Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour 2016
Details
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour, Int. J. Syst. Evol. Microbiol. 66 (2016)
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour 2016
Nomenclature
(Sheu et al.) Dobritsa and Samadpour
Sheu et al.
Dobritsa and Samadpour
2016
ICNP
species
Paraburkholderia dipogonis
Classification
Associations
Descriptions
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour 2016
The description is as provided by Sheu et al. (2015) with the following additional properties. The position in phylogenetic trees based on 16S rRNA gene sequences and the specificities of conserved sequence indels are in accordance with the emended genus description.
Cells are Gram-stain-negative, motile, aerobic, non-spore-forming rods surrounded by a thick capsule. Poly-β-hydroxybutyrate accumulation is observed. Catalase- and oxidase-positive. After 24 h of growth on YEM agar at 25 °C, cells are 0.6–0.8 μm in diameter and 1.8–2.8 μm long. Colonies on YEM agar are pale yellow, circular, smooth and convex with entire edges. Colonies are approximately 1.2–1.8 mm in diameter on YEM agar after 48 h of incubation at 25 °C. Growth occurs at 10–37 °C (optimum, 25–30 °C), at pH 4.0–9.0 (optimum, pH 6.0–7.0) and with 0–2 % (w/v) NaCl (optimum growth in the absence of NaCl). Positive for hydrolysis of Tweens 40 and 60, weakly positive for hydrolysis of CM-cellulose and negative for hydrolysis of DNA, starch, chitin, casein, corn oil, alginate and Tweens 20 and 80. Positive for activities of urease, alkaline phosphatase, C4 esterase, C8 esterase lipase, leucine arylamidase, valine arylamidase, cystine arylamidase, acid phosphatase and naphthol-AS-BI-phosphohydrolase and assimilation of glucose, arabinose, mannose, mannitol, N-acetylglucosamine, gluconate, caprate, adipate and malate; negative for nitrate reduction, indole production, glucose fermentation, hydrolysis of aesculin and gelatin, activities of arginine dihydrolase, C14 lipase, trypsin, α-chymotrypsin, α-galactosidase, β-galactosidase, β-glucuronidase, α-glucosidase, β-glucosidase, N-acetyl-β-glucosaminidase, α-mannosidase and α-fucosidase and assimilation of maltose. Additional chemotaxonomic information can be found in Tables 1 and S2. All known strains are sensitive to chloramphenicol, rifampicin, gentamicin, kanamycin, penicillin G, ampicillin, novobiocin, tetracycline, streptomycin, sulfamethoxazole plus trimethoprim and nalidixic acid. The major fatty acids are C18 : 1ω7c, C16 : 0, C17 : 0 cyclo, summed feature 3 (C16 : 1ω7c and/or C16 : 1ω6c) and C19 : 0 cyclo ω8c. The major respiratory quinone is Q-8. The polar lipid profile consists of a mixture of phosphatidylethanolamine, phosphatidylglycerol, diphosphatidylglycerol, two uncharacterized aminophospholipids and several uncharacterized phospholipids.
The type strain is ICMP 19430T ( = LMG 28415T = HAMBI 3637T), which was isolated from root nodules of Dipogon lignosus in New Zealand
Taxonomic concepts
Burkholderia dipogonis Sheu et al.
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour 2016
Burkholderia dipogonis Sheu et al.
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour 2016
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour
Paraburkholderia dipogonis (Sheu et al. 2015) Dobritsa and Samadpour 2016
Collections
Notes
typification
type strain: ICMP 19430 (isolated in NZ)
Etymology
di.po.go’nis. N.L. gen. masc. n. dipogonis, of Dipogon, a botanical generic name, referring to the isolation of the first strains from Dipogon lignosus
Metadata
3ab60237-226b-497e-a14b-a9e59e5f6f17
scientific name
Names_Fungi
3 April 2022
3 April 2022