首页> 外文期刊>Applied and Environmental Microbiology >Identification and Isolation of Anaerobic, Syntrophic Phthalate Isomer-Degrading Microbes from Methanogenic Sludges Treating Wastewater from Terephthalate Manufacturing
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Identification and Isolation of Anaerobic, Syntrophic Phthalate Isomer-Degrading Microbes from Methanogenic Sludges Treating Wastewater from Terephthalate Manufacturing

机译:从处理对苯二甲酸酯生产废水的产甲烷污泥中鉴定和分离厌氧,可降解的邻苯二甲酸盐异构体的微生物

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The microbial populations responsible for anaerobic degradation of phthalate isomers were investigated by enrichment and isolation of those microbes from anaerobic sludge treating wastewater from the manufacturing of terephthalic acid. Primary enrichments were made with each of three phthalate isomers (ortho-, iso-, and terephthalate) as the sole energy source at 37°C with two sources of anaerobic sludge (both had been used to treat wastewater containing high concentrations of phthalate isomers) as the inoculum. Six methanogenic enrichment cultures were obtained which not only degraded the isomer used for the enrichment but also had the potential to degrade part of other phthalate isomers as well as benzoate with concomitant production of methane, presumably involving strictly syntrophic substrate degradation. Our 16S rRNA gene-cloning analysis combined with fluorescence in situ hybridization revealed that the predominant bacteria in the enrichment cultures were affiliated with a recently recognized non-sulfate-reducing subcluster (subcluster Ih) in the group ‘Desulfotomaculum lineage I' or a clone cluster (group TA) in the class delta-Proteobacteria. Several attempts were made to isolate these microbes, resulting in the isolation of a terephthalate-degrading bacterium, designated strain JT, in pure culture. A coculture of the strain with the hydrogenotrophic methanogen Methanospirillum hungatei converted terephthalate to acetate and methane within 3 months of incubation, whereas strain JT could not degrade terephthalate in pure culture. During the degradation of terephthalate, a small amount of benzoate was transiently accumulated as an intermediate, indicative of decarboxylation of terephthalate to benzoate as the initial step of the degradation. 16S rRNA gene sequence analysis revealed that the strain was a member of subcluster Ih of the group ‘Desulfotomaculum lineage I', but it was only distantly related to other known species.
机译:通过对来自对苯二甲酸生产废水的厌氧污泥中的微生物进行富集和分离,研究了负责邻苯二甲酸酯异构体厌氧降解的微生物种群。在37°C时使用三种邻苯二甲酸酯异构体(原,对苯二甲酸和对苯二甲酸酯)作为唯一能源,并利用两种厌氧污泥进行了一次富集(这两种废水均已用于处理含有高浓度邻苯二甲酸酯异构体的废水)作为接种物。获得了六种产甲烷的富集培养物,它们不仅降解了用于富集的异构体,而且还具有降解其他邻苯二甲酸酯异构体和苯甲酸酯的潜力,并伴有甲烷的产生,大概涉及严格的同养菌底物降解。我们的16S rRNA基因克隆分析与荧光原位杂交相结合,发现富集培养中的主要细菌与“脱硫富马酵母谱系I”或克隆簇中最近公认的非硫酸盐还原亚簇(Ih亚簇)有关。 (TA组)属于delta-Proteobacteria类。进行了数种尝试以分离这些微生物,从而在纯培养物中分离出对苯二甲酸降解细菌,命名为菌株JT。在培养后的3个月内,该菌株与氢营养型产甲烷菌(Methanospirillum Hangatei)的对培养将对苯二甲酸转化为乙酸盐和甲烷,而JT菌株在纯培养中无法降解对苯二甲酸。在对苯二酸酯的降解过程中,少量苯甲酸酯作为中间体短暂积累,表明对苯二酸酯脱羧为苯甲酸酯是降解的起始步骤。 16S rRNA基因序列分析表明,该菌株是Desulfotomaculum谱系I的亚簇Ih的成员,但仅与其他已知物种密切相关。

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