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A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin
Brasilicardin A (BraA) is a promising immunosuppressive compound produced naturally by the pathogenic bacterium Nocardia terpenica IFM 0406. Heterologous host expression of brasilicardin gene cluster showed to be efficient to bypass the safety issues, low production levels and lack of genetic tools...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837296/ https://www.ncbi.nlm.nih.gov/pubmed/33531886 http://dx.doi.org/10.1002/elsc.202000038 |
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author | Wolański, Marcin Krawiec, Michał Schwarz, Paul N. Stegmann, Evi Wohlleben, Wolfgang Buchmann, Anina Gross, Harald Eitel, Michael Koch, Pierre Botas, Alma Méndez, Carmen Núñez, Luz Elena Morís, Francisco Cortés, Jesus Zakrzewska‐Czerwińska, Jolanta |
author_facet | Wolański, Marcin Krawiec, Michał Schwarz, Paul N. Stegmann, Evi Wohlleben, Wolfgang Buchmann, Anina Gross, Harald Eitel, Michael Koch, Pierre Botas, Alma Méndez, Carmen Núñez, Luz Elena Morís, Francisco Cortés, Jesus Zakrzewska‐Czerwińska, Jolanta |
author_sort | Wolański, Marcin |
collection | PubMed |
description | Brasilicardin A (BraA) is a promising immunosuppressive compound produced naturally by the pathogenic bacterium Nocardia terpenica IFM 0406. Heterologous host expression of brasilicardin gene cluster showed to be efficient to bypass the safety issues, low production levels and lack of genetic tools related with the use of native producer. Further improvement of production yields requires better understanding of gene expression regulation within the BraA biosynthetic gene cluster (Bra‐BGC); however, the only so far known regulator of this gene cluster is Bra12. In this study, we discovered the protein LysRNt, a novel member of the LysR‐type transcriptional regulator family, as a regulator of the Bra‐BGC. Using in vitro approaches, we identified the gene promoters which are controlled by LysRNt within the Bra‐BGC. Corresponding genes encode enzymes involved in BraA biosynthesis as well as the key Bra‐BGC regulator Bra12. Importantly, we provide in vivo evidence that LysRNt negatively affects production of brasilicardin congeners in the heterologous host Amycolatopsis japonicum. Finally, we demonstrate that some of the pathway related metabolites, and their chemical analogs, can interact with LysRNt which in turn affects its DNA‐binding activity. |
format | Online Article Text |
id | pubmed-7837296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78372962021-02-01 A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin Wolański, Marcin Krawiec, Michał Schwarz, Paul N. Stegmann, Evi Wohlleben, Wolfgang Buchmann, Anina Gross, Harald Eitel, Michael Koch, Pierre Botas, Alma Méndez, Carmen Núñez, Luz Elena Morís, Francisco Cortés, Jesus Zakrzewska‐Czerwińska, Jolanta Eng Life Sci Research Articles Brasilicardin A (BraA) is a promising immunosuppressive compound produced naturally by the pathogenic bacterium Nocardia terpenica IFM 0406. Heterologous host expression of brasilicardin gene cluster showed to be efficient to bypass the safety issues, low production levels and lack of genetic tools related with the use of native producer. Further improvement of production yields requires better understanding of gene expression regulation within the BraA biosynthetic gene cluster (Bra‐BGC); however, the only so far known regulator of this gene cluster is Bra12. In this study, we discovered the protein LysRNt, a novel member of the LysR‐type transcriptional regulator family, as a regulator of the Bra‐BGC. Using in vitro approaches, we identified the gene promoters which are controlled by LysRNt within the Bra‐BGC. Corresponding genes encode enzymes involved in BraA biosynthesis as well as the key Bra‐BGC regulator Bra12. Importantly, we provide in vivo evidence that LysRNt negatively affects production of brasilicardin congeners in the heterologous host Amycolatopsis japonicum. Finally, we demonstrate that some of the pathway related metabolites, and their chemical analogs, can interact with LysRNt which in turn affects its DNA‐binding activity. John Wiley and Sons Inc. 2020-11-04 /pmc/articles/PMC7837296/ /pubmed/33531886 http://dx.doi.org/10.1002/elsc.202000038 Text en © 2020 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wolański, Marcin Krawiec, Michał Schwarz, Paul N. Stegmann, Evi Wohlleben, Wolfgang Buchmann, Anina Gross, Harald Eitel, Michael Koch, Pierre Botas, Alma Méndez, Carmen Núñez, Luz Elena Morís, Francisco Cortés, Jesus Zakrzewska‐Czerwińska, Jolanta A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
title | A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
title_full | A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
title_fullStr | A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
title_full_unstemmed | A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
title_short | A novel LysR‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
title_sort | novel lysr‐type regulator negatively affects biosynthesis of the immunosuppressant brasilicardin |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837296/ https://www.ncbi.nlm.nih.gov/pubmed/33531886 http://dx.doi.org/10.1002/elsc.202000038 |
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