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Short-chain ketone production by engineered polyketide synthases in Streptomyces albus
Microbial production of fuels and commodity chemicals has been performed primarily using natural or slightly modified enzymes, which inherently limits the types of molecules that can be produced. Type I modular polyketide synthases (PKSs) are multi-domain enzymes that can produce unique and diverse...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6212451/ https://www.ncbi.nlm.nih.gov/pubmed/30385744 http://dx.doi.org/10.1038/s41467-018-07040-0 |
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author | Yuzawa, Satoshi Mirsiaghi, Mona Jocic, Renee Fujii, Tatsuya Masson, Fabrice Benites, Veronica T. Baidoo, Edward E. K. Sundstrom, Eric Tanjore, Deepti Pray, Todd R. George, Anthe Davis, Ryan W. Gladden, John M. Simmons, Blake A. Katz, Leonard Keasling, Jay D. |
author_facet | Yuzawa, Satoshi Mirsiaghi, Mona Jocic, Renee Fujii, Tatsuya Masson, Fabrice Benites, Veronica T. Baidoo, Edward E. K. Sundstrom, Eric Tanjore, Deepti Pray, Todd R. George, Anthe Davis, Ryan W. Gladden, John M. Simmons, Blake A. Katz, Leonard Keasling, Jay D. |
author_sort | Yuzawa, Satoshi |
collection | PubMed |
description | Microbial production of fuels and commodity chemicals has been performed primarily using natural or slightly modified enzymes, which inherently limits the types of molecules that can be produced. Type I modular polyketide synthases (PKSs) are multi-domain enzymes that can produce unique and diverse molecular structures by combining particular types of catalytic domains in a specific order. This catalytic mechanism offers a wealth of engineering opportunities. Here we report engineered microbes that produce various short-chain (C5–C7) ketones using hybrid PKSs. Introduction of the genes into the chromosome of Streptomyces albus enables it to produce >1 g · l(−1) of C6 and C7 ethyl ketones and several hundred mg · l(−1) of C5 and C6 methyl ketones from plant biomass hydrolysates. Engine tests indicate these short-chain ketones can be added to gasoline as oxygenates to increase the octane of gasoline. Together, it demonstrates the efficient and renewable microbial production of biogasolines by hybrid enzymes. |
format | Online Article Text |
id | pubmed-6212451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62124512018-11-05 Short-chain ketone production by engineered polyketide synthases in Streptomyces albus Yuzawa, Satoshi Mirsiaghi, Mona Jocic, Renee Fujii, Tatsuya Masson, Fabrice Benites, Veronica T. Baidoo, Edward E. K. Sundstrom, Eric Tanjore, Deepti Pray, Todd R. George, Anthe Davis, Ryan W. Gladden, John M. Simmons, Blake A. Katz, Leonard Keasling, Jay D. Nat Commun Article Microbial production of fuels and commodity chemicals has been performed primarily using natural or slightly modified enzymes, which inherently limits the types of molecules that can be produced. Type I modular polyketide synthases (PKSs) are multi-domain enzymes that can produce unique and diverse molecular structures by combining particular types of catalytic domains in a specific order. This catalytic mechanism offers a wealth of engineering opportunities. Here we report engineered microbes that produce various short-chain (C5–C7) ketones using hybrid PKSs. Introduction of the genes into the chromosome of Streptomyces albus enables it to produce >1 g · l(−1) of C6 and C7 ethyl ketones and several hundred mg · l(−1) of C5 and C6 methyl ketones from plant biomass hydrolysates. Engine tests indicate these short-chain ketones can be added to gasoline as oxygenates to increase the octane of gasoline. Together, it demonstrates the efficient and renewable microbial production of biogasolines by hybrid enzymes. Nature Publishing Group UK 2018-11-01 /pmc/articles/PMC6212451/ /pubmed/30385744 http://dx.doi.org/10.1038/s41467-018-07040-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yuzawa, Satoshi Mirsiaghi, Mona Jocic, Renee Fujii, Tatsuya Masson, Fabrice Benites, Veronica T. Baidoo, Edward E. K. Sundstrom, Eric Tanjore, Deepti Pray, Todd R. George, Anthe Davis, Ryan W. Gladden, John M. Simmons, Blake A. Katz, Leonard Keasling, Jay D. Short-chain ketone production by engineered polyketide synthases in Streptomyces albus |
title | Short-chain ketone production by engineered polyketide synthases in Streptomyces albus |
title_full | Short-chain ketone production by engineered polyketide synthases in Streptomyces albus |
title_fullStr | Short-chain ketone production by engineered polyketide synthases in Streptomyces albus |
title_full_unstemmed | Short-chain ketone production by engineered polyketide synthases in Streptomyces albus |
title_short | Short-chain ketone production by engineered polyketide synthases in Streptomyces albus |
title_sort | short-chain ketone production by engineered polyketide synthases in streptomyces albus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6212451/ https://www.ncbi.nlm.nih.gov/pubmed/30385744 http://dx.doi.org/10.1038/s41467-018-07040-0 |
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