Brevibacterium marinum sp. nov., isolated from seawater

Lee, Soon Dong

doi:10.1099/ijs.0.65099-0

Cited by 26 publications

(18 citation statements)

References 29 publications

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“…Profiles with the same major acids and similar ratio were also reported for Brevibacterium epidermidis, Brevibacterium linens and Brevibacterium casei (Gruner et al, 1993). Straight-chain fatty acids, such as C 18 : 0 detected by Lee (2008), were not detected in our study.Results of comparative physiological characterization, using identical test conditions in all cases, are given in Table 2 and the species description, using methods described previously (Kämpfer et al, 1991). Strain 01-Je-003 T was grown on nutrient agar for observation of growth at 4, 10, 20, 28, 37, 40 and 45 u C. NaCl and pH tolerance were determined as described by Altenburger et al (1996).…”

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confidence: 47%

“…2). The presence of the predominant lipids diphosphatidylglycerol, phosphatidylglycerol and an unidentified glycolipid was also reported for B. picturae (Heyrman et al, 2004), and B. album, B. marinum and B. oceani have also been shown to contain the major lipids diphosphatidylglycerol and phosphatidylglycerol (Bhadra et al, 2008;Lee, 2008;Tang et al, 2008). Phosphatidylinositol, shown to be present in some Brevibacterium species, could not be detected, but the presence of this lipid has been shown to vary with cultural conditions (Jones & Keddie, 1986).…”

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“…The presence of meso-diaminopimelic acid is common to all brevibacteria examined so far. Also, a quinone system with MK-8(H 2 ) predominating has been reported for representatives of this genus including Brevibacterium samyangense (Lee, 2006), Brevibacterium marinum (Lee, 2008), Brevibacterium album (Tang et al, 2008), Brevibacterium oceani (Bhadra et al, 2008) and B. picturae (Heyrman et al, 2004). The polar lipid profile of strain 01-Je-003 T consisted of the major components diphosphatidylglycerol, phosphatidylglycerol and an unidentified glycolipid, moderate amounts of an unidentified aminophospholipid and minor amounts of three phospholipids and a polar lipid (Fig.…”

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Brevibacterium sandarakinum sp. nov., isolated from a wall of an indoor environment

Kämpfer

Schafer

Lodders

et al. 2010

International Journal of Systematic and Evolutionary Microbiology

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A Gram-stain-positive, rod-shaped, non-endospore-forming, orange-pigmented (coloured) actinobacterium (01-Je-003(T)) was isolated from the wall of an indoor environment primarily colonized with moulds. On the basis of 16S rRNA gene sequence similarity studies, strain 01-Je-003(T) was shown to belong to the genus Brevibacterium and was most similar to the type strains of Brevibacterium picturae (98.8 % similarity), Brevibacterium marinum (97.3 %) and Brevibacterium aurantiacum (97.2 %). Chemotaxonomic data [predominant quinone menaquinone MK-8(H2); polar lipid profile consisting of major compounds diphosphatidylglycerol, phosphatidylglycerol and an unidentified glycolipid; characteristic cell-wall diamino acid meso-diaminopimelic acid; polyamine pattern showing major compounds putrescine and cadaverine; major fatty acids anteiso-C(15 : 0) and anteiso-C(17 : 0)] supported the affiliation of strain 01-Je-003(T) to the genus Brevibacterium. The results of DNA-DNA hybridizations and physiological and biochemical tests allowed genotypic and phenotypic differentiation of strain 01-Je-003(T) from the two most closely related species, B. picturae and B. marinum. Strain 01-Je-003(T) therefore represents a novel species, for which the name Brevibacterium sandarakinum sp. nov. is proposed, with the type strain 01-Je-003(T) (=DSM 22082(T) =CCM 7649(T)).

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Brevibacterium sandarakinum sp. nov., isolated from a wall of an indoor environment

Kämpfer

Schafer

Lodders

et al. 2010

International Journal of Systematic and Evolutionary Microbiology

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“…This species was later emended by Collins et al (1977). Brevibacterium strains have been isolated from diverse environments such as paintings (Heyman et al 2004), brown alga (Ivanova et al 2004), deep sea sediment (Bhadra et al 2008), sea water (Lee 2008), saline soil (Tang et al 2008), human skin (Roux and Raoult 2009), moth caterpillars (Kati et al 2010), indoor wall (Kämpfer et al 2010), salt lakes (Guan et al 2010), poultry manure (Tonouchi et al 2013), river water (Kumar et al 2013) and activated sludge (Cui et al 2013;Kim et al 2013) (LSPN bacterio net; http://www.bacterio.net/). Currently, the genus is comprised of 49 species, including the recently described species Brevibacterium jeotgali (Choi et al 2013).…”

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Brevibacterium metallicus sp. nov., an endophytic bacterium isolated from roots of Prosopis laegivata grown at the edge of a mine tailing in Mexico

Román‐Ponce¹,

Vásquez-Murrieta³

et al. 2015

Arch Microbiol

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A Gram-positive, aerobic, nonmotile strain, NM2E3(T) was identified as Brevibacterium based on the 16S rRNA gene sequence analysis and had the highest similarities to Brevibacterium jeotgali SJ5-8(T) (97.3 %). This novel bacterium was isolated from root tissue of Prosopis laegivata grown at the edge of a mine tailing in San Luis Potosí, Mexico. Its cells were non-spore-forming rods, showing catalase and oxidase activities and were able to grow in LB medium added with 40 mM Cu(2+), 72 mM As(5+) and various other toxic elements. Anteiso-C15:0 (41.6 %), anteiso-C17:0 (30 %) and iso-C15:0 (9.5 %) were the major fatty acids. MK-8(H2) (88.4 %) and MK-7(H2) (11.6 %) were the major menaquinones. The DNA G + C content of the strain NM2E3(T) was 70.8 mol % (Tm). DNA-DNA hybridization showed that the strain NM2E3(T) had 39.8, 21.7 and 20.3 % relatedness with B. yomogidense JCM 17779(T), B. jeotgali JCM 18571(T) and B. salitolerans TRM 45(T), respectively. Based on the phenotypic and genotypic analyses, the strain NM2E3(T) (=CCBAU 101093(T) = HAMBI 3627(T) = LMG 8673(T)) is reported as a novel species of the genus Brevibacterium, for which the name Brevibacterium metallicus sp. nov., is proposed.

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“…Although the genus Brevibacterium is positioned under the phylum Actinobacteria, cells of member of the genus Brevibacterium are single rods that are different from typical actinomycetes organisms with fungal-like morphology. Strains of species of the genus Brevibacterium have been isolated from various habitats, such as paintings (Heyrman et al, 2004), brown alga (Ivanova et al, 2004), deep-sea sediment (Bhadra et al, 2008), seawater (Lee, 2008), soil (Tang et al, 2008), moth caterpillars (Kati et al, 2010) and an indoor wall (Kämpfer et al, 2010). Here, we report the taxonomic study of a novel strain of the genus Brevibacterium obtained from a soil conditioner made from poultry manure in Japan.…”

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Brevibacterium yomogidense sp. nov., isolated from a soil conditioner made from poultry manure

Tonouchi

Kitamura

Fujita

2013

International Journal of Systematic and Evolutionary Microbiology

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A novel Gram-stain-positive rod-shaped actinobacterium was isolated from a soil conditioner made from poultry manure. The isolate, designated strain MN-6-a T , contained anteiso-C 15 : 0 and anteiso-C 17 : 0 as the major fatty acids, and MK-7(H 2 ) and MK-8(H 2 ) as the major menaquinones. Phosphatidylglycerol was a major polar lipid. The G+C content of the genomic DNA was 67.4 mol%. Phylogenetic analysis showed that strain MN-6-a T was closely related to et al., 2010). Here, we report the taxonomic study of a novel strain of the genus Brevibacterium obtained from a soil conditioner made from poultry manure in Japan.The soil conditioner was produced and kindly provided by Sakamoto Youkei Co., Ltd, a poultry farming company, located in Yomogida Village, Aomori Prefecture, Japan. Samples (1 g) of the soil conditioner were suspended in 9.0 ml of sterilized water and serially diluted 10-fold in water. Aliquots of diluents (1 ml) were mixed with 10 ml pre-melted isolation medium (45 u C) and poured onto sterilized plastic plates. The agar plates were incubated at 30 u C for 7 days. The isolation medium consisted of 0.025 % peptone, 0.05 % yeast extract, 0.05 % glucose, 0.003 % MgSO 4 . 7H 2 O, 0.00035 % CaCl 2 . 2H 2 O, 0.01 % cycloheximide and 1.5 % agar. Colonies formed on the plates were transferred to the same medium and then purified. Among the isolates, a Gram-stain-positive rod-shaped bacterium, designated strain MN-6-a T , was selected for the description as a novel species.TSA (Difco) was used for cultivation, maintenance and morphological studies unless otherwise stated. Cultivation was performed at 30 u C. Cell morphology was observed by optical microscopy (Olympus). The absence of flagella was confirmed by transmission electron microscopy (JEM2000EX; JEOL) as described previously (Kitamura et al., 2011). Growth was tested at various temperatures (4, 10, 15, 20, 25, 30, 37, 40 and 45 u C). The pH range for growth was determined using ISP 2 medium adjusted to pH between 5.0 and 11.0 in increments of pH 0.5. NaCl tolerance was determined using ISP 2 medium containing 0 %-20 % NaCl in increments of 1.0 %. Yeast Nitrogen Base (Difco) agar slants (pH 7.0) supplemented with 0.1 % yeast extract were used as the medium for the determination of growth substrates; separately sterilized substrates were added to the sterilized medium to final concentrations of 1.0 %, except sodium salts of organic acids (0.1 %), before making the slants. The DDBJ/EMBL/GenBank accession number for the 16S rRNA gene sequence of Brevibacterium yomogidense MN-6-a T is AB609748.

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Brevibacterium marinum sp. nov., isolated from seawater

Cited by 26 publications

References 29 publications

Brevibacterium sandarakinum sp. nov., isolated from a wall of an indoor environment

Brevibacterium sandarakinum sp. nov., isolated from a wall of an indoor environment

Brevibacterium metallicus sp. nov., an endophytic bacterium isolated from roots of Prosopis laegivata grown at the edge of a mine tailing in Mexico

Brevibacterium yomogidense sp. nov., isolated from a soil conditioner made from poultry manure

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