2012
DOI: 10.1038/ja.2012.45
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Luteimicrobium album sp. nov., a novel actinobacterium isolated from a lichen collected in Japan, and emended description of the genus Luteimicrobium

Abstract: A novel Gram-stain-positive actinobacterium, designated RI148-Li105 T , was isolated from a lichen sample from Rishiri Island, Japan, and its taxonomic position was investigated by a polyphasic approach. 16S rRNA gene sequencing study indicated that strain RI148-Li105 T was related to the type strain of Luteimicrobium subarcticum, with a similarity of 97.8%. Cells of strain RI148-Li105 T exhibited a rod-coccus cycle. The diagnostic cell-wall diamino acid of this organism was lysine and the peptidoglycan type w… Show more

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Cited by 93 publications
(71 citation statements)
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“…Growth at 5 and 10 u C was also evaluated after 14 days of incubation. Cell motility, pH range and NaCl tolerance for growth, anaerobic growth, Gram staining and oxidase and catalase activities were determined using the methods outlined by Hamada et al (2012a). Other physiological and biochemical tests were performed using API ZYM, API Coryne and API 50CH systems (bioMérieux) according to the manufacturer's instructions.…”
mentioning
confidence: 99%
“…Growth at 5 and 10 u C was also evaluated after 14 days of incubation. Cell motility, pH range and NaCl tolerance for growth, anaerobic growth, Gram staining and oxidase and catalase activities were determined using the methods outlined by Hamada et al (2012a). Other physiological and biochemical tests were performed using API ZYM, API Coryne and API 50CH systems (bioMérieux) according to the manufacturer's instructions.…”
mentioning
confidence: 99%
“…These results are summarized in Table 1. The genes encoding 16S rRNA were amplified by PCR using two universal primers, 9 F (5′-GAGTTTGATCCTGGCTCAG-3′) and 1541R (5′-AAGGAGGTGATCCAGCC-3′) [7]. KOD FX (Toyobo Co., Ltd., Tokyo, Japan) was used as described by the manufacturer for the PCR.…”
Section: Organism Informationmentioning
confidence: 99%
“…The amplicon size was 1.5 kb. After purification of the PCR product by AMPure (Beckman Coulter), sequencing was carried out according to an established method [7]. The sequence was deposited into DDBJ under the accession number LC150789.…”
Section: Organism Informationmentioning
confidence: 99%
“…Analyses of sugar composition in whole-cell hydrolysate, amino acids and their isomers in cell-wall hydrolysate and isoprenoid quinones were determined according to the methods described by Hamada et al 15 Polar lipids were investigated by the method of Minnikin et al 16 Cellular fatty acid methyl esters were prepared and analyzed following the standard protocol of MIDI Sherlock Microbial Identification System 17 using ACTINO database (version 4.0; MIDI, Newark, DE, USA) and detected using GC (model 6890N; Agilent Technologies, Santa Clara, CA, USA).…”
Section: Chemotaxonomic Testsmentioning
confidence: 99%