Taxonomy
Morphology
Cultural characteristics
Biochemical characters
Ecology
Pathogenicity
References
Phylum Actinomycetota, Class Actinomycetes, Order Micrococcales, Family Micrococcaceae, Genus Arthrobacter, Arthrobacter alpinus
Ding et al. 2009.
Species description is based on a single isolate.
Gram-positive irregular rods showing a rod-coccus cycle, 0.8-1.0 x 1.3-1.9 µm, and
occurring in pairs as typical V-forms.
Colonies on R2A agar and on nutrient agar are creamy to yellow after 3 days and
yellow after 6 days, round, convex, shiny, and with an entire margin. Colony diameter
is 1–1.5 mm after 3 days at 20 ºC on R2A agar. Growth occurs at 1-25 ºC, with
optimum at 20-25 ºC; no growth at 30 ºC. Grows in the presence of 0-5% (w/v) NaCl.
The pH range for growth is 6-9. Aerobic.
Isolated from an alpine soil in Fuschertörl, Hohe Tauern, Austria.
Sensitive to ampicillin, penicillin G, streptomycin, tetracycline, and chloramphenicol (each 30 µg/ml), but resistant to cyclosporin A
(100 µg/ml).
Undetermined.
- Zhang DC, Schumann P, Liu HC, Xin YH, Zhou YG, Schinner F, Margesin R. Arthrobacter alpinus sp. nov., a psychrophilic bacterium
isolated from alpine soil. Int J Syst Evol Microbiol 2010; 60:2149-2153.
- Hans-Jurgen Busse, 2012. Family I. Micrococcaceae Pribham 1929, 361 AL emend. Stackebrandt, Rainey and Ward-Rainey 1997,
479 in: Bergey’s Manual of Systematic Bacteriology, second edition, Volume Five The Actinobacteria, Part A, Springer, 571-666.
Positive results for acid and alkaline phosphatase, catalase, esculin hydrolysis, esterase (C4), esterase lipase (C8), alpha- and
beta-glucosidase, alpha- and beta-galactosidase, beta-glucuronidase, alpha-mannosidase, leucine arylamidase,
naphthol-AS-BI-phosphohydrolase, starch hydrolysis, and urea hydrolysis.
Can utilize as sole carbon source D-glucose, lactose, L-arabinose, D-maltose, D-mannose, D-mannitol, and N-acetylglucosamine.
Negative results for arginine dihydrolase, casein hydrolysis, alpha-fucosidase, indole production, H2S production, citrate utilization,
lysine dihydrolase, lipase (C14), N-acetyl-beta-glucosaminidase, nitrate reduction, ornithine dihydrolase, oxidase, pyrrolidonyl
arylamidase, trypsin, alpha-chymotrypsin, Tween 80 hydrolysis, acid production from glucose, ribose, xylose, mannitol, maltose,
lactose, sucrose, glycogen, inositol, sorbitol, rhamnose, melibiose, amygdalin, and L-arabinose.
No utilization of citrate, capric acid, adipic acid, and phenylacetic acid.
(c) Costin Stoica