2011
DOI: 10.1016/j.biortech.2011.01.007
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Analysis of microbial communities developed on the fouling layers of a membrane-coupled anaerobic bioreactor applied to wastewater treatment

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Cited by 102 publications
(50 citation statements)
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“…The most abundant biofilm associated archaea included the Methanomicrobia, Methanopyri, Thermoplasmata and Thermococci and Thermoprotei. This was consistent with the previous studies (Calderón et al, 2011;Al Ashhab et al, 2014), indicating that these organisms may be the universal biofilm associated archaea in the membrane-based water purification processes. In comparison with the sludge community, the archaeal communities in biofilms formed a distinct community cluster at low TMP (Fig.…”
Section: Discussionsupporting
confidence: 93%
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“…The most abundant biofilm associated archaea included the Methanomicrobia, Methanopyri, Thermoplasmata and Thermococci and Thermoprotei. This was consistent with the previous studies (Calderón et al, 2011;Al Ashhab et al, 2014), indicating that these organisms may be the universal biofilm associated archaea in the membrane-based water purification processes. In comparison with the sludge community, the archaeal communities in biofilms formed a distinct community cluster at low TMP (Fig.…”
Section: Discussionsupporting
confidence: 93%
“…Besides, the Thermoprotei, Methanopyri, and Thermoplasmata were prevailing in the membrane biofilms in the reverse osmosis membrane system (Al Ashhab et al, 2014). In a pilot-scale membrane-coupled upflow anaerobic sludge blanket bioreactor, the methanogenic archaea, e.g., Methanosarcinales and Methanospirillaceae, persistently composed of the biofouling microbial community, even the membranes were cleaned by the chemical reagents (Calderón et al, 2011). Despite these reports, there is still very little data on the association of archaea with biofilm formation on MBR membranes and their impact on MBR performance (Calderón et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
“…Polymerase chain reaction (PCR) amplification was performed in two steps, following other research on TGGE and DGGE fingerprinting [4,9]. One microliter (2-5 ng) of the DNA extracted was used as a template for all the PCRs.…”
Section: Determination Of Ammonium Nitrite and Nitratementioning
confidence: 99%
“…Culture-dependent methods have sometimes been regarded as inadequate for the analysis of microbial communities in natural environments because of the high numbers of unculturable bacteria. Furthermore, in recent years, molecular methods, based on the sequencing of PCR-amplified the partial 16S rRNA genes from DNA extracted from environmental samples, have been widely used to reveal intrinsic genetic biodiversity [4]. In particular, denaturing gradient gel electrophoresis (DGGE) and temperature gradient gel electrophoresis (TGGE) approaches yield large quantities of data regarding the diversity of microorganisms in their natural habitats.…”
Section: Introductionmentioning
confidence: 99%
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