Cargando…

Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems

Enhanced biological phosphorus removal (EBPR) involves the cycling of biomass through carbon-rich (feast) and carbon-deficient (famine) conditions, promoting the activity of polyphosphate accumulating organisms (PAOs). However, several alternate metabolic strategies, without polyphosphate storage, a...

Descripción completa

Detalles Bibliográficos
Autores principales: McIlroy, Simon J., Onetto, Cristobal A., McIlroy, Bianca, Herbst, Florian-Alexander, Dueholm, Morten S., Kirkegaard, Rasmus H., Fernando, Eustace, Karst, Søren M., Nierychlo, Marta, Kristensen, Jannie M., Eales, Kathryn L., Grbin, Paul R., Wimmer, Reinhard, Nielsen, Per Halkjær
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974061/
https://www.ncbi.nlm.nih.gov/pubmed/29875741
http://dx.doi.org/10.3389/fmicb.2018.01004
_version_ 1783326738569232384
author McIlroy, Simon J.
Onetto, Cristobal A.
McIlroy, Bianca
Herbst, Florian-Alexander
Dueholm, Morten S.
Kirkegaard, Rasmus H.
Fernando, Eustace
Karst, Søren M.
Nierychlo, Marta
Kristensen, Jannie M.
Eales, Kathryn L.
Grbin, Paul R.
Wimmer, Reinhard
Nielsen, Per Halkjær
author_facet McIlroy, Simon J.
Onetto, Cristobal A.
McIlroy, Bianca
Herbst, Florian-Alexander
Dueholm, Morten S.
Kirkegaard, Rasmus H.
Fernando, Eustace
Karst, Søren M.
Nierychlo, Marta
Kristensen, Jannie M.
Eales, Kathryn L.
Grbin, Paul R.
Wimmer, Reinhard
Nielsen, Per Halkjær
author_sort McIlroy, Simon J.
collection PubMed
description Enhanced biological phosphorus removal (EBPR) involves the cycling of biomass through carbon-rich (feast) and carbon-deficient (famine) conditions, promoting the activity of polyphosphate accumulating organisms (PAOs). However, several alternate metabolic strategies, without polyphosphate storage, are possessed by other organisms, which can compete with the PAO for carbon at the potential expense of EBPR efficiency. The most studied are the glycogen accumulating organisms (GAOs), which utilize aerobically stored glycogen to energize anaerobic substrate uptake and storage. In full-scale systems the Micropruina spp. are among the most abundant of the proposed GAO, yet little is known about their ecophysiology. In the current study, genomic and metabolomic studies were performed on Micropruina glycogenica str. Lg2(T) and compared to the in situ physiology of members of the genus in EBPR plants using state-of-the-art single cell techniques. The Micropruina spp. were observed to take up carbon, including sugars and amino acids, under anaerobic conditions, which were partly fermented to lactic acid, acetate, propionate, and ethanol, and partly stored as glycogen for potential aerobic use. Fermentation was not directly demonstrated for the abundant members of the genus in situ, but was strongly supported by the confirmation of anaerobic uptake of carbon and glycogen storage in the absence of detectable polyhydroxyalkanoates or polyphosphate reserves. This physiology is markedly different from the classical GAO model. The amount of carbon stored by fermentative organisms has potentially important implications for phosphorus removal – as they compete for substrates with the Tetrasphaera PAO and stored carbon is not made available to the “Candidatus Accumulibacter” PAO under anaerobic conditions. This study shows that the current models of the competition between PAO and GAO are too simplistic and may need to be revised to take into account the impact of potential carbon storage by fermentative organisms.
format Online
Article
Text
id pubmed-5974061
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-59740612018-06-06 Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems McIlroy, Simon J. Onetto, Cristobal A. McIlroy, Bianca Herbst, Florian-Alexander Dueholm, Morten S. Kirkegaard, Rasmus H. Fernando, Eustace Karst, Søren M. Nierychlo, Marta Kristensen, Jannie M. Eales, Kathryn L. Grbin, Paul R. Wimmer, Reinhard Nielsen, Per Halkjær Front Microbiol Microbiology Enhanced biological phosphorus removal (EBPR) involves the cycling of biomass through carbon-rich (feast) and carbon-deficient (famine) conditions, promoting the activity of polyphosphate accumulating organisms (PAOs). However, several alternate metabolic strategies, without polyphosphate storage, are possessed by other organisms, which can compete with the PAO for carbon at the potential expense of EBPR efficiency. The most studied are the glycogen accumulating organisms (GAOs), which utilize aerobically stored glycogen to energize anaerobic substrate uptake and storage. In full-scale systems the Micropruina spp. are among the most abundant of the proposed GAO, yet little is known about their ecophysiology. In the current study, genomic and metabolomic studies were performed on Micropruina glycogenica str. Lg2(T) and compared to the in situ physiology of members of the genus in EBPR plants using state-of-the-art single cell techniques. The Micropruina spp. were observed to take up carbon, including sugars and amino acids, under anaerobic conditions, which were partly fermented to lactic acid, acetate, propionate, and ethanol, and partly stored as glycogen for potential aerobic use. Fermentation was not directly demonstrated for the abundant members of the genus in situ, but was strongly supported by the confirmation of anaerobic uptake of carbon and glycogen storage in the absence of detectable polyhydroxyalkanoates or polyphosphate reserves. This physiology is markedly different from the classical GAO model. The amount of carbon stored by fermentative organisms has potentially important implications for phosphorus removal – as they compete for substrates with the Tetrasphaera PAO and stored carbon is not made available to the “Candidatus Accumulibacter” PAO under anaerobic conditions. This study shows that the current models of the competition between PAO and GAO are too simplistic and may need to be revised to take into account the impact of potential carbon storage by fermentative organisms. Frontiers Media S.A. 2018-05-23 /pmc/articles/PMC5974061/ /pubmed/29875741 http://dx.doi.org/10.3389/fmicb.2018.01004 Text en Copyright © 2018 McIlroy, Onetto, McIlroy, Herbst, Dueholm, Kirkegaard, Fernando, Karst, Nierychlo, Kristensen, Eales, Grbin, Wimmer and Nielsen. 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) and the copyright owner 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
McIlroy, Simon J.
Onetto, Cristobal A.
McIlroy, Bianca
Herbst, Florian-Alexander
Dueholm, Morten S.
Kirkegaard, Rasmus H.
Fernando, Eustace
Karst, Søren M.
Nierychlo, Marta
Kristensen, Jannie M.
Eales, Kathryn L.
Grbin, Paul R.
Wimmer, Reinhard
Nielsen, Per Halkjær
Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems
title Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems
title_full Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems
title_fullStr Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems
title_full_unstemmed Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems
title_short Genomic and in Situ Analyses Reveal the Micropruina spp. as Abundant Fermentative Glycogen Accumulating Organisms in Enhanced Biological Phosphorus Removal Systems
title_sort genomic and in situ analyses reveal the micropruina spp. as abundant fermentative glycogen accumulating organisms in enhanced biological phosphorus removal systems
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974061/
https://www.ncbi.nlm.nih.gov/pubmed/29875741
http://dx.doi.org/10.3389/fmicb.2018.01004
work_keys_str_mv AT mcilroysimonj genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT onettocristobala genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT mcilroybianca genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT herbstflorianalexander genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT dueholmmortens genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT kirkegaardrasmush genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT fernandoeustace genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT karstsørenm genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT nierychlomarta genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT kristensenjanniem genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT ealeskathrynl genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT grbinpaulr genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT wimmerreinhard genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems
AT nielsenperhalkjær genomicandinsituanalysesrevealthemicropruinasppasabundantfermentativeglycogenaccumulatingorganismsinenhancedbiologicalphosphorusremovalsystems