| Trinickia soli |
Description is based mainly on API 20NE, API ID 32GN and API ZYM results.
Positive results for acid and alkaline phosphatase, catalase, esterase lipase, esterase C4, leucine arylamidase, beta-galactosidase,
beta-glucosidase, nitrate reduction, oxidase, naphthol-AS-BI-phosphohydrolase, Tween 80 hydrolysis, tyrosine hydrolysis and valine
arylamidase.
Can assimilate / utilize: D-xylose, adipic acid, L-arabinose, D-mannose, D-mannitol, potassium gluconate, malic acid, N-
acetylglucosamine, D-ribose, inositol, itaconic acid, lactic acid, L-alanine, glycogen, D-glucose, L-fucose, phenylacetic acid, propionic
acid, L-histidine, 3-hydroxybutyric acid and L-proline.
Negative results for arginine dihydrolase, casein hydrolysis, chitin hydrolysis, carboxymethylcellulose hydoolysis, DNase, esculin
hydrolysis, gelatinase, alpha- and beta-galactosidase (contradiction in article - admin note), beta-glucuronidase, alpha-glucosidase,
H2S production, N-acetyl-beta-glucosaminidase, alpha-mannosidase, alpha-fucosidase, indole production, lipase C14, pectin
hydrolysis, starch hydrolysis, urease, Voges–Proskauer test, cystine arylamidase, trypsin, alpha-chymotrypsin and glucose
fermentation.
No utilization of: erythritol, D-galactose, L-rhamnose, D-sucrose, D-maltose, suberic acid, sodium malonate, sodium acetate, 2- and
5-ketogluconate, 3- and 4-hydroxybenzoic acid, L-serine, salicin, D-melibiose, capric acid, valeric acid and trisodium citrate.
Variable results for the utilization of D-sorbitol and trehalose.
Positive results for acid and alkaline phosphatase, catalase, esterase lipase, esterase C4, leucine arylamidase, beta-galactosidase,
beta-glucosidase, nitrate reduction, oxidase, naphthol-AS-BI-phosphohydrolase, Tween 80 hydrolysis, tyrosine hydrolysis and valine
arylamidase.
Can assimilate / utilize: D-xylose, adipic acid, L-arabinose, D-mannose, D-mannitol, potassium gluconate, malic acid, N-
acetylglucosamine, D-ribose, inositol, itaconic acid, lactic acid, L-alanine, glycogen, D-glucose, L-fucose, phenylacetic acid, propionic
acid, L-histidine, 3-hydroxybutyric acid and L-proline.
Negative results for arginine dihydrolase, casein hydrolysis, chitin hydrolysis, carboxymethylcellulose hydoolysis, DNase, esculin
hydrolysis, gelatinase, alpha- and beta-galactosidase (contradiction in article - admin note), beta-glucuronidase, alpha-glucosidase,
H2S production, N-acetyl-beta-glucosaminidase, alpha-mannosidase, alpha-fucosidase, indole production, lipase C14, pectin
hydrolysis, starch hydrolysis, urease, Voges–Proskauer test, cystine arylamidase, trypsin, alpha-chymotrypsin and glucose
fermentation.
No utilization of: erythritol, D-galactose, L-rhamnose, D-sucrose, D-maltose, suberic acid, sodium malonate, sodium acetate, 2- and
5-ketogluconate, 3- and 4-hydroxybenzoic acid, L-serine, salicin, D-melibiose, capric acid, valeric acid and trisodium citrate.
Variable results for the utilization of D-sorbitol and trehalose.
Taxonomy
Morphology
Cultural characteristics
Biochemical characters
Ecology
Pathogenicity
References
Phylum Pseudomonadota (Proteobacteria), Class Betaproteobacteria, Order Burkholderiales, Family Burkholderiaceae, Genus
Trinickia, Trinickia soli (Yoo et al. 2007) Estrada-de Los Santos et al. 2018.
Old synonyms: Burkholderia soli Yoo et al. 2007, Paraburkholderia soli (Yoo et al. 2007) Sawana et al. 2015.
Species description is based on a single isolate.
Trinickia, Trinickia soli (Yoo et al. 2007) Estrada-de Los Santos et al. 2018.
Old synonyms: Burkholderia soli Yoo et al. 2007, Paraburkholderia soli (Yoo et al. 2007) Sawana et al. 2015.
Species description is based on a single isolate.
Gram-negative rods, 0.5-0.75 x 1.6-3.9 μm. Non-motile.
Colonies are milky, convex and circular with clear margins. Grows at 10-40 ºC
(optimum, 28 ºC), pH 4-8 (optimum, pH 6-7) and 0-2 % (w/v) NaCl. Strictly aerobic.
(optimum, 28 ºC), pH 4-8 (optimum, pH 6-7) and 0-2 % (w/v) NaCl. Strictly aerobic.
Isolated from soil cultivated with Korean ginseng in the Eumseong region of Korea.
Undetermined.
- Yoo S.H., Kim B.Y., Weon H.Y., Kwon S.W., Go S.J. and Stackebrandt E.: Burkholderia soli sp. nov., isolated from soil cultivated
with Korean ginseng. Int. J. Syst. Evol. Microbiol., 2007, 57, 122-125. - Sawana, A., Adeolu, M. and Gupta, R.S. 2014. Molecular signatures and phylogenomic analysis of the genus Burkholderia:
proposal for division of this genus into the emended genus Burkholderia containing pathogenic organisms and a new genus
Paraburkholderia gen. nov. harboring environmental species. Front. Genet., 5, 429. - Sheu S.Y., Chou J.H., Bontemps C., Elliot G.N., Gross E., James E.K., Sprent J.I., Young J.P.W. and Chen W.M.: Burkholderia
symbiotica sp. nov., isolated from root nodules of Mimosa spp. native to north-east Brazil. Int. J. Syst. Evol. Microbiol., 2012, 62,
2272-2278. - Zhu H, Guo J, Chen M, Feng G, Yao Q. Burkholderia dabaoshanensis sp. nov., a heavy-metal-tolerant bacteria isolated from
Dabaoshan mining area soil in China. PLoS One 2012; 7:e50225. - Fu Y, Yan R, Liu D, Jiang S, Cui L, Guo X, Wang X, Zhang J, Xiang W. Trinickia diaoshuihuensis sp. nov., a plant growth promoting
bacterium isolated from soil. Int J Syst Evol Microbiol 2019; 69:291-296. - Gao ZH, Zhong SF, Qin YN, Yang Z, Lv YY, Qiu LH. Trinickia dinghuensis sp. nov. and Trinickia fusca sp. nov., isolated from forest
soil. Int J Syst Evol Microbiol 2019; 69:1390-1397.
(c) Costin Stoica
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