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Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling

BACKGROUND: Butanol is an important biofuel and chemical. The development of butanol-tolerant strains and the identification of functional butanol-tolerant genes is essential for high-yield bio-butanol production due to the toxicity of butanol. RESULTS: Escherichia coli BW25113 was subjected for the...

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Autores principales: He, Xueting, Xue, Tingli, Ma, Yuanyuan, Zhang, Junyan, Wang, Zhiquan, Hong, Jiefang, Hui, Lanfeng, Qiao, Jianjun, Song, Hao, Zhang, Minhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442406/
https://www.ncbi.nlm.nih.gov/pubmed/30976323
http://dx.doi.org/10.1186/s13068-019-1405-z
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author He, Xueting
Xue, Tingli
Ma, Yuanyuan
Zhang, Junyan
Wang, Zhiquan
Hong, Jiefang
Hui, Lanfeng
Qiao, Jianjun
Song, Hao
Zhang, Minhua
author_facet He, Xueting
Xue, Tingli
Ma, Yuanyuan
Zhang, Junyan
Wang, Zhiquan
Hong, Jiefang
Hui, Lanfeng
Qiao, Jianjun
Song, Hao
Zhang, Minhua
author_sort He, Xueting
collection PubMed
description BACKGROUND: Butanol is an important biofuel and chemical. The development of butanol-tolerant strains and the identification of functional butanol-tolerant genes is essential for high-yield bio-butanol production due to the toxicity of butanol. RESULTS: Escherichia coli BW25113 was subjected for the first time to error-prone PCR-based whole-genome shuffling. The resulting mutants BW1847 and BW1857 were found to tolerate 2% (v/v) butanol and short-chain alcohols, including ethanol, isobutanol, and 1-pentanol. The mutants exhibited good stability under butanol stress, indicating that they are potential host strains for the construction of butanol pathways. BW1847 had better butanol tolerance than BW1857 under 0–0.75% (v/v) butanol stress, but showed a lower tolerance than BW1857 under 1.25–2% (v/v) butanol stress. Genome resequencing and PCR confirmation revealed that BW1847 and BW1857 had nine and seven single nucleotide polymorphisms, respectively, and a common 14-kb deletion. Functional complementation experiments of the SNPs and deleted genes demonstrated that the mutations of acrB and rob gene and the deletion of TqsA increased the tolerance of the two mutants to butanol. Genome-wide site-specific mutated strains DT385 (acrB C(1198)T) and DT900 (rob AT(686–7)) also showed significant tolerance to butanol and had higher butanol efflux ability than the control, further demonstrating that their mutations yield an inactive protein that enhances butanol resistance characteristics. CONCLUSIONS: Stable E. coli mutants with enhanced short alcohols and high concentrations of butanol tolerance were obtained through a rapid and effective method. The key genes of butanol tolerance in the two mutants were identified by comparative functional genomic analysis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1405-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-64424062019-04-11 Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling He, Xueting Xue, Tingli Ma, Yuanyuan Zhang, Junyan Wang, Zhiquan Hong, Jiefang Hui, Lanfeng Qiao, Jianjun Song, Hao Zhang, Minhua Biotechnol Biofuels Research BACKGROUND: Butanol is an important biofuel and chemical. The development of butanol-tolerant strains and the identification of functional butanol-tolerant genes is essential for high-yield bio-butanol production due to the toxicity of butanol. RESULTS: Escherichia coli BW25113 was subjected for the first time to error-prone PCR-based whole-genome shuffling. The resulting mutants BW1847 and BW1857 were found to tolerate 2% (v/v) butanol and short-chain alcohols, including ethanol, isobutanol, and 1-pentanol. The mutants exhibited good stability under butanol stress, indicating that they are potential host strains for the construction of butanol pathways. BW1847 had better butanol tolerance than BW1857 under 0–0.75% (v/v) butanol stress, but showed a lower tolerance than BW1857 under 1.25–2% (v/v) butanol stress. Genome resequencing and PCR confirmation revealed that BW1847 and BW1857 had nine and seven single nucleotide polymorphisms, respectively, and a common 14-kb deletion. Functional complementation experiments of the SNPs and deleted genes demonstrated that the mutations of acrB and rob gene and the deletion of TqsA increased the tolerance of the two mutants to butanol. Genome-wide site-specific mutated strains DT385 (acrB C(1198)T) and DT900 (rob AT(686–7)) also showed significant tolerance to butanol and had higher butanol efflux ability than the control, further demonstrating that their mutations yield an inactive protein that enhances butanol resistance characteristics. CONCLUSIONS: Stable E. coli mutants with enhanced short alcohols and high concentrations of butanol tolerance were obtained through a rapid and effective method. The key genes of butanol tolerance in the two mutants were identified by comparative functional genomic analysis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1405-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-01 /pmc/articles/PMC6442406/ /pubmed/30976323 http://dx.doi.org/10.1186/s13068-019-1405-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
He, Xueting
Xue, Tingli
Ma, Yuanyuan
Zhang, Junyan
Wang, Zhiquan
Hong, Jiefang
Hui, Lanfeng
Qiao, Jianjun
Song, Hao
Zhang, Minhua
Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling
title Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling
title_full Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling
title_fullStr Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling
title_full_unstemmed Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling
title_short Identification of functional butanol-tolerant genes from Escherichia coli mutants derived from error-prone PCR-based whole-genome shuffling
title_sort identification of functional butanol-tolerant genes from escherichia coli mutants derived from error-prone pcr-based whole-genome shuffling
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442406/
https://www.ncbi.nlm.nih.gov/pubmed/30976323
http://dx.doi.org/10.1186/s13068-019-1405-z
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