Arthrobacter ruber
Taxonomy
Morphology
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Phylum Actinomycetota, Class Actinomycetes, Order Micrococcales, Family Micrococcaceae, Genus Arthrobacter, Arthrobacter ruber
Liu et al. 2018.
Gram-positive, spherical cells, 1.0–1.2 µm in diameter, occuring singly, in pairs or in
clusters. Non-motile. Non-spore-forming.
Colonies after 4 days incubation on TSA at 28 ºC are red, convex, round and 1.0 mm
in diameter. Growth occurs at 0-34 ºC (optimally at 25-28 ºC), pH 6.0–9.0 (optimally at
pH 7.0) and in the presence of 0-4.0% (w/v) NaCl. Aerobic.
Isolated from ice collected from the ice tongue surface of Midui glacier in Tibet.
Undetermined.
  1. Liu Q, Xin YH, Chen XL, Liu HC, Zhou YG, Chen WX. Arthrobacter ruber sp. nov., isolated from glacier ice. Int J Syst Evol Microbiol
    2018; 68:1616-1621.
Positive results for catalase, citrate utilization, esculin hydrolysis, esterase (C4), esterase lipase (C8), gelatin hydrolysis, alpha- and
beta-galactosidase, alpha- and beta-glucosidase, lipase (C14), leucine arylamidase, valine arylamidase,
naphthol-AS-BI-phosphohydrolase, and VP test.
Can utilize as sole carbon source (Biolog GEN III) dextrin, maltose, trehalose, cellobiose, sucrose, turanose, alpha-D-glucose,
D-mannose, D-fructose, D-galactose, L-rhamnose, inosine, D-sorbitol, D-mannitol, glycerol, D-glucose 6-phosphate, gelatin,
glycyl-L-proline, L-alanine, L-arginine, L-aspartic acid, L-glutamic acid, L-histidine, L-serine, pectin, D-gluconic acid,
phydroxyphenylacetic acid, citric acid, D-malic acid, L-malic acid, bromosuccinic acid, gamma-aminobutryric acid, alpha-ketobutyric
acid, propionic acid, acetic acid; weak reaction for D-fructose 6-phosphate, glucuronamide, alpha-hydroxybutyric acid, acetoacetic
acid and L-lactic acid.

Negative results for arginine dihydrolase, acid and alkaline phosphatase, cystine arylamidase, casein hydrolysis, alpha-fucosidase,
beta-glucuronidase, N-acetyl-beta-glucosaminidase, indole production, H
2S production,  lysine decarboxylase,
alpha-mannosidase, nitrate reduction, ornithine decarboxylase, oxidase starch hydrolysis, Tween 80 hydrolysis, tryptophane
deaminase, trypsin, and alpha-chymotrypsin.
No utilization of gentiobiose, stachyose, D-raffinose, melibiose, methylpyruvate, alpha-ketoglutaric acid, Tween 80, formic acid, and
beta-hydroxy-D,L-butyric acid.
(c) Costin Stoica
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