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The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen

BACKGROUND: The facultatively anaerobic betaproteobacterium Castellaniella defragrans 65Phen utilizes acyclic, monocyclic and bicyclic monoterpenes as sole carbon source under oxic as well as anoxic conditions. A biotransformation pathway of the acyclic β-myrcene required linalool dehydratase-isomer...

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Autores principales: Petasch, Jan, Disch, Eva-Maria, Markert, Stephanie, Becher, Dörte, Schweder, Thomas, Hüttel, Bruno, Reinhardt, Richard, Harder, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109377/
https://www.ncbi.nlm.nih.gov/pubmed/24952578
http://dx.doi.org/10.1186/1471-2180-14-164
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author Petasch, Jan
Disch, Eva-Maria
Markert, Stephanie
Becher, Dörte
Schweder, Thomas
Hüttel, Bruno
Reinhardt, Richard
Harder, Jens
author_facet Petasch, Jan
Disch, Eva-Maria
Markert, Stephanie
Becher, Dörte
Schweder, Thomas
Hüttel, Bruno
Reinhardt, Richard
Harder, Jens
author_sort Petasch, Jan
collection PubMed
description BACKGROUND: The facultatively anaerobic betaproteobacterium Castellaniella defragrans 65Phen utilizes acyclic, monocyclic and bicyclic monoterpenes as sole carbon source under oxic as well as anoxic conditions. A biotransformation pathway of the acyclic β-myrcene required linalool dehydratase-isomerase as initial enzyme acting on the hydrocarbon. An in-frame deletion mutant did not use myrcene, but was able to grow on monocyclic monoterpenes. The genome sequence and a comparative proteome analysis together with a random transposon mutagenesis were conducted to identify genes involved in the monocyclic monoterpene metabolism. Metabolites accumulating in cultures of transposon and in-frame deletion mutants disclosed the degradation pathway. RESULTS: Castellaniella defragrans 65Phen oxidizes the monocyclic monoterpene limonene at the primary methyl group forming perillyl alcohol. The genome of 3.95 Mb contained a 70 kb genome island coding for over 50 proteins involved in the monoterpene metabolism. This island showed higher homology to genes of another monoterpene-mineralizing betaproteobacterium, Thauera terpenica 58Eu(T), than to genomes of the family Alcaligenaceae, which harbors the genus Castellaniella. A collection of 72 transposon mutants unable to grow on limonene contained 17 inactivated genes, with 46 mutants located in the two genes ctmAB (cyclic terpene metabolism). CtmA and ctmB were annotated as FAD-dependent oxidoreductases and clustered together with ctmE, a 2Fe-2S ferredoxin gene, and ctmF, coding for a NADH:ferredoxin oxidoreductase. Transposon mutants of ctmA, B or E did not grow aerobically or anaerobically on limonene, but on perillyl alcohol. The next steps in the pathway are catalyzed by the geraniol dehydrogenase GeoA and the geranial dehydrogenase GeoB, yielding perillic acid. Two transposon mutants had inactivated genes of the monoterpene ring cleavage (mrc) pathway. 2-Methylcitrate synthase and 2-methylcitrate dehydratase were also essential for the monoterpene metabolism but not for growth on acetate. CONCLUSIONS: The genome of Castellaniella defragrans 65Phen is related to other genomes of Alcaligenaceae, but contains a genomic island with genes of the monoterpene metabolism. Castellaniella defragrans 65Phen degrades limonene via a limonene dehydrogenase and the oxidation of perillyl alcohol. The initial oxidation at the primary methyl group is independent of molecular oxygen.
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spelling pubmed-41093772014-07-25 The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen Petasch, Jan Disch, Eva-Maria Markert, Stephanie Becher, Dörte Schweder, Thomas Hüttel, Bruno Reinhardt, Richard Harder, Jens BMC Microbiol Research Article BACKGROUND: The facultatively anaerobic betaproteobacterium Castellaniella defragrans 65Phen utilizes acyclic, monocyclic and bicyclic monoterpenes as sole carbon source under oxic as well as anoxic conditions. A biotransformation pathway of the acyclic β-myrcene required linalool dehydratase-isomerase as initial enzyme acting on the hydrocarbon. An in-frame deletion mutant did not use myrcene, but was able to grow on monocyclic monoterpenes. The genome sequence and a comparative proteome analysis together with a random transposon mutagenesis were conducted to identify genes involved in the monocyclic monoterpene metabolism. Metabolites accumulating in cultures of transposon and in-frame deletion mutants disclosed the degradation pathway. RESULTS: Castellaniella defragrans 65Phen oxidizes the monocyclic monoterpene limonene at the primary methyl group forming perillyl alcohol. The genome of 3.95 Mb contained a 70 kb genome island coding for over 50 proteins involved in the monoterpene metabolism. This island showed higher homology to genes of another monoterpene-mineralizing betaproteobacterium, Thauera terpenica 58Eu(T), than to genomes of the family Alcaligenaceae, which harbors the genus Castellaniella. A collection of 72 transposon mutants unable to grow on limonene contained 17 inactivated genes, with 46 mutants located in the two genes ctmAB (cyclic terpene metabolism). CtmA and ctmB were annotated as FAD-dependent oxidoreductases and clustered together with ctmE, a 2Fe-2S ferredoxin gene, and ctmF, coding for a NADH:ferredoxin oxidoreductase. Transposon mutants of ctmA, B or E did not grow aerobically or anaerobically on limonene, but on perillyl alcohol. The next steps in the pathway are catalyzed by the geraniol dehydrogenase GeoA and the geranial dehydrogenase GeoB, yielding perillic acid. Two transposon mutants had inactivated genes of the monoterpene ring cleavage (mrc) pathway. 2-Methylcitrate synthase and 2-methylcitrate dehydratase were also essential for the monoterpene metabolism but not for growth on acetate. CONCLUSIONS: The genome of Castellaniella defragrans 65Phen is related to other genomes of Alcaligenaceae, but contains a genomic island with genes of the monoterpene metabolism. Castellaniella defragrans 65Phen degrades limonene via a limonene dehydrogenase and the oxidation of perillyl alcohol. The initial oxidation at the primary methyl group is independent of molecular oxygen. BioMed Central 2014-06-21 /pmc/articles/PMC4109377/ /pubmed/24952578 http://dx.doi.org/10.1186/1471-2180-14-164 Text en Copyright © 2014 Petasch et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Petasch, Jan
Disch, Eva-Maria
Markert, Stephanie
Becher, Dörte
Schweder, Thomas
Hüttel, Bruno
Reinhardt, Richard
Harder, Jens
The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen
title The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen
title_full The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen
title_fullStr The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen
title_full_unstemmed The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen
title_short The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen
title_sort oxygen-independent metabolism of cyclic monoterpenes in castellaniella defragrans 65phen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109377/
https://www.ncbi.nlm.nih.gov/pubmed/24952578
http://dx.doi.org/10.1186/1471-2180-14-164
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