2015
DOI: 10.1007/s11743-015-1697-3
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Diesel Oil Degradation Potential of a Bacterium Inhabiting Petroleum Hydrocarbon Contaminated Surface Waters and Characterization of Its Emulsification Ability

Abstract: Degradation of poorly water soluble hydrocarbons, like n‐alkanes and polycyclic aromatic hydrocarbons are challenged by some bacteria through emulsification of hydrocarbons by producing biosurfactants. In diesel oil bioremediation, diesel oil degrading and surfactant producing bacteria are used to eliminate these pollutants from contaminated waters. Therefore, identifying and characterizing bacteria capable of producing surfactant and degrading diesel oil are pivotal. In this study, bacteria isolated from hydr… Show more

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Cited by 25 publications
(12 citation statements)
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“…A 10 mL aliquot was taken and evaporated until constant dryness. Then degradation calculated as explained in Onur, Yilmaz and Icgen ( 2015 ). Degradation of model oil was quantified by separating the extract (1 µL) using gas chromatography (GC; Varian CP3800 fitted with 30 m Zebron ZB-50 column) and individual HCs were detected by a flame ionisation detector (FID).…”
Section: Methodsmentioning
confidence: 99%
“…A 10 mL aliquot was taken and evaporated until constant dryness. Then degradation calculated as explained in Onur, Yilmaz and Icgen ( 2015 ). Degradation of model oil was quantified by separating the extract (1 µL) using gas chromatography (GC; Varian CP3800 fitted with 30 m Zebron ZB-50 column) and individual HCs were detected by a flame ionisation detector (FID).…”
Section: Methodsmentioning
confidence: 99%
“…The universal bacterial 16S rRNA primers, 27F (5′-AGAGTTTGATCCTGGCTCAG-3′) and 1492R (5′-CTACGGCTACCTTGTTACGA-3′) were used to amplify bacterial 16S rDNA [ 22 ]. The PCR product of purified strains was subjected to DNA sequencing by the sequencerABI3730-XL.…”
Section: Materials and Methodologiesmentioning
confidence: 99%
“…The bacterial genomic DNA was extracted using the AxyPrep DNA isolation kit. The universal bacterial 16S rDNA primers, 27F (5′-AGAGTTTGATCCTGGCTCAG-3′) and 1492R (5′-CTACGGCTACCTTGTTACGA-3′) were used to amplify bacterial 16S rDNA [ 26 ]. The PCR product of purified strains was subjected to DNA sequencing by the sequencer ABI3730-XL.…”
Section: Methodsmentioning
confidence: 99%