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首页> 外文期刊>Applied and Environmental Microbiology >Analysis of Diversity and Activity of Sulfate-Reducing Bacterial Communities in Sulfidogenic Bioreactors Using 16S rRNA and dsrB Genes as Molecular Markers
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Analysis of Diversity and Activity of Sulfate-Reducing Bacterial Communities in Sulfidogenic Bioreactors Using 16S rRNA and dsrB Genes as Molecular Markers

机译:使用16S rRNA和dsrB基因作为分子标记分析生硫生物反应器中硫酸盐还原细菌群落的多样性和活性。

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Here we describe the diversity and activity of sulfate-reducing bacteria (SRB) in sulfidogenic bioreactors by using the simultaneous analysis of PCR products obtained from DNA and RNA of the 16S rRNA and dissimilatory sulfite reductase (dsrAB) genes. We subsequently analyzed the amplified gene fragments by using denaturing gradient gel electrophoresis (DGGE). We observed fewer bands in the RNA-based DGGE profiles than in the DNA-based profiles, indicating marked differences in the populations present and in those that were metabolically active at the time of sampling. Comparative sequence analyses of the bands obtained from rRNA and dsrB DGGE profiles were congruent, revealing the same SRB populations. Bioreactors that received either ethanol or isopropanol as an energy source showed the presence of SRB affiliated with Desulfobulbus rhabdoformis and/or Desulfovibrio sulfodismutans, as well as SRB related to the acetate-oxidizing Desulfobacca acetoxidans. The reactor that received wastewater containing a diverse mixture of organic compounds showed the presence of nutritionally versatile SRB affiliated with Desulfosarcina variabilis and another acetate-oxidizing SRB, affiliated with Desulfoarculus baarsii. In addition to DGGE analysis, we performed whole-cell hybridization with fluorescently labeled oligonucleotide probes to estimate the relative abundances of the dominant sulfate-reducing bacterial populations. Desulfobacca acetoxidans-like populations were most dominant (50 to 60%) relative to the total SRB communities, followed by Desulfovibrio-like populations (30 to 40%), and Desulfobulbus-like populations (15 to 20%). This study is the first to identify metabolically active SRB in sulfidogenic bioreactors by using the functional gene dsrAB as a molecular marker. The same approach can also be used to infer the ecological role of coexisting SRB in other habitats.
机译:在这里,我们通过同时分析从16S rRNA的DNA和RNA以及异化亚硫酸盐还原酶(dsrAB)基因获得的PCR产物,描述了在硫化生物反应器中硫酸盐还原细菌(SRB)的多样性和活性。我们随后通过使用变性梯度凝胶电泳(DGGE)分析了扩增的基因片段。我们观察到,基于RNA的DGGE图谱中的条带比基于DNA的图谱中的条带少,这表明存在的种群和采样时具有代谢活性的种群存在明显差异。从rRNA和dsrB DGGE图谱获得的条带的比较序列分析是一致的,揭示了相同的SRB群体。接受乙醇或异丙醇作为能源的生物反应器显示,存在与SRB相关的SRB,而SRB与硫酸盐氧化球菌和乙酸盐相关的SRB有关。接收到包含多种有机化合物混合物的废水的反应器显示,存在着与脱硫弧菌相关的营养丰富的SRB,以及与De弧菌相关的另一种乙酸盐氧化SRB。除DGGE分析外,我们还用荧光标记的寡核苷酸探针进行了全细胞杂交,以估计减少硫酸盐的主要细菌群体的相对丰度。相对于总的SRB群落,类醋酸脱硫杆菌种群最占优势(50%至60%),其次是类脱硫弧菌种群(30%至40%)和类脱硫球菌种群(15%至20%)。这项研究是第一个通过使用功能基因dsrAB作为分子标记物来鉴定具有硫化作用的生物反应器中具有代谢活性的SRB的方法。同样的方法也可以用来推断在其他生境中并存的SRB的生态作用。

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