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...
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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 |
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