Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance

The naturally existing microbial hosts can rarely satisfy industrial requirements, thus there has always been an intense effort in strain engineering to meet the needs of these bioprocesses. Here, in this work, we want to prove the concept that engineering global transcription factor cAMP receptor p...

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Main Authors: Zhang, Hongfang, Chong, Huiqing, Ching, Chi Bun, Jiang, Rongrong
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/98901
http://hdl.handle.net/10220/12722
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-989012020-03-07T11:35:38Z Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance Zhang, Hongfang Chong, Huiqing Ching, Chi Bun Jiang, Rongrong School of Chemical and Biomedical Engineering The naturally existing microbial hosts can rarely satisfy industrial requirements, thus there has always been an intense effort in strain engineering to meet the needs of these bioprocesses. Here, in this work, we want to prove the concept that engineering global transcription factor cAMP receptor protein (CRP) of Escherichia coli can improve cell phenotypes. CRP is one of the global regulatory proteins that can regulate the transcription of over 400 genes in E. coli. The target phenotype in this study is strain osmotolerance. Amino acid mutations were introduced to CRP by either error-prone PCR or DNA shuffling, and the random mutagenesis libraries were subjected to enrichment selection under NaCl stress. Five CRP mutants (MT1–MT5) were selected from the error-prone PCR libraries with enhanced osmotolerance. DNA shuffling technique was employed to generate mutant MT6 with MT1–MT5 as templates. All of these variants showed much better growth in the presence of NaCl compared to the wild type, and MT6 presented the best tolerance towards NaCl. In the presence of 0.9 M NaCl, the growth rate of MT6 is 0.113 h−1, while that of WT is 0.077 h−1. MT6 also exhibited resistance to other osmotic stressors, such as KCl, glucose, and sucrose. DNA microarray analysis showed that genes involved in colanic acid biosynthesis are up-regulated in the absence of salt stress, whereas carbohydrate metabolic genes are differentially expressed under NaCl stress when comparing MT6 to WT. Scanning electron microscopy images confirmed the elongation of both WT and MT6 when exposed to NaCl but the cell surface of MT6 was relatively smooth. 2013-08-01T02:49:11Z 2019-12-06T20:00:56Z 2013-08-01T02:49:11Z 2019-12-06T20:00:56Z 2011 2011 Journal Article Zhang, H., Chong, H., Ching, C. B.,& Jiang, R. (2012). Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance. Biotechnology and Bioengineering, 109(5), 1165-1172. 0006-3592 https://hdl.handle.net/10356/98901 http://hdl.handle.net/10220/12722 10.1002/bit.24411 en Biotechnology and bioengineering
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description The naturally existing microbial hosts can rarely satisfy industrial requirements, thus there has always been an intense effort in strain engineering to meet the needs of these bioprocesses. Here, in this work, we want to prove the concept that engineering global transcription factor cAMP receptor protein (CRP) of Escherichia coli can improve cell phenotypes. CRP is one of the global regulatory proteins that can regulate the transcription of over 400 genes in E. coli. The target phenotype in this study is strain osmotolerance. Amino acid mutations were introduced to CRP by either error-prone PCR or DNA shuffling, and the random mutagenesis libraries were subjected to enrichment selection under NaCl stress. Five CRP mutants (MT1–MT5) were selected from the error-prone PCR libraries with enhanced osmotolerance. DNA shuffling technique was employed to generate mutant MT6 with MT1–MT5 as templates. All of these variants showed much better growth in the presence of NaCl compared to the wild type, and MT6 presented the best tolerance towards NaCl. In the presence of 0.9 M NaCl, the growth rate of MT6 is 0.113 h−1, while that of WT is 0.077 h−1. MT6 also exhibited resistance to other osmotic stressors, such as KCl, glucose, and sucrose. DNA microarray analysis showed that genes involved in colanic acid biosynthesis are up-regulated in the absence of salt stress, whereas carbohydrate metabolic genes are differentially expressed under NaCl stress when comparing MT6 to WT. Scanning electron microscopy images confirmed the elongation of both WT and MT6 when exposed to NaCl but the cell surface of MT6 was relatively smooth.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Zhang, Hongfang
Chong, Huiqing
Ching, Chi Bun
Jiang, Rongrong
format Article
author Zhang, Hongfang
Chong, Huiqing
Ching, Chi Bun
Jiang, Rongrong
spellingShingle Zhang, Hongfang
Chong, Huiqing
Ching, Chi Bun
Jiang, Rongrong
Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance
author_sort Zhang, Hongfang
title Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance
title_short Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance
title_full Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance
title_fullStr Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance
title_full_unstemmed Random mutagenesis of global transcription factor cAMP receptor protein for improved osmotolerance
title_sort random mutagenesis of global transcription factor camp receptor protein for improved osmotolerance
publishDate 2013
url https://hdl.handle.net/10356/98901
http://hdl.handle.net/10220/12722
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