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1.
Water Res ; 144: 561-571, 2018 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-30081336

RESUMEN

Microbial heterotrophic guilds in activated sludge wastewater treatment systems have complex population structures and functions. A previously proposed heterotrophic-specialist model states that heterotrophs consist of sub-guilds specialized in consuming specific classes of compounds, either readily degradable substrate (RDS) or slowly degradable substrate (SDS) according to current mathematical modeling practices for wastewater treatment processes. It follows from metabolic considerations that the levels of RNA and polyhydroxyalkanoate (PHA) are correlated for strains of the same species growing in different environments; a conjecture previously tested. The proposed classification of heterotrophs into RDS or SDS consumers predicts that the same correlation would also be found across heterotrophic species in conventional activated sludge systems; this prediction was tested in the current study. The positive correlation between the RNA and PHA levels was observed in 9 conventional activated sludge plants in two independent sampling times and it was also found stable over a 6-month regular sampling period at one of these plants. Together, these results imply that the levels of RNA and PHA can be used to define heterotrophic-specialist sub-guilds. In order to gain insight in the species composition of the defined sub-guilds, flow cytometry cell sorting was used to further analyze one of the activated sludge samples. Four sorted sub-samples were obtained (high-RNA/high-PHA, low-RNA/high-PHA, high-RNA/low-PHA, and low-RNA/low-PHA), and the phylogenetic composition of each was determined using 16S rRNA gene amplicon pyrosequencing. Heterotrophic genera were identified across 12 phyla, and their representation in each sorted sub-sample showed that the high-RNA/high-PHA and low-RNA/low-PHA groups were most dissimilar. The enriched genera in these sorted sub-samples are suggested to represent the composition of heterotrophic-specialized sub-guilds defined by the kinetics of substrate consumption.


Asunto(s)
Consorcios Microbianos/fisiología , Polihidroxialcanoatos/metabolismo , Aguas del Alcantarillado/química , Aguas del Alcantarillado/microbiología , Reactores Biológicos/microbiología , Citometría de Flujo , Procesos Heterotróficos , Consorcios Microbianos/genética , Modelos Teóricos , Filogenia , ARN Ribosómico 16S/metabolismo , Eliminación de Residuos Líquidos/instrumentación , Eliminación de Residuos Líquidos/métodos , Aguas Residuales/química
2.
Appl Environ Microbiol ; 78(15): 5280-7, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22635995

RESUMEN

The WBC-2 consortium is an organohalide-respiring anaerobic microbial enrichment culture capable of dechlorinating 1,1,2,2-tetrachloroethane (TeCA) to ethene. In the WBC-2 culture, TeCA is first transformed to trans-dichloroethene (tDCE) by dichloroelimination; tDCE is subsequently transformed to vinyl chloride (VC) and then to ethene by hydrogenolysis. Analysis of 16S rRNA gene clone libraries from culture DNA revealed sequences from three putative dechlorinating organisms belonging to Dehalococcoides, Dehalobacter, and Dehalogenimonas genera. Quantitative PCR primers were designed for each of these sequences, and their abundance was quantified in enrichment cultures over time. These data revealed that complete dechlorination of TeCA to ethene involves all three organisms. Dehalobacter spp. grew during the dihaloelimination of TeCA to tDCE, while Dehalococcoides and Dehalogenimonas spp. grew during hydrogenolysis of tDCE to ethene. This is the first time a genus other than Dehalococcoides has been implicated in dechlorination of tDCE to VC.


Asunto(s)
Chloroflexi/metabolismo , Medios de Cultivo/metabolismo , Etano/análogos & derivados , Hidrocarburos Clorados/metabolismo , Chloroflexi/genética , Chloroflexi/crecimiento & desarrollo , Cromatografía de Gases , Cartilla de ADN/genética , Etano/metabolismo , Biblioteca de Genes , Reacción en Cadena de la Polimerasa/métodos , ARN Ribosómico 16S/genética , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos , Especificidad de la Especie
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