Analysis of phosphate-accumulating organisms cultivated under different carbon sources with polymerase chain reaction-denaturing gradient gel electrophoresis assay

To investigate the microbial communities of microorganisms cultivated under different carbon sources, three sequencing batch reactors were operated. They were supplied with sewage, glucose and sodium acetate as carbon sources respectively and showed high phosphorus removal performance. The results o...

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Veröffentlicht in:Journal of environmental sciences (China) 2005, Vol.17 (4), p.611-614
Hauptverfasser: Yu, Shui-Li, Liu, Ya-Nan, Jing, Guo-Lin, Zhao, Bing-Jie, Guo, Si-Yuan
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container_issue 4
container_start_page 611
container_title Journal of environmental sciences (China)
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creator Yu, Shui-Li
Liu, Ya-Nan
Jing, Guo-Lin
Zhao, Bing-Jie
Guo, Si-Yuan
description To investigate the microbial communities of microorganisms cultivated under different carbon sources, three sequencing batch reactors were operated. They were supplied with sewage, glucose and sodium acetate as carbon sources respectively and showed high phosphorus removal performance. The results of denaturing gradient gel electrophoresis(DGGE) of polymerase chain reaction-amplified (PCR) 16S rDNA fragments demonstrated that β-protebacteria, Actinomyces sp. and y-protebactefia only exited in 1# reactor. The microbiological diversity of 1# reactor exceeded the other two reactors. Flavobacterium, Bacillales, Actinomyces, Actinobacteridae and uncultured bacteria(AF527584, AF502204, AY592749, AB076862, AJ619051, AF495454 and AY133070) could be detected in the biological phosphorus removal reactors.
doi_str_mv 10.3321/j.issn:1001-0742.2005.04.017
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subjects 16S
Bacteria - metabolism
Base Sequence
Carbon - metabolism
DNA Primers
Electrophoresis - methods
Molecular Sequence Data
PCR-DGGE
Phosphates - metabolism
Polymerase Chain Reaction - methods
rDNA
生物磷迁移
移动反应
title Analysis of phosphate-accumulating organisms cultivated under different carbon sources with polymerase chain reaction-denaturing gradient gel electrophoresis assay
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