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Proma Plasmids are Instrumental in the Dissemination of Linuron Catabolic Genes between Different Genera

Johannes Werner, Eman Nour, Boyke Bunk, Cathrin Spröer, Kornelia Smalla, Dirk Springael, View ORCID ProfileBaşak Öztürk
doi: https://doi.org/10.1101/831255
Johannes Werner
Department of Biological Oceanography, Leibniz Institute for Baltic Sea Research, Rostock, Germany
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Eman Nour
Institute for Epidemiology and Pathogen Diagnostics, Julius Kühn-Institut, Federal Research Centre for Cultivated Plants (JKI), Braunschweig, Germany
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Boyke Bunk
Bioinformatics Department, Leibniz Institute DSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany
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Cathrin Spröer
Central Services, Leibniz Institute DSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany
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Kornelia Smalla
Institute for Epidemiology and Pathogen Diagnostics, Julius Kühn-Institut, Federal Research Centre for Cultivated Plants (JKI), Braunschweig, Germany
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Dirk Springael
Division of Soil and Water Management, KU Leuven, Leuven, Belgium
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Başak Öztürk
Division of Soil and Water Management, KU Leuven, Leuven, BelgiumJunior Research Group Microbial Biotechnology, Leibniz Institute DSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany
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  • ORCID record for Başak Öztürk
  • For correspondence: basak.oeztuerk@dsmz.de
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ABSTRACT

PromA plasmids are broad host range plasmids, which are often cryptic and hence have an uncertain ecological role. We present three novel PromA γ plasmids which carry genes associated with degradation of the phenylurea herbicide linuron, two (pPBL-H3-2 and pBPS33-2) of which originate from unrelated Hydrogenophaga hosts isolated from different environments, and one (pEN1) which was exogenously captured from an on-farm biopurification system. Both Hydrogenophaga plasmids carry all three necessary gene clusters determining the three main steps for conversion of linuron to Krebs cycle intermediates, while pEN1 only determines the initial linuron hydrolysis step. Linuron catabolic gene clusters that determine the same step were identical on all plasmids, encompassed in differently arranged constellations and characterized by the presence of multiple IS1071 elements. In all plasmids except pEN1, the insertion spot of the catabolic genes in the PromA γ plasmids was the same. Highly similar PromA plasmids carrying the linuron degrading gene cargo at the same insertion spot were were previously identified in linuron degrading Variovorax sp. Interestingly, in both Hydrogenophaga populations not every PromA plasmid copy carries catabolic genes. The results indicate that PromA plasmids are important vehicles of linuron catabolic gene dissemination, rather than being cryptic and only important for the mobilization of other plasmids.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted November 05, 2019.
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Proma Plasmids are Instrumental in the Dissemination of Linuron Catabolic Genes between Different Genera
Johannes Werner, Eman Nour, Boyke Bunk, Cathrin Spröer, Kornelia Smalla, Dirk Springael, Başak Öztürk
bioRxiv 831255; doi: https://doi.org/10.1101/831255
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Proma Plasmids are Instrumental in the Dissemination of Linuron Catabolic Genes between Different Genera
Johannes Werner, Eman Nour, Boyke Bunk, Cathrin Spröer, Kornelia Smalla, Dirk Springael, Başak Öztürk
bioRxiv 831255; doi: https://doi.org/10.1101/831255

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