菌株Pseudomonas sp.JF122降解苯酚同时还原Cr(Ⅵ)的条件优化及生长特性研究

采用富集培养法,从钢铁厂附近河流污泥中分离筛选到1株能同时降解苯酚与还原Cr(Ⅵ)的菌株JF122.在600 mg.L-1苯酚与1.2mg·L-1 Cr(Ⅵ)的条件下,采用单因素实验考察了温度、初始pH、该菌接种量等因素对其同时降解苯酚与还原Cr(Ⅵ)的影响,并通过正交试验L9(33)获得适宜的苯酚降解与Cr(Ⅵ)还原条件.结果表明,菌株JF122降解苯酚与还原Cr(Ⅵ)的适宜条件为:30℃、初始pH=6和接种量1％,此条件下,菌株JF122在56 h内能够降解600 mg·L-1苯酚同时还原1.2 mg·L-1 Cr(Ⅵ).应用响应曲面法建立了菌株JF122的生长与温度、初始pH、接种量等因素间关系的数学模型,并对其生长条件进行了优化.结果表明,菌株JF122最优生长条件与其降解苯酚并同时还原Cr(Ⅵ)的最优条件具有一致性.     

苯酚降解菌CM-HZX1菌株的分离、鉴定及降解性能研究

从污水处理厂的活性污泥中分离出一株以苯酚为唯一碳源生长的高效降解苯酚菌CM-HZX1.通过形态特征、生理生化及16S r DNA基因序列分析,初步鉴定菌株属于红球菌(Rhodococcus sp.),16S r DNA在Gene Bank的登录号为KM014567.实验结果表明,菌株CM-HZX1培养及降解苯酚的最适条件为p H=7.0,温度30℃,转速为150 r·min~(-1).该菌株能耐受4%的盐度,适应性强.0.5 g·L~(-1)苯酚在24 h时的降解率可达93.6%,1.5 g·L~(-1)苯酚在48 h时的降解率在90%以上.研究表明,该菌株在处理工业含酚废水方面具有广阔的应用前景.     

Biodegradation of pendimethalin by Bacillus subtilis Y3

A bacterium strain Y3,capable of efficiently degrading pendimethalin,was isolated from activated sludge and identified as Bacillus subtilis according to its phenotypic features and 16 S rRNA phylogenetic analysis.This strain could grow on pendimethalin as a sole carbon source and degrade 99.5%of 100 mg/L pendimethalin within 2.5 days in batch liquid culture,demonstrating a greater efficiency than any other reported strains.Three metabolic products,6-aminopendimethalin,5-amino-2-methyl-3-nitroso-4-(pentan-3-ylamino) benzoic acid,and 8-amino-2-ethyl-5-(hydroxymethyl)-1,2-dihydroquinoxaline-6-carboxylic acid,were identified by HPLC-MS/MS,and a new microbial degradation pathway was proposed.A nitroreductase catalyzing nitroreduction of pendimethalin to 6-aminopendimethalin was detected in the cell lysate of strain Y3.The cofactor was nicotinamide adenine dinucleotide phosphate(NADPH) or more preferably nicotinamide adenine dinucleotide(NADH).The optimal temperature and pH for the nitroreductase were 30℃ and 7.5,respectively.Hg~(2+),Ni~(2+),Pb~(2+),Co~(2+),Mn~(2+) Cu~(2+),Ag~+,and EDTA severely inhibited the nitroreductase activity,whereas Fe~(2+),Mg~(2+),and Ca~(2+) enhanced it.This study provides an efficient pendimethalin-degrading microorganism and broadens the knowledge of the microbial degradation pathway of pendimethalin.     

Methyl-β-cyclodextrin enhanced biodegradation of polycyclic aromatic hydrocarbons and associated microbial activity in contaminated soil

The contamination of soils by polycyclic aromatic hydrocarbons (PAHs) is a widespread environmental problem and the remediation of PAHs from these areas has been a major concern.The effectiveness of ma...     

耐受铅真菌的筛选及其对Pb2+吸附的初步研究

从铅锌矿周围土壤样品中分离、筛选出一株耐铅真菌(命名为PY),对菌株进行了形态观察、生理生化实验及18SrRNA序列分析,并对该菌株的生物吸附性能进行了分析试验.结果表明,菌株PY为镰刀菌属(JQ267373),该菌株在Pb2+浓度550mg·L-1、湿菌量10g·L-1、pH=5.5、25℃、160r·min-1的条件下振荡吸附75min时,对Pb2+的吸附率可达到84%,吸附量为46.2mg·g-1.在Pb2+浓度为750mg·L-1时,其吸附率为77.9%.在25℃时,菌株PY对Pb2+的吸附模型符合Langmuir和Freundlich吸附等温方程.     

Metabolism of n-C10:0 and n-C11:0 fatty acids by Trichoderma koningii,Penicillium janthinellum and their mixed culture: I. Biomass and CO2 production,and allocation of intracellular lipids

The capacity of two soil fungi, Trichoderma koningii and Penicillium janthinellum, to oxidize n-C_10:0 and n-C_11:0 fatty acids to CO₂ and store intracellular lipids during growth is unknown. This article reports for the first time the metabolism of decanoic acid (DA, C_10:0), undecanoic acid (UDA, n-C_11:0), a mixture of the acids (UDA+DA) and a mixture of UDA+ potato dextrose broth (PDB) by T. koningii and P. janthinellum and their mixed culture. A control PDB complex substrate was used as a substrate control treatment. The fungal cultures were assayed for their capacity to: (1) oxidize n-C_10:0 and n-C_11:0 fatty acids to CO₂ and (2) store lipids intracellularly during growth. On all four fatty acid substrates, the mixed T. koningii and P. janthinellum culture produced more biomass and CO₂ than the individual fungal cultures. Per 150 mL culture, the mixed species culture grown on UDA+PDB and on PDB alone produced the most biomass (7,567 mg and 11,425 mg, respectively). When grown in DA, the mixed species culture produced the least amount of biomass (6,400 mg), a quantity that was lower than those obtained in UDA (7,550 mg) or UDA+DA (7,270 mg). Amounts of CO₂ produced ranged from 210 mg under DA to 618 mg under PDB, and these amounts were highly correlated with biomass (r² = 0.99). Fluorescence microscopy of stained lipids in the mixed fungal cell cultures growing during the exponential phase demonstrated larger fungal cells and higher accumulation of lipids in membranes and storage bodies than those observed during the lag and stationary phases. T. koningii and P. janthinellum grown on n-C_10:0 and n-C_11:0 fatty acids produced lower amounts of biomass and CO₂, but stored higher amounts of intracellular lipids, than when grown on PDB alone.     

Colonization of Penicillium oxalicum SL2 in Pb-contaminated paddy soil and its immobilization effect on soil Pb

Penicillium oxalicum SL2 (SL2) is a previously screened Pb-tolerant fungus that can promote crops growth. The relationship between SL2 colonization and Pb immobilization was studied to provide a theoretical basis for microbial remediation of Pb-contaminated paddy soil. In this study, green fluorescent protein (GFP) labeled SL2 was inoculated into different Pb-contaminated paddy soils (S1-S6). The Pb extracted from the soil by HNO₃, EDTA and CaCl₂ were used to characterize the available Pb. The results showed that the colonization of SL2 was divided into lag phase (0-7 days), growth phase (7-30 days), and mortality phase (30-90 days). SL2 colonized well in sandy soils rich in clay and total phosphorus with initial pH of 4.5-7.0. In addition, SL2 increased soil pH and decreased soil Eh, which was beneficial to immobilize Pb. In different soils, the highest percentages of CaCl₂-Pb, EDTA-Pb, and HNO₃-Pb immobilized by SL2 were 34.34%-40.53%, 17.05%-20.11%, and 7.39%-15.62%, respectively. Pearson correlation analysis showed that the percentages of CaCl₂-Pb and EDTA-Pb immobilized by SL2 were significantly positively correlated with the number of SL2 during the growth phase. SL2 mainly immobilized Pb in the growth phase and a higher peak number of SL2 was beneficial to the immobilization of Pb.     

多效唑的生物降解性研究

利用从多效唑生产废水排放口土壤中富集获得的混合微生物和纯培养菌研究多效唑的生物降解性。结果表明，微生物生物量与多效唑相对浓度之间呈高度负相关（ｒ＝－０９３）。混合微生物降解多效唑较纯培养菌株快，降解的最适温度为３０℃，最适ｐＨ值为７０，对高ｐＨ值有耐受性。好氧和厌氧条件下微生物均能降解多效唑。富集培养物中的主要构成菌为假单孢菌属（Ｐｓｅｕｄｏｍｏｎａｓｓｐ）。降解动力学反应遵循Ｍｏｎｏｄ关系式。     

Mineralization of p-nitrophenol by a new isolate Arthrobacter sp. Y1

Arthrobacter sp. Y1, capable of metabolizing p-nitrophenol (PNP) as the sole carbon, nitrogen and energy source was isolated from activated sludge. The bacterium could tolerate concentrations of PNP up to 600 mg L^{? 1}, and degradation of PNP was achieved within 120 h of incubation. PNP and its metabolites were analyzed by high performance liquid chromatography (HPLC). The metabolite formed indicated that the organism followed the 4-nitrocathechol (4-NC) pathway for metabolism of this compound. The relevant degrading-enzyme was extracellular. Addition of other carbon source (glucose 0～ 30 g L^{? 1}) led to accelerated degradation. If the glucose concentration exceeded 30 g L^{? 1}, however, degradation was repressed. Spectrophotometry assay of the nitrite and genotoxic study showed that strain Y1 could detoxify PNP. Therefore, the present study may provide a basis for the development of the bioremediation strategies to remedy the pollutants in the environment.     

胶网藻对水体中恩诺沙星的毒性响应及去除作用

恩诺沙星是医药及水产养殖业广泛使用的喹诺酮类抗生素,是我国地表水中残留量较多的抗生素种类之一;然而有关该抗生素对水体中浮游植物毒理作用以及后者对其去除作用的研究还鲜见报道.本研究以绿藻门的胶网藻(Dictyosphaerium sp.)为对象,通过12 d室内培养实验,分析在不同浓度(0、 5、 25、 50和100 mg·L~(-1))恩诺沙星暴露的条件下,胶网藻的生长、光合作用活力和胞外多糖的响应变化及其对不同浓度恩诺沙星的去除效率.结果表明,各处理组中胶网藻的生物量和光合色素含量均随培养时间的增加而升高,但与对照组相比,恩诺沙星对胶网藻的生长和光合色素积累均产生显著抑制作用(P0.01).通过拟合分析,计算出恩诺沙星对胶网藻96 h半数致死浓度(LC_(50))为(241.29±7.33) mg·L~(-1),表明胶网藻能够适应高浓度的恩诺沙星胁迫.同时发现,当恩诺沙星浓度5 mg·L~(-1)时,能够促进胶网藻的最大光合速率(F_v/F_m),但浓度5 mg·L~(-1)时则对胶网藻具有抑制作用(P0.01);实际光合速率(Yeild)和最大电子传递速率(ETR_(max))在12 d内呈现先降后升的变化趋势,胶网藻在6 d后可逐渐适应胁迫环境而恢复一定的光合活力.此外,恩诺沙星可刺激胶网藻释放胞外多糖,水溶性多糖(RPS)和胞外胶鞘多糖(CPS)含量均随恩诺沙星浓度升高而增加.实验结束时, 4个无藻对照组(5、 25、 50和100 mg·L~(-1))中恩诺沙星的去除率分别为7.27%、 5.56%、 5.30%和4.88%,而添加胶网藻的处理组其去除率分别为对照组的3.21、 3.01、 2.69和2.83倍,表明胶网藻对于恩诺沙星的去除具有显著的促进作用(P0.01).本研究结果为理解喹诺酮类抗生素对水体初级生产者的生态毒性提供了新资料,同时也为水体抗生素残留的生态去除和淡水微藻的生物资源化利用提供了新的思路.