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Distribution of anammox bacteria in domestic WWTPs and their enrichments evaluated by real-time quantitative PCR

机译:实时污水处理厂中生活污水处理厂中厌氧菌的分布及其富集

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摘要

Enrichment of anaerobic ammonium oxidation (anammox) bacteria using five activated sludges in three domestic wastewater treatment plants (WWTPs) were processed in a short term of 70 days and evaluated by real-time quantitative PCR (RTQ-PCR). Before the enrichment, building phylogenetic trees of Planctomycetes phylum in four reactors of sequencing batch reactor (SBR), anoxic and oxic reactors of anaerobic-anoxic-oxic (A2O) process, and rotating biological contactor (RBC) revealed six groups of distantly relative genera of Planctomyces, Pirellula, Gemmata, Isophaera, Candidatus and putative anammox bacteria. All clones ofCandidatus sp. were affiliated with anammox bacteria and the majority of anammox clones were related to Planctomycete KSU-1 (AB057453). The discovery of anammox bacteria in raw activated sludges provided a partial rationale for the utilization of activated sludge as a seeding source of the anammox process. To verify the activity of anammox bacteria in the activated sludges, enrichment cultivations were conducted using SBRs. The enrichment of anammox bacteria resulted in the significant anammox activity of three samples. Quantification of 16S rRNA gene of anammox bacteria using RTQ-PCR showed the highest concentration of anammox bacteria of 2.48 ± 0.22 × 10~9 copies of 16S rRNA gene/mg-volatile suspended solids (VSS), which was the same order of magnitude as that of the referential granular anammox sludge, 6.23 ± 0.59 × 10~9 copies of 16S rRNA gene/ mg-VSS, taken from an anammox upflow anaerobic sludge blanket (UASB) reactor. The doubling time of anammox bacteria enriched in this study was 1.18 days. The growth yield of anammox bacteria enriched in this study was 4.75 ±0.57 × 10~6 copies of 16S rRNA gene/mg of ammonium- and nitrite-nitrogen, which was similar to 4.50 ±0.61 × 10~6 copies of 16S rRNA gene/mg of ammonium- and nitrite-nitrogen for the referential anammox sludge. Substrate uptake rates of three successful enrichments at the end of the enrichment were comparable to those of granular and suspended anammox sludges. Rapid enrichment of anammox bacteria using activated sludge could offer an alternative method for obtaining a large volume of seeding anammox sludge.
机译:在短短的70天内,在三个家庭污水处理厂(WWTP)中使用五种活性污泥富集了厌氧铵氧化(anammox)细菌,并通过实时定量PCR(RTQ-PCR)进行了评估。在富集之前,在四个顺序分批反应器(SBR),厌氧-缺氧-氧(A2O)过程的缺氧和有氧反应器以及旋转生物接触器(RBC)的四个反应器中构建浮游菌门的系统树。揭示了六组远缘属菌属,Pirellula,Gemmata,Isophaera,Candidatus和假定的厌氧细菌。念珠菌属的所有克隆。与厌氧菌属细菌有关,大多数厌氧菌属克隆与Planctomycete KSU-1(AB057453)有关。原始活性污泥中厌氧菌的发现为利用活性污泥作为厌氧菌工艺的种子来源提供了部分依据。为了验证活性污泥中厌氧氨氧化细菌的活性,使用SBR进行了富集培养。厌氧细菌的富集导致三个样品的明显厌氧活性。使用RTQ-PCR定量分析厌氧细菌的16S rRNA基因显示最高的厌氧细菌浓度为2.48±0.22×10〜9拷贝的16S rRNA基因/ mg挥发性悬浮固体(VSS),数量级与参考厌氧污泥厌氧污泥(UASB)反应器中的16S rRNA基因/ mg-VSS的参考颗粒厌氧污泥的6.23±0.59×10〜9拷贝。在这项研究中富集的厌氧细菌的倍增时间为1.18天。本研究中富集的厌氧细菌的生长产量为4.75±0.57×10〜6拷贝的16S rRNA基因/ mg的铵态氮和亚硝酸盐氮,与4.50±0.61×10〜6拷贝的16S rRNA基因/毫克厌氧氨氮和亚硝酸铵氮。富集结束时,三个成功富集的底物吸收率可与颗粒状和悬浮的厌氧氨污泥相媲美。使用活性污泥快速富集厌氧细菌可以为获得大量接种厌氧菌污泥提供一种替代方法。

著录项

  • 来源
    《Process Biochemistry》 |2010年第3期|323-334|共12页
  • 作者单位

    Energy and Environment Research Division, Korea Institute of Science and Technology, 39-1 Hawolgok-Dong, Seongbuk-Gu, Seoul 136-791, Republic of Korea;

    Energy and Environment Research Division, Korea Institute of Science and Technology, 39-1 Hawolgok-Dong, Seongbuk-Gu, Seoul 136-791, Republic of Korea;

    Energy and Environment Research Division, Korea Institute of Science and Technology, 39-1 Hawolgok-Dong, Seongbuk-Gu, Seoul 136-791, Republic of Korea;

    Energy and Environment Research Division, Korea Institute of Science and Technology, 39-1 Hawolgok-Dong, Seongbuk-Gu, Seoul 136-791, Republic of Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    anaerobic ammonium oxidation; phylogenetic tree; enrichment; real-time quantitative PCR;

    机译:厌氧铵氧化;系统树丰富;实时定量PCR;

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