Chryseobacterium balustinum (Harrison, 1929) Vandamme et al., 1994
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https://doi.org/ 10.12651/JSR.2023.12.4.374 |
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https://treatment.plazi.org/id/03C4879A-FFC0-B248-BCFE-F79DFD33FA55 |
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Felipe |
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Chryseobacterium balustinum |
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Description of Chryseobacterium balustinum View in CoL 16N2F1
Cells are Gram-stain-negative, non-flagellated, and rod shaped. Colonies are smooth, convex, and yellow after incubation for 2 days on R2A at 30°C. In the API 20NE system, positive for nitrate reduction, esculin hydrolysis and gelatin hydrolysis; but negative for indole production, glucose acidification, arginine dihydrolase, urease, β -galactosidase, and cytochrome oxidase. D-Mannose, gluconate, capric acid, adipic acid, malic acid, citrate, and phenyl-acetate are utilized as sole carbon sources; while D-glucose, L-arabinose, D-mannitol, N -acetyl-D-glucosamine, and D-maltose are not. Strain 16N2F1 (= NIBRBAC000509484) was isolated from a sediment soil sample at Chuncheon, Gangwon-do, Republic of Korea.
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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