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Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1
Achieving sustainable chemical synthesis and a circular economy will require process innovation to minimize or recover existing waste streams. Valorization of lignin biomass has the ability to advance this goal. While lignin has proved a recalcitrant feedstock for upgrading, biological approaches ca...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473687/ https://www.ncbi.nlm.nih.gov/pubmed/37662333 http://dx.doi.org/10.1101/2023.08.24.554694 |
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author | Biggs, Bradley W. Tyo, Keith E. J. |
author_facet | Biggs, Bradley W. Tyo, Keith E. J. |
author_sort | Biggs, Bradley W. |
collection | PubMed |
description | Achieving sustainable chemical synthesis and a circular economy will require process innovation to minimize or recover existing waste streams. Valorization of lignin biomass has the ability to advance this goal. While lignin has proved a recalcitrant feedstock for upgrading, biological approaches can leverage native microbial metabolism to simplify complex and heterogeneous feedstocks to tractable starting points for biochemical upgrading. Recently, we demonstrated that one microbe with lignin relevant metabolism, Acinetobacter baylyi ADP1, is both highly engineerable and capable of undergoing rapid design-build-test-learn cycles, making it an ideal candidate for these applications. Here, we utilize these genetic traits and ADP1’s native β-ketoadipate metabolism to convert mock alkali pretreated liquor lignin (APL) to two valuable natural products, vanillin-glucoside and resveratrol. En route, we create strains with up to 22 genetic modifications, including up to 8 heterologously expressed enzymes. Our approach takes advantage of preexisting aromatic species in APL (vanillate, ferulate, and p-coumarate) to create shortened biochemical routes to end products. Together, this work demonstrates ADP1’s potential as a platform for upgrading lignin waste streams and highlights the potential for biosynthetic methods to maximize the existing chemical potential of lignin aromatic monomers. |
format | Online Article Text |
id | pubmed-10473687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104736872023-09-02 Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 Biggs, Bradley W. Tyo, Keith E. J. bioRxiv Article Achieving sustainable chemical synthesis and a circular economy will require process innovation to minimize or recover existing waste streams. Valorization of lignin biomass has the ability to advance this goal. While lignin has proved a recalcitrant feedstock for upgrading, biological approaches can leverage native microbial metabolism to simplify complex and heterogeneous feedstocks to tractable starting points for biochemical upgrading. Recently, we demonstrated that one microbe with lignin relevant metabolism, Acinetobacter baylyi ADP1, is both highly engineerable and capable of undergoing rapid design-build-test-learn cycles, making it an ideal candidate for these applications. Here, we utilize these genetic traits and ADP1’s native β-ketoadipate metabolism to convert mock alkali pretreated liquor lignin (APL) to two valuable natural products, vanillin-glucoside and resveratrol. En route, we create strains with up to 22 genetic modifications, including up to 8 heterologously expressed enzymes. Our approach takes advantage of preexisting aromatic species in APL (vanillate, ferulate, and p-coumarate) to create shortened biochemical routes to end products. Together, this work demonstrates ADP1’s potential as a platform for upgrading lignin waste streams and highlights the potential for biosynthetic methods to maximize the existing chemical potential of lignin aromatic monomers. Cold Spring Harbor Laboratory 2023-08-24 /pmc/articles/PMC10473687/ /pubmed/37662333 http://dx.doi.org/10.1101/2023.08.24.554694 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Biggs, Bradley W. Tyo, Keith E. J. Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 |
title | Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 |
title_full | Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 |
title_fullStr | Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 |
title_full_unstemmed | Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 |
title_short | Aromatic natural products synthesis from aromatic lignin monomers using Acinetobacter baylyi ADP1 |
title_sort | aromatic natural products synthesis from aromatic lignin monomers using acinetobacter baylyi adp1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473687/ https://www.ncbi.nlm.nih.gov/pubmed/37662333 http://dx.doi.org/10.1101/2023.08.24.554694 |
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