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The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol

BACKGROUND: The betaproteobacterium Thauera linaloolentis 47Lol(T) was isolated on the tertiary monoterpene alcohol (R,S)-linalool as sole carbon and energy source under denitrifying conditions. Growth experiments indicated the formation of geraniol and geranial. Thus, a 3,1-hydroxyl-Δ(1)-Δ(2)-mutas...

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Autores principales: Marmulla, Robert, Cala, Edinson Puentes, Markert, Stephanie, Schweder, Thomas, Harder, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847356/
https://www.ncbi.nlm.nih.gov/pubmed/27118314
http://dx.doi.org/10.1186/s12866-016-0693-8
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author Marmulla, Robert
Cala, Edinson Puentes
Markert, Stephanie
Schweder, Thomas
Harder, Jens
author_facet Marmulla, Robert
Cala, Edinson Puentes
Markert, Stephanie
Schweder, Thomas
Harder, Jens
author_sort Marmulla, Robert
collection PubMed
description BACKGROUND: The betaproteobacterium Thauera linaloolentis 47Lol(T) was isolated on the tertiary monoterpene alcohol (R,S)-linalool as sole carbon and energy source under denitrifying conditions. Growth experiments indicated the formation of geraniol and geranial. Thus, a 3,1-hydroxyl-Δ(1)-Δ(2)-mutase (linalool isomerase) activity may initiate the degradation, followed by enzymes of the acyclic terpene utilization (Atu) and leucine/isovalerate utilization (Liu) pathways that were extensively studied in Pseudomonas spp. growing on citronellol or geraniol. RESULTS: A transposon mutagenesis yielded 39 transconjugants that could not grow anaerobically on linalool and nitrate in liquid medium. The deficiencies were apparently based on gene functions required to overcome the toxicity of linalool, but not due to inactivation of genes in the degradation pathway. Growing cultures formed geraniol and geranial transiently, but also geranic acid. Analysis of expressed proteins detected several enzymes of the Atu and Liu pathways. The draft genome of T. linaloolentis 47Lol(T) had atu and liu genes with homology to those of Pseudomonas spp.. CONCLUSION: The in comparison to monoterpenes larger toxicity of monoterpene alcohols is defeated by several modifications of the cellular structure and metabolism in Thauera linaloolentis 47Lol(T). The acyclic terpene utilization pathway is used in T. linaloolentis 47Lol(T) during growth on (R,S)-linalool and nitrate under anoxic conditions. This is the first experimental verification of an active Atu pathway outside of the genus Pseudomonas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0693-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-48473562016-04-28 The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol Marmulla, Robert Cala, Edinson Puentes Markert, Stephanie Schweder, Thomas Harder, Jens BMC Microbiol Research Article BACKGROUND: The betaproteobacterium Thauera linaloolentis 47Lol(T) was isolated on the tertiary monoterpene alcohol (R,S)-linalool as sole carbon and energy source under denitrifying conditions. Growth experiments indicated the formation of geraniol and geranial. Thus, a 3,1-hydroxyl-Δ(1)-Δ(2)-mutase (linalool isomerase) activity may initiate the degradation, followed by enzymes of the acyclic terpene utilization (Atu) and leucine/isovalerate utilization (Liu) pathways that were extensively studied in Pseudomonas spp. growing on citronellol or geraniol. RESULTS: A transposon mutagenesis yielded 39 transconjugants that could not grow anaerobically on linalool and nitrate in liquid medium. The deficiencies were apparently based on gene functions required to overcome the toxicity of linalool, but not due to inactivation of genes in the degradation pathway. Growing cultures formed geraniol and geranial transiently, but also geranic acid. Analysis of expressed proteins detected several enzymes of the Atu and Liu pathways. The draft genome of T. linaloolentis 47Lol(T) had atu and liu genes with homology to those of Pseudomonas spp.. CONCLUSION: The in comparison to monoterpenes larger toxicity of monoterpene alcohols is defeated by several modifications of the cellular structure and metabolism in Thauera linaloolentis 47Lol(T). The acyclic terpene utilization pathway is used in T. linaloolentis 47Lol(T) during growth on (R,S)-linalool and nitrate under anoxic conditions. This is the first experimental verification of an active Atu pathway outside of the genus Pseudomonas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0693-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-27 /pmc/articles/PMC4847356/ /pubmed/27118314 http://dx.doi.org/10.1186/s12866-016-0693-8 Text en © Marmulla et al. 2016 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 Article
Marmulla, Robert
Cala, Edinson Puentes
Markert, Stephanie
Schweder, Thomas
Harder, Jens
The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol
title The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol
title_full The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol
title_fullStr The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol
title_full_unstemmed The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol
title_short The anaerobic linalool metabolism in Thauera linaloolentis 47 Lol
title_sort anaerobic linalool metabolism in thauera linaloolentis 47 lol
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847356/
https://www.ncbi.nlm.nih.gov/pubmed/27118314
http://dx.doi.org/10.1186/s12866-016-0693-8
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