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Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein

BACKGROUND: Though n-butanol has been proposed as a potential transportation biofuel, its toxicity often causes oxidative stress in the host microorganism and is considered one of the bottlenecks preventing its efficient mass production. RESULTS: To relieve the oxidative stress in the host cell, met...

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Autores principales: Chin, Wei-Chih, Lin, Kuo-Hsing, Chang, Jui-Jen, Huang, Chieh-Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848587/
https://www.ncbi.nlm.nih.gov/pubmed/24020941
http://dx.doi.org/10.1186/1754-6834-6-130
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author Chin, Wei-Chih
Lin, Kuo-Hsing
Chang, Jui-Jen
Huang, Chieh-Chen
author_facet Chin, Wei-Chih
Lin, Kuo-Hsing
Chang, Jui-Jen
Huang, Chieh-Chen
author_sort Chin, Wei-Chih
collection PubMed
description BACKGROUND: Though n-butanol has been proposed as a potential transportation biofuel, its toxicity often causes oxidative stress in the host microorganism and is considered one of the bottlenecks preventing its efficient mass production. RESULTS: To relieve the oxidative stress in the host cell, metallothioneins (MTs), which are known as scavengers for reactive oxygen species (ROS), were engineered in E. coli hosts for both cytosolic and outer-membrane-targeted (osmoregulatory membrane protein OmpC fused) expression. Metallothioneins from human (HMT), mouse (MMT), and tilapia fish (TMT) were tested. The host strain expressing membrane-targeted TMT showed the greatest ability to reduce oxidative stresses induced by n-butanol, ethanol, furfural, hydroxymethylfurfural, and nickel. The same strain also allowed for an increased growth rate of recombinant E. coli under n-butanol stress. Further experiments indicated that the TMT-fused OmpC protein could not only function in ROS scavenging but also regulate either glycine betaine (GB) or glucose uptake via osmosis, and the dual functional fusion protein could contribute in an enhancement of the host microorganism’s growth rate. CONCLUSIONS: The abilities of scavenging intracellular or extracellular ROS by these engineering E. coli were examined, and TMT show the best ability among three MTs. Additionally, the membrane-targeted fusion protein, OmpC-TMT, improved host tolerance up to 1.5% n-butanol above that of TMT which is only 1%. These results presented indicate potential novel approaches for engineering stress tolerant microorganism strains.
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spelling pubmed-38485872013-12-05 Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein Chin, Wei-Chih Lin, Kuo-Hsing Chang, Jui-Jen Huang, Chieh-Chen Biotechnol Biofuels Research BACKGROUND: Though n-butanol has been proposed as a potential transportation biofuel, its toxicity often causes oxidative stress in the host microorganism and is considered one of the bottlenecks preventing its efficient mass production. RESULTS: To relieve the oxidative stress in the host cell, metallothioneins (MTs), which are known as scavengers for reactive oxygen species (ROS), were engineered in E. coli hosts for both cytosolic and outer-membrane-targeted (osmoregulatory membrane protein OmpC fused) expression. Metallothioneins from human (HMT), mouse (MMT), and tilapia fish (TMT) were tested. The host strain expressing membrane-targeted TMT showed the greatest ability to reduce oxidative stresses induced by n-butanol, ethanol, furfural, hydroxymethylfurfural, and nickel. The same strain also allowed for an increased growth rate of recombinant E. coli under n-butanol stress. Further experiments indicated that the TMT-fused OmpC protein could not only function in ROS scavenging but also regulate either glycine betaine (GB) or glucose uptake via osmosis, and the dual functional fusion protein could contribute in an enhancement of the host microorganism’s growth rate. CONCLUSIONS: The abilities of scavenging intracellular or extracellular ROS by these engineering E. coli were examined, and TMT show the best ability among three MTs. Additionally, the membrane-targeted fusion protein, OmpC-TMT, improved host tolerance up to 1.5% n-butanol above that of TMT which is only 1%. These results presented indicate potential novel approaches for engineering stress tolerant microorganism strains. BioMed Central 2013-09-11 /pmc/articles/PMC3848587/ /pubmed/24020941 http://dx.doi.org/10.1186/1754-6834-6-130 Text en Copyright © 2013 Chin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chin, Wei-Chih
Lin, Kuo-Hsing
Chang, Jui-Jen
Huang, Chieh-Chen
Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein
title Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein
title_full Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein
title_fullStr Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein
title_full_unstemmed Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein
title_short Improvement of n-butanol tolerance in Escherichia coli by membrane-targeted tilapia metallothionein
title_sort improvement of n-butanol tolerance in escherichia coli by membrane-targeted tilapia metallothionein
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848587/
https://www.ncbi.nlm.nih.gov/pubmed/24020941
http://dx.doi.org/10.1186/1754-6834-6-130
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