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Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis

Dynamic regulation is an effective strategy for fine-tuning metabolic pathways in order to maximize target product synthesis. However, achieving dynamic and autonomous up- and down-regulation of the metabolic modules of interest simultaneously, still remains a great challenge. In this work, we creat...

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Autores principales: Wu, Yaokang, Chen, Taichi, Liu, Yanfeng, Tian, Rongzhen, Lv, Xueqin, Li, Jianghua, Du, Guocheng, Chen, Jian, Ledesma-Amaro, Rodrigo, Liu, Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954435/
https://www.ncbi.nlm.nih.gov/pubmed/31799627
http://dx.doi.org/10.1093/nar/gkz1123
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author Wu, Yaokang
Chen, Taichi
Liu, Yanfeng
Tian, Rongzhen
Lv, Xueqin
Li, Jianghua
Du, Guocheng
Chen, Jian
Ledesma-Amaro, Rodrigo
Liu, Long
author_facet Wu, Yaokang
Chen, Taichi
Liu, Yanfeng
Tian, Rongzhen
Lv, Xueqin
Li, Jianghua
Du, Guocheng
Chen, Jian
Ledesma-Amaro, Rodrigo
Liu, Long
author_sort Wu, Yaokang
collection PubMed
description Dynamic regulation is an effective strategy for fine-tuning metabolic pathways in order to maximize target product synthesis. However, achieving dynamic and autonomous up- and down-regulation of the metabolic modules of interest simultaneously, still remains a great challenge. In this work, we created an autonomous dual-control (ADC) system, by combining CRISPRi-based NOT gates with novel biosensors of a key metabolite in the pathway of interest. By sensing the levels of the intermediate glucosamine-6-phosphate (GlcN6P) and self-adjusting the expression levels of the target genes accordingly with the GlcN6P biosensor and ADC system enabled feedback circuits, the metabolic flux towards the production of the high value nutraceutical N-acetylglucosamine (GlcNAc) could be balanced and optimized in Bacillus subtilis. As a result, the GlcNAc titer in a 15-l fed-batch bioreactor increased from 59.9 g/l to 97.1 g/l with acetoin production and 81.7 g/l to 131.6 g/l without acetoin production, indicating the robustness and stability of the synthetic circuits in a large bioreactor system. Remarkably, this self-regulatory methodology does not require any external level of control such as the use of inducer molecules or switching fermentation/environmental conditions. Moreover, the proposed programmable genetic circuits may be expanded to engineer other microbial cells and metabolic pathways.
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spelling pubmed-69544352020-01-16 Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis Wu, Yaokang Chen, Taichi Liu, Yanfeng Tian, Rongzhen Lv, Xueqin Li, Jianghua Du, Guocheng Chen, Jian Ledesma-Amaro, Rodrigo Liu, Long Nucleic Acids Res Synthetic Biology and Bioengineering Dynamic regulation is an effective strategy for fine-tuning metabolic pathways in order to maximize target product synthesis. However, achieving dynamic and autonomous up- and down-regulation of the metabolic modules of interest simultaneously, still remains a great challenge. In this work, we created an autonomous dual-control (ADC) system, by combining CRISPRi-based NOT gates with novel biosensors of a key metabolite in the pathway of interest. By sensing the levels of the intermediate glucosamine-6-phosphate (GlcN6P) and self-adjusting the expression levels of the target genes accordingly with the GlcN6P biosensor and ADC system enabled feedback circuits, the metabolic flux towards the production of the high value nutraceutical N-acetylglucosamine (GlcNAc) could be balanced and optimized in Bacillus subtilis. As a result, the GlcNAc titer in a 15-l fed-batch bioreactor increased from 59.9 g/l to 97.1 g/l with acetoin production and 81.7 g/l to 131.6 g/l without acetoin production, indicating the robustness and stability of the synthetic circuits in a large bioreactor system. Remarkably, this self-regulatory methodology does not require any external level of control such as the use of inducer molecules or switching fermentation/environmental conditions. Moreover, the proposed programmable genetic circuits may be expanded to engineer other microbial cells and metabolic pathways. Oxford University Press 2020-01-24 2019-12-04 /pmc/articles/PMC6954435/ /pubmed/31799627 http://dx.doi.org/10.1093/nar/gkz1123 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Synthetic Biology and Bioengineering
Wu, Yaokang
Chen, Taichi
Liu, Yanfeng
Tian, Rongzhen
Lv, Xueqin
Li, Jianghua
Du, Guocheng
Chen, Jian
Ledesma-Amaro, Rodrigo
Liu, Long
Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis
title Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis
title_full Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis
title_fullStr Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis
title_full_unstemmed Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis
title_short Design of a programmable biosensor-CRISPRi genetic circuits for dynamic and autonomous dual-control of metabolic flux in Bacillus subtilis
title_sort design of a programmable biosensor-crispri genetic circuits for dynamic and autonomous dual-control of metabolic flux in bacillus subtilis
topic Synthetic Biology and Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954435/
https://www.ncbi.nlm.nih.gov/pubmed/31799627
http://dx.doi.org/10.1093/nar/gkz1123
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