Cargando…

Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes

Some microbes can capture energy through redox reactions with electron flow to solid-phase electron acceptors, such as metal-oxides or poised electrodes, via extracellular electron transfer (EET). While diverse oxide minerals, exhibiting different surface redox potentials, are widely distributed on...

Descripción completa

Detalles Bibliográficos
Autores principales: Ishii, Shun’ichi, Suzuki, Shino, Tenney, Aaron, Nealson, Kenneth H., Bretschger, Orianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246609/
https://www.ncbi.nlm.nih.gov/pubmed/30050163
http://dx.doi.org/10.1038/s41396-018-0238-2
_version_ 1783372365742211072
author Ishii, Shun’ichi
Suzuki, Shino
Tenney, Aaron
Nealson, Kenneth H.
Bretschger, Orianna
author_facet Ishii, Shun’ichi
Suzuki, Shino
Tenney, Aaron
Nealson, Kenneth H.
Bretschger, Orianna
author_sort Ishii, Shun’ichi
collection PubMed
description Some microbes can capture energy through redox reactions with electron flow to solid-phase electron acceptors, such as metal-oxides or poised electrodes, via extracellular electron transfer (EET). While diverse oxide minerals, exhibiting different surface redox potentials, are widely distributed on Earth, little is known about how microbes sense and use the minerals. Here we show electrochemical, metabolic, and transcriptional responses of EET-active microbial communities established on poised electrodes to changes in the surface redox potentials (as electron acceptors) and surrounding substrates (as electron donors). Combination of genome-centric stimulus-induced metatranscriptomics and metabolic pathway investigation revealed that nine Geobacter/Pelobacter microbes performed EET activity differently according to their preferable surface potentials and substrates. While the Geobacter/Pelobacter microbes coded numerous numbers of multi-heme c-type cytochromes and conductive e-pili, wide variations in gene expression were seen in response to altering surrounding substrates and surface potentials, accelerating EET via poised electrode or limiting EET via an open circuit system. These flexible responses suggest that a wide variety of EET-active microbes utilizing diverse EET mechanisms may work together to provide such EET-active communities with an impressive ability to handle major changes in surface potential and carbon source availability.
format Online
Article
Text
id pubmed-6246609
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62466092018-11-21 Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes Ishii, Shun’ichi Suzuki, Shino Tenney, Aaron Nealson, Kenneth H. Bretschger, Orianna ISME J Article Some microbes can capture energy through redox reactions with electron flow to solid-phase electron acceptors, such as metal-oxides or poised electrodes, via extracellular electron transfer (EET). While diverse oxide minerals, exhibiting different surface redox potentials, are widely distributed on Earth, little is known about how microbes sense and use the minerals. Here we show electrochemical, metabolic, and transcriptional responses of EET-active microbial communities established on poised electrodes to changes in the surface redox potentials (as electron acceptors) and surrounding substrates (as electron donors). Combination of genome-centric stimulus-induced metatranscriptomics and metabolic pathway investigation revealed that nine Geobacter/Pelobacter microbes performed EET activity differently according to their preferable surface potentials and substrates. While the Geobacter/Pelobacter microbes coded numerous numbers of multi-heme c-type cytochromes and conductive e-pili, wide variations in gene expression were seen in response to altering surrounding substrates and surface potentials, accelerating EET via poised electrode or limiting EET via an open circuit system. These flexible responses suggest that a wide variety of EET-active microbes utilizing diverse EET mechanisms may work together to provide such EET-active communities with an impressive ability to handle major changes in surface potential and carbon source availability. Nature Publishing Group UK 2018-07-26 2018-12 /pmc/articles/PMC6246609/ /pubmed/30050163 http://dx.doi.org/10.1038/s41396-018-0238-2 Text en © International Society for Microbial Ecology 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ishii, Shun’ichi
Suzuki, Shino
Tenney, Aaron
Nealson, Kenneth H.
Bretschger, Orianna
Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
title Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
title_full Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
title_fullStr Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
title_full_unstemmed Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
title_short Comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
title_sort comparative metatranscriptomics reveals extracellular electron transfer pathways conferring microbial adaptivity to surface redox potential changes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246609/
https://www.ncbi.nlm.nih.gov/pubmed/30050163
http://dx.doi.org/10.1038/s41396-018-0238-2
work_keys_str_mv AT ishiishunichi comparativemetatranscriptomicsrevealsextracellularelectrontransferpathwaysconferringmicrobialadaptivitytosurfaceredoxpotentialchanges
AT suzukishino comparativemetatranscriptomicsrevealsextracellularelectrontransferpathwaysconferringmicrobialadaptivitytosurfaceredoxpotentialchanges
AT tenneyaaron comparativemetatranscriptomicsrevealsextracellularelectrontransferpathwaysconferringmicrobialadaptivitytosurfaceredoxpotentialchanges
AT nealsonkennethh comparativemetatranscriptomicsrevealsextracellularelectrontransferpathwaysconferringmicrobialadaptivitytosurfaceredoxpotentialchanges
AT bretschgerorianna comparativemetatranscriptomicsrevealsextracellularelectrontransferpathwaysconferringmicrobialadaptivitytosurfaceredoxpotentialchanges