首页> 外文会议>WEFTEC 2001;Annual conference & exposition of Water Environment Federation >Quantification of Ammonia- and Nitrite-oxidizing bacteria using competitive PCRin Bench Scale Wastewater Treatment Reactors at Different Biological SolidsRetention Times
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Quantification of Ammonia- and Nitrite-oxidizing bacteria using competitive PCRin Bench Scale Wastewater Treatment Reactors at Different Biological SolidsRetention Times

机译:使用竞争性PCR在不同生物固体保留时间的台式规模废水处理反应器中对氨和亚硝酸盐氧化细菌的定量

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The effect of solids retention time on ammonia- and nitrite-oxidizing bacteria wasmeasured by amoA and Nitrospira 16S rDNA competitive PCR assays in a completemix,bench-scale, activated sludge system. During steady-state operation, nitrificationwas complete in 20-and 10- day BSRT reactors, nearly complete in the 5-day BSRTreactor and incomplete in the 2-day BSRT reactor (80% ammonia removal and 80%nitrite oxidation). Total bacterial 16S rDNA, measured by dot blot hybridizations, rangedfrom 4.0 x 1013 to 1 x 1012 copies per liter, and decreased with decreasing solids retentiontimes. Nitrospira 16S rDNA was 5 to 40 fold higher than amoA and ranged from 3.3 x1010 to 2 x 109 Nitrospira copies per liter and 1 x 1010 to <8 x 107 amoA copies per liter.The data suggest a minimum of 1 x 1010 Nitrospira 16S rDNA and 9 x 108 amoA copiesper liter are need for complete nitrification.
机译:在完全混合,台式规模的活性污泥系统中,通过amoA和Nitrospira 16S rDNA竞争PCR分析法测量了固体保留时间对氨和亚硝酸盐氧化细菌的影响。在稳态运行期间,硝化作用在20天和10天的BSRT反应器中完成,在5天的BSRT反应器中几乎完成,在2天的BSRT反应器中不完全(80%的氨气去除和80%的亚硝酸盐氧化)。通过斑点印迹杂交测量的总细菌16S rDNA,范围为每升4.0 x 1013至1 x 1012拷贝,并随着固体保留时间的减少而降低。 Nitrospira 16S rDNA比amoA高出5至40倍,范围为每升3.3 x1010至2 x 109硝基螺菌拷贝和每升1 x 1010至<8 x 107 amoA拷贝,数据表明至少需要1 x 1010 Nitrospira 16S rDNA完全硝化需要每升9 x 108 amoA拷贝。

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