2003
DOI: 10.1128/aem.69.3.1511-1520.2003
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Bioaugmentation as a Tool To Protect the Structure and Function of an Activated-Sludge Microbial Community against a 3-Chloroaniline Shock Load

Abstract: Bioaugmentation of bioreactors focuses on the removal of xenobiotics, with little attention typically paid to the recovery of disrupted reactor functions such as ammonium-nitrogen removal. Chloroanilines are widely used in industry as a precursor to a variety of products and are occasionally released into wastewater streams. This work evaluated the effects on activated-sludge reactor functions of a 3-chloroaniline (3-CA) pulse and bioaugmentation by inoculation with the 3-CA-degrading strain Comamonas testoste… Show more

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Cited by 230 publications
(153 citation statements)
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“…Microbial community analysis Total DNA of 0.5 g incubation fluid from LAB, SAB and B fractions was extracted as described by Boon et al (2003). A PCR to amplify a fragment of the 16S rRNA gene of the Butyrivibrio group was performed following Boeckaert et al (2008).…”
Section: In Vitro Incubationsmentioning
confidence: 99%
“…Microbial community analysis Total DNA of 0.5 g incubation fluid from LAB, SAB and B fractions was extracted as described by Boon et al (2003). A PCR to amplify a fragment of the 16S rRNA gene of the Butyrivibrio group was performed following Boeckaert et al (2008).…”
Section: In Vitro Incubationsmentioning
confidence: 99%
“…Microbial community (DGGE and HITChip) and metabolic activity analysis (SCFA) The most prominent shifts within the microbiota were monitored via DGGE. After DNA extraction (Boon et al, 2003) and PCR (Muyzer et al, 1993), gels were run using an Ingeny PhorU apparatus (Ingeny International, Goes, The Netherlands). Pearson correlation and UPGMA (Unweighted Pair Group Method using Arithmetic Mean) clustering were used to calculate dendrograms using BioNumerics v5.10 (Applied Maths, Sint-Martens-Latem, Belgium).…”
Section: Experimental Designmentioning
confidence: 99%
“…Quantitative PCR (qPCR) Archaea rRNA gene copies present in the DNA extract of ruminal digesta samples were quantified as described by Boeckaert et al (2007) and Boon et al (2003), using an ABI Prism SDS 7000 instrument (Applied Biosystems, Lennik, Belgium). Amplification reactions were carried out in 25 μl volumes containing 12.5 μl SYBR Green PCR Master Mix (Applied Biosystems, Warrington, UK), 6 μl RNA-free water and 5 μl diluted (1 : 20) DNA extract, as well as the ARCH915 and UNI-b-rev primers at a final concentration of 300 nM each.…”
Section: Vfasmentioning
confidence: 99%