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Nucleic Acids Research Advance Access originally published online on March 13, 2007
Nucleic Acids Research 2007 35(7):2153-2166; doi:10.1093/nar/gkm068
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Nucleic Acids Research, 2007, Vol. 35, No. 7 2153-2166
© 2007 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Computational Biology

Bioinformatic prediction and experimental verification of Fur-regulated genes in the extreme acidophile Acidithiobacillus ferrooxidans

Raquel Quatrini1,*, Claudia Lefimil1, Felipe A. Veloso1, Inti Pedroso1, David S. Holmes1 and Eugenia Jedlicki2

1Center for Bioinformatics and Genome Biology, MIFAB, Life Science Foundation and Andrés Bello University, Santiago, Chile and 2ICBM, Faculty of Medicine, University of Chile, Santiago, Chile

*To whom correspondence should be addressed. Tel: 56 2 237 3014; Fax: 56 2 237 2259; Email: rquatrini{at}yahoo.com.ar

Received December 29, 2006. Revised January 16, 2007. Accepted January 22, 2007.

The {gamma}-proteobacterium Acidithiobacillus ferrooxidans lives in extremely acidic conditions (pH 2) and, unlike most organisms, is confronted with an abundant supply of soluble iron. It is also unusual in that it oxidizes iron as an energy source. Consequently, it faces the challenging dual problems of (i) maintaining intracellular iron homeostasis when confronted with extremely high environmental loads of iron and (ii) of regulating the use of iron both as an energy source and as a metabolic micronutrient. A combined bioinformatic and experimental approach was undertaken to identify Fur regulatory sites in the genome of A. ferrooxidans and to gain insight into the constitution of its Fur regulon. Fur regulatory targets associated with a variety of cellular functions including metal trafficking (e.g. feoPABC, tdr, tonBexbBD, copB, cdf), utilization (e.g. fdx, nif), transcriptional regulation (e.g. phoB, irr, iscR) and redox balance (grx, trx, gst) were identified. Selected predicted Fur regulatory sites were confirmed by FURTA, EMSA and in vitro transcription analyses. This study provides the first model for a Fur-binding site consensus sequence in an acidophilic iron-oxidizing microorganism and lays the foundation for future studies aimed at deepening our understanding of the regulatory networks that control iron uptake, homeostasis and oxidation in extreme acidophiles.


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