真菌-细菌修复石油污染土壤的协同作用机制研究

提出并研究了真菌和细菌协同强化原位修复石油污染土壤.从中原油田石油污染土壤中筛选出刺孢小克银汉霉菌(Cunninghamella echinulata)和阴沟肠杆菌(Enterobacter cloacae),在泥浆体系中考察了Cun.echinulata和E.cloacae的生长及其对石油烃的降解过程.结果表明,混合培养体系中细菌和真菌的数量最高分别为其纯培养体系的3倍和20倍,细胞衰亡则被明显推迟;混合培养体系中石油烃的去除率高于真菌和细菌纯培养体系石油烃去除率的总和;采用多次接种新鲜菌种的培养方式能够强化混合培养体系对石油烃的降解.在石油烃污染土壤中接入由Cun.echinulata和E.Cloacae所组成的真菌-细菌微生物制剂实施原位修复,结果表明,Cun.echinulata和E.Cloacae的生长及其对石油烃的降解不受土著微生物的抑制,最适工艺条件为:水和木屑含量分别为25%和6%(质量分数),Cun.echinulata和E.cloacae接种量分别为2.5×104和2.5 × 107CFU/g.接种上述真菌-细菌40 d后石油烃去除率可达约65%,而土著微生物对石油烃去除率为16.0%.     

麦秸强化微生物降解石油烃及场地试验

在油-盐混合污染耕地的耕作层中施加麦秸以强化水浸洗盐和促进微生物对石油烃的降解.通过实验考察了麦秸添加量对降解石油烃所用的阴沟肠杆菌(Enterobacter cloacae)和刺孢小克银汉霉菌(Cunninghamella echinulata)的生长及其对于石油烃降解行为的影响.结果发现,在土壤中添加5%(质量分数)麦秸可使土壤中的细菌和真菌生物量提高至对照样品的25和3倍;19 d时总石油烃降解率从29.2% 提高到48.0%,其中饱和烃、芳烃的降解率分别从31.5%和39.1%提高到55.7%和55.9%.在中原油田污染耕地现场试验结果表明,石油烃降解菌添加25 d后,添加麦秸的修复土壤中的细菌和真菌生物量为对照土壤的158和9倍;45 d后试验地块中的总石油烃质量分数降至0.3%以下,石油烃降解率最高达到75%.上述结果显示出添加麦秸与真菌-细菌协同修复方法相结合在治理油-盐混合污染耕地中具有很好的应用前景.     

Biodegradation of malathion, α- and β-endosulfan by bacterial strains isolated from agricultural soil in Veracruz,Mexico

The objective of this study was to evaluate the capacity of two bacterial strains isolated, cultivated, and purified from agricultural soils of Veracruz, Mexico, for biodegradation and mineralisation of malathion (diethyl 2-(dimethoxyphosphorothioyl) succinate) and α- and β-endosulfan (6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6-9-methano-2,4,3-benzodioxathiepine-3-oxide). The isolated bacterial strains were identified using biochemical and morphological characterization and the analysis of their 16S rDNA gene, as Enterobacter cloacae strain PMM16 (E1) and E. amnigenus strain XGL214 (M1). The E1 strain was able to degrade endosulfan, whereas the M1 strain was capable of degrading both pesticides. The E1 strain degraded 71.32% of α-endosulfan and 100% of β-endosulfan within 24 days. The absence of metabolites, such as endosulfan sulfate, endosulfan lactone, or endosulfan diol, would suggest degradation of endosulfan isomers through non-oxidative pathways. Malathion was completely eliminated by the M1 strain. The major metabolite was butanedioic acid. There was a time-dependent increase in bacterial biomass, typical of bacterial growth, correlated with the decrease in pesticide concentration. The CO₂ production also increased significantly with the addition of pesticides to the bacterial growth media, demonstrating that, under aerobic conditions, the bacteria utilized endosulfan and malathion as a carbon source. Here, two bacterial strains are shown to metabolize two toxic pesticides into non-toxic intermediates.     

Detection, isolation, and identification of cadmium-resistant bacteria based on PCR-DGGE

This study focused on the screening of cadmium-resistant bacterial strains from Pb-Zn tailing. We investigated the diversity of microbial community inhabiting Dong-san-cha Pb-Zn tailing in Beijing, China, by polymerase chain reaction-denaturing gradient gel electrophoresis （DGGE） of 16S rRNA gene of bacterial strain, and found two dominant strains in the DGGE profile. Using special culture media, we isolated two strong cadmium-resistant bacterial strains. On the basis of morphological, physiological, and biochemical characteristics, BIOLOG, and 16S rDNA sequencing, the two strains were identified as Bacillus cereus and Enterobacter cloacae. Minimal inhibitory concentrations （MICs） of heavy metals for the bacteria were determined. E. cloacae showed higher MIC values for heavy metals and a larger range of antibiotic resistance than B. cereus.     

一株高效广谱染料脱色菌脱色条件的优化

以模拟酸性大红3R染料废水为对象,在单因素实验基础上,选取温度、初始染料浓度、酵母粉浓度三因素为影响因子,以染料脱色率为响应值,利用Box-Behnken设计及响应面分析法研究了各因素对一株广谱型染料脱色菌株Enterobacter cloacae strain M3脱色效果的影响及各因素间交互作用,建立了二次多项式回归方程的预测模型,确定了菌株脱色酸性大红3R废水的优化条件。结果表明：回归方程极显著,拟合性好。最优脱色条件为温度36℃,染料浓度121.12 mg/L,酵母粉浓度1.99%,在此条件下,染料脱色率可达99.21%。经实验验证,实际值与模型预测值拟合良好,偏差仅为0.79%。     

Biodegradation of s-triazine herbicide atrazine by Enterobacter cloacae and Burkholderia cepacia sp. from long-term treated sugarcane-cultivated soils in Kenya

In this study soils from sugarcane-cultivated fields were screened for bacterial species capable of atrazine (6-chloro-N²-ethyl-N⁴-isopropyl-1,3,5-triazine-2,4-diamine) degradation due to long exposure of the soils to this herbicide. To enrich for atrazine degraders, Minimal Salt Medium containing atrazine as the sole N source and glucose as the C source was inoculated with soils impacted with this herbicide and incubated. Bacterial growth was monitored by measuring optical density. The degradation of atrazine was followed by measuring residual atrazine in liquid cultures over a given time period by high performance liquid chromatography. Bacterial strains isolated from the enrichment cultures were characterized by biochemical tests and identified by 16S rRNA gene sequencing. Two bacterial strains coded ISL 8 and ISL 15 isolated from two different fields were shown to have 94 and 96% 16S rRNA gene sequence similarity to Burkholderia cepacia respectively. Another bacterial sp., ISL 14 was closely related to Enterobacter cloacae with a 96% 16S rRNA gene sequence similarity. There was not much difference between the extents of atrazine degradation by the enrichment cultures with communities (79–82% applied amount) from which pure strains were isolated and the pure strains themselves in liquid cultures that showed a degradation of 53–83% of applied amount. The study showed existence of bacterial strains in different sugarcane-cultivated fields which can use atrazine as a nitrogen source. The bacterial strains isolated can be used to enhance the degradation of atrazine in contaminated soils where atrazine is still considered to be recalcitrant.