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A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion

BACKGROUND: Owing to increasing concerns about climate change and the depletion of fossil fuels, the development of efficient microbial processes for biochemical production from lignocellulosic biomass has been a key issue. Because process efficiency is greatly affected by the inherent metabolic act...

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Autores principales: Woo, Sunghwa, Lim, Hyun Gyu, Han, Yong Hee, Park, Sungwoo, Noh, Myung Hyun, Baek, Dongyeop, Moon, Jo Hyun, Seo, Sang Woo, Jung, Gyoo Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134653/
https://www.ncbi.nlm.nih.gov/pubmed/35614459
http://dx.doi.org/10.1186/s13068-022-02157-3
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author Woo, Sunghwa
Lim, Hyun Gyu
Han, Yong Hee
Park, Sungwoo
Noh, Myung Hyun
Baek, Dongyeop
Moon, Jo Hyun
Seo, Sang Woo
Jung, Gyoo Yeol
author_facet Woo, Sunghwa
Lim, Hyun Gyu
Han, Yong Hee
Park, Sungwoo
Noh, Myung Hyun
Baek, Dongyeop
Moon, Jo Hyun
Seo, Sang Woo
Jung, Gyoo Yeol
author_sort Woo, Sunghwa
collection PubMed
description BACKGROUND: Owing to increasing concerns about climate change and the depletion of fossil fuels, the development of efficient microbial processes for biochemical production from lignocellulosic biomass has been a key issue. Because process efficiency is greatly affected by the inherent metabolic activities of host microorganisms, it is essential to utilize a microorganism that can rapidly convert biomass-derived sugars. Here, we report a novel Vibrio-based microbial platform that can rapidly and simultaneously consume three major lignocellulosic sugars (i.e., glucose, xylose, and arabinose) faster than any previously reported microorganisms. RESULTS: The xylose isomerase pathway was constructed in Vibrio sp. dhg, which naturally displays high metabolic activities on glucose and arabinose but lacks xylose catabolism. Subsequent adaptive laboratory evolution significantly improved xylose catabolism of initial strain and led to unprecedently high growth and sugar uptake rate (0.67 h(−1) and 2.15 g g(dry cell weight)(−1) h(−1), respectively). Furthermore, we achieved co-consumption of the three sugars by deletion of PtsG and introduction of GalP. We validated its superior performance and applicability by demonstrating efficient lactate production with high productivity (1.15 g/L/h) and titer (83 g/L). CONCLUSIONS: In this study, we developed a Vibrio-based microbial platform with rapid and simultaneous utilization of the three major sugars from lignocellulosic biomass by applying an integrated approach of rational and evolutionary engineering. We believe that the developed strain can be broadly utilized to accelerate the production of diverse biochemicals from lignocellulosic biomass. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02157-3.
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spelling pubmed-91346532022-05-27 A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion Woo, Sunghwa Lim, Hyun Gyu Han, Yong Hee Park, Sungwoo Noh, Myung Hyun Baek, Dongyeop Moon, Jo Hyun Seo, Sang Woo Jung, Gyoo Yeol Biotechnol Biofuels Bioprod Research BACKGROUND: Owing to increasing concerns about climate change and the depletion of fossil fuels, the development of efficient microbial processes for biochemical production from lignocellulosic biomass has been a key issue. Because process efficiency is greatly affected by the inherent metabolic activities of host microorganisms, it is essential to utilize a microorganism that can rapidly convert biomass-derived sugars. Here, we report a novel Vibrio-based microbial platform that can rapidly and simultaneously consume three major lignocellulosic sugars (i.e., glucose, xylose, and arabinose) faster than any previously reported microorganisms. RESULTS: The xylose isomerase pathway was constructed in Vibrio sp. dhg, which naturally displays high metabolic activities on glucose and arabinose but lacks xylose catabolism. Subsequent adaptive laboratory evolution significantly improved xylose catabolism of initial strain and led to unprecedently high growth and sugar uptake rate (0.67 h(−1) and 2.15 g g(dry cell weight)(−1) h(−1), respectively). Furthermore, we achieved co-consumption of the three sugars by deletion of PtsG and introduction of GalP. We validated its superior performance and applicability by demonstrating efficient lactate production with high productivity (1.15 g/L/h) and titer (83 g/L). CONCLUSIONS: In this study, we developed a Vibrio-based microbial platform with rapid and simultaneous utilization of the three major sugars from lignocellulosic biomass by applying an integrated approach of rational and evolutionary engineering. We believe that the developed strain can be broadly utilized to accelerate the production of diverse biochemicals from lignocellulosic biomass. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02157-3. BioMed Central 2022-05-25 /pmc/articles/PMC9134653/ /pubmed/35614459 http://dx.doi.org/10.1186/s13068-022-02157-3 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
Woo, Sunghwa
Lim, Hyun Gyu
Han, Yong Hee
Park, Sungwoo
Noh, Myung Hyun
Baek, Dongyeop
Moon, Jo Hyun
Seo, Sang Woo
Jung, Gyoo Yeol
A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
title A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
title_full A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
title_fullStr A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
title_full_unstemmed A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
title_short A Vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
title_sort vibrio-based microbial platform for accelerated lignocellulosic sugar conversion
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134653/
https://www.ncbi.nlm.nih.gov/pubmed/35614459
http://dx.doi.org/10.1186/s13068-022-02157-3
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