Facile Production of (+)-Aristolochene and (+)-Bicyclogermacrene in Using Newly Discovered Sesquiterpene Synthases from .

J Agric Food Chem

State Key Laboratory of Bioreactor Engineering, Shanghai Collaborative Innovation Centre for Biomanufacturing, Frontiers Science Center for Materiobiology and Dynamic Chemistry, East China University of Science and Technology, Shanghai 200237, People's Republic of China.

Published: May 2022

AI Article Synopsis

  • Scientists are exploring how a specific type of bacteria can create new chemicals called terpenes, which can be useful in many products.
  • They improved a specific process in the bacteria to help it produce more of these terpenes, leading to the discovery of two new enzymes (TS1 and TS4) that help make different types of terpenes.
  • By using a special technique, they were able to produce a lot more of one terpene than ever before, showing that their method could help make other valuable chemicals in the future.!*

Article Abstract

, producer of a wide array of secondary metabolites, has the potential to be a source of new terpene synthases. In this work, a platform was constructed with BL21(DE3) by enhancing its endogenous 2-methyl-d-erythritol-4-phosphate pathway to supply sufficient terpenoid precursors. Using this precursor-supplying platform, we discovered two sesquiterpene synthases from : TS1, a new (+)-aristolochene synthase, and TS4, the first microbial (+)-bicyclogermacrene synthase. To enhance the sesquiterpene production by TS1, we employed a MBP fusion tag to improve the heterologous protein expression, resulting in the increase of aristolochene production up to 50 mg/L in a 72 h flask culture, which is the highest production reported to date. We also realized the first biosynthesis of (+)-bicyclogermacrene, achieving 188 mg/L in 72 h. This work highlights the great potential of this microbial platform for the discovery of new terpene synthases and opens new ways for the bioproduction of other valuable terpenoids.

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http://dx.doi.org/10.1021/acs.jafc.2c01885DOI Listing

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