2011
DOI: 10.1007/s11783-011-0304-8
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Seasonal microbial community shift in a saline sewage treatment plant

Abstract: Activated sludge was monthly sampled from a saline sewage treatment plant of Hong Kong (China) during to analyze the microbial community shift along with environmental variations using denaturing gradient gel electrophoresis of polymerase chain reaction amplified 16S rDNA fragments. Environmental changes resulted into a seasonal microbial community shift characterized by alterations in species number and abundance in the sewage treatment plant. Correspondence analysis and cluster analysis on community structur… Show more

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Cited by 2 publications
(2 citation statements)
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“…The copy number was normalized to DNA mass and the qPCR procedures were previously described in detail [11] . PCRs of 16S rRNA gene were conducted to check the contamination of chromosomal DNA in the plasmid metagenome by using the primer set of 341F and 518R according to a previous study [45] .…”
Section: Methodsmentioning
confidence: 99%
“…The copy number was normalized to DNA mass and the qPCR procedures were previously described in detail [11] . PCRs of 16S rRNA gene were conducted to check the contamination of chromosomal DNA in the plasmid metagenome by using the primer set of 341F and 518R according to a previous study [45] .…”
Section: Methodsmentioning
confidence: 99%
“…The PCR-amplification in the abovementioned steps were used as templates for PCR with the primers GC358F (with a 40-bp GC clamp at the 5' end of 358F) (Yan et al, 2011) and 517R (Table 1), which span variable region 3 (V3 region) of the 16S rRNA gene. Hot-start and touchdown PCRs were performed to reduce primer-dimer complexes.…”
Section: Dna Extraction and Pcrmentioning
confidence: 99%