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Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems
With over 50.000 identified compounds terpenes are the largest and most structurally diverse group of natural products. They are ubiquitous in bacteria, plants, animals and fungi, conducting several biological functions such as cell wall components or defense mechanisms. Industrial applications enta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433224/ https://www.ncbi.nlm.nih.gov/pubmed/28546842 http://dx.doi.org/10.3762/bjoc.13.85 |
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author | Kemper, Katarina Hirte, Max Reinbold, Markus Fuchs, Monika Brück, Thomas |
author_facet | Kemper, Katarina Hirte, Max Reinbold, Markus Fuchs, Monika Brück, Thomas |
author_sort | Kemper, Katarina |
collection | PubMed |
description | With over 50.000 identified compounds terpenes are the largest and most structurally diverse group of natural products. They are ubiquitous in bacteria, plants, animals and fungi, conducting several biological functions such as cell wall components or defense mechanisms. Industrial applications entail among others pharmaceuticals, food additives, vitamins, fragrances, fuels and fuel additives. Central building blocks of all terpenes are the isoprenoid compounds isopentenyl diphosphate and dimethylallyl diphosphate. Bacteria like Escherichia coli harbor a native metabolic pathway for these isoprenoids that is quite amenable for genetic engineering. Together with recombinant terpene biosynthesis modules, they are very suitable hosts for heterologous production of high value terpenes. Yet, in contrast to the number of extracted and characterized terpenes, little is known about the specific biosynthetic enzymes that are involved especially in the formation of highly functionalized compounds. Novel approaches discussed in this review include metabolic engineering as well as site-directed mutagenesis to expand the natural terpene landscape. Focusing mainly on the validation of successful integration of engineered biosynthetic pathways into optimized terpene producing Escherichia coli, this review shall give an insight in recent progresses regarding manipulation of mostly diterpene synthases. |
format | Online Article Text |
id | pubmed-5433224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-54332242017-05-25 Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems Kemper, Katarina Hirte, Max Reinbold, Markus Fuchs, Monika Brück, Thomas Beilstein J Org Chem Review With over 50.000 identified compounds terpenes are the largest and most structurally diverse group of natural products. They are ubiquitous in bacteria, plants, animals and fungi, conducting several biological functions such as cell wall components or defense mechanisms. Industrial applications entail among others pharmaceuticals, food additives, vitamins, fragrances, fuels and fuel additives. Central building blocks of all terpenes are the isoprenoid compounds isopentenyl diphosphate and dimethylallyl diphosphate. Bacteria like Escherichia coli harbor a native metabolic pathway for these isoprenoids that is quite amenable for genetic engineering. Together with recombinant terpene biosynthesis modules, they are very suitable hosts for heterologous production of high value terpenes. Yet, in contrast to the number of extracted and characterized terpenes, little is known about the specific biosynthetic enzymes that are involved especially in the formation of highly functionalized compounds. Novel approaches discussed in this review include metabolic engineering as well as site-directed mutagenesis to expand the natural terpene landscape. Focusing mainly on the validation of successful integration of engineered biosynthetic pathways into optimized terpene producing Escherichia coli, this review shall give an insight in recent progresses regarding manipulation of mostly diterpene synthases. Beilstein-Institut 2017-05-08 /pmc/articles/PMC5433224/ /pubmed/28546842 http://dx.doi.org/10.3762/bjoc.13.85 Text en Copyright © 2017, Kemper et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Kemper, Katarina Hirte, Max Reinbold, Markus Fuchs, Monika Brück, Thomas Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
title | Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
title_full | Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
title_fullStr | Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
title_full_unstemmed | Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
title_short | Opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
title_sort | opportunities and challenges for the sustainable production of structurally complex diterpenoids in recombinant microbial systems |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433224/ https://www.ncbi.nlm.nih.gov/pubmed/28546842 http://dx.doi.org/10.3762/bjoc.13.85 |
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