Massilia neuiana BT
publication ID |
https://doi.org/ 10.12651/JSR.2020.9.2.085 |
DOI |
https://doi.org/10.5281/zenodo.13140523 |
persistent identifier |
https://treatment.plazi.org/id/5E1987B8-770F-5505-2858-A2472786F853 |
treatment provided by |
Felipe |
scientific name |
Massilia neuiana BT |
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Description of Massilia neuiana BT 239
Cells are Gram-stain-positive, non-flagellated, and rod-shaped. Colonies are pale yellow-colored after 3 days of incubation on R2A at 25°C. In the BIOLOG GEN III, positive for dextrin, D- maltose, gentiobiose, pH 6, L- rhamnose, gelatin, glyctl-L- proline, L- aspartic, L- glutamic acid, lincomycin, D- galacturonic acid, L- galactonic acid lactone, D- glucuronic acid, tetrazolium blue, D- malic acid, L- malic acid, propionic acid, acetic acid and aztreonam; weak positive for D- glucose, D- fructose, D- galactose, D- fucose, 1% sodium lactate, D- fructose-6-PO 4, L- histidine, pectin, glucuronamide, tetrazolium violet, tween 40, β -hydroxy-D, L- butyric acid, acetoacetic acid and formic acid; but negative for D- trehalose, D- cellobiolose, sucrose, D- turanose, stachyose, pH 5, D- raffinose, α - D- lactose, D- melibiose, β - methyl-D- glucoside, D- salicin, N -acetyl-D- glucosamine, N -acetyl- β -mannosamin, N -acetyl-D- galactosamin, N -acetyl neuraminic acid, 1% NaCl, 4% NaCl, 8% NaCl, D- mannose, 3-methyl-glucose, L- fucose, inosine, fusidic acid, D- serine, D- sorbitol, D- mannitol, D- arabitol, myo-inositol, glycerol, D- glucose-6-PO 4, D- aspartic acid, D- serine, troleandomycin, rifamycin SV, minocycline, L- alanine, L- arginine, L- pyroglutamic acid, L- serine, guanidine HCl, niaproof 4, D- gluconic acid, mucic acid, quinic acid, D- saccharic acid, bancomycin, p -hydroxy-pheylacetic acid, methyl pyruvate, D- lactic acid methyl ester, L- lactic acid, citric acid, α -keto-glutaric acid, bromo-succinic acid, nalidixic acid, lithium chloride, potassium tellurite, γ -amino-butryric acid, α -hydroxy-butyric acid, α -keto butyric acid, sodium butyrate and sodium bromate. In API 20NE test, positive for arginine dihydrolase, urease and esculin hydrolysis; but negative for reduction of nitrates (NO 3) to nitrite (NO 2 -), reduction of nitrates (NO 3) to nitrogen (N 2), indole production on tryptophan, glucose fermentation, gelatin hydrolysis, β -galactosidase and D- maltose (weak) were utilized. D- Glucose, D- mannose, D- mannitol, N -acetyl-D- glucosamine, potassium gluconate, capric acid, adipic acid, malic acid, trisodium citrate and phenylacetic acid were not utilized. In API 32GN test, N -acetyl-glucosamine, D- ribose, inositol, D- saccharose (sucrose), itaconic acid, suberic acid, sodium malonate, lactic acid, potassium 5-ketogluconate, 3-hydroxybenzoic acid, D- mannitol, D- glucose, salicin, D- melibiose, D- fucose, D- sorbitol, capric acid, valeric acid, trisodium citrate, L- histidine, potassium 2-ketogluconate and 4-hydroxybenzoic acid were utilized whereas, L- rhamnose, D- maltose, glycogen, L- serine and L- arabinose were not utilized.
Strain BT239 (= NIBRBAC000503018) was isolated from a soil sample, Pocheon City in Gyeonggi Province, 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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