Arthrobacter bussei

Arthrobacter bussei (bus’se.i. N.L. gen. n. bussei, of Busse; named after the German microbiologist Hans-Jürgen Busse) is a pink-coloured, aerobic, coccus-shaped, Gram-stain-positive, oxidase-positive and catalase-positive bacterium isolated from cheese made of cow´s milk. A. bussei is non-motile and does not form spores. Rod–coccus life cycle is not observed. Cells are 1.1–1.5 µm in diameter. On trypticase soy agar it forms pink-coloured, raised and round colonies, which are 1.0 mm in diameter after 5 days at 30 °C The genome of the strain A. bussei KR32T has been fully sequenced.[1]

Arthrobacter bussei
Scientific classification
Domain: Bacteria
Phylum: Actinomycetota
Class: Actinomycetia
Order: Micrococcales
Family: Micrococcaceae
Genus: Arthrobacter
Species:
A. bussei
Binomial name
Arthrobacter bussei
Flegler et al. 2020[1]
Type strain
DSM 109896
KR32
LMG 31480
NCCB 100733

Characteristics

Morphology

The cells of A. bussei are coccus-shaped. The bacterium is Gram-stain-positive. The cells have a diameter of 1.1–1.5 μm. A rod-coccus life cycle is not observed. The species is not flagellated and therefore non-motile. Endospores are not formed. On trypticase soy agar the cells forms very small colonies. Their diameter is 1.0 mm after 5 days at 30 °C. Colonies are pink-coloured, opaque and soft. From above colonies appear round in shape and have a smooth edge. From the side the colonies are raised.[1]

Physiology

The metabolism of A. bussei is based on aerobic respiration. The species is aerobic and needs oxygen to grow. Oxidase test and catalase test are positive. Furthermore, the metabolism can be characterized as chemoorganotrophic and heterotrophic. A. bussei uses organic compounds as an energy source and synthesize substances. Growth occurs at 1–45 °C and pH 7.0–8.0. Tolerates a maximum of 7.5 % NaCl. Growth on Columbia blood agar but not on violet red bile dextrose agar. The bacterium shows no proteolytic or lipolytic activity. Optimal temperature for growth is 27–30 °C. Trypticase soy agar or trypticase soy broth is suitable for cultivation.[1]

A. bussei is able to hydrolyse aesculin but not gelatine. The bacterium is positive for alkaline phosphatase, esterase (C4), esterase lipase (C8), lipase (C14), leucine arylamidase, valine arylamidase, cystine arylamidase, trypsin, naphthol AS-BI-phosphohydrolase, α-galactosidase, β-galactosidase, α-glucosidase, β-glucosidase and α-mannosidase. Negative for α-chymotrypsin, acid phosphatase, β-glucuronidase, N-acetyl-β-glucosaminidase, α-fucosidase, arginine dihydrolase and urease. Within the chemoorgano-heterotrophic metabolism, A. bussei can use a large number of organic compounds as a source of carbon. These include carbohydrates (pentoses, hexoses and oligosaccharides), sugar alcohols and amino acids. Under aerobic conditions, for example, D-glucose is used, but no acid is formed, as would be typical for fermentation. Other usable substrates are glycerol, L-arabinose, D-xylose, D-galactose, D-glucose, D-fructose, D-mannose, L-rhamnose, D-mannitol, N-acetylglucosamine, arbutin, aesculin, salicin, D-cellobiose, D-maltose, D-melibiose, sucrose, D-trehalose, D-raffinose, starch, glycogen, D-turanose, potassium gluconate and potassium 5-ketogluconate. Furthermore amino acids leucine and valine are assimilated.[1]

Carbohydrates that cannot be used are erythritol, D-arabinose, D-ribose, L-xylose, D-ribitol, methyl-β-D-xylopyranoside, L-sorbose, dulcitol, inositol, D-sorbitol, Methly-α-D-mannopyranoside, methly-α-D-glucopyranoside, amygdalin, D-lactose, inulin, D-melezitose, xylitol, gentiobiose, D-lyxose, D-tagatose, fucose, arabitol and potassium 2-ketogluconate. It cannot reduce nitrate to nitrite.[1]

Chemotaxonomy

The fatty acids occurring in the membrane lipids are iso-C14:0, iso-C14:1 cis 9, C14:0, iso-C15:1 cis 9, iso-C15:1 cis 4, iso-C15:0, anteiso-C15:0, iso-C16:1 cis 9, iso-C16:0, C16:1 cis 9, C16:0, C17:1 cis 10/11, C17:1 cis 9, iso-C17:0 and anteiso-C17:0. The main fatty acids are anteiso-C15:0 and iso-C15:0 at 30 °C. At low temperatures (10 °C) monounsaturated fatty acids are produced.[1]

A. bussei produces menaquinone-9 (H2), which is the main quinone in the genus Arthrobacter,[2] menaquinone-8 (H2) and menaquinone-9.[1] The bacterium also produces the polar lipids diphosphatidylglycerol, phosphatidylglycerol, phosphatidylinositol and monoacyldimannosyl-monoacylglycerol.[1]

The pink colouration of the bacterium is caused by the C50 carotenoid bacterioruberin and a number of its mono-, di- and tetraglycosylated derivatives.[1]

Phylogeny

A. bussei is assigned in the "pink Arthrobacter agilis group"[1] within the "Arthrobacter agilis group",[2] which forms a stable clade. The "pink Arthrobacter agilis group" includes the species Arthrobacter agilis,[3] Arthrobacter ruber[4] and Arthrobacter echini,[5] which all have a pink pigmentation. Other species of the Arthrobacter agilis group’, Arthrobacter flavus,[6] Arthrobacter tecti,[7] Arthrobacter parietis[7] and Arthrobacter tumbae[7] are yellow or yellow-orange pigmented.[1]

Genome

The genome of strain A. bussei KR32T was fully sequenced in 2019 and has a size of 3.63 megabase pairs. There are 3086 proteins annotated. The genome contains, inter alia, genes for the biosynthesis of carotenoids and two putative acyl-CoA desaturases, by which the bacterium can synthesize monounsaturated fatty acids. The genomic DNA G+C content of the type strain is 69.14 mol%, based on the whole genome sequence.[1]

Culture collections

The type strain A. bussei KR32T (=DSM 109896T =LMG 31480T =NCCB 100733T ) is available for scientific and commercial purposes.

References

  1. Alexander Flegler; Katharina Runzheimer; Vanessa Kombeitz; Anna Tatjana Mänz; David Heidler von Heilborn; Lara Etzbach; Andreas Schieber; Georg Hölzl; Bruno Hüttel; Christian Woehle; André Lipski (2020). "Arthrobacter bussei sp. nov., a pink-coloured organism isolated from cheese made of cow's milk". International Journal of Systematic and Evolutionary Microbiology (in German). 70 (5): 3027–3036. doi:10.1099/ijsem.0.004125. ISSN 1466-5026. PMID 32223834.
  2. Hans-Jürgen Busse (2016). "Review of the taxonomy of the genus Arthrobacter, emendation of the genus Arthrobacter sensu lato, proposal to reclassify selected species of the genus Arthrobacter in the novel genera Glutamicibacter gen. nov., Paeniglutamicibacter gen. nov., Pseudoglutamicibacter gen. nov., Paenarthrobacter gen. nov. and Pseudarthrobacter gen. nov., and emended description of Arthrobacter roseus". International Journal of Systematic and Evolutionary Microbiology (in German). 66 (1): 9–37. doi:10.1099/ijsem.0.000702. ISSN 1466-5026. PMID 26486726.
  3. Cathrin Koch; Peter Schumann; Erko Stackebrandt (1995). "Reclassification of Micrococcus agilis (Ali-Cohen 1889) to the Genus Arthrobacter as Arthrobacter agilis comb. nov. and Emendation of the Genus Arthrobacter". International Journal of Systematic and Evolutionary Microbiology (in German). 45 (4): 837–839. doi:10.1099/00207713-45-4-837. ISSN 1466-5026. PMID 7547308.
  4. Qing Liu; Yu-Hua Xin; Xiu-Ling Chen; Hong-Can Liu; Yu-Guang Zhou (2018). "Arthrobacter ruber sp. nov., isolated from glacier ice". International Journal of Systematic and Evolutionary Microbiology (in German). 68 (5): 1616–1621. doi:10.1099/ijsem.0.002719. ISSN 1466-5026. PMID 29561255.
  5. June-Young Lee; Dong-Wook Hyun; Pil Soo Kim; Hyun Sik Kim; Na-Ri Shin (2016). "Arthrobacter echini sp. nov., isolated from the gut of a purple sea urchin, Heliocidaris crassispina". International Journal of Systematic and Evolutionary Microbiology (in German). 66 (4): 1887–1893. doi:10.1099/ijsem.0.000965. ISSN 1466-5026. PMID 26868361.
  6. Reddy, G S; Aggarwal, R K; Matsumoto, G I; Shivaji, S (2000). "Arthrobacter flavus sp. nov., a psychrophilic bacterium isolated from a pond in McMurdo Dry Valley, Antarctica". International Journal of Systematic and Evolutionary Microbiology. 50 (4): 1553–1561. doi:10.1099/00207713-50-4-1553. ISSN 1466-5026. PMID 10939663.
  7. Heyrman, Jeroen; Verbeeren, Jens; Schumann, Peter; Swings, Jean; De Vos, Paul (2005). "Six novel Arthrobacter species isolated from deteriorated mural paintings". International Journal of Systematic and Evolutionary Microbiology. 55 (4): 1457–1464. doi:10.1099/ijs.0.63358-0. ISSN 1466-5026. PMID 16014466.
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