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Identification and
molecular analysis of mercury resistant bacteria in Kor
River, Iran
Mehdi Kargar1, Mohammad Zareain Jahromi1*,
Mahmood Najafian1, Parastoo Khajeaian1,
Reza Nahavandi2,3,
Sareh Raeiszadeh Jahromi1 and
Mohammad
Firoozinia1
1Department
of Biology, Islamic Azad University, Jahrom Branch, Jahrom,
Iran.
2Laboratory
of Marine biotechnology, Institute of Bioscience, University
Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
3Iranian
Fisheries Research
Organization (I.F.R.O.), P.O. Box 14155-6116,
Tehran, Iran.
*Corresponding author.
E-mail:
obeidatgh@yahoo.com. Tel:
+962775609847. Fax: +96253530469.
Accepted 17 February, 2012
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Mercury (Hg) is one of the most important toxic pollutants
widespread in the environment. It is being extensively used
in industrial applications (chlor-alkali electrolysis,
fungicides, disinfectants, dental products, etc), resulting
in local hot spots of pollution and serious effects on biota
and humans. The aim of this study was to identify mercury
resistant bacteria and extract their plasmids and DNA.
In this study, mercury-resistant bacteria were isolated and
characterized from mercury-polluted sediments in Kor River
in Iran. The samples were cultured in different media
cultures, identified using biochemical tests, and due to the
relationship between antibiotic and mercury resistance, they
were isolated based on these two factors. The plasmids and
DNA were extracted from the most resistant bacteria to both
antibiotic and mercury and the sizes were determined using
agarose gel electrophoresis. A 12.3 Kb plasmid from Serattia
sp. and Escherichia coli and using Sau3A1 enzyme,
some DNA fragments (4, 6, 8 and 10 Kb) from Pseudomonas
sp., Serattia sp. and Escherichia coli were
also extracted.
Key words:
Mercury, resistant, bacteria, DNA, plasmid extraction,
restriction endonuclease. |