Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>

<p>Abstract</p> <p>Background</p> <p><it>Acidithiobacillus ferrooxidans </it>gains energy from the oxidation of ferrous iron and various reduced inorganic sulfur compounds at very acidic pH. Although an initial model for the electron pathways involved in iro...

Full description

Bibliographic Details
Main Authors: Holmes David S, Jedlicki Eugenia, Denis Yann, Appia-Ayme Corinne, Quatrini Raquel, Bonnefoy Violaine
Format: Article
Language:English
Published: BMC 2009-08-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/10/394
id doaj-45560e683e8346a888ca5d5a04ee8804
record_format Article
spelling doaj-45560e683e8346a888ca5d5a04ee88042020-11-24T21:33:40ZengBMCBMC Genomics1471-21642009-08-0110139410.1186/1471-2164-10-394Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>Holmes David SJedlicki EugeniaDenis YannAppia-Ayme CorinneQuatrini RaquelBonnefoy Violaine<p>Abstract</p> <p>Background</p> <p><it>Acidithiobacillus ferrooxidans </it>gains energy from the oxidation of ferrous iron and various reduced inorganic sulfur compounds at very acidic pH. Although an initial model for the electron pathways involved in iron oxidation has been developed, much less is known about the sulfur oxidation in this microorganism. In addition, what has been reported for both iron and sulfur oxidation has been derived from different <it>A. ferrooxidans </it>strains, some of which have not been phylogenetically characterized and some have been shown to be mixed cultures. It is necessary to provide models of iron and sulfur oxidation pathways within one strain of <it>A. ferrooxidans </it>in order to comprehend the full metabolic potential of the pangenome of the genus.</p> <p>Results</p> <p>Bioinformatic-based metabolic reconstruction supported by microarray transcript profiling and quantitative RT-PCR analysis predicts the involvement of a number of novel genes involved in iron and sulfur oxidation in <it>A. ferrooxidans </it>ATCC23270. These include for iron oxidation: <it>cup </it>(copper oxidase-like), <it>ctaABT </it>(heme biogenesis and insertion), <it>nuoI </it>and <it>nuoK </it>(NADH complex subunits), <it>sdrA1 </it>(a NADH complex accessory protein) and <it>atpB </it>and <it>atpE </it>(ATP synthetase F0 subunits). The following new genes are predicted to be involved in reduced inorganic sulfur compounds oxidation: a gene cluster (<it>rhd, tusA, dsrE, hdrC, hdrB, hdrA, orf2, hdrC, hdrB</it>) encoding three sulfurtransferases and a heterodisulfide reductase complex, <it>sat </it>potentially encoding an ATP sulfurylase and <it>sdrA2 </it>(an accessory NADH complex subunit). Two different regulatory components are predicted to be involved in the regulation of alternate electron transfer pathways: 1) a gene cluster (<it>ctaRUS</it>) that contains a predicted iron responsive regulator of the Rrf2 family that is hypothesized to regulate cytochrome <it>aa</it><sub>3 </sub>oxidase biogenesis and 2) a two component sensor-regulator of the RegB-RegA family that may respond to the redox state of the quinone pool.</p> <p>Conclusion</p> <p>Bioinformatic analysis coupled with gene transcript profiling extends our understanding of the iron and reduced inorganic sulfur compounds oxidation pathways in <it>A. ferrooxidans </it>and suggests mechanisms for their regulation. The models provide unified and coherent descriptions of these processes within the type strain, eliminating previous ambiguity caused by models built from analyses of multiple and divergent strains of this microorganism.</p> http://www.biomedcentral.com/1471-2164/10/394
collection DOAJ
language English
format Article
sources DOAJ
author Holmes David S
Jedlicki Eugenia
Denis Yann
Appia-Ayme Corinne
Quatrini Raquel
Bonnefoy Violaine
spellingShingle Holmes David S
Jedlicki Eugenia
Denis Yann
Appia-Ayme Corinne
Quatrini Raquel
Bonnefoy Violaine
Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>
BMC Genomics
author_facet Holmes David S
Jedlicki Eugenia
Denis Yann
Appia-Ayme Corinne
Quatrini Raquel
Bonnefoy Violaine
author_sort Holmes David S
title Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>
title_short Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>
title_full Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>
title_fullStr Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>
title_full_unstemmed Extending the models for iron and sulfur oxidation in the extreme Acidophile <it>Acidithiobacillus ferrooxidans</it>
title_sort extending the models for iron and sulfur oxidation in the extreme acidophile <it>acidithiobacillus ferrooxidans</it>
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2009-08-01
description <p>Abstract</p> <p>Background</p> <p><it>Acidithiobacillus ferrooxidans </it>gains energy from the oxidation of ferrous iron and various reduced inorganic sulfur compounds at very acidic pH. Although an initial model for the electron pathways involved in iron oxidation has been developed, much less is known about the sulfur oxidation in this microorganism. In addition, what has been reported for both iron and sulfur oxidation has been derived from different <it>A. ferrooxidans </it>strains, some of which have not been phylogenetically characterized and some have been shown to be mixed cultures. It is necessary to provide models of iron and sulfur oxidation pathways within one strain of <it>A. ferrooxidans </it>in order to comprehend the full metabolic potential of the pangenome of the genus.</p> <p>Results</p> <p>Bioinformatic-based metabolic reconstruction supported by microarray transcript profiling and quantitative RT-PCR analysis predicts the involvement of a number of novel genes involved in iron and sulfur oxidation in <it>A. ferrooxidans </it>ATCC23270. These include for iron oxidation: <it>cup </it>(copper oxidase-like), <it>ctaABT </it>(heme biogenesis and insertion), <it>nuoI </it>and <it>nuoK </it>(NADH complex subunits), <it>sdrA1 </it>(a NADH complex accessory protein) and <it>atpB </it>and <it>atpE </it>(ATP synthetase F0 subunits). The following new genes are predicted to be involved in reduced inorganic sulfur compounds oxidation: a gene cluster (<it>rhd, tusA, dsrE, hdrC, hdrB, hdrA, orf2, hdrC, hdrB</it>) encoding three sulfurtransferases and a heterodisulfide reductase complex, <it>sat </it>potentially encoding an ATP sulfurylase and <it>sdrA2 </it>(an accessory NADH complex subunit). Two different regulatory components are predicted to be involved in the regulation of alternate electron transfer pathways: 1) a gene cluster (<it>ctaRUS</it>) that contains a predicted iron responsive regulator of the Rrf2 family that is hypothesized to regulate cytochrome <it>aa</it><sub>3 </sub>oxidase biogenesis and 2) a two component sensor-regulator of the RegB-RegA family that may respond to the redox state of the quinone pool.</p> <p>Conclusion</p> <p>Bioinformatic analysis coupled with gene transcript profiling extends our understanding of the iron and reduced inorganic sulfur compounds oxidation pathways in <it>A. ferrooxidans </it>and suggests mechanisms for their regulation. The models provide unified and coherent descriptions of these processes within the type strain, eliminating previous ambiguity caused by models built from analyses of multiple and divergent strains of this microorganism.</p>
url http://www.biomedcentral.com/1471-2164/10/394
work_keys_str_mv AT holmesdavids extendingthemodelsforironandsulfuroxidationintheextremeacidophileitacidithiobacillusferrooxidansit
AT jedlickieugenia extendingthemodelsforironandsulfuroxidationintheextremeacidophileitacidithiobacillusferrooxidansit
AT denisyann extendingthemodelsforironandsulfuroxidationintheextremeacidophileitacidithiobacillusferrooxidansit
AT appiaaymecorinne extendingthemodelsforironandsulfuroxidationintheextremeacidophileitacidithiobacillusferrooxidansit
AT quatriniraquel extendingthemodelsforironandsulfuroxidationintheextremeacidophileitacidithiobacillusferrooxidansit
AT bonnefoyviolaine extendingthemodelsforironandsulfuroxidationintheextremeacidophileitacidithiobacillusferrooxidansit
_version_ 1725952672271433728