Chryseobacterium carnipullorum, Charimba et al., 2013
publication ID |
https://doi.org/ 10.12651/JSR.2020.9.1.026 |
DOI |
https://doi.org/10.5281/zenodo.12792953 |
persistent identifier |
https://treatment.plazi.org/id/03D987A7-8603-502A-4A83-F8FEFB84FA20 |
treatment provided by |
Felipe |
scientific name |
Chryseobacterium carnipullorum |
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Description of Chryseobacterium carnipullorum 18S4 T 3
Cells are Gram-stain-negative, non-flagellated, non-pigmented, and rod-shaped. Colonies are circular, convex, smooth, and yellow colored after incubation for 2 days on MH at 30℃. Positive for indole production, esculin hydrolysis, and gelatin hydrolysis, but negative for nitrate reduction, glucose fermentation, arginine dihydrolase, urease, and β-galactosidase in API 20NE. D-Glucose, D-mannose, N -acetyl-glucosamine, potassium gluconate, D-maltose, malic acid, trisodium citrate, adipic acid and phenylacetic acid are utilized as sole carbon sources, but not L-arabinose, D-mannitol and capric acid. Strain 18S4 T 3 (= GFMCBAC000000191) was isolated from soil sampled at Goyang, Gyeonggi-do. The GenBank accession number for the 16S rRNA gene sequence of strain 18S4 T 3 is MK 204572.
T |
Tavera, Department of Geology and Geophysics |
MH |
Naturhistorisches Museum, Basel |
MK |
National Museum of Kenya |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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