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Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis

BACKGROUND: The catabolite repressor/activator protein (FruR) is a global regulatory protein known to control the expression of several genes concerned with carbon utilization and energy metabolism. This study aimed to illustrate effects of the FruR mutant on the (L-)phenylalanine ((L-)PHE) producin...

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Autores principales: Chen, Minliang, Liang, Hengyu, Han, Chao, Zhou, Peng, Xing, Zhiwei, Chen, Qianqian, Liu, Yongyu, Xie, Gou-an, Xie, Rufei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609185/
https://www.ncbi.nlm.nih.gov/pubmed/36289548
http://dx.doi.org/10.1186/s12934-022-01954-7
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author Chen, Minliang
Liang, Hengyu
Han, Chao
Zhou, Peng
Xing, Zhiwei
Chen, Qianqian
Liu, Yongyu
Xie, Gou-an
Xie, Rufei
author_facet Chen, Minliang
Liang, Hengyu
Han, Chao
Zhou, Peng
Xing, Zhiwei
Chen, Qianqian
Liu, Yongyu
Xie, Gou-an
Xie, Rufei
author_sort Chen, Minliang
collection PubMed
description BACKGROUND: The catabolite repressor/activator protein (FruR) is a global regulatory protein known to control the expression of several genes concerned with carbon utilization and energy metabolism. This study aimed to illustrate effects of the FruR mutant on the (L-)phenylalanine ((L-)PHE) producing strain PHE01. RESULTS: Random mutagenesis libraries of fruR generated in vitro were first integrated into the chromosome of PHE01 by CRISPR/Cas9 technique, and then the best mutant PHE07 (FruR(E173K)) was obtained. With this mutant, a final (L-)PHE concentration of 70.50 ± 1.02 g/L was achieved, which was 23.34% higher than that of PHE01. To better understand the mechanism, both transcriptomes and metabolomes of PHE07 were carried out and compared to that of PHE01. Specifically, the transcript levels of genes involved in gluconeogenesis pathway, pentose phosphate pathway, Krebs cycle, and glyoxylate shunt were up-regulated in the FruR(E173K) mutant, whereas genes aceEF, acnB, and icd were down-regulated. From the metabolite level, the FruR(E173K) mutation led to an accumulation of pentose phosphate pathway and Krebs cycle products, whereas the products of pyruvate metabolism pathway: acetyl-CoA and cis-aconic acid, were down-regulated. As a result of the altered metabolic flows, the utilization of carbon sources was improved and the supply of precursors (phosphoenolpyruvate and erythrose 4-phosphate) for (L-)PHE biosynthesis was increased, which together led to the enhanced production of (L-)PHE. CONCLUSION: A novel strategy for (L-)PHE overproduction by modification of the global transcription factor FruR in E. coli was reported. Especially, these findings expand the scope of pathways affected by the fruR regulon and illustrate its importance as a global regulator in (L-)PHE production. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01954-7.
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spelling pubmed-96091852022-10-28 Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis Chen, Minliang Liang, Hengyu Han, Chao Zhou, Peng Xing, Zhiwei Chen, Qianqian Liu, Yongyu Xie, Gou-an Xie, Rufei Microb Cell Fact Research BACKGROUND: The catabolite repressor/activator protein (FruR) is a global regulatory protein known to control the expression of several genes concerned with carbon utilization and energy metabolism. This study aimed to illustrate effects of the FruR mutant on the (L-)phenylalanine ((L-)PHE) producing strain PHE01. RESULTS: Random mutagenesis libraries of fruR generated in vitro were first integrated into the chromosome of PHE01 by CRISPR/Cas9 technique, and then the best mutant PHE07 (FruR(E173K)) was obtained. With this mutant, a final (L-)PHE concentration of 70.50 ± 1.02 g/L was achieved, which was 23.34% higher than that of PHE01. To better understand the mechanism, both transcriptomes and metabolomes of PHE07 were carried out and compared to that of PHE01. Specifically, the transcript levels of genes involved in gluconeogenesis pathway, pentose phosphate pathway, Krebs cycle, and glyoxylate shunt were up-regulated in the FruR(E173K) mutant, whereas genes aceEF, acnB, and icd were down-regulated. From the metabolite level, the FruR(E173K) mutation led to an accumulation of pentose phosphate pathway and Krebs cycle products, whereas the products of pyruvate metabolism pathway: acetyl-CoA and cis-aconic acid, were down-regulated. As a result of the altered metabolic flows, the utilization of carbon sources was improved and the supply of precursors (phosphoenolpyruvate and erythrose 4-phosphate) for (L-)PHE biosynthesis was increased, which together led to the enhanced production of (L-)PHE. CONCLUSION: A novel strategy for (L-)PHE overproduction by modification of the global transcription factor FruR in E. coli was reported. Especially, these findings expand the scope of pathways affected by the fruR regulon and illustrate its importance as a global regulator in (L-)PHE production. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01954-7. BioMed Central 2022-10-26 /pmc/articles/PMC9609185/ /pubmed/36289548 http://dx.doi.org/10.1186/s12934-022-01954-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Minliang
Liang, Hengyu
Han, Chao
Zhou, Peng
Xing, Zhiwei
Chen, Qianqian
Liu, Yongyu
Xie, Gou-an
Xie, Rufei
Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis
title Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis
title_full Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis
title_fullStr Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis
title_full_unstemmed Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis
title_short Engineering of global transcription factor FruR to redirect the carbon flow in Escherichia coli for enhancing l-phenylalanine biosynthesis
title_sort engineering of global transcription factor frur to redirect the carbon flow in escherichia coli for enhancing l-phenylalanine biosynthesis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609185/
https://www.ncbi.nlm.nih.gov/pubmed/36289548
http://dx.doi.org/10.1186/s12934-022-01954-7
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