2012
DOI: 10.1128/jb.01848-12
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Complete Genome Sequence of Acidovorax sp. Strain KKS102, a Polychlorinated-Biphenyl Degrader

Abstract: bWe report the complete genome sequence of Acidovorax sp. strain KKS102, a polychlorinated-biphenyl-degrading strain isolated from a soil sample in Tokyo. The genome contains a single circular 5,196,935-bp chromosome and no plasmids.

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Cited by 121 publications
(109 citation statements)
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“…Draft genome sequencing was carried out using the HiSeq 1000 sequencing system (Illumina, San Diego, CA) and the 454 GS FLX titanium system (Roche, Mannheim, Germany), and mutation sites were identified by using ShortReadManager software (34). An RNeasy minikit (Qiagen, Hilden, Germany) was used to prepare total cellular RNA from B. multivorans cells cultivated in liquid medium.…”
Section: Methodsmentioning
confidence: 99%
“…Draft genome sequencing was carried out using the HiSeq 1000 sequencing system (Illumina, San Diego, CA) and the 454 GS FLX titanium system (Roche, Mannheim, Germany), and mutation sites were identified by using ShortReadManager software (34). An RNeasy minikit (Qiagen, Hilden, Germany) was used to prepare total cellular RNA from B. multivorans cells cultivated in liquid medium.…”
Section: Methodsmentioning
confidence: 99%
“…Acidovorax is a common environmental isolate, with some species known to cause plant disease (Acidovorax citrulii) (Burdman and Walcott 2012), and others known to reduce nitrogen (Ohtsubo et al 2012;Chakraborty and Picardal 2013). The Acidovorax OTU which accounts for almost all of the sequences in the genera was BLAST-matched to A. valerianellae, which has been implicated in disease in the edible plant species Valerianellae locusta (commonly called Corn Salad) (Gardan et al 2003;Thiele et al 2012).…”
Section: Discussionmentioning
confidence: 99%
“…The 799 Mb paired-end sequences were assembled into 259 scaffolds larger than 500 bp using Newbler v2.6 (Roche Applied Science, Branford, CT, USA) with the default parameters. Subsequently, each sequence gap in scaffolds was checked and re-assembled using sequence reads belonging to gap extremes by GenoFinisher [13]. Branching contigs, one connected to multiple other contigs, were also examined and misassembled linkages were corrected.…”
Section: Genome Sequencing Informationmentioning
confidence: 99%