Issue 13, 2023

Building Streptomyces albus as a chassis for synthesis of bacterial terpenoids

Abstract

Terpenoids comprise the most chemically and structurally diverse family of natural products. In contrast to the huge numbers of terpenoids discovered from plants and fungi, only a relatively small number of terpenoids were reported from bacteria. Recent genomic data in bacteria suggest that a large number of biosynthetic gene clusters encoding terpenoids remain uncharacterized. In order to enable the functional characterization of terpene synthase and relevant tailoring enzymes, we selected and optimized an expression system based on a Streptomyces chassis. Through genome mining, 16 distinct bacterial terpene biosynthetic gene clusters were selected and 13 of them were successfully expressed in the Streptomyces chassis, leading to characterization of 11 terpene skeletons including three new ones, representing an ∼80% success rate. In addition, after functional expression of tailoring genes, 18 novel distinct terpenoids were isolated and characterized. This work demonstrates the advantages of a Streptomyces chassis which not only enabled the successful production of bacterial terpene synthases, but also enabled functional expression of tailoring genes, especially P450, for terpenoid modification.

Graphical abstract: Building Streptomyces albus as a chassis for synthesis of bacterial terpenoids

Supplementary files

Article information

Article type
Edge Article
Submitted
01 Nov 2022
Accepted
03 Mar 2023
First published
06 Mar 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2023,14, 3661-3667

Building Streptomyces albus as a chassis for synthesis of bacterial terpenoids

Y. L. Hu, Q. Zhang, S. H. Liu, J. L. Sun, F. Z. Yin, Z. R. Wang, J. Shi, R. H. Jiao and H. M. Ge, Chem. Sci., 2023, 14, 3661 DOI: 10.1039/D2SC06033G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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