Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge

Bacterial communities were examined in replicate lab-scale activated sludge reactors after a period of several months of enrichment with non-ionic nonylphenol ethoxylate (NPE) surfactants. Four sequential batch reactors were fed with synthetic sewage, two of which received additionally NPE. Small su...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Figuerola, Eva Lucía Margarita, Itria, Raúl Fabio, Erijman, Leonardo
Publicado: 2006
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14622912_v8_n4_p625_Lozada
http://hdl.handle.net/20.500.12110/paper_14622912_v8_n4_p625_Lozada
Aporte de:
id paper:paper_14622912_v8_n4_p625_Lozada
record_format dspace
spelling paper:paper_14622912_v8_n4_p625_Lozada2023-06-08T16:16:14Z Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge Figuerola, Eva Lucía Margarita Itria, Raúl Fabio Erijman, Leonardo bacterial RNA ethylene glycol derivative ribosome DNA RNA 16S surfactant terics article bacterium bioreactor classification fluorescence in situ hybridization genetics growth, development and aging instrumentation methodology microbiology phylogeny reverse transcription polymerase chain reaction sewage two dimensional gel electrophoresis water management Bacteria Bioreactors DNA, Ribosomal Electrophoresis, Gel, Two-Dimensional Ethylene Glycols In Situ Hybridization, Fluorescence Phylogeny Reverse Transcriptase Polymerase Chain Reaction RNA, Bacterial RNA, Ribosomal, 16S Sewage Soil Microbiology Surface-Active Agents Water Purification Acidobacteria Alphaproteobacteria Bacteria (microorganisms) Betaproteobacteria Burkholderiales Gammaproteobacteria Sphingomonas Bacterial communities were examined in replicate lab-scale activated sludge reactors after a period of several months of enrichment with non-ionic nonylphenol ethoxylate (NPE) surfactants. Four sequential batch reactors were fed with synthetic sewage, two of which received additionally NPE. Small subunit rDNA-derived denaturing gel gradient electrophoresis (DGGE) profiles and 16S rDNA clone libraries were dominated by clones of Gammaproteobacteria class. Sequences of the other codominant rDNA phylotypes observed only in DGGE from NPE-amended reactors were, respectively, associated with the Group III of the Acidobacteria phylum. Intriguingly, 16S rRNA content from abundant Gammaproteobacteria cells was unexpectedly low. In addition to Acidobacteria, rRNA-derived DGGE profiles were dominated by members of the order Burkholderiales (of the Betaproteobacteria) and of the genus Sphingomonas (a member of the Alphaproteobacteria). Specific oligonucleotide probes for the selected ribotypes were designed and applied for quantitative real time polymerase chain reaction and fluorescence in situ hybridization, confirming their dominance in treated reactors. The parallel abundance of unique phylotypes in replicate reactors implies a distinctive selection of dominant organisms, which are better adapted to specialized niches in the highly selective environment. © 2005 Society for Applied Microbiology and Blackwell Publishing Ltd. Fil:Figuerola, E.L.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Itria, R.F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Erijman, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2006 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14622912_v8_n4_p625_Lozada http://hdl.handle.net/20.500.12110/paper_14622912_v8_n4_p625_Lozada
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic bacterial RNA
ethylene glycol derivative
ribosome DNA
RNA 16S
surfactant
terics
article
bacterium
bioreactor
classification
fluorescence in situ hybridization
genetics
growth, development and aging
instrumentation
methodology
microbiology
phylogeny
reverse transcription polymerase chain reaction
sewage
two dimensional gel electrophoresis
water management
Bacteria
Bioreactors
DNA, Ribosomal
Electrophoresis, Gel, Two-Dimensional
Ethylene Glycols
In Situ Hybridization, Fluorescence
Phylogeny
Reverse Transcriptase Polymerase Chain Reaction
RNA, Bacterial
RNA, Ribosomal, 16S
Sewage
Soil Microbiology
Surface-Active Agents
Water Purification
Acidobacteria
Alphaproteobacteria
Bacteria (microorganisms)
Betaproteobacteria
Burkholderiales
Gammaproteobacteria
Sphingomonas
spellingShingle bacterial RNA
ethylene glycol derivative
ribosome DNA
RNA 16S
surfactant
terics
article
bacterium
bioreactor
classification
fluorescence in situ hybridization
genetics
growth, development and aging
instrumentation
methodology
microbiology
phylogeny
reverse transcription polymerase chain reaction
sewage
two dimensional gel electrophoresis
water management
Bacteria
Bioreactors
DNA, Ribosomal
Electrophoresis, Gel, Two-Dimensional
Ethylene Glycols
In Situ Hybridization, Fluorescence
Phylogeny
Reverse Transcriptase Polymerase Chain Reaction
RNA, Bacterial
RNA, Ribosomal, 16S
Sewage
Soil Microbiology
Surface-Active Agents
Water Purification
Acidobacteria
Alphaproteobacteria
Bacteria (microorganisms)
Betaproteobacteria
Burkholderiales
Gammaproteobacteria
Sphingomonas
Figuerola, Eva Lucía Margarita
Itria, Raúl Fabio
Erijman, Leonardo
Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
topic_facet bacterial RNA
ethylene glycol derivative
ribosome DNA
RNA 16S
surfactant
terics
article
bacterium
bioreactor
classification
fluorescence in situ hybridization
genetics
growth, development and aging
instrumentation
methodology
microbiology
phylogeny
reverse transcription polymerase chain reaction
sewage
two dimensional gel electrophoresis
water management
Bacteria
Bioreactors
DNA, Ribosomal
Electrophoresis, Gel, Two-Dimensional
Ethylene Glycols
In Situ Hybridization, Fluorescence
Phylogeny
Reverse Transcriptase Polymerase Chain Reaction
RNA, Bacterial
RNA, Ribosomal, 16S
Sewage
Soil Microbiology
Surface-Active Agents
Water Purification
Acidobacteria
Alphaproteobacteria
Bacteria (microorganisms)
Betaproteobacteria
Burkholderiales
Gammaproteobacteria
Sphingomonas
description Bacterial communities were examined in replicate lab-scale activated sludge reactors after a period of several months of enrichment with non-ionic nonylphenol ethoxylate (NPE) surfactants. Four sequential batch reactors were fed with synthetic sewage, two of which received additionally NPE. Small subunit rDNA-derived denaturing gel gradient electrophoresis (DGGE) profiles and 16S rDNA clone libraries were dominated by clones of Gammaproteobacteria class. Sequences of the other codominant rDNA phylotypes observed only in DGGE from NPE-amended reactors were, respectively, associated with the Group III of the Acidobacteria phylum. Intriguingly, 16S rRNA content from abundant Gammaproteobacteria cells was unexpectedly low. In addition to Acidobacteria, rRNA-derived DGGE profiles were dominated by members of the order Burkholderiales (of the Betaproteobacteria) and of the genus Sphingomonas (a member of the Alphaproteobacteria). Specific oligonucleotide probes for the selected ribotypes were designed and applied for quantitative real time polymerase chain reaction and fluorescence in situ hybridization, confirming their dominance in treated reactors. The parallel abundance of unique phylotypes in replicate reactors implies a distinctive selection of dominant organisms, which are better adapted to specialized niches in the highly selective environment. © 2005 Society for Applied Microbiology and Blackwell Publishing Ltd.
author Figuerola, Eva Lucía Margarita
Itria, Raúl Fabio
Erijman, Leonardo
author_facet Figuerola, Eva Lucía Margarita
Itria, Raúl Fabio
Erijman, Leonardo
author_sort Figuerola, Eva Lucía Margarita
title Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
title_short Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
title_full Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
title_fullStr Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
title_full_unstemmed Replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
title_sort replicability of dominant bacterial populations after long-term surfactant-enrichment in lab-scale activated sludge
publishDate 2006
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14622912_v8_n4_p625_Lozada
http://hdl.handle.net/20.500.12110/paper_14622912_v8_n4_p625_Lozada
work_keys_str_mv AT figuerolaevaluciamargarita replicabilityofdominantbacterialpopulationsafterlongtermsurfactantenrichmentinlabscaleactivatedsludge
AT itriaraulfabio replicabilityofdominantbacterialpopulationsafterlongtermsurfactantenrichmentinlabscaleactivatedsludge
AT erijmanleonardo replicabilityofdominantbacterialpopulationsafterlongtermsurfactantenrichmentinlabscaleactivatedsludge
_version_ 1768542332096872448