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In vivo production of pederin by labrenzin pathway expansion

Pederin is a potent polyketide toxin that causes severe skin lesions in humans after contact with insects of genus Paederus. Due to its potent anticancer activities, pederin family compounds have raised the interest of pharmaceutical industry. Despite the extensive studies on the cluster of biosynth...

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Autores principales: Kačar, Dina, Schleissner, Carmen, Cañedo, Librada M., Rodríguez, Pilar, de la Calle, Fernando, Cuevas, Carmen, Galán, Beatriz, García, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062313/
https://www.ncbi.nlm.nih.gov/pubmed/35517715
http://dx.doi.org/10.1016/j.mec.2022.e00198
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author Kačar, Dina
Schleissner, Carmen
Cañedo, Librada M.
Rodríguez, Pilar
de la Calle, Fernando
Cuevas, Carmen
Galán, Beatriz
García, José Luis
author_facet Kačar, Dina
Schleissner, Carmen
Cañedo, Librada M.
Rodríguez, Pilar
de la Calle, Fernando
Cuevas, Carmen
Galán, Beatriz
García, José Luis
author_sort Kačar, Dina
collection PubMed
description Pederin is a potent polyketide toxin that causes severe skin lesions in humans after contact with insects of genus Paederus. Due to its potent anticancer activities, pederin family compounds have raised the interest of pharmaceutical industry. Despite the extensive studies on the cluster of biosynthetic genes responsible for the production of pederin, it has not yet been possible to isolate and cultivate its bacterial endosymbiont producer. However, the marine bacterium Labrenzia sp. PHM005 was recently reported to produce labrenzin, the closest pederin analog. By cloning a synthetic pedO gene encoding one of the three O-methyltraferase of the pederin cluster into Labrenzia sp. PHM005 we have been able to produce pederin for the first time by fermentation in the new recombinant strain.
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spelling pubmed-90623132022-05-04 In vivo production of pederin by labrenzin pathway expansion Kačar, Dina Schleissner, Carmen Cañedo, Librada M. Rodríguez, Pilar de la Calle, Fernando Cuevas, Carmen Galán, Beatriz García, José Luis Metab Eng Commun Short communication Pederin is a potent polyketide toxin that causes severe skin lesions in humans after contact with insects of genus Paederus. Due to its potent anticancer activities, pederin family compounds have raised the interest of pharmaceutical industry. Despite the extensive studies on the cluster of biosynthetic genes responsible for the production of pederin, it has not yet been possible to isolate and cultivate its bacterial endosymbiont producer. However, the marine bacterium Labrenzia sp. PHM005 was recently reported to produce labrenzin, the closest pederin analog. By cloning a synthetic pedO gene encoding one of the three O-methyltraferase of the pederin cluster into Labrenzia sp. PHM005 we have been able to produce pederin for the first time by fermentation in the new recombinant strain. Elsevier 2022-04-25 /pmc/articles/PMC9062313/ /pubmed/35517715 http://dx.doi.org/10.1016/j.mec.2022.e00198 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short communication
Kačar, Dina
Schleissner, Carmen
Cañedo, Librada M.
Rodríguez, Pilar
de la Calle, Fernando
Cuevas, Carmen
Galán, Beatriz
García, José Luis
In vivo production of pederin by labrenzin pathway expansion
title In vivo production of pederin by labrenzin pathway expansion
title_full In vivo production of pederin by labrenzin pathway expansion
title_fullStr In vivo production of pederin by labrenzin pathway expansion
title_full_unstemmed In vivo production of pederin by labrenzin pathway expansion
title_short In vivo production of pederin by labrenzin pathway expansion
title_sort in vivo production of pederin by labrenzin pathway expansion
topic Short communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062313/
https://www.ncbi.nlm.nih.gov/pubmed/35517715
http://dx.doi.org/10.1016/j.mec.2022.e00198
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