Three bacterial isolates identified as Alcanivorax borkumensis
SK2, Rhodococcus erythropolis HS4 and Pseudomonas
stutzeri SDM, based on 16S rRNA gene sequences, were isolated from
crude oil enrichments of natural seawater. Single strains and four bacterial
consortia designed by mixing the single bacterial cultures respectively in the
following ratios: (Alcanivorax: Pseudomonas, 1:1),
(Alcanivorax: Rhodococcus, 1:1),
(Pseudomonas: Rhodococcus, 1:1), and
(Alcanivorax: Pseudomonas:
Rhodococcus, 1:1:1), were analyzed in order to evaluate
their oil degrading capability. All experiments were carried out in microcosms
systems containing seawater (with and without addition of inorganic nutrients)
and crude oil (unique carbon source). Measures of total and live bacterial
abundance, Card-FISH and quali-, quantitative analysis of hydrocarbons (GC-FID)
were carried out in order to elucidate the co-operative action of mixed
microbial populations in the process of biodegradation of crude oil. All data
obtained confirmed the fundamental role of bacteria belonging to
Alcanivorax genus in the degradation of linear hydrocarbons
in oil polluted environments.
The purpose of present study was the simulation of an oil spill accompanied by burial of significant amount of petroleum hydrocarbons (PHs) in coastal sediments. Approximately 1000 kg of sediments collected in Messina harbor were spiked with Bunker C furnace fuel oil (6500 ppm). The rapid consumption of oxygen by aerobic heterotrophs created highly reduced conditions in the sediments with subsequent recession of biodegradation rates. As follows, after 3 months of ageing, the anaerobic sediments did not exhibit any significant levels of biodegradation and more than 80% of added Bunker C fuel oil remained buried. Anaerobic microbial community exhibited a strong enrichment in sulfate-reducing PHs-degrading and PHs-associated Deltaproteobacteria. As an effective bioremediation strategy to clean up these contaminated sediments, we applied a Modular Slurry System (MSS) allowing the containment of sediments and their physical–chemical treatment, e.g., aeration. Aeration for 3 months has increased the removal of main PHs contaminants up to 98%. As revealed by CARD-FISH, qPCR, and 16S rRNA gene clone library analyses, addition of Bunker C fuel oil initially affected the activity of autochthonous aerobic obligate marine hydrocarbonoclastic bacteria (OMHCB), and after 1 month more than the third of microbial population was represented by Alcanivorax-, Cycloclasticus-, and Marinobacter-related organisms. In the end of the experiment, the microbial community composition has returned to a status typically observed in pristine marine ecosystems with no detectable OMHCB present. Eco-toxicological bioassay revealed that the toxicity of sediments after treatment was substantially decreased. Thus, our studies demonstrated that petroleum-contaminated anaerobic marine sediments could efficiently be cleaned through an in situ oxygenation which stimulates their self-cleaning potential due to reawakening of allochtonous aerobic OMHCB.
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