Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1
The anaerobic isolate Enterobacter lignolyticus SCF1 was initially cultivated based on anaerobic growth on lignin as sole carbon source. The source of the isolated bacteria was from tropical forest soils that decompose litter rapidly with low and fluctuating redox potentials, making it likely that b...
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doaj-e945aa4a2c1a461db86844277c5d8b842020-11-25T00:04:59ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2013-09-01410.3389/fmicb.2013.0028059376Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1Kristen M DeAngelis0Deepak eSharma1Rebecca eVarney2Blake A Simmons3Blake A Simmons4Nancy G Isern5Lye Meng eMarkillie6Carrie D Nicora7Angela D Norbeck8Ronald C Taylor9Joshua T Aldrich10Errol W Robinson11University of Massachusetts AmherstUniversity of Massachusetts AmherstUniversity of Massachusetts AmherstSandia National LaboratoryJoint BioEnergy InstituteEnvrionmental Molecular Sciences LaboratoryEnvrionmental Molecular Sciences LaboratoryEnvrionmental Molecular Sciences LaboratoryEnvrionmental Molecular Sciences LaboratoryEnvrionmental Molecular Sciences LaboratoryEnvrionmental Molecular Sciences LaboratoryEnvrionmental Molecular Sciences LaboratoryThe anaerobic isolate Enterobacter lignolyticus SCF1 was initially cultivated based on anaerobic growth on lignin as sole carbon source. The source of the isolated bacteria was from tropical forest soils that decompose litter rapidly with low and fluctuating redox potentials, making it likely that bacteria using oxygen-independent enzymes play an important role in decomposition. We have used transcriptomics and proteomics to examine the increased growth of the anaerobic isolate Enterobacter lignolyticus SCF1 when grown on media amended with lignin compared to unamended growth. Proteomics revealed accelerated xylose uptake and metabolism under lignin-amended growth, and lignin degradation via the 4-hydroxyphenylacetate degradation pathway, catalase/peroxidase enzymes, and the glutathione biosynthesis and glutathione S-transferase proteins. We also observed increased production of NADH-quinone oxidoreductase, other electron transport chain proteins, and ATP synthase and ATP-binding cassette (ABC) transporters. We detected significant lignin degradation over time by absorbance, and also used metabolomics to demonstrate increased xylose utilization in lignin-amended compared to unamended growth. Our data shows the advantages of a multi-omics approach, where incomplete pathways identified by genomics were completed, and new observations made on coping with poor carbon availability. The fast growth, high efficiency and specificity of enzymes employed in bacterial anaerobic litter deconstruction makes these soils useful templates for improving biofuel production.http://journal.frontiersin.org/Journal/10.3389/fmicb.2013.00280/fullCatalaseEnterobacterGlutathioneLigninPeroxidaseProteomics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kristen M DeAngelis Deepak eSharma Rebecca eVarney Blake A Simmons Blake A Simmons Nancy G Isern Lye Meng eMarkillie Carrie D Nicora Angela D Norbeck Ronald C Taylor Joshua T Aldrich Errol W Robinson |
spellingShingle |
Kristen M DeAngelis Deepak eSharma Rebecca eVarney Blake A Simmons Blake A Simmons Nancy G Isern Lye Meng eMarkillie Carrie D Nicora Angela D Norbeck Ronald C Taylor Joshua T Aldrich Errol W Robinson Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1 Frontiers in Microbiology Catalase Enterobacter Glutathione Lignin Peroxidase Proteomics |
author_facet |
Kristen M DeAngelis Deepak eSharma Rebecca eVarney Blake A Simmons Blake A Simmons Nancy G Isern Lye Meng eMarkillie Carrie D Nicora Angela D Norbeck Ronald C Taylor Joshua T Aldrich Errol W Robinson |
author_sort |
Kristen M DeAngelis |
title |
Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1 |
title_short |
Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1 |
title_full |
Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1 |
title_fullStr |
Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1 |
title_full_unstemmed |
Evidence supporting dissimilatory and assimilatory lignin degradation in Enterobacter lignolyticus SCF1 |
title_sort |
evidence supporting dissimilatory and assimilatory lignin degradation in enterobacter lignolyticus scf1 |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Microbiology |
issn |
1664-302X |
publishDate |
2013-09-01 |
description |
The anaerobic isolate Enterobacter lignolyticus SCF1 was initially cultivated based on anaerobic growth on lignin as sole carbon source. The source of the isolated bacteria was from tropical forest soils that decompose litter rapidly with low and fluctuating redox potentials, making it likely that bacteria using oxygen-independent enzymes play an important role in decomposition. We have used transcriptomics and proteomics to examine the increased growth of the anaerobic isolate Enterobacter lignolyticus SCF1 when grown on media amended with lignin compared to unamended growth. Proteomics revealed accelerated xylose uptake and metabolism under lignin-amended growth, and lignin degradation via the 4-hydroxyphenylacetate degradation pathway, catalase/peroxidase enzymes, and the glutathione biosynthesis and glutathione S-transferase proteins. We also observed increased production of NADH-quinone oxidoreductase, other electron transport chain proteins, and ATP synthase and ATP-binding cassette (ABC) transporters. We detected significant lignin degradation over time by absorbance, and also used metabolomics to demonstrate increased xylose utilization in lignin-amended compared to unamended growth. Our data shows the advantages of a multi-omics approach, where incomplete pathways identified by genomics were completed, and new observations made on coping with poor carbon availability. The fast growth, high efficiency and specificity of enzymes employed in bacterial anaerobic litter deconstruction makes these soils useful templates for improving biofuel production. |
topic |
Catalase Enterobacter Glutathione Lignin Peroxidase Proteomics |
url |
http://journal.frontiersin.org/Journal/10.3389/fmicb.2013.00280/full |
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