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Engineered polyketides: Synergy between protein and host level engineering

Metabolic engineering efforts toward rewiring metabolism of cells to produce new compounds often require the utilization of non-native enzymatic machinery that is capable of producing a broad range of chemical functionalities. Polyketides encompass one of the largest classes of chemically diverse na...

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Detalles Bibliográficos
Autores principales: Barajas, Jesus F., Blake-Hedges, Jacquelyn M., Bailey, Constance B., Curran, Samuel, Keasling, Jay. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655351/
https://www.ncbi.nlm.nih.gov/pubmed/29318196
http://dx.doi.org/10.1016/j.synbio.2017.08.005
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author Barajas, Jesus F.
Blake-Hedges, Jacquelyn M.
Bailey, Constance B.
Curran, Samuel
Keasling, Jay. D.
author_facet Barajas, Jesus F.
Blake-Hedges, Jacquelyn M.
Bailey, Constance B.
Curran, Samuel
Keasling, Jay. D.
author_sort Barajas, Jesus F.
collection PubMed
description Metabolic engineering efforts toward rewiring metabolism of cells to produce new compounds often require the utilization of non-native enzymatic machinery that is capable of producing a broad range of chemical functionalities. Polyketides encompass one of the largest classes of chemically diverse natural products. With thousands of known polyketides, modular polyketide synthases (PKSs) share a particularly attractive biosynthetic logic for generating chemical diversity. The engineering of modular PKSs could open access to the deliberate production of both existing and novel compounds. In this review, we discuss PKS engineering efforts applied at both the protein and cellular level for the generation of a diverse range of chemical structures, and we examine future applications of PKSs in the production of medicines, fuels and other industrially relevant chemicals.
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spelling pubmed-56553512018-01-09 Engineered polyketides: Synergy between protein and host level engineering Barajas, Jesus F. Blake-Hedges, Jacquelyn M. Bailey, Constance B. Curran, Samuel Keasling, Jay. D. Synth Syst Biotechnol Article Metabolic engineering efforts toward rewiring metabolism of cells to produce new compounds often require the utilization of non-native enzymatic machinery that is capable of producing a broad range of chemical functionalities. Polyketides encompass one of the largest classes of chemically diverse natural products. With thousands of known polyketides, modular polyketide synthases (PKSs) share a particularly attractive biosynthetic logic for generating chemical diversity. The engineering of modular PKSs could open access to the deliberate production of both existing and novel compounds. In this review, we discuss PKS engineering efforts applied at both the protein and cellular level for the generation of a diverse range of chemical structures, and we examine future applications of PKSs in the production of medicines, fuels and other industrially relevant chemicals. KeAi Publishing 2017-09-07 /pmc/articles/PMC5655351/ /pubmed/29318196 http://dx.doi.org/10.1016/j.synbio.2017.08.005 Text en http://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 Article
Barajas, Jesus F.
Blake-Hedges, Jacquelyn M.
Bailey, Constance B.
Curran, Samuel
Keasling, Jay. D.
Engineered polyketides: Synergy between protein and host level engineering
title Engineered polyketides: Synergy between protein and host level engineering
title_full Engineered polyketides: Synergy between protein and host level engineering
title_fullStr Engineered polyketides: Synergy between protein and host level engineering
title_full_unstemmed Engineered polyketides: Synergy between protein and host level engineering
title_short Engineered polyketides: Synergy between protein and host level engineering
title_sort engineered polyketides: synergy between protein and host level engineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655351/
https://www.ncbi.nlm.nih.gov/pubmed/29318196
http://dx.doi.org/10.1016/j.synbio.2017.08.005
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