Fagervold Sonja K, Watts Joy E M, May Harold D, Sowers Kevin R
Center of Marine Biotechnology, University of Maryland Biotechnology Institute, Baltimore, MD 21202, USA.
Appl Environ Microbiol. 2005 Dec;71(12):8085-90. doi: 10.1128/AEM.71.12.8085-8090.2005.
Three species within a deeply branching cluster of the Chloroflexi are the only microorganisms currently known to anaerobically transform polychlorinated biphenyls (PCBs) by the mechanism of reductive dechlorination. A selective PCR primer set was designed that amplifies the 16S rRNA genes of a monophyletic group within the Chloroflexi including Dehalococcoides spp. and the o-17/DF-1 group. Assays for both qualitative and quantitative analyses by denaturing gradient gel electrophoresis and most probable number-PCR, respectively, were developed to assess sediment microcosm enrichments that reductively dechlorinated PCBs 101 (2,2',4,5,5'-CB) and 132 (2,2',3,3',4,6'-CB). PCB 101 was reductively dechlorinated at the para-flanked meta position to PCB 49 (2,2',4,5'-CB) by phylotype DEH10, which belongs to the Dehalococcoides group. This same species reductively dechlorinated the para- and ortho-flanked meta-chlorine of PCB 132 to PCB 91 (2,2',3',4,6'-CB). However, another phylotype designated SF1, which is more closely related to the o-17/DF-1 group, was responsible for the subsequent dechlorination of PCB 91 to PCB 51 (2,2',4,6'-CB). Using the selective primer set, an increase in 16S rRNA gene copies was observed only with actively dechlorinating cultures, indicating that PCB-dechlorinating activities by both phylotype DEH10 and SF1 were linked to growth. The results suggest that individual species within the Chloroflexi exhibit a limited range of congener specificities and that a relatively diverse community of species within a deeply branching group of Chloroflexi with complementary congener specificities is likely required for the reductive dechlorination of different PCBs congeners in the environment.
绿弯菌门一个深度分支簇中的三个物种是目前已知的仅有的通过还原脱氯机制厌氧转化多氯联苯(PCBs)的微生物。设计了一套选择性PCR引物,可扩增绿弯菌门内一个单系类群的16S rRNA基因,该类群包括脱卤球菌属物种以及o-17/DF-1类群。分别开发了通过变性梯度凝胶电泳进行定性分析以及通过最大可能数-PCR进行定量分析的方法,以评估对PCBs 101(2,2',4,5,5'-CB)和132(2,2',3,3',4,6'-CB)进行还原脱氯的沉积物微观生态系统富集情况。PCBs 101在侧翼对位的间位被属于脱卤球菌类群的DEH10系统型还原脱氯为PCBs 49(2,2',4,5'-CB)。同一物种将PCBs 132侧翼对位和邻位的间位氯还原脱氯为PCBs 91(2,2',,3',4,6'-CB)。然而,另一个与o-17/DF-1类群关系更密切的名为SF1的系统型,负责将PCBs 91进一步脱氯为PCBs 51(2,2',4,6'-CB)。使用该选择性引物组,仅在进行活跃脱氯的培养物中观察到16S rRNA基因拷贝数增加,这表明DEH10和SF1这两个系统型的PCBs脱氯活性均与生长相关。结果表明,绿弯菌门内的单个物种表现出有限的同系物特异性范围,并且环境中不同PCBs同系物的还原脱氯可能需要绿弯菌门一个深度分支类群内具有互补同系物特异性的相对多样的物种群落。