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Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)

Leptospirillum ferriphilum plays a major role in acidic, metal-rich environments, where it represents one of the most prevalent iron oxidizers. These milieus include acid rock and mine drainage as well as biomining operations. Despite its perceived importance, no complete genome sequence of the type...

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Autores principales: Christel, Stephan, Herold, Malte, Bellenberg, Sören, El Hajjami, Mohamed, Buetti-Dinh, Antoine, Pivkin, Igor V., Sand, Wolfgang, Wilmes, Paul, Poetsch, Ansgar, Dopson, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772234/
https://www.ncbi.nlm.nih.gov/pubmed/29150517
http://dx.doi.org/10.1128/AEM.02091-17
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author Christel, Stephan
Herold, Malte
Bellenberg, Sören
El Hajjami, Mohamed
Buetti-Dinh, Antoine
Pivkin, Igor V.
Sand, Wolfgang
Wilmes, Paul
Poetsch, Ansgar
Dopson, Mark
author_facet Christel, Stephan
Herold, Malte
Bellenberg, Sören
El Hajjami, Mohamed
Buetti-Dinh, Antoine
Pivkin, Igor V.
Sand, Wolfgang
Wilmes, Paul
Poetsch, Ansgar
Dopson, Mark
author_sort Christel, Stephan
collection PubMed
description Leptospirillum ferriphilum plays a major role in acidic, metal-rich environments, where it represents one of the most prevalent iron oxidizers. These milieus include acid rock and mine drainage as well as biomining operations. Despite its perceived importance, no complete genome sequence of the type strain of this model species is available, limiting the possibilities to investigate the strategies and adaptations that Leptospirillum ferriphilum DSM 14647(T) (here referred to as Leptospirillum ferriphilum(T)) applies to survive and compete in its niche. This study presents a complete, circular genome of Leptospirillum ferriphilum(T) obtained by PacBio single-molecule real-time (SMRT) long-read sequencing for use as a high-quality reference. Analysis of the functionally annotated genome, mRNA transcripts, and protein concentrations revealed a previously undiscovered nitrogenase cluster for atmospheric nitrogen fixation and elucidated metabolic systems taking part in energy conservation, carbon fixation, pH homeostasis, heavy metal tolerance, the oxidative stress response, chemotaxis and motility, quorum sensing, and biofilm formation. Additionally, mRNA transcript counts and protein concentrations were compared between cells grown in continuous culture using ferrous iron as the substrate and those grown in bioleaching cultures containing chalcopyrite (CuFeS(2)). Adaptations of Leptospirillum ferriphilum(T) to growth on chalcopyrite included the possibly enhanced production of reducing power, reduced carbon dioxide fixation, as well as elevated levels of RNA transcripts and proteins involved in heavy metal resistance, with special emphasis on copper efflux systems. Finally, the expression and translation of genes responsible for chemotaxis and motility were enhanced. IMPORTANCE Leptospirillum ferriphilum is one of the most important iron oxidizers in the context of acidic and metal-rich environments during moderately thermophilic biomining. A high-quality circular genome of Leptospirillum ferriphilum(T) coupled with functional omics data provides new insights into its metabolic properties, such as the novel identification of genes for atmospheric nitrogen fixation, and represents an essential step for further accurate proteomic and transcriptomic investigation of this acidophile model species in the future. Additionally, light is shed on adaptation strategies of Leptospirillum ferriphilum(T) for growth on the copper mineral chalcopyrite. These data can be applied to deepen our understanding and optimization of bioleaching and biooxidation, techniques that present sustainable and environmentally friendly alternatives to many traditional methods for metal extraction.
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spelling pubmed-57722342018-01-29 Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T) Christel, Stephan Herold, Malte Bellenberg, Sören El Hajjami, Mohamed Buetti-Dinh, Antoine Pivkin, Igor V. Sand, Wolfgang Wilmes, Paul Poetsch, Ansgar Dopson, Mark Appl Environ Microbiol Evolutionary and Genomic Microbiology Leptospirillum ferriphilum plays a major role in acidic, metal-rich environments, where it represents one of the most prevalent iron oxidizers. These milieus include acid rock and mine drainage as well as biomining operations. Despite its perceived importance, no complete genome sequence of the type strain of this model species is available, limiting the possibilities to investigate the strategies and adaptations that Leptospirillum ferriphilum DSM 14647(T) (here referred to as Leptospirillum ferriphilum(T)) applies to survive and compete in its niche. This study presents a complete, circular genome of Leptospirillum ferriphilum(T) obtained by PacBio single-molecule real-time (SMRT) long-read sequencing for use as a high-quality reference. Analysis of the functionally annotated genome, mRNA transcripts, and protein concentrations revealed a previously undiscovered nitrogenase cluster for atmospheric nitrogen fixation and elucidated metabolic systems taking part in energy conservation, carbon fixation, pH homeostasis, heavy metal tolerance, the oxidative stress response, chemotaxis and motility, quorum sensing, and biofilm formation. Additionally, mRNA transcript counts and protein concentrations were compared between cells grown in continuous culture using ferrous iron as the substrate and those grown in bioleaching cultures containing chalcopyrite (CuFeS(2)). Adaptations of Leptospirillum ferriphilum(T) to growth on chalcopyrite included the possibly enhanced production of reducing power, reduced carbon dioxide fixation, as well as elevated levels of RNA transcripts and proteins involved in heavy metal resistance, with special emphasis on copper efflux systems. Finally, the expression and translation of genes responsible for chemotaxis and motility were enhanced. IMPORTANCE Leptospirillum ferriphilum is one of the most important iron oxidizers in the context of acidic and metal-rich environments during moderately thermophilic biomining. A high-quality circular genome of Leptospirillum ferriphilum(T) coupled with functional omics data provides new insights into its metabolic properties, such as the novel identification of genes for atmospheric nitrogen fixation, and represents an essential step for further accurate proteomic and transcriptomic investigation of this acidophile model species in the future. Additionally, light is shed on adaptation strategies of Leptospirillum ferriphilum(T) for growth on the copper mineral chalcopyrite. These data can be applied to deepen our understanding and optimization of bioleaching and biooxidation, techniques that present sustainable and environmentally friendly alternatives to many traditional methods for metal extraction. American Society for Microbiology 2018-01-17 /pmc/articles/PMC5772234/ /pubmed/29150517 http://dx.doi.org/10.1128/AEM.02091-17 Text en Copyright © 2018 Christel et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Evolutionary and Genomic Microbiology
Christel, Stephan
Herold, Malte
Bellenberg, Sören
El Hajjami, Mohamed
Buetti-Dinh, Antoine
Pivkin, Igor V.
Sand, Wolfgang
Wilmes, Paul
Poetsch, Ansgar
Dopson, Mark
Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)
title Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)
title_full Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)
title_fullStr Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)
title_full_unstemmed Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)
title_short Multi-omics Reveals the Lifestyle of the Acidophilic, Mineral-Oxidizing Model Species Leptospirillum ferriphilum(T)
title_sort multi-omics reveals the lifestyle of the acidophilic, mineral-oxidizing model species leptospirillum ferriphilum(t)
topic Evolutionary and Genomic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772234/
https://www.ncbi.nlm.nih.gov/pubmed/29150517
http://dx.doi.org/10.1128/AEM.02091-17
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