Strain identifier

BacDive ID: 164191

Type strain: Yes

Species: Dongshaea marina

Strain Designation: DM2

Culture col. no.: JCM 32096, BCRC 81069

Strain history: W. Y. Shieh; Inst. of Oceanogr., Natl. Taiwan Univ., Taiwan; DM2.

NCBI tax ID(s): 2047966 (species)

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Dongshaea marina DM2 is a facultative anaerobe, halophilic, chemoheterotroph bacterium that forms circular colonies and was isolated from Lagoon sediment sample of Dongsha Island.

  1. colony-forming
  2. Gram-negative
  3. rod-shaped
  4. chemoheterotroph
  5. facultative anaerobe
  6. halophilic
  7. mesophilic
  8. 16S sequence
  9. Bacteria
  10. genome sequence
  • Information on isolation source, the sampling and environmental conditions Isolation, sampling and environmental informationarrow_down
  • [Ref.: #67770] Sample type/isolated from Lagoon sediment sample of Dongsha Island
    [Ref.: #67770] Country Taiwan, Province of China
    [Ref.: #67770] Country ISO 3 Code TWN
    [Ref.: #67770] Continent Asia
     
    [Ref.: #67775] Sample type/isolated from lagoon sediment sample
    [Ref.: #67775] Geographic location (country and/or sea, region) Dongsha Island
    [Ref.: #67775] Country Taiwan, Province of China
    [Ref.: #67775] Country ISO 3 Code TWN
    [Ref.: #67775] Continent Asia
    [Ref.: #67775] Enrichment culture temperature 25  ̊C
    [Ref.: #67775] Isolation/enrichment procedure Some wet mass (2 g) of each sample was taken and vigorously shaken in 98 ml sterile NaCl-Tris buffer (30 g NaCl and 0.24 g Tris in 1 l deionized water, pH 8.0). The shaken solutions were decimally diluted with the same buffer. Aliquots (1 ml) of the dilutions (10-3 to 10-5) were transferred to rimless tubes containing PYG medium (5 ml) in triplicate. All cultures were set in anaerobic jars (Difco) and incubated at 25°C in the dark for 3-7 days. The air in each anaerobic jar was replaced by N2 before incubation. The gas replacement was performed by flushing the anaerobic jar 30 times with high-purity N2 (99.9 %). Oxygen-free or nearly oxygen-free conditions could be established in the culturesystem throughout such a gas replacement treatment. Cultures that developed visible turbidity were streaked (one loopful) onto the PY plate medium and the plates were incubated at 25°C in the dark for 2-3 days under aerobic conditions. Individual colonies appearing on the plates were picked off and purified by successive streaking on PY plates.
    * marker position based on {}

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