2009
DOI: 10.1007/s11274-008-9952-7
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The dominant bacteria shifted from the order “Lactobacillales” to Bacillales and Actinomycetales during a start-up period of large-scale, completely-mixed composting reactor using plastic bottle flakes as bulking agent

Abstract: Bacterial community succession in the start-up of a large-scale, completely-mixed composting reactor was analyzed by 16S rRNA gene (16S rDNA) clone analysis and denaturing gradient gel electrophoresis (DGGE) combined with measurements of temperature, pH, moisture contents, and decomposing rate. DGGE analysis and physicochemical parameters showed that bacterial community succession occurred in four phases; (1) at the start of operation and pH decreasing period (day 0-3), (2) pH decreased and increased period (d… Show more

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Cited by 27 publications
(16 citation statements)
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“…Genomic DNA was isolated from at least 1 g of three replicate mixed soils using the PowerSoil DNA Isolation Kit (MoBio) according to the manufacturer's instructions. Extracted DNA was stored at −20 • C. To amplify a 16S rRNA gene fragment of the appropriate size and sequence variability for 454 pyrosequencing, primers 27F (5 -AGAGTTTGATCCTGGCTCAG-3 , Escherichia coli position 9-27) and 515R (5 -TTACCGCGGCTGCTGGCAC-3 , E. coli position 533-515) were chosen (Watanabe et al 2009), and the primers 27F and B515R contained the 454 Life Sciences(R) adaptors B and A respectively. Based on these, the V1-V3 region of bacterial 16S rRNA genes was amplified.…”
Section: Dna Extraction Pcr and 454 Pyrosequencingmentioning
confidence: 99%
“…Genomic DNA was isolated from at least 1 g of three replicate mixed soils using the PowerSoil DNA Isolation Kit (MoBio) according to the manufacturer's instructions. Extracted DNA was stored at −20 • C. To amplify a 16S rRNA gene fragment of the appropriate size and sequence variability for 454 pyrosequencing, primers 27F (5 -AGAGTTTGATCCTGGCTCAG-3 , Escherichia coli position 9-27) and 515R (5 -TTACCGCGGCTGCTGGCAC-3 , E. coli position 533-515) were chosen (Watanabe et al 2009), and the primers 27F and B515R contained the 454 Life Sciences(R) adaptors B and A respectively. Based on these, the V1-V3 region of bacterial 16S rRNA genes was amplified.…”
Section: Dna Extraction Pcr and 454 Pyrosequencingmentioning
confidence: 99%
“…The bar-coded primers 27F and 533R containing A and B sequencing adaptors (454 Life Sciences) were used. The forward primer (B-27F) was 5′- CCTATCCCCTGTGTGCCTTGGCAGTCGACT AG AGTTTGATCCTGGCTCAG-3′, where the sequence of the B adaptor is shown in italics and underline, the reverse primer (A-533R) was 5′- CCATCTCATCCCTGCGTGTCTCCGACGACT NNNNNNNNNNTTACCGCGGCTGCTGGCAC-3′, where the sequence of the A adaptor is shown in italics and underlined and the Ns represent a ten-base sample specific barcode sequence [26] .…”
Section: Methodsmentioning
confidence: 99%
“…The proliferation of Actinobacteria during the late period may be related to the decomposition of cellulose [31,42,45]. The shift of bacteria community to Bacillales and Actinomycetales in the composting process was also proved by the molecular method of 16S rRNA DGGE analysis [44]. Component analysis of the quinone profile further indicated the change of microbial community structure and its variation with different raw materials (Fig.…”
Section: Change Of Microbial Properties During Composting Processmentioning
confidence: 96%