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Spatial and temporal changes in Actinobacterial dominance in experimental artificial groundwater recharge

机译:实验性人工地下水补给中放线菌优势的时空变化

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Artificial groundwater recharge (AGR) is used in the drinking water industry to supplement groundwater resources and to minimise the use of chemicals in water treatment. This study analysed the spatial and temporal changes of microbial communities in AGR using two test systems: a nutrient-amended fluidized-bed reactor (FBR) and a sand column. Structural changes in the feed lake water (Lake Roine), FBR, and sand column bacterial communities were determined by denaturing gradient gel electrophoresis (DGGE) and the length heterogeneity analysis of amplified 16S rRNA genes (LH-PCR). Two clone libraries were created to link the LH-PCR results to the dominant bacterial groups. The lake water bacterial community was relatively stable, with three bands dominating in all LH-PCR products. The most dominant fragment accounted for up to 72% and was derived from Actinobacteria. Based on the clone libraries and LH-PCR data, Actinobacteria also dominated in the unattached bacterial community of the FBR, whereas several Proteobacterial groups were more abundant on the FBR carrier particles. In the stabilised AGR system a major change in the community structure of the lake water bacteria took place during passage within the first 0.6 m in the sand column as the community composition shifted from Actinobacteria-dominated populations to a diverse, mainly Proteobacterial communities. Concurrently, most of the dissolved organic carbon (DOC) was removed at this stage. In summary, the study showed that the make-up of microbial communities in experimental AGR systems responded to changes in their environment. LH-PCR showed potential as a method to determine microbial community dynamics in long-term studies at real-scale AGR sites. This is the first step to provide data on microbial community dynamics in AGR for drinking water production.
机译:饮用水工业中使用人工地下水补给(AGR)来补充地下水资源,并最大程度地减少水处理中化学药品的使用。这项研究使用两个测试系统分析了AGR中微生物群落的时空变化:营养改良流化床反应器(FBR)和砂柱。通过变性梯度凝胶电泳(DGGE)和扩增的16S rRNA基因的长度异质性分析(LH-PCR),确定了饲料湖水(Lake Roine),FBR和沙柱细菌群落的结构变化。创建了两个克隆文库,以将LH-PCR结果链接到优势细菌群。湖水细菌群落相对稳定,在所有LH-PCR产品中均以三个谱带为主。最主要的片段占多达72%,来自放线菌。根据克隆文库和LH-PCR数据,放线菌在FBR的未附着细菌群落中也占主导地位,而FBR载体颗粒上的几个变形细菌基团更为丰富。在稳定的AGR系统中,湖水细菌群落的主要结构发生了变化,在沙柱的前0.6 m内通过,这是因为群落组成从放线菌为主的种群转移到了多样化的,主要是蛋白质细菌群落。同时,在此阶段去除了大部分溶解的有机碳(DOC)。总而言之,研究表明,实验性AGR系统中微生物群落的组成对环境的变化有反应。 LH-PCR在确定实际AGR站点的长期研究中显示了确定微生物群落动态的方法的潜力。这是提供用于饮用水生产的AGR中微生物群落动态数据的第一步。

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