Dietzia cinnamea KYW
publication ID |
https://doi.org/ 10.12651/JSR.2016.5.1.001 |
DOI |
https://doi.org/10.5281/zenodo.8120413 |
persistent identifier |
https://treatment.plazi.org/id/E838BC0C-FF94-FFB2-7ACA-3C6A0EB74849 |
treatment provided by |
Felipe |
scientific name |
Dietzia cinnamea KYW |
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Description of Dietzia cinnamea KYW View in CoL View at ENA 853
Cells are Gram-staining-negative, non-flagellated and rodshaped. Colonies are opaque, round, smooth, convex and orangecolored after 2 days of incubation on MA at 25℃. Negative reactions are obtained for nitrate reduction, indole production, glucose fermentation, arginine dihydrolase, urease, esculin hydrolysis, gelatinase and β-galactosidase in API 20NE. Does not utilize Dglucose, Larabinose, Dmannose, Dmannitol, N acetylglucosamine, Dmaltose, potassium gluconate, capric acid, adipic acid, malic acid, trisodium citrate and phenylacetic acid. Strain KYW853 (= NIBRBA 0000114113) was isolated from a sea water sample, Gwangyang Bay, Gwangyang, Korea.
Description of Mycobacterium frederiksbergense SPE 2-2
Cells are Gram-staining-positive, non-flagellated and rodshaped. Colonies are round, smooth and yellowcolored after 2 days of incubation on R2 A at 30℃. Positive reactions are obtained for nitrate reduction, glucose fermentation, esculin hydrolysis and β-galactosidase in API 20NE, and negative reactions are obtained for indole production, arginine dihydrolase, urease and gelatinase. Dglucose, Larabinose, Dmannose, Dmannitol, N acetylglucosamine, potassium gluconate, adipic acid, malic acid, trisodium citrate and phenylacetic acid are utilized. Does not utilize Dmaltose and capric acid. Strain SPE2 2 (= NIBRBA0000113880 ) was isolated from a plant root sample, Chungnam National University, Daejeon, 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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