Current understanding and biotechnological application of the bacterial diterpene synthase CotB2

Ronja Driller, Daniel Garbe, Norbert Mehlmer, Monika Fuchs, Keren Raz, Dan Thomas Major, Thomas Brück, Bernhard Loll

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)2355-2368
Number of pages14
JournalBeilstein Journal of Organic Chemistry
Volume15
DOIs
StatePublished - 2 Oct 2019

Keywords

  • Biotechnology
  • CotB2
  • Crystal structure
  • Cyclooctatin
  • Diterpene
  • Reaction mechanism
  • Terpene synthase

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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