Search

Background: Polycyclic aromatic hydrocarbons are a large group of oil contaminants with carcinogenic, mutagenic and teratogenic effects. The release of these compounds in soil destroys animals, plants and microbial diversity and has several negative impacts on physical properties of the soil including the destruction of soil aggregates reduction in pores, and increase in soil bulk density. Many strains of microorganisms isolated have the phenanthrene-degrading ability but this study focused on isolation and identification of a phenanthrene-degrader bacterium for bioremediation of contaminated soils. Background: Polycyclic aromatic hydrocarbons are a large group of oil contaminants with carcinogenic, mutagenic and teratogenic effects. The release of these compounds in soil destroys animals, plants and microbial diversity and has several negative impacts on physical properties of the soil including the destruction of soil aggregates reduction in pores, and increase in soil bulk density. Many strains of microorganisms isolated have the phenanthrene-degrading ability but this study focused on isolation and identification of a phenanthrene-degrader bacterium for bioremediation of contaminated soils. Materials and Methods: Enrichment technique was used for isolation and the most effective isolates, were named pseudomonas aeruginosa ZF1 and Serratia marcescens ZF2. The degradation experiments were conducted in the mineral salt medium (MSM) containing phenanthrene as the sole source of carbon and energy. The selection was based on phenanthrene biodegradation abilities. The isolates were identified using morphological, biochemical tests and 16S rDNA sequencing and after 10 days’ incubation at 30 °C and pH = 7, the bacterial growth and Phe-degrading rate were evaluated by protein assay (Bradford) and gas chromatography (GC), respectively. Results: Biochemical tests and 16s rDNA gene sequence analysis revealed that isolated bacteria are similar to Pseudomonas aeruginosa ZF1 and Serratia marcescens ZF2 with 99% similarity. The results showed a mixture of ZF1 and ZF2 bacteria could degrade 83% at minimum concentrations of 200 ppm of phenanthrene whereas single strain culture of two bacteria had poor degradation abilities (less than 15%). Conclusion: Results showed that isolated co-culture bacteria have high potential to degrade phenanthrene with the best results achieved when the enriched consortium was used and this mixture was shown to be an appropriate candidate for bioremediation purposes.

Background: This study focused on isolation and identification of a Phenanthrene (Phe) degrader bacterium and optimization of environmental conditions for Phe degradation. Materials and Methods: Enrichment technique was used for isolation and the most effective isolate; named AP was selected based on its Phe biodegradation abilities. The isolate was identified using morphological and biochemical tests as well as16S rDNA sequencing. The effects of various factors such as temperature, pH and C/N on bacterial growth and Phe degradation were investigated using protein assay (Bradford) and Gas Chromatography (GC), respectively. Results: The selected isolate was identified as Dietzia cinnamea AP. It was able to degrade Phe at pH 6-10 (optimum at 8), temperatures of 25 -45 °C (optimum at 35 °C) and NH4Cl concentrations of 0.5-2.5 gL-1 (optimum at 2 g L-1). By optimization of environmental parameters, within 10 days of fermentation, Phe degradation rate increased by more than 1.2 fold (from 60% to 73%). Conclusion: D. cinnamea AP was found to be an appropriate candidate for bioremediation applications. To the best of our knowledge, this is the first report of D. cinnamea species that can degrade Phe.