Steinberg Lisa M, Regan John M
Department of Civil and Environmental Engineering, The Pennsylvania State University, University Park, PA 16802, USA.
Appl Environ Microbiol. 2008 Nov;74(21):6663-71. doi: 10.1128/AEM.00553-08. Epub 2008 Sep 5.
Methanogens play a critical role in the decomposition of organics under anaerobic conditions. The methanogenic consortia in saturated wetland soils are often subjected to large temperature fluctuations and acidic conditions, imposing a selective pressure for psychro- and acidotolerant community members; however, methanogenic communities in engineered digesters are frequently maintained within a narrow range of mesophilic and circumneutral conditions to retain system stability. To investigate the hypothesis that these two disparate environments have distinct methanogenic communities, the methanogens in an oligotrophic acidic fen and a mesophilic anaerobic digester treating municipal wastewater sludge were characterized by creating clone libraries for the 16S rRNA and methyl coenzyme M reductase alpha subunit (mcrA) genes. A quantitative framework was developed to assess the differences between these two communities by calculating the average sequence similarity for 16S rRNA genes and mcrA within a genus and family using sequences of isolated and characterized methanogens within the approved methanogen taxonomy. The average sequence similarities for 16S rRNA genes within a genus and family were 96.0 and 93.5%, respectively, and the average sequence similarities for mcrA within a genus and family were 88.9 and 79%, respectively. The clone libraries of the bog and digester environments showed no overlap at the species level and almost no overlap at the family level. Both libraries were dominated by clones related to uncultured methanogen groups within the Methanomicrobiales, although members of the Methanosarcinales and Methanobacteriales were also found in both libraries. Diversity indices for the 16S rRNA gene library of the bog and both mcrA libraries were similar, but these indices indicated much lower diversity in the 16S digester library than in the other three libraries.
产甲烷菌在厌氧条件下的有机物分解过程中起着关键作用。饱和湿地土壤中的产甲烷菌群落经常面临较大的温度波动和酸性条件,这对耐低温和耐酸的群落成员施加了选择压力;然而,工程化消化器中的产甲烷菌群落通常维持在较窄的中温及近中性条件范围内,以保持系统稳定性。为了研究这两个截然不同的环境具有不同产甲烷菌群落这一假设,通过构建16S rRNA和甲基辅酶M还原酶α亚基(mcrA)基因的克隆文库,对贫营养酸性沼泽和处理城市污水污泥的中温厌氧消化器中的产甲烷菌进行了表征。通过使用已批准的产甲烷菌分类法中分离和表征的产甲烷菌序列,计算属和科内16S rRNA基因和mcrA的平均序列相似性,建立了一个定量框架来评估这两个群落之间的差异。属内和科内16S rRNA基因的平均序列相似性分别为96.0%和93.5%,属内和科内mcrA的平均序列相似性分别为88.9%和79%。沼泽和消化器环境的克隆文库在物种水平上没有重叠,在科水平上几乎也没有重叠。两个文库都以与未培养的甲烷微菌目产甲烷菌群相关的克隆为主,尽管在两个文库中也都发现了甲烷八叠球菌目和甲烷杆菌目的成员。沼泽的16S rRNA基因文库和两个mcrA文库的多样性指数相似,但这些指数表明消化器16S文库中的多样性远低于其他三个文库。