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Shared PKS Module in Biosynthesis of Synergistic Laxaphycins

Cyanobacteria produce a wide range of lipopeptides that exhibit potent membrane-disrupting activities. Laxaphycins consist of two families of structurally distinct macrocyclic lipopeptides that act in a synergistic manner to produce antifungal and antiproliferative activities. Laxaphycins are produc...

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Autores principales: Heinilä, Lassi Matti Petteri, Fewer, David P., Jokela, Jouni Kalevi, Wahlsten, Matti, Jortikka, Anna, Sivonen, Kaarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524897/
https://www.ncbi.nlm.nih.gov/pubmed/33042096
http://dx.doi.org/10.3389/fmicb.2020.578878
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author Heinilä, Lassi Matti Petteri
Fewer, David P.
Jokela, Jouni Kalevi
Wahlsten, Matti
Jortikka, Anna
Sivonen, Kaarina
author_facet Heinilä, Lassi Matti Petteri
Fewer, David P.
Jokela, Jouni Kalevi
Wahlsten, Matti
Jortikka, Anna
Sivonen, Kaarina
author_sort Heinilä, Lassi Matti Petteri
collection PubMed
description Cyanobacteria produce a wide range of lipopeptides that exhibit potent membrane-disrupting activities. Laxaphycins consist of two families of structurally distinct macrocyclic lipopeptides that act in a synergistic manner to produce antifungal and antiproliferative activities. Laxaphycins are produced by range of cyanobacteria but their biosynthetic origins remain unclear. Here, we identified the biosynthetic pathways responsible for the biosynthesis of the laxaphycins produced by Scytonema hofmannii PCC 7110. We show that these laxaphycins, called scytocyclamides, are produced by this cyanobacterium and are encoded in a single biosynthetic gene cluster with shared polyketide synthase enzymes initiating two distinct non-ribosomal peptide synthetase pathways. The unusual mechanism of shared enzymes synthesizing two distinct types of products may aid future research in identifying and expressing natural product biosynthetic pathways and in expanding the known biosynthetic logic of this important family of natural products.
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spelling pubmed-75248972020-10-09 Shared PKS Module in Biosynthesis of Synergistic Laxaphycins Heinilä, Lassi Matti Petteri Fewer, David P. Jokela, Jouni Kalevi Wahlsten, Matti Jortikka, Anna Sivonen, Kaarina Front Microbiol Microbiology Cyanobacteria produce a wide range of lipopeptides that exhibit potent membrane-disrupting activities. Laxaphycins consist of two families of structurally distinct macrocyclic lipopeptides that act in a synergistic manner to produce antifungal and antiproliferative activities. Laxaphycins are produced by range of cyanobacteria but their biosynthetic origins remain unclear. Here, we identified the biosynthetic pathways responsible for the biosynthesis of the laxaphycins produced by Scytonema hofmannii PCC 7110. We show that these laxaphycins, called scytocyclamides, are produced by this cyanobacterium and are encoded in a single biosynthetic gene cluster with shared polyketide synthase enzymes initiating two distinct non-ribosomal peptide synthetase pathways. The unusual mechanism of shared enzymes synthesizing two distinct types of products may aid future research in identifying and expressing natural product biosynthetic pathways and in expanding the known biosynthetic logic of this important family of natural products. Frontiers Media S.A. 2020-09-16 /pmc/articles/PMC7524897/ /pubmed/33042096 http://dx.doi.org/10.3389/fmicb.2020.578878 Text en Copyright © 2020 Heinilä, Fewer, Jokela, Wahlsten, Jortikka and Sivonen. 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) and the copyright owner(s) 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
Heinilä, Lassi Matti Petteri
Fewer, David P.
Jokela, Jouni Kalevi
Wahlsten, Matti
Jortikka, Anna
Sivonen, Kaarina
Shared PKS Module in Biosynthesis of Synergistic Laxaphycins
title Shared PKS Module in Biosynthesis of Synergistic Laxaphycins
title_full Shared PKS Module in Biosynthesis of Synergistic Laxaphycins
title_fullStr Shared PKS Module in Biosynthesis of Synergistic Laxaphycins
title_full_unstemmed Shared PKS Module in Biosynthesis of Synergistic Laxaphycins
title_short Shared PKS Module in Biosynthesis of Synergistic Laxaphycins
title_sort shared pks module in biosynthesis of synergistic laxaphycins
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524897/
https://www.ncbi.nlm.nih.gov/pubmed/33042096
http://dx.doi.org/10.3389/fmicb.2020.578878
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