Affiliation(s)
1. Laboratory of Aquaculture and Bioremediation (AquaBior), Department of Biotechnology, Faculty of Nature and Life Sciences, University of Oran 1 Ahmed Ben Bella, Oran 31000, Algeria
2. Higher School of Biological Sciences of Oran, Oran 31000, Algeria
ABSTRACT
Petroleum contaminants caused great damages to environment and human
health. Among, the port of Oran is subject of pollution mainly by PAHs (Polycyclic Aromatic
Hydrocarbons) as a result of the
large flow of ships. Thus bioremediation by indigenous microorganisms is an
important means for their reduction and elimination. In the present work, a
hydrocarbonoclastic bacterium strain SP49F2 was considered, firstly isolated
from the contaminated marine sediments and seawater at the port of Oran
(Algeria), using Bushnell-Hass mineral salt medium, and identified on the basis
of morphological and biochemical characteristics and molecular tools by
analysis of partial 16S rRNA gene sequence, using the Basic Local Alignment
Search Tool program on the data base of NCBI (National Centre for Biotechnology
Information), and the EzBioCloud 16S rRNA database. Kinetic of growth of this
isolate on crude oil during 20 days of culture was studied at temperature 25 °C, 3% (w/v)
of NaCl concentration and pH 7, at 140 rpm (Revolutions Per Minute). Strain SP49F2 was identified molecularly as Acinetobacter johnsonii, and might
support high concentrations of crude oil (up to 10%, v/v). Results of growth
kinetic on crude oil as sole energy and carbon source by the isolate strain
showed that the stationary phase was attained at day 12. Thus, train Acinetobacter johnsonii SP49F2 could
efficiently utilize crude oil as its sole carbon and energy source, and could
be used as a wonderful native biological alternative for the bioremediation of
the port of Oran, and marine area polluted by petroleum hydrocarbons, as an
eco-friendly efficacy degrader, and may be suitable for biotechnological
applications.
KEYWORDS
Crude oil, Acinetobacter
johnsonii, bioremediation, marine sediments, 16S rDNA.
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