Cargando…

Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment

Thermal swamps are unique ecosystems where geothermally warmed waters mix with decomposing woody biomass, hosting novel biogeochemical-cycling and lignin-degrading microbial consortia. Assembly of shotgun metagenome libraries resolved 351 distinct genomes from hot-spring (30–45 °C) and mesophilic (1...

Descripción completa

Detalles Bibliográficos
Autores principales: Levy-Booth, David J., Hashimi, Ameena, Roccor, Raphael, Liu, Li-Yang, Renneckar, Scott, Eltis, Lindsay D., Mohn, William W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027834/
https://www.ncbi.nlm.nih.gov/pubmed/33139871
http://dx.doi.org/10.1038/s41396-020-00820-x
_version_ 1783675877450579968
author Levy-Booth, David J.
Hashimi, Ameena
Roccor, Raphael
Liu, Li-Yang
Renneckar, Scott
Eltis, Lindsay D.
Mohn, William W.
author_facet Levy-Booth, David J.
Hashimi, Ameena
Roccor, Raphael
Liu, Li-Yang
Renneckar, Scott
Eltis, Lindsay D.
Mohn, William W.
author_sort Levy-Booth, David J.
collection PubMed
description Thermal swamps are unique ecosystems where geothermally warmed waters mix with decomposing woody biomass, hosting novel biogeochemical-cycling and lignin-degrading microbial consortia. Assembly of shotgun metagenome libraries resolved 351 distinct genomes from hot-spring (30–45 °C) and mesophilic (17 °C) sediments. Annotation of 39 refined draft genomes revealed metabolism consistent with oligotrophy, including pathways for degradation of aromatic compounds, such as syringate, vanillate, p-hydroxybenzoate, and phenol. Thermotolerant Burkholderiales, including Rubrivivax ssp., were implicated in diverse biogeochemical and aromatic transformations, highlighting their broad metabolic capacity. Lignin catabolism was further investigated using metatranscriptomics of sediment incubated with milled or Kraft lignin at 45 °C. Aromatic compounds were depleted from lignin-amended sediment over 148 h. The metatranscriptomic data revealed upregulation of des/lig genes predicted to specify the catabolism of syringate, vanillate, and phenolic oligomers in the sphingomonads Altererythrobacter ssp. and Novosphingobium ssp., as well as in the Burkholderiales genus, Rubrivivax. This study demonstrates how temperature structures biogeochemical cycling populations in a unique ecosystem, and combines community-level metagenomics with targeted metatranscriptomics to identify pathways with potential for bio-refinement of lignin-derived aromatic compounds. In addition, the diverse aromatic catabolic pathways of Altererythrobacter ssp. may serve as a source of thermotolerant enzymes for lignin valorization.
format Online
Article
Text
id pubmed-8027834
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-80278342021-04-21 Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment Levy-Booth, David J. Hashimi, Ameena Roccor, Raphael Liu, Li-Yang Renneckar, Scott Eltis, Lindsay D. Mohn, William W. ISME J Article Thermal swamps are unique ecosystems where geothermally warmed waters mix with decomposing woody biomass, hosting novel biogeochemical-cycling and lignin-degrading microbial consortia. Assembly of shotgun metagenome libraries resolved 351 distinct genomes from hot-spring (30–45 °C) and mesophilic (17 °C) sediments. Annotation of 39 refined draft genomes revealed metabolism consistent with oligotrophy, including pathways for degradation of aromatic compounds, such as syringate, vanillate, p-hydroxybenzoate, and phenol. Thermotolerant Burkholderiales, including Rubrivivax ssp., were implicated in diverse biogeochemical and aromatic transformations, highlighting their broad metabolic capacity. Lignin catabolism was further investigated using metatranscriptomics of sediment incubated with milled or Kraft lignin at 45 °C. Aromatic compounds were depleted from lignin-amended sediment over 148 h. The metatranscriptomic data revealed upregulation of des/lig genes predicted to specify the catabolism of syringate, vanillate, and phenolic oligomers in the sphingomonads Altererythrobacter ssp. and Novosphingobium ssp., as well as in the Burkholderiales genus, Rubrivivax. This study demonstrates how temperature structures biogeochemical cycling populations in a unique ecosystem, and combines community-level metagenomics with targeted metatranscriptomics to identify pathways with potential for bio-refinement of lignin-derived aromatic compounds. In addition, the diverse aromatic catabolic pathways of Altererythrobacter ssp. may serve as a source of thermotolerant enzymes for lignin valorization. Nature Publishing Group UK 2020-11-02 2021-03 /pmc/articles/PMC8027834/ /pubmed/33139871 http://dx.doi.org/10.1038/s41396-020-00820-x Text en © The Author(s) 2020 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
Levy-Booth, David J.
Hashimi, Ameena
Roccor, Raphael
Liu, Li-Yang
Renneckar, Scott
Eltis, Lindsay D.
Mohn, William W.
Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
title Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
title_full Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
title_fullStr Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
title_full_unstemmed Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
title_short Genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
title_sort genomics and metatranscriptomics of biogeochemical cycling and degradation of lignin-derived aromatic compounds in thermal swamp sediment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027834/
https://www.ncbi.nlm.nih.gov/pubmed/33139871
http://dx.doi.org/10.1038/s41396-020-00820-x
work_keys_str_mv AT levyboothdavidj genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment
AT hashimiameena genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment
AT roccorraphael genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment
AT liuliyang genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment
AT renneckarscott genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment
AT eltislindsayd genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment
AT mohnwilliamw genomicsandmetatranscriptomicsofbiogeochemicalcyclinganddegradationofligninderivedaromaticcompoundsinthermalswampsediment