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Validation of arsenic resistance in Bacillus cereus strain AG27 by comparative protein modeling of arsC gene product.
- Source :
-
The protein journal [Protein J] 2011 Feb; Vol. 30 (2), pp. 91-101. - Publication Year :
- 2011
-
Abstract
- The ars gene system provides arsenic resistance to a variety of microorganisms and can be chromosomal or plasmid-borne. The arsC gene, which codes for an arsenate reductase is essential for arsenate resistance and transforms arsenate into arsenite, which is extruded from the cell. Therefore, arsC gene from Bacillus cereus strain AG27 isolated from soil was amplified, cloned and sequenced. The strain exhibited a minimum inhibitory concentration of 40 and 35 mM to sodium arsenate and sodium arsenite, respectively. Homology of the sequence, when compared with available database using BLASTn search showed that 300 bp amplicons obtained possess partial arsC gene sequence which codes for arsenate reductase, an enzyme involved in the reduction of arsenate to arsenite which is then effluxed out of the cell, thereby indicating the presence of efflux mechanism of resistance in strain. The efflux mechanism was further confirmed by atomic absorption spectroscopy and scanning electron microscopy studies. Moreover, three dimensional structure of modeled arsC from Bacillus cereus strain shares significant structural similarity with arsenate reductase protein of B.subtilis, consisting of, highly similar overall fold with single α/β domain containing a central four stranded, parallel, open-twisted β-sheet flanked by α-helices on both sides. The structure harbors the arsenic binding motif AB loop or P-loop that is highly conserved in arsenate reductase family.
- Subjects :
- Amino Acid Sequence
Arsenate Reductases genetics
Arsenate Reductases metabolism
Arsenates chemistry
Arsenates metabolism
Arsenic chemistry
Arsenites chemistry
Arsenites metabolism
Computer Simulation
Microbial Sensitivity Tests
Models, Molecular
Molecular Sequence Data
Protein Folding
Protein Structure, Secondary
RNA, Ribosomal, 16S chemistry
RNA, Ribosomal, 16S genetics
Arsenate Reductases chemistry
Arsenic toxicity
Bacillus cereus drug effects
Bacillus cereus enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1875-8355
- Volume :
- 30
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The protein journal
- Publication Type :
- Academic Journal
- Accession number :
- 21258851
- Full Text :
- https://doi.org/10.1007/s10930-011-9305-5