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Current understanding and biotechnological application of the bacterial diterpene synthase CotB2

CotB2 catalyzes the first committed step in cyclooctatin biosynthesis of the soil bacterium Streptomyces melanosporofaciens. To date, CotB2 represents the best studied bacterial diterpene synthase. Its reaction mechanism has been addressed by isoptope labeling, targeted mutagenesis and theoretical c...

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Autores principales: Driller, Ronja, Garbe, Daniel, Mehlmer, Norbert, Fuchs, Monika, Raz, Keren, Major, Dan Thomas, Brück, Thomas, Loll, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6808215/
https://www.ncbi.nlm.nih.gov/pubmed/31666870
http://dx.doi.org/10.3762/bjoc.15.228
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author Driller, Ronja
Garbe, Daniel
Mehlmer, Norbert
Fuchs, Monika
Raz, Keren
Major, Dan Thomas
Brück, Thomas
Loll, Bernhard
author_facet Driller, Ronja
Garbe, Daniel
Mehlmer, Norbert
Fuchs, Monika
Raz, Keren
Major, Dan Thomas
Brück, Thomas
Loll, Bernhard
author_sort Driller, Ronja
collection PubMed
description CotB2 catalyzes the first committed step in cyclooctatin biosynthesis of the soil bacterium Streptomyces melanosporofaciens. To date, CotB2 represents the best studied bacterial diterpene synthase. Its reaction mechanism has been addressed by isoptope labeling, targeted mutagenesis and theoretical computations in the gas phase, as well as full enzyme molecular dynamic simulations. By X-ray crystallography different snapshots of CotB2 from the open, inactive, to the closed, active conformation have been obtained in great detail, allowing us to draw detailed conclusions regarding the catalytic mechanism at the molecular level. Moreover, numerous alternative geranylgeranyl diphosphate cyclization products obtained by CotB2 mutagenesis have exciting applications for the sustainable production of high value bioactive substances.
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spelling pubmed-68082152019-10-30 Current understanding and biotechnological application of the bacterial diterpene synthase CotB2 Driller, Ronja Garbe, Daniel Mehlmer, Norbert Fuchs, Monika Raz, Keren Major, Dan Thomas Brück, Thomas Loll, Bernhard Beilstein J Org Chem Review CotB2 catalyzes the first committed step in cyclooctatin biosynthesis of the soil bacterium Streptomyces melanosporofaciens. To date, CotB2 represents the best studied bacterial diterpene synthase. Its reaction mechanism has been addressed by isoptope labeling, targeted mutagenesis and theoretical computations in the gas phase, as well as full enzyme molecular dynamic simulations. By X-ray crystallography different snapshots of CotB2 from the open, inactive, to the closed, active conformation have been obtained in great detail, allowing us to draw detailed conclusions regarding the catalytic mechanism at the molecular level. Moreover, numerous alternative geranylgeranyl diphosphate cyclization products obtained by CotB2 mutagenesis have exciting applications for the sustainable production of high value bioactive substances. Beilstein-Institut 2019-10-02 /pmc/articles/PMC6808215/ /pubmed/31666870 http://dx.doi.org/10.3762/bjoc.15.228 Text en Copyright © 2019, Driller 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). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Driller, Ronja
Garbe, Daniel
Mehlmer, Norbert
Fuchs, Monika
Raz, Keren
Major, Dan Thomas
Brück, Thomas
Loll, Bernhard
Current understanding and biotechnological application of the bacterial diterpene synthase CotB2
title Current understanding and biotechnological application of the bacterial diterpene synthase CotB2
title_full Current understanding and biotechnological application of the bacterial diterpene synthase CotB2
title_fullStr Current understanding and biotechnological application of the bacterial diterpene synthase CotB2
title_full_unstemmed Current understanding and biotechnological application of the bacterial diterpene synthase CotB2
title_short Current understanding and biotechnological application of the bacterial diterpene synthase CotB2
title_sort current understanding and biotechnological application of the bacterial diterpene synthase cotb2
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6808215/
https://www.ncbi.nlm.nih.gov/pubmed/31666870
http://dx.doi.org/10.3762/bjoc.15.228
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