2014
DOI: 10.1016/j.biortech.2014.05.043
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Effect of phenol on the nitrogen removal performance and microbial community structure and composition of an anammox reactor

Abstract: The effects of phenol on the nitrogen removal performance of a sequencing batch reactor (SBR) with anammox activity and on the microbial community within the reactor were evaluated. A phenol concentration of 300 mg L(-1) reduced the ammonium-nitrogen removal efficiency of the SBR from 96.5% to 47%. The addition of phenol changed the microbial community structure and composition considerably, as shown by denaturing gradient gel electrophoresis and 454 pyrosequencing of 16S rRNA genes. Some phyla, such as Proteo… Show more

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Cited by 104 publications
(43 citation statements)
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“…Even when the phenol is biodegraded, its kinetics is often slow, and biodegradation occurs only at low concentration due to the inhibition [8,9]. In contrast, advanced oxidation process (AOP) is a robust method to break down large organic molecules, including aromatic compounds.…”
Section: Introductionmentioning
confidence: 98%
“…Even when the phenol is biodegraded, its kinetics is often slow, and biodegradation occurs only at low concentration due to the inhibition [8,9]. In contrast, advanced oxidation process (AOP) is a robust method to break down large organic molecules, including aromatic compounds.…”
Section: Introductionmentioning
confidence: 98%
“…For these reasons, 454-pyrosequencing has gained interest in the study of complex microbial communities such as those of wastewater treatment environments (Hu et al, 2012;Xie et al, 2013). Despite the potential of 454-pyrosequencing, the use of this novel technique with anammox reactors is still scarce (Costa et al, 2014;Pereira et al, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…DGGE is one of the most popular and used techniques for biodiversity assessment in bioreactor samples (Boon et al 2002;Arooj et al 2007;Connaughton et al 2006;Miura et al 2007;Pereira et al 2014;Ramos et al 2014). DGGE protocols are relatively simple and straightforward and produce results in relatively short time: after extraction of genomic DNA or RNA, target gene sequences (mostly 16S rRNA gene fragments, or functional genes) are amplified using specially designed primers with GC clamps in the PCR reaction, and PCR amplicons of equal length are separated electrophoretically in a denaturing gradient gel (Muyzer et al 1993) (Fig.…”
Section: Dgge As One Of the Most Popular And Used Molecular Tool For mentioning
confidence: 98%