2013
DOI: 10.1016/j.sajb.2013.01.007
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An evaluation of the endophytic colonies present in pathogenic and non-pathogenic Vanguerieae using electron microscopy

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Cited by 6 publications
(5 citation statements)
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“…The cellular morphology of BUN14 was visualized using a JCM-5700 Scanning Electron Microscope, resolution 0.6 nm, specimen size 5 mm ∅ × 0.6 mm high, with a Gatan Digital Micrograph imaging system and SE & BS detectors 53 . BUN14 cultures were centrifuged (10 min 14,000 g ) and bacterial biomass was fixed in 2.5% gluteraldehyde in 0.075 M K-phosphate buffer (pH 7.4) for 2 h at room temperature.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The cellular morphology of BUN14 was visualized using a JCM-5700 Scanning Electron Microscope, resolution 0.6 nm, specimen size 5 mm ∅ × 0.6 mm high, with a Gatan Digital Micrograph imaging system and SE & BS detectors 53 . BUN14 cultures were centrifuged (10 min 14,000 g ) and bacterial biomass was fixed in 2.5% gluteraldehyde in 0.075 M K-phosphate buffer (pH 7.4) for 2 h at room temperature.…”
Section: Methodsmentioning
confidence: 99%
“…BUN14 cultures were centrifuged (10 min 14,000 g ) and bacterial biomass was fixed in 2.5% gluteraldehyde in 0.075 M K-phosphate buffer (pH 7.4) for 2 h at room temperature. The preparation of the Scanning Electron Microscope (SEM) was performed according to Stanton et al 53 . To test the ability of strain BUN14 to utilize hydrocarbon substrates as the sole carbon and energy source, the organism was inoculated onto solid ONR7a agar media containing individual hydrocarbons (pristane, phenanthrene, pyrene, naphthalene, fluoranthene, dibenzothiophene, dibenzofuran, squalene, and carbazole: 50 mM final concentration) and incubated for 7 days at 30 ± 1 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Cultures of BU33N were centrifuged (10 min 14.000 g) and bacterial biomass was fixed in 2.5% gluteraldehyde in 0.075 M K-phosphate buffer (pH 7.4) for 2 h at room temperature. The preparation of the Scanning Electron Microscope (SEM) was performed according to Stanton et al [26], and samples visualized using a JCM-5700 Scanning Electron Microscope, resolution 0.6nm, specimen size 5 mm ∅ × 0.6 mm high, with a Gatan Digital Micrograph imaging system and SE & BS detectors.…”
Section: Methodsmentioning
confidence: 99%
“…For scanning electron microscopy, BU72 cultures were grown in Tryptic Soy Broth (TSB) for 48 at 28°C until exponential growth phase (OD600 around 0.5). Preparations for scanning electron microscope were performed according to Stanton et al (2013). Cultures was were/was centrifuged and bacterial biomass was xed in 2.5% glutaraldehyde in K-phosphate buffer (0.075 M, pH 7.4) for 2 h at room temperature.…”
Section: Characterization Of Bu72 By Scanning Electron Microscopy And...mentioning
confidence: 99%
“…The Scanning Electron Microscope (SEM) used was a JCM-5700SEM, resolution 0.6 nm, specimen size 5 mm dia x 0.6 mm high, heating (1200°C) and cooling (N2(l)) stages, Gatan Digital Micrograph imaging system, SE & BS detectors (Stanton et al 2013).…”
Section: Characterization Of Bu72 By Scanning Electron Microscopy And...mentioning
confidence: 99%