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1.
Bioprocess Biosyst Eng ; 42(12): 2035-2046, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31506821

ABSTRACT

The aim of this study was to understand how the microbial community adapted to changes, including a pH perturbation, occurring during the start-up and operation processes in a full-scale methanogenic UASB reactor designed to treat dairy wastewater. The reactor performance, prokaryotic community, and lipid degradation capacity were monitored over a 9-month period. The methanogenic community was studied by mcrA/mrtA gene copy-number quantification and methanogenic activity tests. A diverse prokaryotic community characterized the seeding sludge as assessed by sequencing the V4 region of the 16S rRNA gene. As the feeding began, the bacterial community was dominated by Firmicutes, Synergistetes, and Proteobacteria phyla. After an accidental pH increase that affected the microbial community structure, a sharp increase in the relative abundance of Clostridia and a decrease in the mcrA/mrtA gene copy number and methanogenic activity were observed. After a recovery period, the microbial population regained diversity and methanogenic activity. Alkaline shocks are likely to happen in dairy wastewater treatment because of the caustic soda usage. In this work, the plasticity of the prokaryotic community was key to surviving changes to the external environment and supporting biogas production in the reactor.


Subject(s)
Bioreactors/microbiology , Sewage/microbiology , Waste Disposal, Fluid , Water Microbiology , Water Purification , Anaerobiosis , Archaea/metabolism , Bacteria, Anaerobic/classification , Biofuels , Clostridium/classification , Dairying , Euryarchaeota/metabolism , Firmicutes/classification , Hydrogen-Ion Concentration , Methane/metabolism , Microbiota , Proteobacteria/classification , RNA, Ribosomal, 16S/genetics , Wastewater
2.
Bioresour Technol ; 264: 290-297, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29852419

ABSTRACT

The aim of the present work was to investigate the dynamics of microbial community at DNA and RNA level and the role of bamA and mcrA gene during anaerobic digestion of phenol and p-cresol. Anaerobic digestion was conducted in batch reactors and microbial community dynamics was analysed. Results showed that active microbial community was quite dissimilar in comparison to the total microbial community. Syntrophorhabdus and Bacillus were the dominant active bacterial genera whereas Methanosaeta together with Methanobacterium showed the highest potential activity in the Archaea domain indicating a relevant role of these microorganisms in the anaerobic process. Ecological Networks revealed dissimilar interactions at DNA and RNA level, being the latter a better descriptor of the known roles of dominant OTUs. QRT-PCR results showed that expression of bamA gene correlated positively with instantaneous degradation rate proving for first time its functionality and its relationship with the kinetics of the process.


Subject(s)
Archaea/genetics , Cresols/metabolism , Genes, Bacterial , Phenol/metabolism , Anaerobiosis , Archaea/metabolism , Bioreactors , Methane , RNA, Ribosomal, 16S
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