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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-3848587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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