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Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z

BACKGROUND: Ectoine (1,3,4,5-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) is an attractive compatible solute because of its wide industrial applications. Previous studies on the microbial production of ectoine have focused on sugar fermentation. Alternatively, methane can be used as an inexpensi...

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Autores principales: Cho, Sukhyeong, Lee, Yun Seo, Chai, Hanyu, Lim, Sang Eun, Na, Jeong Geol, Lee, Jinwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759281/
https://www.ncbi.nlm.nih.gov/pubmed/35418141
http://dx.doi.org/10.1186/s13068-022-02104-2
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author Cho, Sukhyeong
Lee, Yun Seo
Chai, Hanyu
Lim, Sang Eun
Na, Jeong Geol
Lee, Jinwon
author_facet Cho, Sukhyeong
Lee, Yun Seo
Chai, Hanyu
Lim, Sang Eun
Na, Jeong Geol
Lee, Jinwon
author_sort Cho, Sukhyeong
collection PubMed
description BACKGROUND: Ectoine (1,3,4,5-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) is an attractive compatible solute because of its wide industrial applications. Previous studies on the microbial production of ectoine have focused on sugar fermentation. Alternatively, methane can be used as an inexpensive and abundant resource for ectoine production by using the halophilic methanotroph, Methylomicrobium alcaliphilum 20Z. However, there are some limitations, including the low production of ectoine from methane and the limited tools for the genetic manipulation of methanotrophs to facilitate their use as industrial strains. RESULTS: We constructed M. alcaliphilum 20ZDP with a high conjugation efficiency and stability of the episomal plasmid by the removal of its native plasmid. To improve the ectoine production in M. alcaliphilum 20Z from methane, the ectD (encoding ectoine hydroxylase) and ectR (transcription repressor of the ectABC-ask operon) were deleted to reduce the formation of by-products (such as hydroxyectoine) and induce ectoine production. When the double mutant was batch cultured with methane, ectoine production was enhanced 1.6-fold compared to that obtained with M. alcaliphilum 20ZDP (45.58 mg/L vs. 27.26 mg/L) without growth inhibition. Notably, a maximum titer of 142.32 mg/L was reached by the use of an optimized medium for ectoine production containing 6% NaCl and 0.05 μM of tungsten without hydroxyectoine production. This result demonstrates the highest ectoine production from methane to date. CONCLUSIONS: Ectoine production was significantly enhanced by the disruption of the ectD and ectR genes in M. alcaliphilum 20Z under optimized conditions favoring ectoine accumulation. We demonstrated effective genetic engineering in a methanotrophic bacterium, with enhanced production of ectoine from methane as the sole carbon source. This study suggests a potentially transformational path to commercial sugar-based ectoine production. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02104-2.
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spelling pubmed-87592812022-01-18 Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z Cho, Sukhyeong Lee, Yun Seo Chai, Hanyu Lim, Sang Eun Na, Jeong Geol Lee, Jinwon Biotechnol Biofuels Bioprod Research BACKGROUND: Ectoine (1,3,4,5-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) is an attractive compatible solute because of its wide industrial applications. Previous studies on the microbial production of ectoine have focused on sugar fermentation. Alternatively, methane can be used as an inexpensive and abundant resource for ectoine production by using the halophilic methanotroph, Methylomicrobium alcaliphilum 20Z. However, there are some limitations, including the low production of ectoine from methane and the limited tools for the genetic manipulation of methanotrophs to facilitate their use as industrial strains. RESULTS: We constructed M. alcaliphilum 20ZDP with a high conjugation efficiency and stability of the episomal plasmid by the removal of its native plasmid. To improve the ectoine production in M. alcaliphilum 20Z from methane, the ectD (encoding ectoine hydroxylase) and ectR (transcription repressor of the ectABC-ask operon) were deleted to reduce the formation of by-products (such as hydroxyectoine) and induce ectoine production. When the double mutant was batch cultured with methane, ectoine production was enhanced 1.6-fold compared to that obtained with M. alcaliphilum 20ZDP (45.58 mg/L vs. 27.26 mg/L) without growth inhibition. Notably, a maximum titer of 142.32 mg/L was reached by the use of an optimized medium for ectoine production containing 6% NaCl and 0.05 μM of tungsten without hydroxyectoine production. This result demonstrates the highest ectoine production from methane to date. CONCLUSIONS: Ectoine production was significantly enhanced by the disruption of the ectD and ectR genes in M. alcaliphilum 20Z under optimized conditions favoring ectoine accumulation. We demonstrated effective genetic engineering in a methanotrophic bacterium, with enhanced production of ectoine from methane as the sole carbon source. This study suggests a potentially transformational path to commercial sugar-based ectoine production. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02104-2. BioMed Central 2022-01-13 /pmc/articles/PMC8759281/ /pubmed/35418141 http://dx.doi.org/10.1186/s13068-022-02104-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cho, Sukhyeong
Lee, Yun Seo
Chai, Hanyu
Lim, Sang Eun
Na, Jeong Geol
Lee, Jinwon
Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
title Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
title_full Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
title_fullStr Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
title_full_unstemmed Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
title_short Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
title_sort enhanced production of ectoine from methane using metabolically engineered methylomicrobium alcaliphilum 20z
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759281/
https://www.ncbi.nlm.nih.gov/pubmed/35418141
http://dx.doi.org/10.1186/s13068-022-02104-2
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