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Real-time monitoring of ammonia-oxidizing activity in a nitrifying biofilm by amoA mRNA analysis

机译:通过amoA mRNA分析实时监测硝化生物膜中氨氧化活性

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Ammonia monooxygenase encoding mRNA (amoA mRNA) transcription in the wastewater treatment process was investigated using reverse transcription PCR (RT-PCR) as the model indicating specific function and activity in nitrifying processes. The dynamic response of amoA mRNA transcription and ammonia-oxidizing activity to the change of environmental conditions such as pH and concentration of ammonia was examined to determine the inductive factor and the inhibitor for amoA mRNA expression. Furthermore, we semiquantitatively investigated the response of amoA mRNA transcription to the pH fluctuation in a continuous fed nitrifying reactor. AS a result, amoA mRNA oriented analysis enabled real-time assay of ammonia-oxidizing activity within 2 h as a response time. In contrast, rRNA and amoA encoding DNA were constantly detected at almost the same amount throughout the experiment. mRNA transcription was regulated by the many environmental conditions: ammonia seems to be one of the strong inducers for transcription of amoA mRNA, whereas low pH seems to be a strong inhibitor. These factors simultaneously affected the mRNA transcription and enzymatic activity leading to the complex phenomena of ammonia-oxidizing activity and amoA mRNA transcription in the continuous feeding reactors. [References: 3]
机译:使用逆转录PCR(RT-PCR)作为模型来研究废水处理过程中编码mRNA(amoA mRNA)转录的氨单加氧酶,该模型表明了硝化过程中的特定功能和活性。检查amoA mRNA转录和氨氧化活性对环境条件(例如pH和氨浓度)变化的动态响应,以确定amoA mRNA表达的诱导因子和抑制剂。此外,我们在连续进料硝化反应器中半定量研究了amoA mRNA转录对pH波动的响应。结果,通过amoA mRNA定向分析,可以在2小时内实时测定氨氧化活性作为响应时间。相反,在整个实验过程中,经常以几乎相同的量检测到rRNA和amoA编码DNA。 mRNA的转录受许多环境条件的调节:氨似乎是amoA mRNA转录的强诱导剂之一,而低pH似乎是强抑制剂。这些因素同时影响mRNA的转录和酶促活性,导致连续进料反应器中氨氧化活性和amoA mRNA的转录复杂现象。 [参考:3]

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