2010
DOI: 10.1099/ijs.0.016832-0
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Brevundimonas halotolerans sp. nov., Brevundimonas poindexterae sp. nov. and Brevundimonas staleyi sp. nov., prosthecate bacteria from aquatic habitats

Abstract: In a previous study, caulobacteria from a broad range of freshwater, brackish water, marine and soil habitats (Anast & Smit, 1988;MacRae & Smit, 1991;Segers et al., 1994) were studied using a polyphasic approach. As a result, the descriptions of the genera Caulobacter and Brevundimonas were emended and a number of Caulobacter species were transferred to the genus Brevundimonas (Abraham et al., 1999). We report here on three novel species within the genus Brevundimonas which emerged from this study.Strains used… Show more

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Cited by 39 publications
(15 citation statements)
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“…Brevundimonas spp. have been isolated from multiple environments, including soils [ 9–21 ], deep subsea floor sediment [ 22 ] activated sludge,[ 23 ] black sand, [ 24 ], deep subsea floor sediment [ 25 ] numerous aquatic habitats [ 26 ], purified water [ 27 ] and also from the condensation water of a Russian space laboratory [ 28 ].…”
Section: Introductionmentioning
confidence: 99%
“…Brevundimonas spp. have been isolated from multiple environments, including soils [ 9–21 ], deep subsea floor sediment [ 22 ] activated sludge,[ 23 ] black sand, [ 24 ], deep subsea floor sediment [ 25 ] numerous aquatic habitats [ 26 ], purified water [ 27 ] and also from the condensation water of a Russian space laboratory [ 28 ].…”
Section: Introductionmentioning
confidence: 99%
“…Calculations were carried out according to Mesbah et al , (1989), with non-methylated lambda-phage DNA (Sigma) as a standard. Amplification of the 16S rRNA gene and sequencing was done as described previously (Abraham et al , 2010). The phylogenetic position of strain MCS 33 T was determined by analysis of the 16S rRNA gene sequence (Abraham et al , 1999) using the software clustal w (Thompson et al , 1997).…”
mentioning
confidence: 99%
“…Subsequently, several Caulobacter species and subspecies were transferred to the genus Brevundimonas as Brevundimonas alba , B. aurantiaca , B. bacteroides , B. intermedia , B. subvibrioides and B. variabilis (Abraham et al , 1999). Additionally, over a dozen Brevundimonas species, B. nasdae (Li et al , 2004), B. mediterranea (Fritz et al , 2005), B. kwangchunensis (Yoon et al , 2006a), B. terrae (Yoon et al , 2006b), B. aveniformis (Ryu et al , 2007), B. lenta (Yoon et al , 2007), B. naejangsanensis , B. bullata (Kang et al , 2009), B. basaltis (Choi et al , 2010), B. halotolerans , B. poindexterae , B. staleyi (Abraham et al , 2010), B. vancanneytii (Estrela & Abraham, 2010) and B. viscosa (Wang et al , 2012), have been described or reclassified. In this study, we report on a novel Brevundimonas -like dimorphic prosthecate bacterial strain, TAR-001 T , which was isolated from a deep-subsea floor sediment sample at a depth of 11 m below the sea floor (mbsf) off the Shimokita Peninsula of Japan in the north-western Pacific Ocean (Site C9001: 1180 m water depth).…”
mentioning
confidence: 99%
“…1,2-Di- O -acyl-3- O -α- d -glucopyranuronosyl glycerol (MGDOx), phosphatidylglycerol (PG), 1,2-di- O -acyl-3- O -α- d -glucopyranosyl glycerol (MGD) and 1,2-di- O -acyl-3- O -[ d -glucopyranosyl-(1→4)-α- d -glucopyranuronosyl]glycerol (DGL) were the major polar lipid constitutions (Table S2). The cellular fatty acid profile of strain TAR-001 T consisted of straight-chain unsaturated fatty acids and saturated fatty acids, and small amounts of hydroxy fatty acids, a typical pattern for the genus Brevundimonas (Abraham et al , 1999, 2010; Li et al , 2004; Fritz et al , 2005; Yoon et al , 2006a, b, 2007; Ryu et al , 2007; Kang et al , 2009; Choi et al , 2010; Wang et al , 2012). The dominant cellular fatty acid of strain TAR-001 T and these two Brevundimonas strains was C18 : 1ω7 c .…”
mentioning
confidence: 99%