Journal of Bioremediation & Biodegradation
Open Access

Research Article

Molecular Assessment of Microbial Species Involved in the Biodegradation of Crude Oil in Saline Niger Delta Sediments Using Bioreactors

Purpose: At elevated salinities conventional microbiological processes are not very effective, therefore clean up of contaminants using bioremediation strategy will involve the use of halophilic and halo-tolerant bacterial species. This research therefore aimed at isolating and identifying potential halophilic and halo-tolerant bacterial species capable of hydrocarbon degradation during bioreactor based treatment with exogenous nutrients. Methods: The diversity of indigenous bacterial species with potential to degrade hydrocarbons was investigated using both culture-dependent and independent techniques. Bioremediation of hydrocarbon contaminated saline sediments was carried out using seven 2.5 liter bioslurry bioreactors operated over a 64-day period. Physicochemical parameters monitored were pH, nitrate, phosphate, total petroleum hydrocarbon (TPH), polycyclic aromatic hydrocarbon (PAH), temperature, salinity, and total organic carbon (%TOC). Results: The baseline TPH, PAH and pH of the sediments were 19 ppm, 3.1 ppm and 7.0 respectively. The baseline salinity of the sediment was 10% thus the sediment was adjudged moderately saline. TPH ranged from 97 ppm-105 ppm on day zero and decreased to an average of 5.62 ppm on day 64, while PAH ranged from 56 ppm-61 ppm on day zero and decreased to an average of 4.02 ppm on day 64. The bacterial species identified as potential hydrocarbon degraders includes Halomonas lutea, Achromobacter spp, Aquitalea magnusonii, Bacillus sp, Sphingobacterium sp, Shewanella sp, Brevundimonas naejangsanensis, Pseudomonas pseudoalcaligenes, Pseudomonas aeruginosa, unidentified bacterium BH23 and Gordonia sp. The genus Pseudomonas formed majority of the isolates successfully sequenced and exhibited similarity values ranging from 91% to 100% with sequences deposited in GenBank. A combination of both molecular and culture based technique allowed the identification to species level of twelve isolates. One isolate could not be identified while the remaining isolates were identified to their generic level. Treatment BCD recorded highest total culturable heterotrophic bacteria (TCHB) count (7.1 × 108 cfu/g) and total culturable hydrocarbon utilizing bacteria (TCHUB) count (6.7 × 108 cfu/g). There was a significant difference at P<0.05 in TCHUB bacteria counts between the unamended bioreactor slurries and those amended with organic and inorganic nutrients. There were also significant differences in TCHUB counts when the bioaugumented slurry was compared with those amended with NPK, Urea and cow dung using one way ANOVA and Tukey’s multiple comparison tests. Conclusion: This study revealed potentially novel bacterial species and previously described hydrocarbon degrading bacterial species that can be characterized further to determine their role in hydrocarbon degradation as well as their salt tolerance level prior to application in bioremediation of saline environments.

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