2003
DOI: 10.1099/ijs.0.02242-0
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Psychrobacter jeotgali sp. nov., isolated from jeotgal, a traditional Korean fermented seafood

Abstract: Two Gram-negative, non-motile, non-spore-forming and moderately halophilic cocci (strains T and YKJ-105) were isolated from the traditional Korean fermented seafood, jeotgal. The two strains grew optimally at 25-30˚C and grew at 4 and 36˚C, but not above 37˚C. They grew in the presence of 0-10 % (w/v) NaCl with an optimum of 2-3 % (w/v) NaCl.

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Cited by 258 publications
(183 citation statements)
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“…The 16S rRNA gene was amplified by PCR as described previously (Yoon et al, 1998) using two universal primers (59-GAGTTTGATCCTGGCTCAG-39 and 59-AC-GGTTACCTTGTTACGACTT-39). Sequencing of the amplified 16S rRNA gene and phylogenetic analysis were performed as described by Yoon et al (2003).…”
mentioning
confidence: 99%
“…The 16S rRNA gene was amplified by PCR as described previously (Yoon et al, 1998) using two universal primers (59-GAGTTTGATCCTGGCTCAG-39 and 59-AC-GGTTACCTTGTTACGACTT-39). Sequencing of the amplified 16S rRNA gene and phylogenetic analysis were performed as described by Yoon et al (2003).…”
mentioning
confidence: 99%
“…The 16S rRNA gene was amplified by PCR as described previously (Yoon et al, 1998) using two universal primers, 9F (59-GAGTTTGA-TCCTGGCTCAG-39) and 1512R (59-ACGGTTACCTT-GTTACGACTT-39), and the PCR products were purified by using a QIAquick PCR purification kit (Qiagen). Sequencing of the amplified 16S rRNA gene and phylogenetic analysis were performed as described by Yoon et al (2003). Isoprenoid quinones were extracted according to the method of Komagata & Suzuki (1987) and analysed using reversed-phase HPLC and a YMC ODS-A (25064.6 mm) column.…”
mentioning
confidence: 99%
“…The 16S rRNA gene was amplified by PCR using two universal primers (59-GAGTTTGATCC-TGGCTCAG-39 and 59-AGAAAGGAGGTGATCCAGCC-39) as described previously (Yoon et al, 1998), and the PCR products were purified by using a QIAquick PCR purification kit (Qiagen). Sequencing of the amplified 16S rRNA gene and phylogenetic analysis were performed as described by Yoon et al, (2003). Alignment of sequences was carried out with CLUSTAL W software (Thompson et al, 1994).…”
mentioning
confidence: 99%