2009
DOI: 10.1099/ijs.0.006163-0
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Sphingobium vermicomposti sp. nov., isolated from vermicompost

Abstract: Strain VC-230T was isolated from homemade vermicompost produced from kitchen waste. The isolate was a Gram-negative-staining, catalase-and oxidase-positive, motile rod-shaped bacterium able to grow at 15-37 6C and pH 6-8. On the basis of 16S rRNA gene sequence analysis, strain VC-230 T was determined to belong to the family Sphingomonadaceae by its clustering with type strains of the genus Sphingobium, with Sphingobium chlorophenolicum ATCC 33790 T (97.7 %) and Sphingobium herbicidovorans DSM 11019 T (97.4 %) … Show more

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Cited by 28 publications
(8 citation statements)
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“…PCR amplification of the 16S rRNA gene fragments was performed using primers 27F (5 -AGAGTTTGATCCTGGCTCAG-3 ) and 1492R (5 -GGTTACCTTGTTACGACTT-3 ), as described by Vaz-Moreira et al [18]. Products of PCR were purified with the GenElute PCR Clean-Up Kit (Sigma) and used as templates.…”
Section: S Rrna Sequencingmentioning
confidence: 99%
“…PCR amplification of the 16S rRNA gene fragments was performed using primers 27F (5 -AGAGTTTGATCCTGGCTCAG-3 ) and 1492R (5 -GGTTACCTTGTTACGACTT-3 ), as described by Vaz-Moreira et al [18]. Products of PCR were purified with the GenElute PCR Clean-Up Kit (Sigma) and used as templates.…”
Section: S Rrna Sequencingmentioning
confidence: 99%
“…Bacterial isolates were identified to the species level on the basis of analysis of the 16S rRNA gene sequence. The 16S rRNA gene was amplified and sequenced with primers 27F and 1492R (26) according to the method of Vaz-Moreira et al (40). The nucleotide sequences were used to query the EzTaxon library (7).…”
mentioning
confidence: 99%
“…The DNA was extracted according to the protocols for total DNA purification from Gram-positive or -negative bacteria of the GRS genomic DNA Kit (Grisp, Porto, Portugal). The primers used for the amplification of the gene fragments for the 16s rRNA identification were 27F (5′-AGAGTTTGATCCTGGCTCAG-3′) and 1492R (5′-GGTTACCTTGTTACGACTT-3′) [ 29 ]. For the preparation of the master mix, the following solutions were used: dNTP (10 mM), Taq buffer KCl (10×), MgCl2 (25 mM), primers 27F and 1492R (100 μM each), Taq polymerase (1 U/mL), and 2 μL of bacterial DNA.…”
Section: Methodsmentioning
confidence: 99%