氏（75．46％）优于Ag（62．55％）。     

Biological treatment specific for an industrial wastewater containing s-triazines

Mixed cultures of bacteria grew in medium containing real s-triazine wastes as nitrogen source. About 80% of the s-triazine waste could be degraded as determined by HPLC and by measurements of dissolved nitrogen. The culture required an added carbon source in order to degrade s-triazines. A temperature optimum near 40 degrees C was observed and a salt concentration above about 4% markedly retarded growth and the degradation of s-triazines. This system was examined as a biological treatment for wastes from syntheses of s-triazines.     

Peroxidase mediated decolorization and remediation of wastewater containing industrial dyes: a review

In this article an effort has been made to review literature based on the role of peroxidases in the treatment and decolorization of a wide spectrum aromatic dyes from polluted water. Peroxidases can catalyze degradation/transformation of aromatic dyes either by precipitation or by opening the aromatic ring structure. Peroxidases from plant sources; horseradish, turnip, tomato, soybean, bitter gourd, white radish and Saccharum uvarum and microbial sources; lignin peroxidases, manganese peroxidases, vanadium haloperoxidases, versatile peroxidases, dye decolorizing peroxidases have been employed for the remediation of commercial dyes. Soluble and immobilized peroxidases have been successfully exploited in batch as well as in continuous processes for the treatment of synthetic dyes with complex aromatic molecular structures present in industrial effluents at large scale. However, recalcitrant dyes were also decolorized by the action of peroxidases in the presence of redox mediators.     

Diversity and distribution of bacteria in a multistage surface flow constructed wetland to treat swine wastewater in sediments

Applied Microbiology and Biotechnology - Managing waste produced from swine farming operations is a significant agricultural and environmental challenge. Confined animal feeding operations...     

Biodegradation of phenolic industrial wastewater in a fluidized bed bioreactor with immobilized cells of Pseudomonas putida

The paper presents the main results obtained from the study of the biodegradation of phenolic industrial wastewaters by a pure culture of immobilized cells of Pseudomonas putida ATCC 17484. The experiments were carried out in batch and continuous mode. The maximum degradation capacity and the influence of the adaptation of the microorganism to the substrate were studied in batch mode. Industrial wastewater with a phenol concentration of 1000 mg/l was degraded when the microorganism was adapted to the toxic chemical. The presence in the wastewater of compounds other than phenol was noted and it was found that Pseudomonas putida was able to degrade these compounds. In continuous mode, a fluidized-bed bioreactor was operated and the influence of the organic loading rate on the removal efficiency of phenol was studied. The bioreactor showed phenol degradation efficiencies higher than 90%, even for a phenol loading rate of 0.5 g phenol/ld (corresponding to 0.54 g TOC/ld).     

Use of horizontal subsurface flow constructed wetlands to treat reverse osmosis concentrate of rolling wastewater

According to the characteristics of the reverse osmosis concentrate (ROC) generated from iron and steel company, we used three sets of parallel horizontal subsurface flow (HSF) constructed wetlands (CWs) with different plants and substrate layouts to treat the high-salinity wastewater. The plant growth and removal efficiencies under saline condition were evaluated. The evaluation was based entirely on routinely collected water quality data and the physical and chemical characteristics of the plants (Phragmites australis, Typha latifolia, Iris wilsonii, and Scirpus planiculmis). The principal parameters of concern in the effluent were chemical oxygen demand (COD), total nitrogen (TN), and total phosphorus (TP). The results showed that the CWs were able to remove COD, TN, and TP from ROC. S. planiculmis was not suitable for the treatment of high-saline wastewater. The sequence of metals accumulated in CW plants was K>Ca>Na>Mg>Zn>Cu. More than 70% of metals were accumulated in the aboveground of P. australis. The CW filled with gravel and manganese ore and planted with P. australis and T. latifolia had the best performance of pollutant removal, with average removal of 49.96%, 39.45%, and 72.01% for COD, TN, and TP, respectively. The effluent water quality met the regulation in China. These results suggested that HSF CW planted with P. australis and T. latifolia can be applied for ROC pollutants removal.     

工业废水中阿特拉津降解细菌的遗传和生理多样性

【目的】通过遗传学和生理学实验,揭示分离自工业废水的阿特拉津降解细菌具有遗传和生理多样性,为阐明阿特拉津生物降解的分子机理和阿特拉津降解细菌在污染环境生物修复中的应用提供新见解。【方法】用普通PCR方法检测菌株的阿特拉津降解基因,分析其降解基因组成;用基因组重复序列PCR技术(rep-PCR)分析降解菌株的基因组类型;用Western blot方法检测菌株阿特拉津降解途径的第一个酶三嗪水解酶(TrzN);用不同氮源(阿特拉津、莠灭净、扑草净、西玛津、氰草净、阿特拉通和氰尿酸)和碳源(蔗糖、葡萄糖、麦芽糖、乳糖、柠檬酸钠、乙酸钠和琥珀酸钠)培养降解菌株,通过检测培养液的OD600值,证明菌株能够利用的氮源和碳源种类。【结果】对分离自工业废水的27个阿特拉津降解菌株所进行的阿特拉津降解基因PCR检测表明,其降解基因组成分别为trzN-atzBC、trzN-atzABC和atzADEF;通过rep-PCR实验将27个阿特拉津降解菌株分为7个群;Western blot结果表明,27个菌株中有24个含有三嗪水解酶TrzN;氮源利用实验表明,2个菌株能够利用所有7种氮源生长,其余25个菌株只能利用其中的2-6种;碳源利用实验表明,10个菌株能够利用所有7种碳源生长,其余17个菌株只能利用其中的3-6种。【结论】分离自某工业废水的27株阿特拉津降解功能菌存在相当广泛的遗传和生理学上的多样性,trzN-atzABC降解基因组成为首次发现。     

Use of an industrial effluent as a carbon source for denitrification of a high-strength wastewater

Denitrification of a high-strength synthetic wastewater (150 g NO^- ₃ l^-1) was carried out using a wine distillery effluent as an example of an industrial carbon source (22.7 g chemical oxygen demand l^-1). Two configurations were tested: one consisted of an acidogenesis reactor followed by a denitrifying reactor and the other was a single reactor directly fed with the raw effluents. In both cases, denitrification was achieved at a nitrate load of 9.54 g NO^- ₃ l^-1 day^-1 (2.19 g N as NO^- ₃ l^-1 day^-1) with good specific reduction rates: 32.6 mg and 35.2 mg N as NO _x  g volatile suspended solids h^-1, calculated on a single day, for the two-step and the one-step process respectively. Dissimilatory nitrate reduction to ammonium did not occur, even in the one-step process. Received: 26 October 1995/Received revision: 15 February 1996/Accepted: 20 February 1996     

The adsorption of bacteria to immobilized lectins

R.A. PATCHETT, A.F. KELLY AND R.G. KROLL. 1991. The agglutination of a selection of bacteria by some lectins was examined. The lectin from Codium fragile agglutinated seven strains of Salmonella typhimurium. The lectin from Helix pomatia agglutinated eight of 12 strains of Listeria monocytogenes and a further two strains gave a weak agglutination reaction. Helix pomatia lectin conjugated to magnetic microspheres enabled the adsorption of L. monocytogenes from suspension with subsequent elution by the competing ligand N -acetyl galactosamine. Affinity chromatography of a suspension of L. monocytogenes through a column of H. pomatia lectin immobilized on agarose, also adsorbed cells and enabled subsequent elution with N -acetyl galactosamine. The column technique enabled the more rapid adsorption of bacteria perhaps because of improved interactions between bacteria and immobilized lectin.     

The adsorption of bacteria to immobilized lectins

The agglutination of a selection of bacteria by some lectins was examined. The lectin from Codium fragile agglutinated seven strains of Salmonella typhimurium. The lectin from Helix pomatia agglutinated eight of 12 strains of Listeria monocytogenes and a further two strains gave a weak agglutination reaction. Helix pomatia lectin conjugated to magnetic microspheres enabled the adsorption of L. monocytogenes from suspension with subsequent elution by the competing ligand N-acetyl galactosamine. Affinity chromatography of a suspension of L. monocytogenes through a column of H. pomatia lectin immobilized on agarose, also adsorbed cells and enabled subsequent elution with N-acetyl galactosamine. The column technique enabled the more rapid adsorption of bacteria perhaps because of improved interactions between bacteria and immobilized lectin.     

Long-term surveillance of sulfate-reducing bacteria in highly saline industrial wastewater evaporation ponds

Abundance and seasonal dynamics of sulfate-reducing bacteria (SRB), in general, and of extreme halophilic SRB (belonging to Desulfocella halophila) in particular, were examined in highly saline industrial wastewater evaporation ponds over a forty one month period. Industrial wastewater was sampled and the presence of SRB was determined by quantitative real-time PCR (qPCR) with a set of primers designed to amplify the dissimilatory sulfite reductase (dsrA) gene. SRB displayed higher abundance during the summer (10⁶–10⁸ targets ml^-1) and lower abundance from the autumn-spring (10³–10⁵ targets ml^-1). However, addition of concentrated dissolved organic matter into the evaporation ponds during winter immediately resulted in a proliferation of SRB, despite the lower wastewater temperature (12–14°C). These results indicate that the qPCR approach can be used for rapid measurement of SRB to provide valuable information about the abundance of SRB in harsh environments, such as highly saline industrial wastewaters. Low level of H₂S has been maintained over five years, which indicates a possible inhibition of SRB activity, following artificial salination (≈16% w/v of NaCl) of wastewater evaporation ponds, despite SRB reproduction being detected by qPCR.     

光合细菌利用工业有机废水产生5-氨基乙酰丙酸

[目的]利用本实验室筛选的5-氨基乙酰丙酸(5-aminolevulinic acid,ALA)高产紫色非硫红假单胞菌株,以味精、柠檬酸、啤酒和豆制品生产废水作为底物,进行光合细菌利用废水产生ALA并去除化学需氧量(CODcr)的研究.[方法]光合细菌培养温度为30℃,光照强度为3000 Lux,进行乙酰丙酸、甘氨酸、琥珀酸的添加与否和废水灭菌与否的处理,用比色法测定菌液光密度,ALA检测采用Ehrlich'S试剂分光光度检测法.[结果]在不添加乙酰丙酸(levulinic acid,LA)、甘氨酸和琥珀酸的条件下,菌株99-28的菌体生长在72～96 h达到稳定期,ALA产量在96h最高,在4种废水中,味精废水的ALA产量最高,CODcr去除率也最高;添加LA、甘氨酸和琥珀酸显著提高ALA产量,但CODcr去除效果不好.废水不灭菌略微降低99-28菌株的生长和CODcr的去除能力,在添加LA、甘氨酸和琥珀酸的条件下的,ALA产量明显下降.ALA高产突变菌株L-1在有机废水中的生长状况、对有机废水的CODcr去除与菌株99-28表现一致,在不添加和添加LA、甘氨酸和琥珀酸的条件下,突变株L-1的ALA产量明显比菌株99-28高.[结论]本实验室筛选的紫色非硫红假单胞菌株能利用有机废水作为底物产生ALA并降解CODcr.