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Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose

BACKGROUND: 5-Ketofructose (5-KF) has recently been identified as a promising non-nutritive natural sweetener. Gluconobacter oxydans strains have been developed that allow efficient production of 5-KF from fructose by plasmid-based expression of the fructose dehydrogenase genes fdhSCL of Gluconobact...

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Autores principales: Battling, Svenja, Wohlers, Karen, Igwe, Chika, Kranz, Angela, Pesch, Matthias, Wirtz, Astrid, Baumgart, Meike, Büchs, Jochen, Bott, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055074/
https://www.ncbi.nlm.nih.gov/pubmed/32131833
http://dx.doi.org/10.1186/s12934-020-01310-7
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author Battling, Svenja
Wohlers, Karen
Igwe, Chika
Kranz, Angela
Pesch, Matthias
Wirtz, Astrid
Baumgart, Meike
Büchs, Jochen
Bott, Michael
author_facet Battling, Svenja
Wohlers, Karen
Igwe, Chika
Kranz, Angela
Pesch, Matthias
Wirtz, Astrid
Baumgart, Meike
Büchs, Jochen
Bott, Michael
author_sort Battling, Svenja
collection PubMed
description BACKGROUND: 5-Ketofructose (5-KF) has recently been identified as a promising non-nutritive natural sweetener. Gluconobacter oxydans strains have been developed that allow efficient production of 5-KF from fructose by plasmid-based expression of the fructose dehydrogenase genes fdhSCL of Gluconobacter japonicus. As plasmid-free strains are preferred for industrial production of food additives, we aimed at the construction of efficient 5-KF production strains with the fdhSCL genes chromosomally integrated. RESULTS: For plasmid-free 5-KF production, we selected four sites in the genome of G. oxydans IK003.1 and inserted the fdhSCL genes under control of the strong P264 promoter into each of these sites. All four recombinant strains expressed fdhSCL and oxidized fructose to 5-KF, but site-specific differences were observed suggesting that the genomic vicinity influenced gene expression. For further improvement, a second copy of the fdhSCL genes under control of P264 was inserted into the second-best insertion site to obtain strain IK003.1::fdhSCL(2). The 5-KF production rate and the 5-KF yield obtained with this double-integration strain were considerably higher than for the single integration strains and approached the values of IK003.1 with plasmid-based fdhSCL expression. CONCLUSION: We identified four sites in the genome of G. oxydans suitable for expression of heterologous genes and constructed a strain with two genomic copies of the fdhSCL genes enabling efficient plasmid-free 5-KF production. This strain will serve as basis for further metabolic engineering strategies aiming at the use of alternative carbon sources for 5-KF production and for bioprocess optimization.
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spelling pubmed-70550742020-03-10 Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose Battling, Svenja Wohlers, Karen Igwe, Chika Kranz, Angela Pesch, Matthias Wirtz, Astrid Baumgart, Meike Büchs, Jochen Bott, Michael Microb Cell Fact Research BACKGROUND: 5-Ketofructose (5-KF) has recently been identified as a promising non-nutritive natural sweetener. Gluconobacter oxydans strains have been developed that allow efficient production of 5-KF from fructose by plasmid-based expression of the fructose dehydrogenase genes fdhSCL of Gluconobacter japonicus. As plasmid-free strains are preferred for industrial production of food additives, we aimed at the construction of efficient 5-KF production strains with the fdhSCL genes chromosomally integrated. RESULTS: For plasmid-free 5-KF production, we selected four sites in the genome of G. oxydans IK003.1 and inserted the fdhSCL genes under control of the strong P264 promoter into each of these sites. All four recombinant strains expressed fdhSCL and oxidized fructose to 5-KF, but site-specific differences were observed suggesting that the genomic vicinity influenced gene expression. For further improvement, a second copy of the fdhSCL genes under control of P264 was inserted into the second-best insertion site to obtain strain IK003.1::fdhSCL(2). The 5-KF production rate and the 5-KF yield obtained with this double-integration strain were considerably higher than for the single integration strains and approached the values of IK003.1 with plasmid-based fdhSCL expression. CONCLUSION: We identified four sites in the genome of G. oxydans suitable for expression of heterologous genes and constructed a strain with two genomic copies of the fdhSCL genes enabling efficient plasmid-free 5-KF production. This strain will serve as basis for further metabolic engineering strategies aiming at the use of alternative carbon sources for 5-KF production and for bioprocess optimization. BioMed Central 2020-03-04 /pmc/articles/PMC7055074/ /pubmed/32131833 http://dx.doi.org/10.1186/s12934-020-01310-7 Text en © The Author(s) 2020 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/. 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 in a credit line to the data.
spellingShingle Research
Battling, Svenja
Wohlers, Karen
Igwe, Chika
Kranz, Angela
Pesch, Matthias
Wirtz, Astrid
Baumgart, Meike
Büchs, Jochen
Bott, Michael
Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
title Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
title_full Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
title_fullStr Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
title_full_unstemmed Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
title_short Novel plasmid-free Gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
title_sort novel plasmid-free gluconobacter oxydans strains for production of the natural sweetener 5-ketofructose
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055074/
https://www.ncbi.nlm.nih.gov/pubmed/32131833
http://dx.doi.org/10.1186/s12934-020-01310-7
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