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TherRNAt/rDNA ratio as a measure of nitrite oxidizing activity.

机译:TherRNAt / rDNA比率可衡量亚硝酸盐的氧化活性。

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摘要

A bench scale nitrification reactor (BSNR) containing the genus Nitrobacter (1 x 1010/L; 5 to 20% of bacteria) was used to assess the ribosomal RNA transcript (rRNAt) to ribosomal RNA gene (rDNA) ratio as a nitrite oxidizing activity metric. Upper (1.8) and lower (0.69) prediction intervals were established for the ratio in the BSNR during 10 consecutive weeks of high nitrification efficiency. It was hypothesized that during NOB inhibition the ratio would decline below 0.69 and during unlimited nitrite oxidation exceed 1.8. When the ratio was measured in a batch nitrite oxidation experiment, the value increased monotonically from less than 0.10 during nitrite starvation to more than 3.0 eight hours after unlimited nitrite oxidation began. The metric declined monotonically back to 0.10 within 4 hours of nitrite exhaustion. The response was mediated by rRNAt abundance that varied as the growth prospect changed from unfavorable (nitrite starvation: 5 x 108 copies/L), to favorable (excess nitrite: 3 x 10 10 copies/L), and back to unfavorable (nitrite starvation: 5 x 10 8 copies/L). Batch inhibition experiments supported a hypothesized negative monotonic correlation between the ratio and the inhibitor concentration and fraction inhibition level. For all inhibitors studied, the ratio was significantly reduced ( 0.69) after 4.5 hours of exposure to concentrations that extensively inhibited nitrite oxidation, though the response varied at the same inhibition level for different inhibitors and was absent after a sudden pH change to 4.5. Despite being widely reported in the literature, free ammonia did not significantly reduce nitrite oxidation rates if ammonia oxidizing bacteria (AOB) were inhibited; however, the metric reflected ( 0.69) the virtual absence of nitrite oxidizing activity at low free ammonia concentrations when the AOB activity level was high. In a staged BSNR inhibition experiment, the ratio dropped significantly ( 0.69) 22 hours before the nitrification efficiency fell below 90%. When nitrite oxidizing activity was later recovered, the ratio increased significantly (> 0.69) before this was apparent in soluble nitrogen data. In summary, a range of experiments suggested the rRNAt/rDNA ratio was an effective monitor for nitrite oxidizing activity that could feasibly identify and forecast wastewater treatment instability.
机译:使用包含硝化细菌(1 x 1010 / L;细菌的5至20%)的台式硝化反应器(BSNR)评估核糖体RNA转录本(rRNAt)与核糖体RNA基因(rDNA)的比率,作为亚硝酸盐的氧化活性指标。在连续10周的高硝化效率期间,BSNR的比率已确定较高的预测间隔(1.8)和较低的预测间隔(0.69)。假设在NOB抑制期间该比率将下降至0.69以下,而在无限制的亚硝酸盐氧化期间该比率将超过1.8。在分批亚硝酸盐氧化实验中测量该比率时,该值从亚硝酸盐饥饿期间的不足0.10单调增加到无限次亚硝酸盐氧化开始后8小时的3.0以上。在亚硝酸盐耗尽4小时内,该指标单调下降至0.10。 rRNAt丰度介导了响应,rRNAt丰度随着生长前景从不利(亚硝酸盐饥饿:5 x 108拷贝/升),有利(亚硝酸盐过量:3 x 10 10拷贝/升)和回到不利(亚硝酸盐饥饿)而变化。 :5 x 10 8份/ L)。批量抑制实验支持比率与抑制剂浓度和组分抑制水平之间的假设负单调相关性。对于所有研究的抑制剂,暴露于4.5小时后,其浓度均显着降低(<0.69),而该浓度可广泛抑制亚硝酸盐氧化,尽管对于不同的抑制剂,其响应在相同的抑制水平下会发生变化,并且在pH突然变为4.5后消失。尽管在文献中有广泛报道,但是如果抑制了氨氧化细菌(AOB),则游离氨并不会显着降低亚硝酸盐的氧化速率。但是,该度量标准反映了(<0.69)当AOB活性水平较高时,在低游离氨浓度下几乎没有亚硝酸盐氧化活性。在分阶段的BSNR抑制实验中,该比率在硝化效率降至90%以下之前22小时显着下降(<0.69)。当稍后恢复亚硝酸盐的氧化活性时,该比例显着增加(> 0.69),然后在可溶性氮数据中变得明显。总而言之,一系列实验表明,rRNAt / rDNA比率是亚硝酸盐氧化活性的有效监测器,可以有效地识别和预测废水处理的不稳定性。

著录项

  • 作者

    Hawkins, Shawn Allen.;

  • 作者单位

    The University of Tennessee.;

  • 授予单位 The University of Tennessee.;
  • 学科 Biology Molecular.; Biology Microbiology.; Chemistry Biochemistry.; Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 402 p.
  • 总页数 402
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;微生物学;生物化学;环境污染及其防治;
  • 关键词

  • 入库时间 2022-08-17 11:41:30

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