Cargando…

Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli

BACKGROUND: Glycolate is an important α-hydroxy carboxylic acid widely used in industrial and consumer applications. The production of glycolate from glucose in Escherichia coli is generally carried out by glycolysis and glyoxylate shunt pathways, followed by reduction to glycolate. Glycolate accumu...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Kangjia, Li, Guohui, Wei, Ren, Mao, Yin, Zhao, Yunying, He, Aiyong, Bai, Zhonghu, Deng, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449901/
https://www.ncbi.nlm.nih.gov/pubmed/30988698
http://dx.doi.org/10.1186/s13036-019-0159-2
_version_ 1783408945506811904
author Zhu, Kangjia
Li, Guohui
Wei, Ren
Mao, Yin
Zhao, Yunying
He, Aiyong
Bai, Zhonghu
Deng, Yu
author_facet Zhu, Kangjia
Li, Guohui
Wei, Ren
Mao, Yin
Zhao, Yunying
He, Aiyong
Bai, Zhonghu
Deng, Yu
author_sort Zhu, Kangjia
collection PubMed
description BACKGROUND: Glycolate is an important α-hydroxy carboxylic acid widely used in industrial and consumer applications. The production of glycolate from glucose in Escherichia coli is generally carried out by glycolysis and glyoxylate shunt pathways, followed by reduction to glycolate. Glycolate accumulation was significantly affected by nitrogen sources and isocitrate dehydrogenase (ICDH), which influenced carbon flux distribution between the tricarboxylic acid (TCA) cycle and the glyoxylate shunt, however, the mechanism was unclear. RESULTS: Herein, we used RNA-Seq to explore the effects of nitrogen sources and ICDH knockout on glycolate production. The Mgly534 strain and the Mgly624 strain (with the ICDH deletion in Mgly534), displaying different phenotypes on organic nitrogen sources, were also adopted for the exploration. Though the growth of Mgly534 was improved on organic nitrogen sources, glycolate production decreased and acetate accumulated, while Mgly624 achieved a balance between cell growth and glycolate production, reaching 0.81 g glycolate/OD (2.6-fold higher than Mgly534). To further study Mgly624, the significant changed genes related to N-regulation, oxidative stress response and iron transport were analyzed. Glutamate and serine were found to increase the biomass and productivity respectively. Meanwhile, overexpressing the arginine transport gene argT accelerated the cell growth rate and increased the biomass. Further, the presence of Fe(2+) also speeded up the cells growth and compensated for the lack of reducing equivalents. CONCLUSION: Our studies identified that ICDH knockout strain was more suitable for glycolate production. RNA-Seq provided a better understanding of the ICDH knockout on cellular physiology and glycolate production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13036-019-0159-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6449901
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-64499012019-04-15 Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli Zhu, Kangjia Li, Guohui Wei, Ren Mao, Yin Zhao, Yunying He, Aiyong Bai, Zhonghu Deng, Yu J Biol Eng Research BACKGROUND: Glycolate is an important α-hydroxy carboxylic acid widely used in industrial and consumer applications. The production of glycolate from glucose in Escherichia coli is generally carried out by glycolysis and glyoxylate shunt pathways, followed by reduction to glycolate. Glycolate accumulation was significantly affected by nitrogen sources and isocitrate dehydrogenase (ICDH), which influenced carbon flux distribution between the tricarboxylic acid (TCA) cycle and the glyoxylate shunt, however, the mechanism was unclear. RESULTS: Herein, we used RNA-Seq to explore the effects of nitrogen sources and ICDH knockout on glycolate production. The Mgly534 strain and the Mgly624 strain (with the ICDH deletion in Mgly534), displaying different phenotypes on organic nitrogen sources, were also adopted for the exploration. Though the growth of Mgly534 was improved on organic nitrogen sources, glycolate production decreased and acetate accumulated, while Mgly624 achieved a balance between cell growth and glycolate production, reaching 0.81 g glycolate/OD (2.6-fold higher than Mgly534). To further study Mgly624, the significant changed genes related to N-regulation, oxidative stress response and iron transport were analyzed. Glutamate and serine were found to increase the biomass and productivity respectively. Meanwhile, overexpressing the arginine transport gene argT accelerated the cell growth rate and increased the biomass. Further, the presence of Fe(2+) also speeded up the cells growth and compensated for the lack of reducing equivalents. CONCLUSION: Our studies identified that ICDH knockout strain was more suitable for glycolate production. RNA-Seq provided a better understanding of the ICDH knockout on cellular physiology and glycolate production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13036-019-0159-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-04 /pmc/articles/PMC6449901/ /pubmed/30988698 http://dx.doi.org/10.1186/s13036-019-0159-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhu, Kangjia
Li, Guohui
Wei, Ren
Mao, Yin
Zhao, Yunying
He, Aiyong
Bai, Zhonghu
Deng, Yu
Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli
title Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli
title_full Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli
title_fullStr Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli
title_full_unstemmed Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli
title_short Systematic analysis of the effects of different nitrogen source and ICDH knockout on glycolate synthesis in Escherichia coli
title_sort systematic analysis of the effects of different nitrogen source and icdh knockout on glycolate synthesis in escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449901/
https://www.ncbi.nlm.nih.gov/pubmed/30988698
http://dx.doi.org/10.1186/s13036-019-0159-2
work_keys_str_mv AT zhukangjia systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT liguohui systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT weiren systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT maoyin systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT zhaoyunying systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT heaiyong systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT baizhonghu systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli
AT dengyu systematicanalysisoftheeffectsofdifferentnitrogensourceandicdhknockoutonglycolatesynthesisinescherichiacoli