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Regulation of electron transfer processes affects phototrophic mat structure and activity

Phototrophic microbial mats are among the most diverse ecosystems in nature. These systems undergo daily cycles in redox potential caused by variations in light energy input and metabolic interactions among the microbial species. In this work, solid electrodes with controlled potentials were placed...

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Autores principales: Ha, Phuc T., Renslow, Ryan S., Atci, Erhan, Reardon, Patrick N., Lindemann, Stephen R., Fredrickson, James K., Call, Douglas R., Beyenal, Haluk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558538/
https://www.ncbi.nlm.nih.gov/pubmed/26388853
http://dx.doi.org/10.3389/fmicb.2015.00909
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author Ha, Phuc T.
Renslow, Ryan S.
Atci, Erhan
Reardon, Patrick N.
Lindemann, Stephen R.
Fredrickson, James K.
Call, Douglas R.
Beyenal, Haluk
author_facet Ha, Phuc T.
Renslow, Ryan S.
Atci, Erhan
Reardon, Patrick N.
Lindemann, Stephen R.
Fredrickson, James K.
Call, Douglas R.
Beyenal, Haluk
author_sort Ha, Phuc T.
collection PubMed
description Phototrophic microbial mats are among the most diverse ecosystems in nature. These systems undergo daily cycles in redox potential caused by variations in light energy input and metabolic interactions among the microbial species. In this work, solid electrodes with controlled potentials were placed under mats to study the electron transfer processes between the electrode and the microbial mat. The phototrophic microbial mat was harvested from Hot Lake, a hypersaline, epsomitic lake located near Oroville (Washington, USA). We operated two reactors: graphite electrodes were polarized at potentials of -700 mV(Ag/AgCl) [cathodic (CAT) mat system] and +300 mV(Ag/AgCl) [anodic (AN) mat system] and the electron transfer rates between the electrode and mat were monitored. We observed a diel cycle of electron transfer rates for both AN and CAT mat systems. Interestingly, the CAT mats generated the highest reducing current at the same time points that the AN mats showed the highest oxidizing current. To characterize the physicochemical factors influencing electron transfer processes, we measured depth profiles of dissolved oxygen (DO) and sulfide in the mats using microelectrodes. We further demonstrated that the mat-to-electrode and electrode-to-mat electron transfer rates were light- and temperature-dependent. Using nuclear magnetic resonance (NMR) imaging, we determined that the electrode potential regulated the diffusivity and porosity of the microbial mats. Both porosity and diffusivity were higher in the CAT mats than in the AN mats. We also used NMR spectroscopy for high-resolution quantitative metabolite analysis and found that the CAT mats had significantly higher concentrations of osmoprotectants such as betaine and trehalose. Subsequently, we performed amplicon sequencing across the V4 region of the 16S rRNA gene of incubated mats to understand the impact of electrode potential on microbial community structure. These data suggested that variation in the electrochemical conditions under which mats were generated significantly impacted the relative abundances of mat members and mat metabolism.
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spelling pubmed-45585382015-09-18 Regulation of electron transfer processes affects phototrophic mat structure and activity Ha, Phuc T. Renslow, Ryan S. Atci, Erhan Reardon, Patrick N. Lindemann, Stephen R. Fredrickson, James K. Call, Douglas R. Beyenal, Haluk Front Microbiol Microbiology Phototrophic microbial mats are among the most diverse ecosystems in nature. These systems undergo daily cycles in redox potential caused by variations in light energy input and metabolic interactions among the microbial species. In this work, solid electrodes with controlled potentials were placed under mats to study the electron transfer processes between the electrode and the microbial mat. The phototrophic microbial mat was harvested from Hot Lake, a hypersaline, epsomitic lake located near Oroville (Washington, USA). We operated two reactors: graphite electrodes were polarized at potentials of -700 mV(Ag/AgCl) [cathodic (CAT) mat system] and +300 mV(Ag/AgCl) [anodic (AN) mat system] and the electron transfer rates between the electrode and mat were monitored. We observed a diel cycle of electron transfer rates for both AN and CAT mat systems. Interestingly, the CAT mats generated the highest reducing current at the same time points that the AN mats showed the highest oxidizing current. To characterize the physicochemical factors influencing electron transfer processes, we measured depth profiles of dissolved oxygen (DO) and sulfide in the mats using microelectrodes. We further demonstrated that the mat-to-electrode and electrode-to-mat electron transfer rates were light- and temperature-dependent. Using nuclear magnetic resonance (NMR) imaging, we determined that the electrode potential regulated the diffusivity and porosity of the microbial mats. Both porosity and diffusivity were higher in the CAT mats than in the AN mats. We also used NMR spectroscopy for high-resolution quantitative metabolite analysis and found that the CAT mats had significantly higher concentrations of osmoprotectants such as betaine and trehalose. Subsequently, we performed amplicon sequencing across the V4 region of the 16S rRNA gene of incubated mats to understand the impact of electrode potential on microbial community structure. These data suggested that variation in the electrochemical conditions under which mats were generated significantly impacted the relative abundances of mat members and mat metabolism. Frontiers Media S.A. 2015-09-03 /pmc/articles/PMC4558538/ /pubmed/26388853 http://dx.doi.org/10.3389/fmicb.2015.00909 Text en Copyright © 2015 Ha, Renslow, Atci, Reardon, Lindemann, Fredrickson, Call and Beyenal. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Ha, Phuc T.
Renslow, Ryan S.
Atci, Erhan
Reardon, Patrick N.
Lindemann, Stephen R.
Fredrickson, James K.
Call, Douglas R.
Beyenal, Haluk
Regulation of electron transfer processes affects phototrophic mat structure and activity
title Regulation of electron transfer processes affects phototrophic mat structure and activity
title_full Regulation of electron transfer processes affects phototrophic mat structure and activity
title_fullStr Regulation of electron transfer processes affects phototrophic mat structure and activity
title_full_unstemmed Regulation of electron transfer processes affects phototrophic mat structure and activity
title_short Regulation of electron transfer processes affects phototrophic mat structure and activity
title_sort regulation of electron transfer processes affects phototrophic mat structure and activity
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558538/
https://www.ncbi.nlm.nih.gov/pubmed/26388853
http://dx.doi.org/10.3389/fmicb.2015.00909
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