固定化微生物絮凝菌在废水脱色中的应用

从筛选到的微生物絮凝菌中构建出比单一菌群产生更高絮凝活性絮凝剂的复合菌群,并对其进行固定化,将固定化后的细胞应用于染料废水的处理。研究发现,利用海藻酸钙包埋絮凝菌能较长时间保持细胞高的活性,且固定化菌群对染料废水具有较好的脱色效果,并在一定程度上可以达到连续生产絮凝剂的目的。     

生物铁-复合菌处理牛仔布印染废水

针对生化池1种或几种菌种启动慢、抗冲击负荷能力差和污泥处理效率低的问题,提出用生物铁法结合生物强化技术、投加复合优势菌的处理方法,应用于牛仔布染整废水处理,COD去除率、脱色率分别达到96%、99%,产泥量可减少80%以上,每吨水节约成本60%,吨水处理费用1.6~1.9元,无二次污染,可推广应用。     

土壤甲胺磷抗性细菌种群特征脂肪酸生物标记的分析（Characteristics of PLFA Biomarkers for Acephatemet Resistant Bacteria Isolated from the Soils）

应用高浓度甲胺磷培养基,对农药厂排污口土壤微生物进行分离,鉴定出21株细菌,分属13个细菌属.对甲胺磷抗性细菌脂肪酸的分析,共测定到38个脂肪酸生物标记(PLFA),这些生物标记分为4种类型,即1)高频次分布的生物标记,普遍存在于细菌类群,属于细菌总体类群(Bacteriaingeneral)的生物标记;2)中频次分布的生物标记,在细菌种出现概率中等,可以用于代表细菌属类群(Bacteriumgenus)识别生物标记;3)低频次分布的生物标记,在细菌中的分布概率较小,可以用于指示特定细菌种间差异的生物标记;4)微频次分布的生物标记,这种生物标记仅在一种细菌种类出现,是细菌种特征生物标记.利用脂肪酸生物标记分析同属细菌不同种的差异,可将假单胞杆菌属分为2类,第1类包括了铜绿假单胞菌、荧光假单胞菌、丁香假单胞菌,其特征为17:0CYCLO生物标记含量小于3.60%;第2类包含了伞菌假单胞菌、威隆假单胞菌、恶臭假单胞菌、温哥华假单胞菌,其特征为17:0CYCLO生物标记含量大于5.99%.利用脂肪酸生物标记的差异对甲胺磷抗性细菌种的聚类分析,能有效地将细菌类群分为3类,微生物群落中存在着稳定的生物标记和受环境影响的生物标记,论文提供了一种脂肪酸生物标记的分析方法,结合细菌的生物学特性研究,可以解释微生物在环境中的变化,对于土壤微生物群落的研究具有重要意义.     

人工湿地污水处理系统春季空气微生物群落结构分析?

通过构建16S/18S rDNA基因文库,分析自由表面流人工湿地污水处理系统春季空气细菌和空气真菌群落结构特征.结果表明,空气细菌分布在变形菌门(Proteobacteria)、放线菌门(Actinobacteria)、浮霉菌门(Planctomycetes)、蓝藻门(Cyanophyta)、绿弯菌门(Chloroflexi)、拟杆菌门(Bacteroidetes)和厚壁菌门(Firmicutes),主要为β-变形菌纲(71.04%)、γ-变形菌纲(12.03%)、α-变形菌纲(3.83%)、蓝藻纲(4.38%)、芽孢杆菌纲(3.28%)和鞘脂杆菌纲(2.19%),优势菌属是马赛菌属(Massilia 66.66%)、假单胞菌属(Pseudomonas 4.37%)、蓝丝细菌属(Cyanothece 3.83%)和沙雷氏菌属(Serratia 3.28%).空气真菌主要类群为座囊菌纲(Dothideomycetes 61.18%),其次是接合菌纲(Zygomycetes 16.47%)、盘菌纲(Discomycetes 14.12%),优势菌属是核腔菌属(Pyrenophora 48.31%)、被孢霉属(Mortierella 15.7%)、缘刺盘菌属(Cheilymenia 12.4%)、Boothiomyces (4.5%).人工湿地空气微生物中未检测出大肠杆菌(Escherichia coli)、沙门氏菌(Salmonella spp.)和产气荚膜梭菌(Clostridium perfringens),但存在粘质沙雷氏菌(S. marcescens)、恶臭假单胞菌(P. putida)、表皮葡萄球菌(Staphylococcus epidermidis)等致病菌或条件致病菌.     

北京大气降水中细菌气溶胶的多样性研究

利用16S rRNA基因测序分类学技术,分别以北京市区2011及2012年不同月份的降水样品中细菌的基因组DNA为模板,通过克隆、测序构建基因组文库,研究了北京市大气降水中细菌的群落结构组成及多样性变化.系统发育分析结果表明,变形菌门(Proteobacteria) (α-,β-,γ-)是北京市降水样品中细菌的优势菌群(75.6%~100%),另外包括拟杆菌门(Bacteroidetes)、放线菌门(Actinobacteria)、异常球菌门(Deinococcus-Thermus)、蓝藻门(Cyanobacteria)、硝化螺菌门(Nitrospira)、厚壁菌门(Firmicutes)共7个主要门类的细菌,以及未定菌(TM7).多样性指数分析结果显示,不同的降水样品,细菌群落结构组成及多样性均存在着差异性,冬季12月份雪水样品细菌群落结构多样性明显高于其他季节的样品,细菌群落多样性(Shannon, H)特点是,冬季>秋季>夏季.     

不同时期条纹环沟藻可培养藻际细菌研究

通过梯度稀释法分离出条纹环沟藻5个生长时期的可培养藻际细菌,利用基于单菌落16S rDNA V3区序列测定对细菌进行了分子分类鉴定,与GenBank上的相似菌株序列构建了邻接系统发育树并计算遗传距离,同时对不同时期的细菌进行了定量分析.结果表明,在分离培养出的32株细菌中,有12株不同种属细菌.12株细菌分属于a-变形菌纲(Alphaproteobacteria)、g-变形菌纲(Gammaproteobacteria)、拟杆菌门(Bacteroidetes)和放线菌门(Actinobacteria)4大细菌类群,在种类和数量上均以α-变形菌纲为主,其次为g-变形菌纲和拟杆菌门.每个生长时期可培养藻际细菌的种类数为5~8种,其中稳定生长期细菌种类数较为丰富,而在迟滞期和衰亡后期细菌种类较少.从各时期的细菌总数来看,对数生长期细菌数量最低,仅为2.83×106CFU/mL;在衰亡前期细菌数量最高,达到1.72×109CFU/mL;衰亡后期虽然细菌数量有所降低,但仍达到1.37×108CFU/mL.聚类分析和多维尺度分析结果显示,衰亡前期细菌群落结构与其它时期差异较大,而藻细胞快速生长阶段的对数生长期和稳定生长期菌落结构相近.衰亡前期特异性菌株鲍氏不动杆菌(Acinetobacter baumannii)的大量出现,可能与藻类迅速进入衰亡阶段有关;而各个时期均出现的一株麦氏交替单胞菌(Alteromonas macleodii)可能对条纹环沟藻的种群竞争起作用.在条纹环沟藻不同生长时期藻际细菌的种类与数量有所差异,藻际细菌的群落结构可能对条纹环沟藻的生长、种群竞争以及赤潮的生消具有重要作用.     

Characterization of CANON reactor performance and microbial community shifts with elevated COD/N ratios under a continuous aeration mode

COD/N at low ratios (0–0.82) improved N removals of CANON. CANON performance decreased after COD/N up to 0.82. The relative abundance of AOB decreased continuously with increasing COD/N. AOB outcompeted at a high COD load led to CANON failure. The relative abundance of AnAOB decreased and increased with increasing COD/N. The effects of increasing COD/N on nitrogen removal performance and microbial structure were investigated in a SBR adopting a completely autotrophic nitrogen removal over nitrite process with a continuous aeration mode (DO at approximately 0.15–0.2 mg/L). As the COD/N increased from 0.1 to≤0.59, the nitrogen removal efficiency (NRE) increased from 88.7% to 95.5%; while at COD/N ratios of 0.59–0.82, the NRE remained at 90.7%–95.5%. As the COD/N increased from 0.82 to 1.07, the NRE decreased continuously until reaching 60.1%. Nitrosomonas sp. (AOB) and Candidatus Jettenia (anammox bacteria) were the main functional genera in the SBR. As the COD/N increased from 0.10 to 1.07, the relative abundance of Nitrosomonas decreased from 13.4% to 2.0%, while that of Candidatus Jettenia decreased from 35% to 9.9% with COD/N<0.82 then increased to 45.4% at a COD/N of 1.07. Aerobic heterotrophic bacteria outcompeted AOB at high COD loadings (650 mg/L) because of oxygen competition, which ultimately led to deteriorated nitrogen removal performance.     

养殖水体复合功能菌的分离及其性能

针对养殖水体中因氨态氮、硫化氢和小分子有机酸富营养化引起的污染问题,分离筛选出硝化细菌、反硝化细菌、光合细菌、硫化细菌和生物絮凝菌等具有不同生理功能的污染物治理菌株,经优化配伍制备出性能优良的复合功能菌,结果表明:硝化细菌对氨态氮的去除率达97.8%,亚硝态氮的去除率达95.7%,反硝化细菌对硝态氮的去除率为96.4%,光合细菌和硫化细菌对硫化氢的去除率为55%,微生物絮凝菌的絮凝效率为83%;复合功能菌对CODCr、NH4+-N,总氮、硫化物的去除率分别可达94.3%,89.6%,88.7%和71.3%。     

Effect of nitrobenzene on the performance and bacterial community in an expanded granular sludge bed reactor treating high-sulfate organic wastewater

Less than 50 mg/L nitrobenzene brought little effect on anaerobic sulfate reduction. Kinetics of sulfate reduction under different nitrobenzene contents was studied. Increased nitrobenzene contents greatly changed the bacterial community structure. Genus Desulfovibrio played the key role in anaerobic sulfate reduction process. Nitrobenzene (NB) is frequently found in wastewaters containing sulfate and may affect biological sulfate reduction process, but information is limited on the responses of sulfate reduction efficiency and microbial community to the increased NB contents. In this study, a laboratory-scale expanded granular sludge bed reactor was operated continuously to treat high-sulfate organic wastewater with increased NB contents. Results successfully demonstrated that the presence of more than 50 mg/L NB depressed sulfate reduction and such inhibition was partly reversible. Bath experiments showed that the maximum specific desulfuration activity (SDA) decreased from 135.80 mg SO₄^2?/gVSS/d to 30.78 mg SO₄^2?/gVSS/d when the NB contents increased from none to 400 mg/L. High-throughput sequencing showed that NB also greatly affected bacterial community structure. Bacteroidetes dominated in the bioreactor. The abundance of Proteobacteria increased with NB addition while Firmicutes presented an opposite trend. Proteobacteria gradually replaced Firmicutes for the dominance in response to the increase of influent NB concentrations. The genus Desulfovibrio was the dominant sulfate-reducing bacteria (SRB) with absence or presence of NB, but was inhibited under high content of NB. The results provided better understanding for the biological sulfate reduction under NB stress.     

Elimination of antibiotic resistance genes and control of horizontal transfer risk by UV-based treatment of drinking water: A mini review

Antibiotic-resistant bacteria and antibiotic resistance genes are in water bodies. UV/chlorination method is better to remove ARGs than UV or chlorination alone. Research on UV/hydrogen peroxide to eliminate ARGs is forthcoming. UV-based photocatalytic processes are effective to degrade ARGs. Antibiotic-resistant bacteria (ARB) and antibiotic resistance genes (ARGs) have been recognized as one of the biggest public health issues of the 21st century. Both ARB and ARGs have been determined in water after treatment with conventional disinfectants. Ultraviolet (UV) technology has been seen growth in application to disinfect the water. However, UV method alone is not adequate to degrade ARGs in water. Researchers are investigating the combination of UV with other oxidants (chlorine, hydrogen peroxide (H₂O₂), peroxymonosulfate (PMS), and photocatalysts) to harness the high reactivity of produced reactive species (Clž·, ClOž·ž, Clž₂·ž⁻, žž·OH, and SOž₄ž·⁻€) in such processes with constituents of cell (e.g., deoxyribonucleic acid (DNA) and its components) in order to increase the degradation efficiency of ARGs. This paper briefly reviews the current status of different UV-based treatments (UV/chlorination, UV/H₂O₂, UV/PMS, and UV-photocatalysis) to degrade ARGs and to control horizontal gene transfer (HGT) in water. The review also provides discussion on the mechanism of degradation of ARGs and application of q-PCR and gel electrophoresis to obtain insights of the fate of ARGs during UV-based treatment processes.