Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783588639546015744 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7524897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT heinilalassimattipetteri sharedpksmoduleinbiosynthesisofsynergisticlaxaphycins AT fewerdavidp sharedpksmoduleinbiosynthesisofsynergisticlaxaphycins AT jokelajounikalevi sharedpksmoduleinbiosynthesisofsynergisticlaxaphycins AT wahlstenmatti sharedpksmoduleinbiosynthesisofsynergisticlaxaphycins AT jortikkaanna sharedpksmoduleinbiosynthesisofsynergisticlaxaphycins AT sivonenkaarina sharedpksmoduleinbiosynthesisofsynergisticlaxaphycins |