Cargando…

Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB

BACKGROUND: Escherichia coli has been proved to be one promising platform chassis for the production of various natural products, such as biofuels. Product toxicity is one of the main bottlenecks for achieving maximum production of biofuels. Host strain engineering is an effective approach to allevi...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Guochao, Wu, Anning, Xiao, Lin, Han, Ruizhi, Ni, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598250/
https://www.ncbi.nlm.nih.gov/pubmed/31297152
http://dx.doi.org/10.1186/s13068-019-1507-7
_version_ 1783430730999660544
author Xu, Guochao
Wu, Anning
Xiao, Lin
Han, Ruizhi
Ni, Ye
author_facet Xu, Guochao
Wu, Anning
Xiao, Lin
Han, Ruizhi
Ni, Ye
author_sort Xu, Guochao
collection PubMed
description BACKGROUND: Escherichia coli has been proved to be one promising platform chassis for the production of various natural products, such as biofuels. Product toxicity is one of the main bottlenecks for achieving maximum production of biofuels. Host strain engineering is an effective approach to alleviate solvent toxicity issue in fermentation. RESULTS: Thirty chaperones were overexpressed in E. coli JM109, and SecB recombinant strain was identified with the highest n-butanol tolerance. The tolerance (T) of E. coli overexpressing SecB, calculated by growth difference in the presence and absence of solvents, was determined to be 9.13% at 1.2% (v/v) butanol, which was 3.2-fold of the control strain. Random mutagenesis of SecB was implemented and homologously overexpressed in E. coli, and mutant SecB(T10A) was identified from 2800 variants rendering E. coli the highest butanol tolerance. Saturation mutagenesis on T10 site revealed that hydrophobic residues were required for high butanol tolerance of E. coli. Compared with wild-type (WT) SecB, the T of SecB(T10A) strain was further increased from 9.14 to 14.4% at 1.2% butanol, which was 5.3-fold of control strain. Remarkably, E. coli engineered with SecB(T10A) could tolerate as high as 1.8% butanol (~ 14.58 g/L). The binding affinity of SecB(T10A) toward model substrate unfolded maltose binding protein (preMBP) was 11.9-fold of that of WT SecB as determined by isothermal titration calorimetry. Residue T10 locates at the entrance of hydrophobic substrate binding groove of SecB, and might play an important role in recognition and binding of cargo proteins. CONCLUSIONS: SecB chaperone was identified by chaperone mining to be effective in enhancing butanol tolerance of E. coli. Maximum butanol tolerance of E. coli could reach 1.6% and 1.8% butanol by engineering single gene of SecB or SecB(T10A). Hydrophobic interaction is vital for enhanced binding affinity between SecB and cargo proteins, and therefore improved butanol tolerance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1507-7) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6598250
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-65982502019-07-11 Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB Xu, Guochao Wu, Anning Xiao, Lin Han, Ruizhi Ni, Ye Biotechnol Biofuels Research BACKGROUND: Escherichia coli has been proved to be one promising platform chassis for the production of various natural products, such as biofuels. Product toxicity is one of the main bottlenecks for achieving maximum production of biofuels. Host strain engineering is an effective approach to alleviate solvent toxicity issue in fermentation. RESULTS: Thirty chaperones were overexpressed in E. coli JM109, and SecB recombinant strain was identified with the highest n-butanol tolerance. The tolerance (T) of E. coli overexpressing SecB, calculated by growth difference in the presence and absence of solvents, was determined to be 9.13% at 1.2% (v/v) butanol, which was 3.2-fold of the control strain. Random mutagenesis of SecB was implemented and homologously overexpressed in E. coli, and mutant SecB(T10A) was identified from 2800 variants rendering E. coli the highest butanol tolerance. Saturation mutagenesis on T10 site revealed that hydrophobic residues were required for high butanol tolerance of E. coli. Compared with wild-type (WT) SecB, the T of SecB(T10A) strain was further increased from 9.14 to 14.4% at 1.2% butanol, which was 5.3-fold of control strain. Remarkably, E. coli engineered with SecB(T10A) could tolerate as high as 1.8% butanol (~ 14.58 g/L). The binding affinity of SecB(T10A) toward model substrate unfolded maltose binding protein (preMBP) was 11.9-fold of that of WT SecB as determined by isothermal titration calorimetry. Residue T10 locates at the entrance of hydrophobic substrate binding groove of SecB, and might play an important role in recognition and binding of cargo proteins. CONCLUSIONS: SecB chaperone was identified by chaperone mining to be effective in enhancing butanol tolerance of E. coli. Maximum butanol tolerance of E. coli could reach 1.6% and 1.8% butanol by engineering single gene of SecB or SecB(T10A). Hydrophobic interaction is vital for enhanced binding affinity between SecB and cargo proteins, and therefore improved butanol tolerance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1507-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-28 /pmc/articles/PMC6598250/ /pubmed/31297152 http://dx.doi.org/10.1186/s13068-019-1507-7 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
Xu, Guochao
Wu, Anning
Xiao, Lin
Han, Ruizhi
Ni, Ye
Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB
title Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB
title_full Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB
title_fullStr Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB
title_full_unstemmed Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB
title_short Enhancing butanol tolerance of Escherichia coli reveals hydrophobic interaction of multi-tasking chaperone SecB
title_sort enhancing butanol tolerance of escherichia coli reveals hydrophobic interaction of multi-tasking chaperone secb
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598250/
https://www.ncbi.nlm.nih.gov/pubmed/31297152
http://dx.doi.org/10.1186/s13068-019-1507-7
work_keys_str_mv AT xuguochao enhancingbutanoltoleranceofescherichiacolirevealshydrophobicinteractionofmultitaskingchaperonesecb
AT wuanning enhancingbutanoltoleranceofescherichiacolirevealshydrophobicinteractionofmultitaskingchaperonesecb
AT xiaolin enhancingbutanoltoleranceofescherichiacolirevealshydrophobicinteractionofmultitaskingchaperonesecb
AT hanruizhi enhancingbutanoltoleranceofescherichiacolirevealshydrophobicinteractionofmultitaskingchaperonesecb
AT niye enhancingbutanoltoleranceofescherichiacolirevealshydrophobicinteractionofmultitaskingchaperonesecb