Cargando…

Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass

BACKGROUND: Clostridium thermocellum is capable of solubilizing and converting lignocellulosic biomass into ethanol. Although much of the work-to-date has centered on characterizing this microbe’s growth on model cellulosic substrates, such as cellobiose, Avicel, or filter paper, it is vitally impor...

Descripción completa

Detalles Bibliográficos
Autores principales: Poudel, Suresh, Giannone, Richard J., Rodriguez, Miguel, Raman, Babu, Martin, Madhavi Z., Engle, Nancy L., Mielenz, Jonathan R., Nookaew, Intawat, Brown, Steven D., Tschaplinski, Timothy J., Ussery, David, Hettich, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223564/
https://www.ncbi.nlm.nih.gov/pubmed/28077967
http://dx.doi.org/10.1186/s13068-016-0697-5
_version_ 1782493193826205696
author Poudel, Suresh
Giannone, Richard J.
Rodriguez, Miguel
Raman, Babu
Martin, Madhavi Z.
Engle, Nancy L.
Mielenz, Jonathan R.
Nookaew, Intawat
Brown, Steven D.
Tschaplinski, Timothy J.
Ussery, David
Hettich, Robert L.
author_facet Poudel, Suresh
Giannone, Richard J.
Rodriguez, Miguel
Raman, Babu
Martin, Madhavi Z.
Engle, Nancy L.
Mielenz, Jonathan R.
Nookaew, Intawat
Brown, Steven D.
Tschaplinski, Timothy J.
Ussery, David
Hettich, Robert L.
author_sort Poudel, Suresh
collection PubMed
description BACKGROUND: Clostridium thermocellum is capable of solubilizing and converting lignocellulosic biomass into ethanol. Although much of the work-to-date has centered on characterizing this microbe’s growth on model cellulosic substrates, such as cellobiose, Avicel, or filter paper, it is vitally important to understand its metabolism on more complex, lignocellulosic substrates to identify relevant industrial bottlenecks that could undermine efficient biofuel production. To this end, we have examined a time course progression of C. thermocellum grown on switchgrass to assess the metabolic and protein changes that occur during the conversion of plant biomass to ethanol. RESULTS: The most striking feature of the metabolome was the observed accumulation of long-chain, branched fatty acids over time, implying an adaptive restructuring of C. thermocellum’s cellular membrane as the culture progresses. This is undoubtedly a response to the gradual accumulation of lignocellulose-derived inhibitory compounds as the organism deconstructs the switchgrass to access the embedded cellulose. Corroborating the metabolomics data, proteomic analysis revealed a corresponding time-dependent increase in various enzymes, including those involved in the interconversion of branched amino acids valine, leucine, and isoleucine to iso- and anteiso-fatty acid precursors. Additionally, the metabolic accumulation of hemicellulose-derived sugars and sugar alcohols concomitant with increased abundance of enzymes involved in C5 sugar metabolism/pentose phosphate pathway indicates that C. thermocellum shifts glycolytic intermediates to alternate pathways to modulate overall carbon flux in response to C5 sugar metabolites that increase during lignocellulose deconstruction. CONCLUSIONS: Integrated omic platforms provided complementary systems biological information that highlight C. thermocellum’s specific response to cytotoxic inhibitors released during the deconstruction and utilization of switchgrass. These additional viewpoints allowed us to fully realize the level to which the organism adapts to an increasingly challenging culture environment—information that will prove critical to C. thermocellum’s industrial efficacy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0697-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5223564
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-52235642017-01-11 Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass Poudel, Suresh Giannone, Richard J. Rodriguez, Miguel Raman, Babu Martin, Madhavi Z. Engle, Nancy L. Mielenz, Jonathan R. Nookaew, Intawat Brown, Steven D. Tschaplinski, Timothy J. Ussery, David Hettich, Robert L. Biotechnol Biofuels Research BACKGROUND: Clostridium thermocellum is capable of solubilizing and converting lignocellulosic biomass into ethanol. Although much of the work-to-date has centered on characterizing this microbe’s growth on model cellulosic substrates, such as cellobiose, Avicel, or filter paper, it is vitally important to understand its metabolism on more complex, lignocellulosic substrates to identify relevant industrial bottlenecks that could undermine efficient biofuel production. To this end, we have examined a time course progression of C. thermocellum grown on switchgrass to assess the metabolic and protein changes that occur during the conversion of plant biomass to ethanol. RESULTS: The most striking feature of the metabolome was the observed accumulation of long-chain, branched fatty acids over time, implying an adaptive restructuring of C. thermocellum’s cellular membrane as the culture progresses. This is undoubtedly a response to the gradual accumulation of lignocellulose-derived inhibitory compounds as the organism deconstructs the switchgrass to access the embedded cellulose. Corroborating the metabolomics data, proteomic analysis revealed a corresponding time-dependent increase in various enzymes, including those involved in the interconversion of branched amino acids valine, leucine, and isoleucine to iso- and anteiso-fatty acid precursors. Additionally, the metabolic accumulation of hemicellulose-derived sugars and sugar alcohols concomitant with increased abundance of enzymes involved in C5 sugar metabolism/pentose phosphate pathway indicates that C. thermocellum shifts glycolytic intermediates to alternate pathways to modulate overall carbon flux in response to C5 sugar metabolites that increase during lignocellulose deconstruction. CONCLUSIONS: Integrated omic platforms provided complementary systems biological information that highlight C. thermocellum’s specific response to cytotoxic inhibitors released during the deconstruction and utilization of switchgrass. These additional viewpoints allowed us to fully realize the level to which the organism adapts to an increasingly challenging culture environment—information that will prove critical to C. thermocellum’s industrial efficacy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0697-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-10 /pmc/articles/PMC5223564/ /pubmed/28077967 http://dx.doi.org/10.1186/s13068-016-0697-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Poudel, Suresh
Giannone, Richard J.
Rodriguez, Miguel
Raman, Babu
Martin, Madhavi Z.
Engle, Nancy L.
Mielenz, Jonathan R.
Nookaew, Intawat
Brown, Steven D.
Tschaplinski, Timothy J.
Ussery, David
Hettich, Robert L.
Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
title Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
title_full Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
title_fullStr Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
title_full_unstemmed Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
title_short Integrated omics analyses reveal the details of metabolic adaptation of Clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
title_sort integrated omics analyses reveal the details of metabolic adaptation of clostridium thermocellum to lignocellulose-derived growth inhibitors released during the deconstruction of switchgrass
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223564/
https://www.ncbi.nlm.nih.gov/pubmed/28077967
http://dx.doi.org/10.1186/s13068-016-0697-5
work_keys_str_mv AT poudelsuresh integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT giannonerichardj integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT rodriguezmiguel integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT ramanbabu integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT martinmadhaviz integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT englenancyl integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT mielenzjonathanr integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT nookaewintawat integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT brownstevend integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT tschaplinskitimothyj integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT usserydavid integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass
AT hettichrobertl integratedomicsanalysesrevealthedetailsofmetabolicadaptationofclostridiumthermocellumtolignocellulosederivedgrowthinhibitorsreleasedduringthedeconstructionofswitchgrass