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Exploring novel bacterial terpene synthases
Terpenes are the largest class of natural products with extensive structural diversity and are widely used as pharmaceuticals, herbicides, flavourings, fragrances, and biofuels. While they have mostly been isolated from plants and fungi, the availability and analysis of bacterial genome sequence dat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192455/ https://www.ncbi.nlm.nih.gov/pubmed/32353014 http://dx.doi.org/10.1371/journal.pone.0232220 |
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author | Reddy, Gajendar Komati Leferink, Nicole G. H. Umemura, Maiko Ahmed, Syed T. Breitling, Rainer Scrutton, Nigel S. Takano, Eriko |
author_facet | Reddy, Gajendar Komati Leferink, Nicole G. H. Umemura, Maiko Ahmed, Syed T. Breitling, Rainer Scrutton, Nigel S. Takano, Eriko |
author_sort | Reddy, Gajendar Komati |
collection | PubMed |
description | Terpenes are the largest class of natural products with extensive structural diversity and are widely used as pharmaceuticals, herbicides, flavourings, fragrances, and biofuels. While they have mostly been isolated from plants and fungi, the availability and analysis of bacterial genome sequence data indicates that bacteria also possess many putative terpene synthase genes. In this study, we further explore this potential for terpene synthase activity in bacteria. Twenty two potential class I terpene synthase genes (TSs) were selected to represent the full sequence diversity of bacterial synthase candidates and recombinantly expressed in E. coli. Terpene synthase activity was detected for 15 of these enzymes, and included mono-, sesqui- and diterpene synthase activities. A number of confirmed sesquiterpene synthases also exhibited promiscuous monoterpene synthase activity, suggesting that bacteria are potentially a richer source of monoterpene synthase activity then previously assumed. Several terpenoid products not previously detected in bacteria were identified, including aromandendrene, acora-3,7(14)-diene and longiborneol. Overall, we have identified promiscuous terpene synthases in bacteria and demonstrated that terpene synthases with substrate promiscuity are widely distributed in nature, forming a rich resource for engineering terpene biosynthetic pathways for biotechnology. |
format | Online Article Text |
id | pubmed-7192455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71924552020-05-11 Exploring novel bacterial terpene synthases Reddy, Gajendar Komati Leferink, Nicole G. H. Umemura, Maiko Ahmed, Syed T. Breitling, Rainer Scrutton, Nigel S. Takano, Eriko PLoS One Research Article Terpenes are the largest class of natural products with extensive structural diversity and are widely used as pharmaceuticals, herbicides, flavourings, fragrances, and biofuels. While they have mostly been isolated from plants and fungi, the availability and analysis of bacterial genome sequence data indicates that bacteria also possess many putative terpene synthase genes. In this study, we further explore this potential for terpene synthase activity in bacteria. Twenty two potential class I terpene synthase genes (TSs) were selected to represent the full sequence diversity of bacterial synthase candidates and recombinantly expressed in E. coli. Terpene synthase activity was detected for 15 of these enzymes, and included mono-, sesqui- and diterpene synthase activities. A number of confirmed sesquiterpene synthases also exhibited promiscuous monoterpene synthase activity, suggesting that bacteria are potentially a richer source of monoterpene synthase activity then previously assumed. Several terpenoid products not previously detected in bacteria were identified, including aromandendrene, acora-3,7(14)-diene and longiborneol. Overall, we have identified promiscuous terpene synthases in bacteria and demonstrated that terpene synthases with substrate promiscuity are widely distributed in nature, forming a rich resource for engineering terpene biosynthetic pathways for biotechnology. Public Library of Science 2020-04-30 /pmc/articles/PMC7192455/ /pubmed/32353014 http://dx.doi.org/10.1371/journal.pone.0232220 Text en © 2020 Reddy 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 | Research Article Reddy, Gajendar Komati Leferink, Nicole G. H. Umemura, Maiko Ahmed, Syed T. Breitling, Rainer Scrutton, Nigel S. Takano, Eriko Exploring novel bacterial terpene synthases |
title | Exploring novel bacterial terpene synthases |
title_full | Exploring novel bacterial terpene synthases |
title_fullStr | Exploring novel bacterial terpene synthases |
title_full_unstemmed | Exploring novel bacterial terpene synthases |
title_short | Exploring novel bacterial terpene synthases |
title_sort | exploring novel bacterial terpene synthases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192455/ https://www.ncbi.nlm.nih.gov/pubmed/32353014 http://dx.doi.org/10.1371/journal.pone.0232220 |
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