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Linking genotype and phenotype in an economically viable propionic acid biosynthesis process

BACKGROUND: Propionic acid (PA) is used as a food preservative and increasingly, as a precursor for the synthesis of monomers. PA is produced mainly through hydrocarboxylation of ethylene, also known as the ‘oxo-process’; however, Propionibacterium species are promising biological PA producers nativ...

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Autores principales: Luna-Flores, Carlos H., Stowers, Chris C., Cox, Brad M., Nielsen, Lars K., Marcellin, Esteban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090647/
https://www.ncbi.nlm.nih.gov/pubmed/30123322
http://dx.doi.org/10.1186/s13068-018-1222-9
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author Luna-Flores, Carlos H.
Stowers, Chris C.
Cox, Brad M.
Nielsen, Lars K.
Marcellin, Esteban
author_facet Luna-Flores, Carlos H.
Stowers, Chris C.
Cox, Brad M.
Nielsen, Lars K.
Marcellin, Esteban
author_sort Luna-Flores, Carlos H.
collection PubMed
description BACKGROUND: Propionic acid (PA) is used as a food preservative and increasingly, as a precursor for the synthesis of monomers. PA is produced mainly through hydrocarboxylation of ethylene, also known as the ‘oxo-process’; however, Propionibacterium species are promising biological PA producers natively producing PA as their main fermentation product. However, for fermentation to be competitive, a PA yield of at least 0.6 g/g is required. RESULTS: A new strain able to reach the required yield was obtained using genome shuffling. To gain insight into the changes leading to the improved phenotype, the genome of the new strain was sequenced, and metabolomics and transcriptomics data were obtained. In combination, the data revealed three key mutations: (i) a mutation in the promoter region of a sugar transporter which enables an increase in the uptake rate of sucrose; (ii) a mutation in a polar amino acid transporter which improves consumption of amino acids and acid tolerance; and (iii) a mutation in a gene annotated as a cytochrome C biogenesis gene, which is likely responsible for the coupling of the Wood–Werkman cycle to ATP production were responsible for the phenotype. The bioprocess was further enhanced with a feeding strategy that achieved 70 g/L of product. The proposed bioprocess is expected to outperform the economics of the current ‘oxo-process’ by 2020. CONCLUSIONS: In this study, using genome shuffling, we obtained a strain capable of producing PA exceeding the commercial needs. The multiomics comparison between the novel strain and the wild type revealed overexpression of amino acid pathways, changes in sucrose transporters and an increased activity in the methylglyoxal and the glucuronate interconversion pathways. The analysis also suggests that a mutation in the cytochrome C biogenesis gene, coupled with ATP production through the Wood–Werkman cycle, may be responsible for the increased PA production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1222-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-60906472018-08-17 Linking genotype and phenotype in an economically viable propionic acid biosynthesis process Luna-Flores, Carlos H. Stowers, Chris C. Cox, Brad M. Nielsen, Lars K. Marcellin, Esteban Biotechnol Biofuels Research BACKGROUND: Propionic acid (PA) is used as a food preservative and increasingly, as a precursor for the synthesis of monomers. PA is produced mainly through hydrocarboxylation of ethylene, also known as the ‘oxo-process’; however, Propionibacterium species are promising biological PA producers natively producing PA as their main fermentation product. However, for fermentation to be competitive, a PA yield of at least 0.6 g/g is required. RESULTS: A new strain able to reach the required yield was obtained using genome shuffling. To gain insight into the changes leading to the improved phenotype, the genome of the new strain was sequenced, and metabolomics and transcriptomics data were obtained. In combination, the data revealed three key mutations: (i) a mutation in the promoter region of a sugar transporter which enables an increase in the uptake rate of sucrose; (ii) a mutation in a polar amino acid transporter which improves consumption of amino acids and acid tolerance; and (iii) a mutation in a gene annotated as a cytochrome C biogenesis gene, which is likely responsible for the coupling of the Wood–Werkman cycle to ATP production were responsible for the phenotype. The bioprocess was further enhanced with a feeding strategy that achieved 70 g/L of product. The proposed bioprocess is expected to outperform the economics of the current ‘oxo-process’ by 2020. CONCLUSIONS: In this study, using genome shuffling, we obtained a strain capable of producing PA exceeding the commercial needs. The multiomics comparison between the novel strain and the wild type revealed overexpression of amino acid pathways, changes in sucrose transporters and an increased activity in the methylglyoxal and the glucuronate interconversion pathways. The analysis also suggests that a mutation in the cytochrome C biogenesis gene, coupled with ATP production through the Wood–Werkman cycle, may be responsible for the increased PA production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1222-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-13 /pmc/articles/PMC6090647/ /pubmed/30123322 http://dx.doi.org/10.1186/s13068-018-1222-9 Text en © The Author(s) 2018 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
Luna-Flores, Carlos H.
Stowers, Chris C.
Cox, Brad M.
Nielsen, Lars K.
Marcellin, Esteban
Linking genotype and phenotype in an economically viable propionic acid biosynthesis process
title Linking genotype and phenotype in an economically viable propionic acid biosynthesis process
title_full Linking genotype and phenotype in an economically viable propionic acid biosynthesis process
title_fullStr Linking genotype and phenotype in an economically viable propionic acid biosynthesis process
title_full_unstemmed Linking genotype and phenotype in an economically viable propionic acid biosynthesis process
title_short Linking genotype and phenotype in an economically viable propionic acid biosynthesis process
title_sort linking genotype and phenotype in an economically viable propionic acid biosynthesis process
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090647/
https://www.ncbi.nlm.nih.gov/pubmed/30123322
http://dx.doi.org/10.1186/s13068-018-1222-9
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