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Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli

Polyketides are a class of specialised metabolites synthesised by both eukaryotes and prokaryotes. These chemically and structurally diverse molecules are heavily used in the clinic and include frontline antimicrobial and anticancer drugs such as erythromycin and doxorubicin. To replenish the clinic...

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Autores principales: Cummings, Matthew, Peters, Anna D., Whitehead, George F. S., Menon, Binuraj R. K., Micklefield, Jason, Webb, Simon J., Takano, Eriko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6638757/
https://www.ncbi.nlm.nih.gov/pubmed/31318855
http://dx.doi.org/10.1371/journal.pbio.3000347
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author Cummings, Matthew
Peters, Anna D.
Whitehead, George F. S.
Menon, Binuraj R. K.
Micklefield, Jason
Webb, Simon J.
Takano, Eriko
author_facet Cummings, Matthew
Peters, Anna D.
Whitehead, George F. S.
Menon, Binuraj R. K.
Micklefield, Jason
Webb, Simon J.
Takano, Eriko
author_sort Cummings, Matthew
collection PubMed
description Polyketides are a class of specialised metabolites synthesised by both eukaryotes and prokaryotes. These chemically and structurally diverse molecules are heavily used in the clinic and include frontline antimicrobial and anticancer drugs such as erythromycin and doxorubicin. To replenish the clinicians’ diminishing arsenal of bioactive molecules, a promising strategy aims at transferring polyketide biosynthetic pathways from their native producers into the biotechnologically desirable host Escherichia coli. This approach has been successful for type I modular polyketide synthases (PKSs); however, despite more than 3 decades of research, the large and important group of type II PKSs has until now been elusive in E. coli. Here, we report on a versatile polyketide biosynthesis pipeline, based on identification of E. coli–compatible type II PKSs. We successfully express 5 ketosynthase (KS) and chain length factor (CLF) pairs—e.g., from Photorhabdus luminescens TT01, Streptomyces resistomycificus, Streptoccocus sp. GMD2S, Pseudoalteromonas luteoviolacea, and Ktedonobacter racemifer—as soluble heterodimeric recombinant proteins in E. coli for the first time. We define the anthraquinone minimal PKS components and utilise this biosynthetic system to synthesise anthraquinones, dianthrones, and benzoisochromanequinones (BIQs). Furthermore, we demonstrate the tolerance and promiscuity of the anthraquinone heterologous biosynthetic pathway in E. coli to act as genetically applicable plug-and-play scaffold, showing it to function successfully when combined with enzymes from phylogenetically distant species, endophytic fungi and plants, which resulted in 2 new-to-nature compounds, neomedicamycin and neochaetomycin. This work enables plug-and-play combinatorial biosynthesis of aromatic polyketides using bacterial type II PKSs in E. coli, providing full access to its many advantages in terms of easy and fast genetic manipulation, accessibility for high-throughput robotics, and convenient biotechnological scale-up. Using the synthetic and systems biology toolbox, this plug-and-play biosynthetic platform can serve as an engine for the production of new and diversified bioactive polyketides in an automated, rapid, and versatile fashion.
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spelling pubmed-66387572019-07-25 Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli Cummings, Matthew Peters, Anna D. Whitehead, George F. S. Menon, Binuraj R. K. Micklefield, Jason Webb, Simon J. Takano, Eriko PLoS Biol Methods and Resources Polyketides are a class of specialised metabolites synthesised by both eukaryotes and prokaryotes. These chemically and structurally diverse molecules are heavily used in the clinic and include frontline antimicrobial and anticancer drugs such as erythromycin and doxorubicin. To replenish the clinicians’ diminishing arsenal of bioactive molecules, a promising strategy aims at transferring polyketide biosynthetic pathways from their native producers into the biotechnologically desirable host Escherichia coli. This approach has been successful for type I modular polyketide synthases (PKSs); however, despite more than 3 decades of research, the large and important group of type II PKSs has until now been elusive in E. coli. Here, we report on a versatile polyketide biosynthesis pipeline, based on identification of E. coli–compatible type II PKSs. We successfully express 5 ketosynthase (KS) and chain length factor (CLF) pairs—e.g., from Photorhabdus luminescens TT01, Streptomyces resistomycificus, Streptoccocus sp. GMD2S, Pseudoalteromonas luteoviolacea, and Ktedonobacter racemifer—as soluble heterodimeric recombinant proteins in E. coli for the first time. We define the anthraquinone minimal PKS components and utilise this biosynthetic system to synthesise anthraquinones, dianthrones, and benzoisochromanequinones (BIQs). Furthermore, we demonstrate the tolerance and promiscuity of the anthraquinone heterologous biosynthetic pathway in E. coli to act as genetically applicable plug-and-play scaffold, showing it to function successfully when combined with enzymes from phylogenetically distant species, endophytic fungi and plants, which resulted in 2 new-to-nature compounds, neomedicamycin and neochaetomycin. This work enables plug-and-play combinatorial biosynthesis of aromatic polyketides using bacterial type II PKSs in E. coli, providing full access to its many advantages in terms of easy and fast genetic manipulation, accessibility for high-throughput robotics, and convenient biotechnological scale-up. Using the synthetic and systems biology toolbox, this plug-and-play biosynthetic platform can serve as an engine for the production of new and diversified bioactive polyketides in an automated, rapid, and versatile fashion. Public Library of Science 2019-07-18 /pmc/articles/PMC6638757/ /pubmed/31318855 http://dx.doi.org/10.1371/journal.pbio.3000347 Text en © 2019 Cummings et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Methods and Resources
Cummings, Matthew
Peters, Anna D.
Whitehead, George F. S.
Menon, Binuraj R. K.
Micklefield, Jason
Webb, Simon J.
Takano, Eriko
Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli
title Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli
title_full Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli
title_fullStr Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli
title_full_unstemmed Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli
title_short Assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in Escherichia coli
title_sort assembling a plug-and-play production line for combinatorial biosynthesis of aromatic polyketides in escherichia coli
topic Methods and Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6638757/
https://www.ncbi.nlm.nih.gov/pubmed/31318855
http://dx.doi.org/10.1371/journal.pbio.3000347
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