Sun Weimin, Sun Xiaxuo, Cupples Alison M
Department of Civil and Environmental Engineering, A135 Research Engineering Complex, Michigan State University, East Lansing, MI, 48824, USA.
Biodegradation. 2014 Apr;25(2):189-203. doi: 10.1007/s10532-013-9651-4. Epub 2013 Jun 2.
The study investigates two functional genes for toluene degradation across three redox conditions (nitrate and sulfate amended and methanogenic). The genes targeted include benzylsuccinate synthase α-subunit (bssA) and a gene recently identified as being a strong indicator of anaerobic aromatic degradation, called 6-oxocylcohex-1-ene-1-carbonyl-CoA hydrolase (bamA). In all, sixteen different anaerobic toluene degrading microcosms were investigated using several primers sets targeting bssA and one primer set targeting bamA. One bssA primer set (7772f/8546r) was the most successful in producing a strong amplicon (eight from sixteen) with the other bssA primers sets producing strong amplicons in six or less samples. In contrast, the bamA primer set (bam-sp9 and bam-asp1) produced a strong amplicon in DNA extracted from all except one microcosm. Partial bssA and bamA sequences were obtained for a number of samples and compared to those available in GenBank. The partial bssA sequences (from nitrate amended and methanogenic microcosms) were most similar to Thauera sp. DNT-1, Thauera aromatica, Aromatoleum aromaticum EbN1 and bssA clones from a study involving sulfate reducing toluene degradation. The bamA sequences obtained could be placed into five previously defined clades (bamA-clade 1, Georgfuchsia/Azoarcus, Magnetospirillum/Thauera Syntrophus and Geobacter clades), with the placement generally depending on redox conditions. Gene numbers were also correlated with toluene degradation and the final gene number for both genes differed considerably between the range of redox conditions. The work is the first in depth investigation of bamA diversity over a range of redox conditions and inoculum sources.
该研究调查了在三种氧化还原条件(硝酸盐和硫酸盐添加条件以及产甲烷条件)下用于甲苯降解的两个功能基因。所靶向的基因包括苄基琥珀酸合酶α亚基(bssA)和一个最近被确定为厌氧芳香族化合物降解的强指示基因,即6-氧代环己-1-烯-1-羰基-CoA水解酶(bamA)。总共使用了几套靶向bssA的引物和一套靶向bamA的引物,对16个不同的厌氧甲苯降解微观世界进行了研究。一套bssA引物(7772f/8546r)在产生强扩增子方面最为成功(16个中有8个),而其他bssA引物组在6个或更少的样本中产生强扩增子。相比之下,bamA引物组(bam-sp9和bam-asp1)在除一个微观世界之外的所有样本提取的DNA中都产生了强扩增子。获得了许多样本的部分bssA和bamA序列,并与GenBank中可用的序列进行了比较。部分bssA序列(来自硝酸盐添加和产甲烷微观世界)与陶厄氏菌属DNT-1、芳香陶厄氏菌、芳香油杆菌EbN1以及一项涉及硫酸盐还原甲苯降解研究中的bssA克隆最为相似。获得的bamA序列可归入五个先前定义的进化枝(bamA进化枝1、乔治富氏菌属/固氮弧菌属、嗜磁螺菌属/陶厄氏菌属互营杆菌属和地杆菌属进化枝),其归属通常取决于氧化还原条件。基因数量也与甲苯降解相关,并且在不同氧化还原条件范围内,这两个基因的最终基因数量差异很大。这项工作是首次在一系列氧化还原条件和接种物来源下对bamA多样性进行的深入研究。