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A combined strategy for the overproduction of complex ergot alkaloid agroclavine

Microbial cell factories (MCFs) and cell-free systems (CFSs) are generally considered as two unrelated approaches for the biosynthesis of biomolecules. In the current study, two systems were combined together for the overproduction of agroclavine (AC), a structurally complex ergot alkaloid. The whol...

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Autores principales: Yu, Zhi-Pu, An, Chunyan, Yao, Yongpeng, Wang, Chang-Yun, Sun, Zhoutong, Cui, Chengsen, Liu, Ling, Gao, Shu-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428804/
https://www.ncbi.nlm.nih.gov/pubmed/36092273
http://dx.doi.org/10.1016/j.synbio.2022.08.003
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author Yu, Zhi-Pu
An, Chunyan
Yao, Yongpeng
Wang, Chang-Yun
Sun, Zhoutong
Cui, Chengsen
Liu, Ling
Gao, Shu-Shan
author_facet Yu, Zhi-Pu
An, Chunyan
Yao, Yongpeng
Wang, Chang-Yun
Sun, Zhoutong
Cui, Chengsen
Liu, Ling
Gao, Shu-Shan
author_sort Yu, Zhi-Pu
collection PubMed
description Microbial cell factories (MCFs) and cell-free systems (CFSs) are generally considered as two unrelated approaches for the biosynthesis of biomolecules. In the current study, two systems were combined together for the overproduction of agroclavine (AC), a structurally complex ergot alkaloid. The whole biosynthetic pathway for AC was split into the early pathway and the late pathway at the point of the FAD-linked oxidoreductase EasE, which was reconstituted in an MCF (Aspergillus nidulans) and a four-enzyme CFS, respectively. The final titer of AC of this combined system is 1209 mg/L, which is the highest one that has been reported so far, to the best of our knowledge. The development of such a combined route could potentially avoid the limitations of both MCF and CFS systems, and boost the production of complex ergot alkaloids with polycyclic ring systems.
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spelling pubmed-94288042022-09-08 A combined strategy for the overproduction of complex ergot alkaloid agroclavine Yu, Zhi-Pu An, Chunyan Yao, Yongpeng Wang, Chang-Yun Sun, Zhoutong Cui, Chengsen Liu, Ling Gao, Shu-Shan Synth Syst Biotechnol Article Microbial cell factories (MCFs) and cell-free systems (CFSs) are generally considered as two unrelated approaches for the biosynthesis of biomolecules. In the current study, two systems were combined together for the overproduction of agroclavine (AC), a structurally complex ergot alkaloid. The whole biosynthetic pathway for AC was split into the early pathway and the late pathway at the point of the FAD-linked oxidoreductase EasE, which was reconstituted in an MCF (Aspergillus nidulans) and a four-enzyme CFS, respectively. The final titer of AC of this combined system is 1209 mg/L, which is the highest one that has been reported so far, to the best of our knowledge. The development of such a combined route could potentially avoid the limitations of both MCF and CFS systems, and boost the production of complex ergot alkaloids with polycyclic ring systems. KeAi Publishing 2022-08-20 /pmc/articles/PMC9428804/ /pubmed/36092273 http://dx.doi.org/10.1016/j.synbio.2022.08.003 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Yu, Zhi-Pu
An, Chunyan
Yao, Yongpeng
Wang, Chang-Yun
Sun, Zhoutong
Cui, Chengsen
Liu, Ling
Gao, Shu-Shan
A combined strategy for the overproduction of complex ergot alkaloid agroclavine
title A combined strategy for the overproduction of complex ergot alkaloid agroclavine
title_full A combined strategy for the overproduction of complex ergot alkaloid agroclavine
title_fullStr A combined strategy for the overproduction of complex ergot alkaloid agroclavine
title_full_unstemmed A combined strategy for the overproduction of complex ergot alkaloid agroclavine
title_short A combined strategy for the overproduction of complex ergot alkaloid agroclavine
title_sort combined strategy for the overproduction of complex ergot alkaloid agroclavine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428804/
https://www.ncbi.nlm.nih.gov/pubmed/36092273
http://dx.doi.org/10.1016/j.synbio.2022.08.003
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