Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance

Organic solvents are often applied in biphasic biocatalysis or involved in bioremediation, but native microorganisms usually have low tolerance toward these organic solvents and cannot survive in the stressful environment. Here, we aimed to improve the organic solvent tolerance of Escherichia coli b...

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Main Authors: Basak, Souvik, Song, Hao, Jiang, Rongrong
Other Authors: School of Chemical and Biomedical Engineering
Format: Journal Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/97922
http://hdl.handle.net/10220/12336
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author Basak, Souvik
Song, Hao
Jiang, Rongrong
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Basak, Souvik
Song, Hao
Jiang, Rongrong
author_sort Basak, Souvik
collection NTU
description Organic solvents are often applied in biphasic biocatalysis or involved in bioremediation, but native microorganisms usually have low tolerance toward these organic solvents and cannot survive in the stressful environment. Here, we aimed to improve the organic solvent tolerance of Escherichia coli by engineering its global transcription factor cAMP receptor protein (CRP). Toluene was chosen as model organic solvent. The mutated crp genes were generated via error-prone PCR and three toluene-tolerant mutants M1–M3 were isolated from random mutagenesis libraries by enrichment selection. All mutants exhibited much better growth than the wild type upon exposure to 0.2–0.23% (v/v) toluene, with M2 the best. When toluene concentration was at 0.2%, M1–M3 shared similar growth rate at 0.68 h−1 despite the elongated 20-h lag phase, with WT exhibiting null growth. In 0.23% toluene, the growth rate of M2 was found to be 0.51 h−1 while the growth of WT was completely inhibited. M2 also demonstrated excellent growth in other organic solvents such as n-hexane, cyclohexane and p-xylene as compared to the wild type. Our quantitative real-time reverse transcription PCR analysis with organic-solvent stress associated genes indicated that amino acid mutations in CRP would lead to changes in the expression level of genes that are not regulated by CRP. The field emission scanning electron microscopy images revealed that both wild type and M2, though combating toluene stress, did not have any significant changes in their cellular size and shape.
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spelling ntu-10356/979222020-03-07T11:35:36Z Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance Basak, Souvik Song, Hao Jiang, Rongrong School of Chemical and Biomedical Engineering Organic solvents are often applied in biphasic biocatalysis or involved in bioremediation, but native microorganisms usually have low tolerance toward these organic solvents and cannot survive in the stressful environment. Here, we aimed to improve the organic solvent tolerance of Escherichia coli by engineering its global transcription factor cAMP receptor protein (CRP). Toluene was chosen as model organic solvent. The mutated crp genes were generated via error-prone PCR and three toluene-tolerant mutants M1–M3 were isolated from random mutagenesis libraries by enrichment selection. All mutants exhibited much better growth than the wild type upon exposure to 0.2–0.23% (v/v) toluene, with M2 the best. When toluene concentration was at 0.2%, M1–M3 shared similar growth rate at 0.68 h−1 despite the elongated 20-h lag phase, with WT exhibiting null growth. In 0.23% toluene, the growth rate of M2 was found to be 0.51 h−1 while the growth of WT was completely inhibited. M2 also demonstrated excellent growth in other organic solvents such as n-hexane, cyclohexane and p-xylene as compared to the wild type. Our quantitative real-time reverse transcription PCR analysis with organic-solvent stress associated genes indicated that amino acid mutations in CRP would lead to changes in the expression level of genes that are not regulated by CRP. The field emission scanning electron microscopy images revealed that both wild type and M2, though combating toluene stress, did not have any significant changes in their cellular size and shape. 2013-07-26T01:57:31Z 2019-12-06T19:48:23Z 2013-07-26T01:57:31Z 2019-12-06T19:48:23Z 2012 2012 Journal Article Basak, S., Song, H., & Jiang, R. (2012). Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance. Process Biochemistry, 47(12), 2152-2158. 1359-5113 https://hdl.handle.net/10356/97922 http://hdl.handle.net/10220/12336 10.1016/j.procbio.2012.08.006 en Process biochemistry © 2012 Elsevier Ltd.
spellingShingle Basak, Souvik
Song, Hao
Jiang, Rongrong
Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance
title Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance
title_full Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance
title_fullStr Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance
title_full_unstemmed Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance
title_short Error-prone PCR of global transcription factor cyclic AMP receptor protein for enhanced organic solvent (toluene) tolerance
title_sort error prone pcr of global transcription factor cyclic amp receptor protein for enhanced organic solvent toluene tolerance
url https://hdl.handle.net/10356/97922
http://hdl.handle.net/10220/12336
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AT songhao errorpronepcrofglobaltranscriptionfactorcyclicampreceptorproteinforenhancedorganicsolventtoluenetolerance
AT jiangrongrong errorpronepcrofglobaltranscriptionfactorcyclicampreceptorproteinforenhancedorganicsolventtoluenetolerance