Shewanella putrefaciens CN32非饱和生物膜对环境压力的响应以及与铬的作用

Shewanella putrefaciens CN32模拟在非饱和环境中生长的生物膜,探究不同环境条件对非饱和生物膜胞内外大分子物质的影响,以及生物膜对重金属Cr的作用.在84 h、219 mmol·L^-1 NaCl、pH6.2和35℃条件下,生物膜分泌胞外聚合物的量达到最大,每片生物膜胞外聚合物总量为400.6μg;生长12 h的每片生物膜中胞外聚合物吸附了9.77μg Cr,占生物膜总吸附量的63.8%;三维荧光光谱表明,生物膜吸附Cr后胞外聚合物中色氨酸蛋白类物质与酪氨酸蛋白类物质荧光强度明显降低.结果表明,一定强度的渗透压、低pH和高温能促进生物膜分泌更多的胞外聚合物.非饱和生物膜中,胞外聚合物是重金属Cr的主要结合区域,并且胞外聚合物中的色氨酸蛋白类物质与酪氨酸蛋白类物质可能在与Cr络合中起重要作用.     

自然水体生物膜有机组分对Cd2+的吸附特征

室内模拟研究了长春南湖水生物膜中有机组分即胞外聚合物、微生物非活性细胞和微生物活性细胞对Cd^2＋的吸附特征及其影响因素。结果表明：3种有机组分对Cd^2＋的吸附过程分为快速和慢速阶段，达到吸附平衡的时间分别为360、100和100min；Cd^2＋的吸附最均在pH为6h达到最佳；在实验所选温度范围内，胞外聚合物在30℃时对Cd^2＋的吸附量最大．而温度对Cd^2＋在微生物非活性细胞和活性细胞的影响不显著；Cd^2＋在3种有机组分上的吸附均符合Langmuir和Freundlish热力学方程，吸附能力为胞外聚合物〉微生物非活性细胞〉微生物活性细胞。在有Pb^2＋共存的条件下，Langmuir和Freundlish热力学方程仍然适合描述3种有机组分对Cd^2＋的热力学吸附过程，但Cd^2＋的吸附量和饱和吸附最均减小。     

群感效应与信号分子在污泥颗粒化过程中的作用研究进展

好氧颗粒污泥具有良好的沉降性能和较好的污水处理效果等优点.本文综述好氧颗粒污泥的形成过程,重点分析在污泥颗粒化过程中群感效应和细胞信号分子的作用.研究发现,群感效应和细胞信号分子在污泥颗粒化过程中发挥着重要作用,群感效应可以加快污泥胞外聚合物合成和提高微生物表面附着能力,信号分子可以促进微生物分泌胞外聚合物并影响生物膜的形成.举例说明信号分子中的c-di-GMP作为第二信使在污泥颗粒化过程中的重要作用,c-di-GMP可以将细菌从单细胞游走型转变为多细胞黏附型——生物膜状态.投加钙离子会促进能够分泌c-diGMP的菌群生长从而加快好氧颗粒污泥的形成,投加锰离子会减少好氧颗粒污泥中c-di-GMP的含量导致好氧颗粒污泥解体.最后进行前景展望,认为从群感效应和信号分子的角度去解析好氧颗粒污泥形成机理,可为确立好氧颗粒污泥形成机制奠定理论基础,对其进一步的工程化应用具有现实意义.     

低温生物膜和活性污泥的生物活性比较

通过 (5± 1)℃下生物膜系统 (BF)和活性污泥系统 (AS)处理生活污水长达 8个多月的运行 ,对比研究了两系统的生物活性 .结果表明 ,活性污泥不仅生物活性较高 ,而且具有更有利的传质条件 .在水力停留时间HRT =8h的条件下 ,生物膜和活性污泥胞外分泌物中的还原糖含量分别为 1.75 %及 1.9% ,挥发性污泥组分 (VSS)中的ATP含量分别为 1.0 8mg/ g及 1.4 3mg/g ;电镜检测结果表明 ,生物膜结构致密 ,而活性污泥疏松多孔有利于物质传递 .图 5表 2参 14     

生物膜及其组分对4-氯酚的吸附速率研究

研究了４－氯酚在生物膜不同组分上的吸附速率特征．本实验中生物膜不同组分包括生长有生物膜外壳的模拟水体悬浮颗粒物(高岭土)、细菌细胞、胞外多糖、高岭土及有胞外多糖存在的高岭土５个部分．结果表明,生物膜及其不同组分均对４－氯酚发生吸附,以细菌细胞更为显著,但它们的时间动力学过程不同． 在所研究的５种吸附体系中,生长有生物膜外壳的高岭上体系较快地达到近平衡状态．并且吸附时间过程受ｐＨ值的影响．     

有机底物对活性污泥胞外聚合物的影响

研究了城市污水中常见的具有不同特性的有机底物(蛋白胨、葡萄糖、乙酸钠,以及乙酸钠和葡萄糖的混合物)分别在四个相同的反应器中所培养的活性污泥胞外聚合物的量和组成．结果表明：有机底物的特性影响胞外聚合物的组成和量,在乙酸钠为底物的污泥中,胞外多糖占大部分(糖类／蛋白质的比值为1．7—8.6,质量比),而以蛋白胨为底物时,胞外蛋白质占主要成分(糖类／蛋白质的比值为0.2-0.5);以乙酸钠为底物形成的胞外聚合物的总量较多,通过扫描电子显微镜和原子力显微镜对活性污泥进行观测,确证了胞外聚合物的存在及其形式,并得到了胞外聚合物层的大致尺寸．     

生物膜及其组分对4—氯酚的吸附速率研究^1）

研究了4－氯酚在生物膜不同组分上的吸附速率特征,本实验中生物膜不同组组分包括生长有生的膜外壳的模拟水体悬浮颗粒物（高岭土）,细胞细胞,胞外多糖高岭土及有胞外多糖存在的高岭土5个部分,结果表明,生物膜及其不同组分均对4氯酚发生吸附,以细菌细胞更为显著,但它们的时间动力学过程不同,在研究的5种吸附体系中,生长有生物膜外壳的高岭土体系较快地达到近平衡状态,并且吸附时间过程受pH值的影响。     

好氧颗粒污泥胞外聚合物的产生及其分布

考察了不同操作条件和基质条件对好氧颗粒污泥中胞外聚合物(EPS)产生的影响及其在污泥和体系上清液中的分布.结果表明:随体系操作条件和基质条件的变化,好氧颗粒污泥内部和上清液中的EPS含量呈规律性变化.相对而言,好氧颗粒污泥中EPS含量的变化幅度较小,过多的EPS则释放到上清液中.大量EPS的释放只发生在颗粒污泥解体时,而酸性条件和不适当的C/N比不利于好氧颗粒污泥的形成及形态保持.体系溶解氧为4.5 mg·l-1,pH为中性,污泥负荷小于等于0.37kgCOD·kg-1MLSS·d-1,碳氮比为20∶ 1时,好氧颗粒污泥中EPS的含量约占污泥总质量的9%-12%,与厌氧颗粒污泥(0.6%-20%)相近,但远低于絮状活性污泥(80%),此时,EPS在上清液中的含量最低或接近最低,为14-26 mg·l-1.     

武汉东湖秋季水体中光合自氧生物膜的生长特性

利用一种自行设计的光合自氧生物膜采样装置,在武汉东湖(重富营养化湖泊)20和100 cm水深处自然培养和收集光合自氧生物膜,研究其生长发育及活性特点.结果表明:富营养化水体中光合自氧生物膜生长经历了潜伏适应期、增长期、脱落期和恢复生长期4个阶段;光合自氧生物膜生物量、胞外多糖含量、COD含量和脱氢酶活性随培养时间延长呈稳定增长趋势;20 cm水深处光合自氧生物膜生长总体上快于100 cm水深处,并且其生物量和活性也较高;光合自氧生物膜的生理特征与一般天然水体中生长的相似,说明重富营养化水体对生物膜的胁迫作用不明显.     

再生水环境中杀菌剂对SS316L表面生物膜活性与电化学行为影响

本文应用生物化学和电化学分析方法研究了发电厂循环水系统常用杀菌剂NaClO和十二烷基二甲基苄基氯化铵(1227)对硫酸盐还原菌(SRB)脱氢酶活性,胞外聚合物(EPS)以及对不锈钢SS316L表面生物膜电化学行为的影响.结果表明,2种杀菌剂均有效地降低了细菌脱氢酶活性和细菌代谢产物EPS中多糖和蛋白质的含量.其中NaClO和1227对多糖削减水平相当,平均降幅均为72 mass%;NaClO对蛋白质削减效果较为明显,平均降幅为60 mass%,而1227对蛋白质的平均降幅为48 mass%.添加2种杀菌剂后,SS316电极表面溶解电流随时间缓慢下降,表明这两种杀菌剂在一定程度上能够减缓SRB生物膜对SS316L表面的电化学腐蚀.1227能够维持SS316电极表面较为稳定的溶解电流和钝化区间.     

The role of extracellular polymeric substances on the sorption of pentachlorophenol onto natural biofilms in different incubation times: a fluorescence study

Extracellular polymeric substances (EPS) have been regarded as the most significant components in sorbing organic contaminants onto natural biofilms. However, few investigations have reported the effects of EPS on the sorption of organic contaminants onto biofilms in different incubation times. Here, pentachlorophenol (PCP), selected as a model organic pollutant, was sorbed by biofilms and EPS-free biofilms cultured for 15, 30, and 45 days, to evaluate the role of EPS in the sorption process. EPS were extracted from biofilms to investigate the binding mechanism of PCP to the fluorescence matters in EPS by fluorescence quenching titration. Results showed that EPS, bound with biofilms or released to water, could increase or decrease the sorption amounts of PCP on biofilms in various incubation times. The presence of bound EPS in biofilms enhanced the sorption amounts of 30-day biofilms (6.0?±?0.11?μmol?g^?1) because of the formation of the EPS-PCP complex between PCP and fluorescence matters in EPS, such as protein-like matters. In contrast, the release of PCP-bound EPS in 15- and 45-day biofilms decreased the sorption amounts of PCP on biofilms. All the results suggested that EPS dominated the sorption of PCP onto biofilms.     

Extracellular polymeric substances (EPS) from cyanobacterial mats: characterisation and isolation method optimisation

Extracellular polymeric substances (EPS) play an important role in bacterial mat formation and sediment stabilisation of coastal zones. The analysis of these secretion products on a molecular level is a prerequisite to understand their formation mechanisms and ecological function in microbial consortia. The present study focuses on the optimisation of EPS isolation and characterisation from cohesive cyanobacterial mats. Extracted EPS were analysed for quantity, content of total organic carbon and nitrogen, and bulk contents of neutral sugars, uronic acids, and proteins. These criteria are strongly influenced by the extraction conditions applied and therefore, the effects of different extraction media (NaCl or artificial seawater), addition of EDTA, centrifugal force, and purification via repeated ethanol precipitation on extraction success were determined. From this an optimised extraction procedure for EPS resulted. When using fresh mat samples, the yield of EPS amounted to 3.3 ± 0.8 mg g⁻¹ mat (dw). The isolated EPS were composed of nearly equal amounts of proteins and uronic acids (12.7 ± 1.5 and 11.8 ± 1.1%, respectively) and the bulk content of neutral sugars was 30.5 ± 2.6%. High contents of TOC and TN indicated relatively pure EPS and only a low contribution of inorganic compounds. Furthermore, low contents of 2-keto-3-deoxyoctonate and the small protein/polysaccharide-ratio in the EPS extracted by our method, signified low contaminations by intracellular polymers and hence a low rupture of cells. Our method provides an useful tool to evaluate further investigations of the composition, characteristics and properties of EPS on a sound basis.     

水溶性有机酸对萘溶解度及迁移性能的影响

通过热力学的方法,研究了水溶性有机酸对萘的溶解度及迁移性能的影响,结果表明,萘的溶解度和萘由纯水向不同浓度有机酸溶液的迁移能力随着有机酸浓度的增加而增加,但这种趋势并非简单的线性增加,当有机酸浓度超过一定数值后,萘的溶解度会突然增大,迁移趋势会明显增加.这种变化与在稀溶液中形成的水包有机酸笼合物结构有关.     

胞外聚合物物理法提取过程的优化

对物理法提取活性污泥中的胞外聚合物(EPS)进行了优化.分别考察了超声时间、振摇时间、离心速度和时间以及加热时间对EPS的松散附着(LB)和紧密粘附(TB)提取的影响,得出污泥EPS物理法提取的优化方案.     

Characterization of the dissolved organic matter in sewage effluent of sequence batch reactor: the impact of carbon source

Dissolved organic matter (DOM) transformation in sequence batch reactor (SBR) fed with carbon sources of different biodegradability was investigated. During the biologic degradation process, the low molecular weight (MW) fraction (< 1 kDa) gradually decreased, while the refractory compounds with higher aromaticity were aggregated. Size exclusion chromatography (SEC) and fluorescence of excitation emission matrices (EEM) demonstrated that more biopolymers (polysaccharides or proteins) and humic-like substances were presented in the extracellular polymeric substance (EPS) extracted from the SBR fed with sodium acetate or glucose, while the EPS from SBR fed with slowly biodegradable dissolved organic carbon (DOC) substratestarch had relatively less biopolymers. Comparing the EfOM in sewage effluent of three SBRs, the effluent from SBR fed with starch is more aromatic. Organic carbon with MW>1 kDa as well as the hydrophobic fraction in DOM gradually increased with the carbon sources changing from sodium acetate to glucose and starch. The DOC fractionation and the EEM all demonstrated that EfOM from the effluent of the SBR fed with starch contained more fulvic acid-like substances comparing with the SBR fed with sodium acetate and glucose.     

Influence of aeration intensity on the performance of A/O-type sequencing batch MBR system treating azo dye wastewater

Among the numerous parameters affecting the membrane bioreactor (MBR) performance, the aeration intensity is one of the most important factors. In the present investigation, an anoxic/aerobic-type (A/O-type) sequencing batch MBR system, added anoxic process as a pretreatment to improve the biodegradability of azo dye wastewater, was investigated under different aeration intensities and the impact of the aeration intensity on effluent quantity, sludge properties, extracellular polymeric substances (EPS) amount generated as well as the change of permeation flux were examined. Neither lower nor higher aeration intensities could improve A/O-type sequencing batch MBR performances. The results showed 0.15 m³·h^-1 aeration intensity was promising for treatment of azo dye wastewater under the conditions examined. Under this aeration intensity, chemical oxygen demand (COD), ammonium nitrogen and color removal as well as membrane flux amounted to 97.8%, 96.5%, 98.7% and 6.21 L·m^-2·h^-1, respectively. The effluent quality, with 25.0 mg·L^-1COD, 0.84 mg·L^-1 ammonium nitrogen and 8 chroma, could directly meet the reuse standard in China. In the meantime, the sludge relative hydrophobicity, the bound EPS, soluble EPS and EPS amounts contained in the membrane fouling layer were 70.3%, 52.0 mg·g^-1VSS, 38.8 mg·g^-1VSS and 90.8 mg·g^-1VSS, respectively, which showed close relationships to both pollutant removals and membrane flux.     

Characterisation of an extracellular polysaccharide produced by Bacillus mucilaginosus MY6-2 and its application in metal biosorption

A novel extracellular bioflocculant from Bacillus mucilaginosus MY6-2 was obtained by alcohol precipitation, dialysis and lyophilisation. The chemical analysis indicated that the bioflocculant was mainly composed of extracellular polysaccharide (named EPS MY6-2). Monosacchride composition result analysed by Gas chromatography indicated that EPS MY6-2 was mainly composed of Man, Glc, Gal, GlcA and GalA. The result of flocculating characteristics indicated that pH, EPS dosage and cation supplement had evident effect on flocculating activity of EPS MY6-2. The biosorption of iron ions from aqueous solution was tested with respect to pH, initial metal ion concentration and EPS dosage. The optimum biosorption conditions were as follows: pH 5.0, initial ion concentration from 200 to 800 mg/L and EPS dosage of 60 mg/L ion solution. The adsorption rates are maintained above 95% under these conditions. The adsorption data provided an excellent fit to both Langmuir and Freundlich isotherms, implying that the binding of the iron ions took place as a monolayer on the surface of the EPS.     

有机质腐解对穗花狐尾藻生长及磷积累的影响

在室内以原沉积物（处理1）和分别添加0.5%与1%有机质（植物残体）（处理2和处理3）的沉积物作为底质培养沉水植物,研究了植物残体的腐解对穗花狐尾藻生长及各器官磷积累的影响。结果表明：在试验的早期阶段,植物残体的腐解对狐尾藻的生长及磷积累有一定的抑制,其干质量积累量与磷积累量均表现为处理1〉处理2〉处理3,与处理1相比,处理2和处理3植株干质量积累量分别降低了16.9%和24.35%,磷积累量降低了24.38%和44.18%;但在培养的中后期,则表现为处理2〉处理3〉处理1,与处理1相比,处理2和处理3的穗花狐尾藻干质量和磷积累量分别增加了22.45%和7.48%、75.53%和17.21%。整个培养实验结果表明低含量植物残体的残留,促进了植株生长及磷积累,但当植物残体残留过高时,沉水植物的生长及磷积累受到抑制。3个处理不同器官干质量和磷分配比均表现为叶〉茎〉根,叶是穗花狐尾藻主要的磷累积器官。     

珠江三角洲第四纪各地层生成与存储天然铵能力的探讨与对比

珠江三角洲第四纪底部含水层当中的天异常高然铵,来自于第四纪沉积当中的有机质在厌氧条件下的矿化。珠江三角洲第四纪晚期的沉积序列,主要包括两层海相沉积层（M1和 M2）,以及两层陆相沉积层（T1和 T2）。然而,截至目前,上述地层对天然铵的生成与存储作用,尚不明确。从三角洲的内陆到近岸,选取重点钻孔BJ8、SD1、SD14和MZ4,利用准确的定年数据,以及钻孔剖面各类铵以及总有机碳等数据,探讨与比较了珠江三角洲第四纪各地层生成与储存天然铵的能力。结果表明：全新世时期的海相沉积层（M1）,具有高达17.4 g·kg-1的沉积有机质质量分数。对 SD14钻孔剖面上高精度的有机碳分析表明,M1、M2层平均有机质质量分数分别为11.7和10.1 g·kg-1。因此,相对于晚更新世时期的海相沉积层（M2）来说,全新世海相沉积层M1具备生成更多铵的能力。对SD14钻孔剖面上各类铵的分析表明,M1和M2总铵质量分数的平均值分别为0.41和0.31 g·kg-1;M1、M2和T2各地层单位面积所储存铵的平均值分别为28.6、11.25和0.34 kg·m-2。而不同地层铵含量的差异,在该研究关注的其他钻孔 BJ8,SD1和 MZ4也非常明显。因此得出结论,全新世海相沉积层M1,是主要的储铵层,而M2则是次要的储铵层。两个陆相沉积层T1和T2,不论在生铵和储铵的功能上,远远小于两个海相沉积层。在 M1层中,铵的量呈现随深度增加而升高的趋势,原因在于铵不断生成累积,并通过扩散作用向下运移。而M2层中铵的含量呈现由上至下递减的趋势,说明M2层中的铵主要来自于上部M1层的扩散,其本身生成铵的量比M1少。M1层在珠江三角洲广泛发育,M2层经过长期的风化和剥蚀,在珠江三角洲许多地方已缺失。珠江三角洲底部含水层中天然高铵的浓度,主要由M1层生成与存储的铵的总量所决定。     

微耗损固相微萃取技术及其在有机污染物自由溶解态浓度测定中的应用

自由溶解态浓度可用于评价污染物的生物有效性,评估污染物的环境风险.本文介绍了微耗损固相微萃取(nd-SPME)技术测定自由溶解态浓度的原理、测定条件和基质干扰等影响因素,并着重总结归纳了nd-SPME技术在在环境基质和生物基质中有机污染物自由溶解态浓度测定中的应用.