Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP)
The limited isobutanol tolerance of Escherichia coli is a major drawback during fermentative isobutanol production. Different from classical strain engineering approaches, this work was initiated to improve E. coli isobutanol tolerance from its transcriptional level by engineering its global transcr...
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sg-ntu-dr.10356-1027922020-03-07T11:40:23Z Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) Zhang, Hongfang Song, Hao Huang, Lei Jiang, Rongrong Chong, Huiqing Geng, Hefang School of Chemical and Biomedical Engineering DRNTU::Engineering::Bioengineering The limited isobutanol tolerance of Escherichia coli is a major drawback during fermentative isobutanol production. Different from classical strain engineering approaches, this work was initiated to improve E. coli isobutanol tolerance from its transcriptional level by engineering its global transcription factor cAMP receptor protein (CRP). Random mutagenesis libraries were generated by error-prone PCR of crp, and the libraries were subjected to isobutanol stress for selection. Variant IB2 (S179P, H199R) was isolated and exhibited much better growth (0.18 h−1) than the control (0.05 h−1) in 1.2% (v/v) isobutanol (9.6 g/L). Genome-wide DNA microarray analysis revealed that 58 and 308 genes in IB2 had differential expression (>2-fold, p < 0.05) in the absence and presence of 1% (v/v) isobutanol, respectively. When challenged with isobutanol, genes related to acid resistance (gadABCE, hdeABD), nitrate reduction (narUZYWV), flagella and fimbrial activity (lfhA, yehB, ycgR, fimCDF), and sulfate reduction and transportation (cysIJH, cysC, cysN) were the major functional groups that were up-regulated, whereas most of the down-regulated genes were enzyme (tnaA) and transporters (proVWX, manXYZ). As demonstrated by single-gene knockout experiments, gadX, nirB, rhaS, hdeB, and ybaS were found associated with strain isobutanol resistance. The intracellular reactive oxygen species (ROS) level in IB2 was only half of that of the control when facing stress, indicating that IB2 can withstand toxic isobutanol much better than the control. Biotechnol. Biotechnol. 2014-04-07T05:04:16Z 2019-12-06T21:00:15Z 2014-04-07T05:04:16Z 2019-12-06T21:00:15Z 2013 2013 Journal Article Chong, H., Geng, H., Zhang, H., Song, H., Huang, L., & Jiang, R. (2014). Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP). Biotechnology and Bioengineering, 111(4), 700-708. 0006-3592 https://hdl.handle.net/10356/102792 http://hdl.handle.net/10220/19150 10.1002/bit.25134 en Biotechnology and bioengineering © 2013 Wiley Periodicals, Inc. |
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DRNTU::Engineering::Bioengineering Zhang, Hongfang Song, Hao Huang, Lei Jiang, Rongrong Chong, Huiqing Geng, Hefang Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) |
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The limited isobutanol tolerance of Escherichia coli is a major drawback during fermentative isobutanol production. Different from classical strain engineering approaches, this work was initiated to improve E. coli isobutanol tolerance from its transcriptional level by engineering its global transcription factor cAMP receptor protein (CRP). Random mutagenesis libraries were generated by error-prone PCR of crp, and the libraries were subjected to isobutanol stress for selection. Variant IB2 (S179P, H199R) was isolated and exhibited much better growth (0.18 h−1) than the control (0.05 h−1) in 1.2% (v/v) isobutanol (9.6 g/L). Genome-wide DNA microarray analysis revealed that 58 and 308 genes in IB2 had differential expression (>2-fold, p < 0.05) in the absence and presence of 1% (v/v) isobutanol, respectively. When challenged with isobutanol, genes related to acid resistance (gadABCE, hdeABD), nitrate reduction (narUZYWV), flagella and fimbrial activity (lfhA, yehB, ycgR, fimCDF), and sulfate reduction and transportation (cysIJH, cysC, cysN) were the major functional groups that were up-regulated, whereas most of the down-regulated genes were enzyme (tnaA) and transporters (proVWX, manXYZ). As demonstrated by single-gene knockout experiments, gadX, nirB, rhaS, hdeB, and ybaS were found associated with strain isobutanol resistance. The intracellular reactive oxygen species (ROS) level in IB2 was only half of that of the control when facing stress, indicating that IB2 can withstand toxic isobutanol much better than the control. Biotechnol. Biotechnol. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Zhang, Hongfang Song, Hao Huang, Lei Jiang, Rongrong Chong, Huiqing Geng, Hefang |
format |
Article |
author |
Zhang, Hongfang Song, Hao Huang, Lei Jiang, Rongrong Chong, Huiqing Geng, Hefang |
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Zhang, Hongfang |
title |
Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) |
title_short |
Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) |
title_full |
Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) |
title_fullStr |
Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) |
title_full_unstemmed |
Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP) |
title_sort |
enhancing e. coli isobutanol tolerance through engineering its global transcription factor camp receptor protein (crp) |
publishDate |
2014 |
url |
https://hdl.handle.net/10356/102792 http://hdl.handle.net/10220/19150 |
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