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Guentas2016
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<p id="par0010">Description of <em>Burkholderia novacaledonica</em> sp. nov.</p> <p id="par0015"><em>Burkholderia novacaledonica</em> sp. nov. (no.va. L. adj. for new,ca.le.do’nica. L. n. <em>Caledonia</em> Latin name for the Scottish Highlands; L.adj. <em>novacaledonica</em> of New Caledonia from where the strains were isolated).</p> <p id="par0020">Cells are Gram-negative, non-sporulating, straight rods. The temperature range for growth is 15–37 °C, with an optimum at 28 °C, growth not occurred at 40 °C. The optimum pH for growth is 5–6. Strain grew optimally at 0–1% NaCl. The strains werecatalase-positive but oxidase, nitrate reductase negative. Theyare able to produce alkaline phosphatase, leucine arylamidase, Naphtol AS-BI-phosphohydrolase, urease, β-galactosidase and arginine dihydrolase but unable to produce C14-lipase, cysteine arylamidase, α-chymotrypsin, α-galactosidase, β-galactosidase, β-glucuronidase, <em>N</em>-acetyl-β-glucosaminidase, α-mannosidase, α-fucosidase. The strain was positive for the assimilation of α-<span class="small-caps">d</span>-glucose, <span class="small-caps">d</span>-fructose, <em>N</em>-acetyl-glucosamine, dextrin, potassium gluconate, malate, tri-sodium citrate, 1% sodium lactate, <span class="small-caps">d</span>-fructose-6-phosphate, potassium telurite. The following carbon sources are not utilized: adipic acid, sucrose, stachyose, <span class="small-caps">d</span>-raffinose, <em>N</em>-acetyl-mannosamine, <em>N</em>-acetyl-neuraminic acid, <span class="small-caps">d</span>-malic-acid, γ-amino-butyric acid, <span class="small-caps">d</span>-aspartic acid, sodium bromate, l-arginine, l-histidine, l-pyroglutamic acid, <span class="small-caps">d</span>-saccharic acid. The strains are unable to ferment glucose. The other car-bon sources and enzyme activities were strain-dependent. The strains are sensitive to chloramphenicol, gentamycin, tetracycline, kanamycin, nalidixic acid, and streptomycin but resistant to penicillin, ampicillin and aztreonam (Supplemental Table 5). The major cellular fatty acids present in strain STM10272<sup>T</sup> were C18:1<sup>ω7c</sup> (40.9%), C16:0 (17.1%), cyclo C17: 0 (5.9%), C16: 3OH (4.1%), C14: 0 (3.8%) and C16: 2OH (2.3%) (Supplemental Table 6). The whole genome DNA–DNA hybridization experiments were performed between the strain STM10272<sup>T</sup> and the type strains of the nearest phylogenetic neighbours: <em>Burkholderia zhejiangensis</em> [30], <em>B. grimmiae</em> [45] and <em>B. glathei</em> [46]. The percentage of DNA–DNA similarity reached 48.4% between strain STM10272<sup>T</sup> and <em>B. zhejiangensis</em> DSM 28073<sup>T</sup>, 34.0% between strain STM10272<sup>T</sup> and <em>B. grimmiae</em> DSM 25160<sup>T</sup> and 22.9% between strain STM10272<sup>T</sup>and <em>B. glathei</em> DSM 50014<sup>T</sup>. The G + C content for the type strain STM20272<sup>T</sup> is 63.6 mol%. The type strain is STM10272<sup>T</sup> = CIP110887<sup>T</sup> = LMG28615<sup>T</sup>. The 16SrRNA gene sequence was deposited in the EMBL database under accession number FR872397.</p>
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