Cargando…

In silico profiling of cell growth and succinate production in Escherichia coli NZN111

BACKGROUND: Succinic acid is a valuable product due to its wide-ranging utilities. To improve succinate production and reduce by-products formation, Escherichia coli NZN111 was constructed by insertional inactivation of lactate dehydrogenase (LDH) and pyruvate formate lyase (PFL) encoded by the gene...

Descripción completa

Detalles Bibliográficos
Autores principales: Jian, Xingxing, Li, Ningchuan, Zhang, Cheng, Hua, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110578/
https://www.ncbi.nlm.nih.gov/pubmed/27909649
http://dx.doi.org/10.1186/s40643-016-0125-5
_version_ 1782467709732126720
author Jian, Xingxing
Li, Ningchuan
Zhang, Cheng
Hua, Qiang
author_facet Jian, Xingxing
Li, Ningchuan
Zhang, Cheng
Hua, Qiang
author_sort Jian, Xingxing
collection PubMed
description BACKGROUND: Succinic acid is a valuable product due to its wide-ranging utilities. To improve succinate production and reduce by-products formation, Escherichia coli NZN111 was constructed by insertional inactivation of lactate dehydrogenase (LDH) and pyruvate formate lyase (PFL) encoded by the genes ldhA and pflB, respectively. However, this double-deletion mutant is incapable of anaerobically growing on glucose in rich or minimal medium even with acetate supplementation. A widespread hold view is that the inactivation of NADH-dependent LDH limits the regeneration of NAD(+) and consequently disables proper growth under anaerobic conditions. RESULTS: In this study, genome-scale metabolic core model of E. coli was reconstructed and employed to perform all simulations in silico according to the reconstruction of engineered strain E. coli NZN111. Non-optimized artificial centering hit-and-run (ACHR) method and metabolite flux-sum analysis were utilized to evaluate metabolic characteristics of strains. Thus, metabolic characteristics of the strains wild-type E. coli, ldhA mutant, pflB mutant, and NZN111 under anaerobic conditions were successfully unraveled. CONCLUSIONS: We found a viewpoint contrary to the widespread realization that an NADH/NAD(+) in NZN111 mainly resulted from the inactivation of PFL rather than the inactivation of LDH. In addition, the two alternative anaerobic fermentation pathways, lactate and ethanol production pathways, were blocked owing to the disruption of ldhA and pflB, resulting in insufficient NAD(+) regeneration to oxidize or metabolize glucose for cell growth. Furthermore, we speculated reaction NADH16, the conversion of ubiquinone-8 (q8) to ubiquinol-8 (q8h2), as a potential amplification target for anaerobically improving cell growth and succinate production in NZN111. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40643-016-0125-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5110578
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-51105782016-11-29 In silico profiling of cell growth and succinate production in Escherichia coli NZN111 Jian, Xingxing Li, Ningchuan Zhang, Cheng Hua, Qiang Bioresour Bioprocess Research BACKGROUND: Succinic acid is a valuable product due to its wide-ranging utilities. To improve succinate production and reduce by-products formation, Escherichia coli NZN111 was constructed by insertional inactivation of lactate dehydrogenase (LDH) and pyruvate formate lyase (PFL) encoded by the genes ldhA and pflB, respectively. However, this double-deletion mutant is incapable of anaerobically growing on glucose in rich or minimal medium even with acetate supplementation. A widespread hold view is that the inactivation of NADH-dependent LDH limits the regeneration of NAD(+) and consequently disables proper growth under anaerobic conditions. RESULTS: In this study, genome-scale metabolic core model of E. coli was reconstructed and employed to perform all simulations in silico according to the reconstruction of engineered strain E. coli NZN111. Non-optimized artificial centering hit-and-run (ACHR) method and metabolite flux-sum analysis were utilized to evaluate metabolic characteristics of strains. Thus, metabolic characteristics of the strains wild-type E. coli, ldhA mutant, pflB mutant, and NZN111 under anaerobic conditions were successfully unraveled. CONCLUSIONS: We found a viewpoint contrary to the widespread realization that an NADH/NAD(+) in NZN111 mainly resulted from the inactivation of PFL rather than the inactivation of LDH. In addition, the two alternative anaerobic fermentation pathways, lactate and ethanol production pathways, were blocked owing to the disruption of ldhA and pflB, resulting in insufficient NAD(+) regeneration to oxidize or metabolize glucose for cell growth. Furthermore, we speculated reaction NADH16, the conversion of ubiquinone-8 (q8) to ubiquinol-8 (q8h2), as a potential amplification target for anaerobically improving cell growth and succinate production in NZN111. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40643-016-0125-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-11-15 2016 /pmc/articles/PMC5110578/ /pubmed/27909649 http://dx.doi.org/10.1186/s40643-016-0125-5 Text en © The Author(s) 2016 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.
spellingShingle Research
Jian, Xingxing
Li, Ningchuan
Zhang, Cheng
Hua, Qiang
In silico profiling of cell growth and succinate production in Escherichia coli NZN111
title In silico profiling of cell growth and succinate production in Escherichia coli NZN111
title_full In silico profiling of cell growth and succinate production in Escherichia coli NZN111
title_fullStr In silico profiling of cell growth and succinate production in Escherichia coli NZN111
title_full_unstemmed In silico profiling of cell growth and succinate production in Escherichia coli NZN111
title_short In silico profiling of cell growth and succinate production in Escherichia coli NZN111
title_sort in silico profiling of cell growth and succinate production in escherichia coli nzn111
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110578/
https://www.ncbi.nlm.nih.gov/pubmed/27909649
http://dx.doi.org/10.1186/s40643-016-0125-5
work_keys_str_mv AT jianxingxing insilicoprofilingofcellgrowthandsuccinateproductioninescherichiacolinzn111
AT liningchuan insilicoprofilingofcellgrowthandsuccinateproductioninescherichiacolinzn111
AT zhangcheng insilicoprofilingofcellgrowthandsuccinateproductioninescherichiacolinzn111
AT huaqiang insilicoprofilingofcellgrowthandsuccinateproductioninescherichiacolinzn111