Dyella dinghuensis, Ou & Gao & Chen & Bi & Qiu, 2019

Ou, Fang-hong, Gao, Zeng-hong, Chen, Mei-hong, Bi, Jie-yi & Qiu, Li-hong, 2019, Dyella dinghuensis sp. nov. and Dyella choica sp. nov., isolated from forest soil, International Journal of Systematic and Evolutionary Microbiology 69 (5), pp. 1496-1503 : 1501-1502

publication ID

https://doi.org/ 10.1099/ijsem.0.003356

DOI

https://doi.org/10.5281/zenodo.6314481

persistent identifier

https://treatment.plazi.org/id/A64D8E2E-0E3C-E558-4342-FC4391D736E2

treatment provided by

Felipe

scientific name

Dyella dinghuensis
status

sp. nov.

DESCRIPTION OF DYELLA DINGHUENSIS SP. NOV.

Dyella dinghuensis (ding.hu.en′ sis. N.L. fem. adj. dinghuensis referring to Dinghu Mountain, where the organism was isolated).

Cells are Gram-stain-negative, aerobic, non-motile, and rod-shaped (0.3–0.6×1.0–2.3 µm). Colonies are circular, convex with clear margin and yellow-coloured after 4 days on R2A agar. Growth was observed on trypticase soy agar, R2A agar and Luria–Bertani agar, but not MacConkey agar. Growth on R2A agar occurs at 12–37 Ǫ C, pH 4.5–7.0 and in the presence of 0–1.0 % (w/v) NaCl. Optimum growth occurs at 28 Ǫ C, pH 5.0–6.0 and without NaCl supplement. Catalase-positive and oxidase-positive. Nitrate is not reduced to nitrite. Casein is hydrolysed, but gelatin, starch and Tween 80 are not. H 2 S and indole are not produced. The following substrates can be used as sole carbon sources for growth: adipic acid, arbutin, amygdalin, D- xylose, D- galactose, D- glucose, D- fructose, D- mannose, D- mannitol, cellobiose, maltose, inulin, malic acid, methyl Oi- D- glucopyranoside, N -acetyl-D- glucosamine and phenylacetic acid. The following substrates are not utilized for growth: aesculin ferric citrate, capric acid, D- adonitol, D- arabinose, D- arabitol, D- fucose, D- gentiobiose, lactose, D- lyxose, melezitose, melibiose, raffinose, D- ribose, D- sorbitol, sucrose, D- tagatose, trehalose, turanose, dulcitol, erythritol, glycerol, glycogen, inositol, L- arabinose, L- arabitol, L- fucose, L- rhamnose, L- sorbose, L- xylose, methyl Oi - D- mannopyranoside, methyl β - D- xylopyranoside, potassium 2-ketogluconate, potassium 5- ketogluconate, potassium gluconate, salicin, starch and xylitol. The following enzyme activities are positive: alkaline phosphatase, acidphosphatase, arginine dihydrolase, cystine arylamidase, Oi -galactosidase, Oi -glucosidase, Oi -fucosidase, Oi -mannosidase, β -galactosidase, β -glucosidase, esterase (C4), esterase (C8), leucine arylamidase, naphthol-AS-BIphosphohydrolase, N -acetyl- β -glucosaminidase, urease and valine arylamidase. Trypsin is weakly positive. The following enzyme activities are negative: Oi -chymotrypsin, β -glucuronidase and lipase (C14). Ubiquinone-8 is the only respiratory quinone, and iso-C 15: 0, iso-C 16: 0, iso-C 17: 0, iso- C 17: 1 Ɯ 9 c are the major cellular fatty acids (>10 %). The G+C content of the genomic DNA is 59.1 mol%. The major polar lipids consist of phosphatidylethanolamine, phosphatidylglycerol, diphosphatidylglycerol, phosphatidylmethylethanolamine, one unidentified aminophospholipid, two unidentified aminolipids, one unidentified phospholipid and lipid.

The type strain, DHOA06 T (=KCTC 52129 T =NBRC 111978 T), was isolated from forest soil sampled at Dinghushan Biosphere Reserve , Guangdong Province, PR China. The 16S rRNA gene sequence and whole genome sequence of strain DHOA06 T have been deposited in DDBJ/EMBL/ GenBank under accession numbers KY194795 View Materials and RYZR00000000, respectively.

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