Qiu Yan-Ling, Sekiguchi Yuji, Imachi Hiroyuki, Kamagata Yoichi, Tseng I-Cheng, Cheng Sheng-Shung, Ohashi Akiyoshi, Harada Hideki
Department of Environmental Systems Engineering, Nagaoka University of Technology, Nagaoka, Niigata 940-2188, Japan.
Appl Environ Microbiol. 2004 Mar;70(3):1617-26. doi: 10.1128/AEM.70.3.1617-1626.2004.
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 degrees 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.
通过从处理对苯二甲酸生产废水的厌氧污泥中富集和分离微生物,研究了负责邻苯二甲酸异构体厌氧降解的微生物群落。以三种邻苯二甲酸异构体(邻苯二甲酸、间苯二甲酸和对苯二甲酸)中的每一种作为唯一能源,在37℃下,以两种厌氧污泥来源(均已用于处理含有高浓度邻苯二甲酸异构体的废水)作为接种物进行初步富集。获得了六种产甲烷富集培养物,它们不仅能降解用于富集的异构体,还具有降解部分其他邻苯二甲酸异构体以及苯甲酸盐的潜力,并伴随甲烷的产生,推测这涉及严格的互营底物降解。我们的16S rRNA基因克隆分析与荧光原位杂交相结合表明,富集培养物中的主要细菌隶属于“脱硫肠状菌谱系I”组中一个最近被认可的非硫酸盐还原亚群(亚群Ih)或δ-变形菌纲中的一个克隆簇(TA组):多次尝试分离这些微生物,最终获得了一株对苯二甲酸降解菌的纯培养物,命名为JT菌株。该菌株与氢营养型产甲烷菌Hungate甲烷螺菌的共培养物在培养3个月内将对苯二甲酸转化为乙酸盐和甲烷,而JT菌株在纯培养中不能降解对苯二甲酸。在对苯二甲酸降解过程中,少量苯甲酸盐作为中间产物短暂积累,表明对苯二甲酸脱羧生成苯甲酸盐是降解的第一步。16S rRNA基因序列分析表明,该菌株是“脱硫肠状菌谱系I”组亚群Ih的成员,但与其他已知物种的关系较远。