Analysis of Gene Expression as Marker of Relevant Metabolisms, in Three Acidithiobacillus ferrooxidans Strains, in Different Growth Conditions

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Acidithiobacillus ferrooxidans is a chemiolithoautotrophic Gram-negative bacterium widely spread in ambient temperature bioleaching processes. Several strains of At. ferrooxidans were isolated and studied and, some time later, questions arise about whether it was a species with a wide metabolic variation or a group of closely related species. Advances in molecular biology, phylogeny and genomics have shed some light on At. ferrooxidans strains and allows their grouping according to their relations. However, significant challenges remains to be met, such as understanding how a particular strain faces environmental challenges and how a particular kind of adaptive response affects the growth and activity of the strain. The purpose of this study was to identify differential expression signals between At. ferrooxidans strains −with different abundances and dynamics− present in the bioleaching system at Escondida mine. Culture characterization and DNA macroarrays techniques provided some answers. Analysis of growth curves showed that IESL 32 had the highest anaerobic growth rate, while aerobic growth was similar for all strains. It was shown that though the phylogenetic analysis based on 16S rRNA sequences suggested a close relation between IESL 32 and the type strain ATCC 23270, the growth curves and the expression profile showed that the type strain and strain D2 had the closest similarity. Growth experiments under different conditions, together with the comparative analysis of gene expressions in At. ferrooxidans, could be a springboard for future investigations of strain characterization to broaden our knowledge about adaptation, metabolic strategies, regulation and microbial diversity in industrial processes.

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166-171

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October 2013

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[1] M. Dopson, C. Baker-Austin and P.L. Bond, Analysis of differential protein expression during growth states of Ferroplasma strains and insights into electron transport for iron oxidation. Microbiology. 151 (2005) 4127-4137.

DOI: 10.1099/mic.0.28362-0

Google Scholar

[2] R. Quatrini, C. Appia-Ayme, Y. Denis, E. Jedlicki, D. Holmes and V. Bonnefoy. Extending the models for iron and sulfur oxidation in the extreme acidophile Acidithiobacillus ferrooxidans. BMC Genom. 10 (2009): 394.

DOI: 10.1186/1471-2164-10-394

Google Scholar

[3] C. Demergasso, F. Galleguillos, P. Soto, M. Serón and V. Iturriaga, Microbial succession during a heap bioleaching cycle of low grade copper sulfides: Does this knowledge mean a real input for industrial process design and control? Hydrometallurgy, 104 (2010).

DOI: 10.1016/j.hydromet.2010.04.016

Google Scholar

[4] P. A. Galleguillos, K. B. Hallberg and D. B. Johnson, Microbial diversity and genetic response to stress conditions of extremophilic bacteria isolated from the Escondida copper mine, Adv. Mat. Res. 71-73 (2009) 55-58.

DOI: 10.4028/www.scientific.net/amr.71-73.55

Google Scholar

[5] C. Salazar, M. Acosta, P. Galleguillos, A. Shmaryahu, R. Quatrini, D.S. Holmes and, C. Demergasso, Analysis of gene expression in response to copper stress in Acidithiobacillus ferrooxidans strain D2, isolated from a copper bioleaching operation. In this issue.

DOI: 10.4028/www.scientific.net/amr.825.157

Google Scholar

[6] P. A. Galleguillos, Biodiversity and stress response of extremophilic prokaryotes isolated from the Escondida copper mine, Chile. PhD Thesis, Bangor University, (2011).

Google Scholar

[7] C.S. Davis-Belmar and P.R. Norris, Ferrous and pyrite oxidation by Acidimicrobium, species, Adv. Mat. Res. 71-73 (2009) 271-274.

DOI: 10.4028/www.scientific.net/amr.71-73.271

Google Scholar

[8] M. Acosta, S. Beard, J. Ponce, M. Vera, J.C. Mobarec and C.A. Jerez. Identification of putative sulfurtransferase genes in the extremophilic Acidithiobacillus ferrooxidans ATCC 23270 genome: structural and functional characterization of the proteins, OMICS. 9 (2005).

DOI: 10.1089/omi.2005.9.13

Google Scholar

[9] M. Vera, F. Pagliani, N. Guiliani, C. Jerez. The chemolithoautotroph Acidithiobacillus ferrooxidans can survive under phosphate-limiting conditions by expressing a C-P lyase operon that allows it to grow on phosphonates. Appl. Environ. Microbiol. 74 (2008).

DOI: 10.1128/aem.02101-07

Google Scholar

[10] D. K. Button, Kinetics of nutrient-limited transport and microbial growth, Microbiol. Rev. 49 (1985) 270-296.

DOI: 10.1128/mr.49.3.270-297.1985

Google Scholar

[11] M. Esparza, J.P. Cárdenas, B. Bowien, E. Jedlicki and D.S. Holmes, Genes and pathways for CO fixation in the obligate, chemolithoautotrophic acidophile, Acidithiobacillus ferrooxidans, carbon fixation in A. ferrooxidans. BMC Microbiol. 10 (2010).

DOI: 10.1186/1471-2180-10-229

Google Scholar

[12] K.C. Costa, P.M. Wong, T. Wang, T.J. Lie, J.A. Dodsworth, I. Swanson, J.A. Burn, M. Hackett and J.A. Leigh, Protein complexing in a methanogen suggests electron bifurcation and electron delivery from formate to heterodisulfide reductase. Proc Natl Acad Sci U S A. 107 (2010).

DOI: 10.1073/pnas.1003653107

Google Scholar

[13] H. Osorio, S. Mangold, Y. Denis, I. Nancucheo, M. Esparza, D.B. Johnson, V. Bonnefoy, M. Dopson and D.S. Holmes, Anaerobic Sulfur Metabolism Coupled to Dissimilatory Iron Reduction in the Extremophile Acidithiobacillus ferrooxidans. Appl. Environ. Microbiol. 79 (2013).

DOI: 10.1128/aem.03057-12

Google Scholar

[14] R.G. Sawers, Formate and its role in hydrogen production in Escherichia coli, Biochem. Soc. T. 33 (2005) 42–46.

DOI: 10.1042/bst0330042

Google Scholar

[15] S. Hedrich and D. B. Johnson, Acidithiobacillus ferridurans, sp. nov.; an acidophilic iron- , sulfur- and hydrogen-metabolizing chemolithotrophic Gammaproteobacterium. Int J Syst Evol Microbiol (2013) doi: 10. 1099 /ijs. 0. 049759-0.

DOI: 10.1099/ijs.0.049759-0

Google Scholar