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Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels

The emetic toxin cereulide produced by Bacillus cereus is synthesized by the modular enzyme complex Ces that is encoded on a pXO1-like megaplasmid. To decipher the role of the genes adjacent to the structural genes cesA/cesB, coding for the non-ribosomal peptide synthetase (NRPS), gene inactivation-...

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Autores principales: Lücking, Genia, Frenzel, Elrike, Rütschle, Andrea, Marxen, Sandra, Stark, Timo D., Hofmann, Thomas, Scherer, Siegfried, Ehling-Schulz, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602138/
https://www.ncbi.nlm.nih.gov/pubmed/26528255
http://dx.doi.org/10.3389/fmicb.2015.01101
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author Lücking, Genia
Frenzel, Elrike
Rütschle, Andrea
Marxen, Sandra
Stark, Timo D.
Hofmann, Thomas
Scherer, Siegfried
Ehling-Schulz, Monika
author_facet Lücking, Genia
Frenzel, Elrike
Rütschle, Andrea
Marxen, Sandra
Stark, Timo D.
Hofmann, Thomas
Scherer, Siegfried
Ehling-Schulz, Monika
author_sort Lücking, Genia
collection PubMed
description The emetic toxin cereulide produced by Bacillus cereus is synthesized by the modular enzyme complex Ces that is encoded on a pXO1-like megaplasmid. To decipher the role of the genes adjacent to the structural genes cesA/cesB, coding for the non-ribosomal peptide synthetase (NRPS), gene inactivation- and overexpression mutants of the emetic strain F4810/72 were constructed and their impact on cereulide biosynthesis was assessed. The hydrolase CesH turned out to be a part of the complex regulatory network controlling cereulide synthesis on a transcriptional level, while the ABC transporter CesCD was found to be essential for post-translational control of cereulide synthesis. Using a gene inactivation approach, we show that the NRPS activating function of the phosphopantetheinyl transferase (PPtase) embedded in the ces locus was complemented by a chromosomally encoded Sfp-like PPtase, representing an interesting example for the functional interaction between a plasmid encoded NRPS and a chromosomally encoded activation enzyme. In summary, our results highlight the complexity of cereulide biosynthesis and reveal multiple levels of toxin formation control. ces operon internal genes were shown to play a pivotal role by acting at different levels of toxin production, thus complementing the action of the chromosomal key transcriptional regulators AbrB and CodY.
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spelling pubmed-46021382015-11-02 Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels Lücking, Genia Frenzel, Elrike Rütschle, Andrea Marxen, Sandra Stark, Timo D. Hofmann, Thomas Scherer, Siegfried Ehling-Schulz, Monika Front Microbiol Microbiology The emetic toxin cereulide produced by Bacillus cereus is synthesized by the modular enzyme complex Ces that is encoded on a pXO1-like megaplasmid. To decipher the role of the genes adjacent to the structural genes cesA/cesB, coding for the non-ribosomal peptide synthetase (NRPS), gene inactivation- and overexpression mutants of the emetic strain F4810/72 were constructed and their impact on cereulide biosynthesis was assessed. The hydrolase CesH turned out to be a part of the complex regulatory network controlling cereulide synthesis on a transcriptional level, while the ABC transporter CesCD was found to be essential for post-translational control of cereulide synthesis. Using a gene inactivation approach, we show that the NRPS activating function of the phosphopantetheinyl transferase (PPtase) embedded in the ces locus was complemented by a chromosomally encoded Sfp-like PPtase, representing an interesting example for the functional interaction between a plasmid encoded NRPS and a chromosomally encoded activation enzyme. In summary, our results highlight the complexity of cereulide biosynthesis and reveal multiple levels of toxin formation control. ces operon internal genes were shown to play a pivotal role by acting at different levels of toxin production, thus complementing the action of the chromosomal key transcriptional regulators AbrB and CodY. Frontiers Media S.A. 2015-10-13 /pmc/articles/PMC4602138/ /pubmed/26528255 http://dx.doi.org/10.3389/fmicb.2015.01101 Text en Copyright © 2015 Lücking, Frenzel, Rütschle, Marxen, Stark, Hofmann, Scherer and Ehling-Schulz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Lücking, Genia
Frenzel, Elrike
Rütschle, Andrea
Marxen, Sandra
Stark, Timo D.
Hofmann, Thomas
Scherer, Siegfried
Ehling-Schulz, Monika
Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels
title Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels
title_full Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels
title_fullStr Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels
title_full_unstemmed Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels
title_short Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels
title_sort ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic bacillus cereus on multiple levels
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602138/
https://www.ncbi.nlm.nih.gov/pubmed/26528255
http://dx.doi.org/10.3389/fmicb.2015.01101
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