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Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum

Clostridium autoethanogenum and Clostridium ljungdahlii are physiologically and genetically very similar strict anaerobic acetogens capable of growth on carbon monoxide as sole carbon source. While exact nutritional requirements have not been reported, we observed that for growth, the addition of vi...

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Autores principales: Annan, Florence J., Al-Sinawi, Bakir, Humphreys, Christopher M., Norman, Rupert, Winzer, Klaus, Köpke, Michael, Simpson, Sean D., Minton, Nigel P., Henstra, Anne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505512/
https://www.ncbi.nlm.nih.gov/pubmed/30972463
http://dx.doi.org/10.1007/s00253-019-09763-6
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author Annan, Florence J.
Al-Sinawi, Bakir
Humphreys, Christopher M.
Norman, Rupert
Winzer, Klaus
Köpke, Michael
Simpson, Sean D.
Minton, Nigel P.
Henstra, Anne M.
author_facet Annan, Florence J.
Al-Sinawi, Bakir
Humphreys, Christopher M.
Norman, Rupert
Winzer, Klaus
Köpke, Michael
Simpson, Sean D.
Minton, Nigel P.
Henstra, Anne M.
author_sort Annan, Florence J.
collection PubMed
description Clostridium autoethanogenum and Clostridium ljungdahlii are physiologically and genetically very similar strict anaerobic acetogens capable of growth on carbon monoxide as sole carbon source. While exact nutritional requirements have not been reported, we observed that for growth, the addition of vitamins to media already containing yeast extract was required, an indication that these are fastidious microorganisms. Elimination of complex components and individual vitamins from the medium revealed that the only organic compounds required for growth were pantothenate, biotin and thiamine. Analysis of the genome sequences revealed that three genes were missing from pantothenate and thiamine biosynthetic pathways, and five genes were absent from the pathway for biotin biosynthesis. Prototrophy in C. autoethanogenum and C. ljungdahlii for pantothenate was obtained by the introduction of plasmids carrying the heterologous gene clusters panBCD from Clostridium acetobutylicum, and for thiamine by the introduction of the thiC-purF operon from Clostridium ragsdalei. Integration of panBCD into the chromosome through allele-coupled exchange also conveyed prototrophy. C. autoethanogenum was converted to biotin prototrophy with gene sets bioBDF and bioHCA from Desulfotomaculum nigrificans strain CO-1-SRB, on plasmid and integrated in the chromosome. The genes could be used as auxotrophic selection markers in recombinant DNA technology. Additionally, transformation with a subset of the genes for pantothenate biosynthesis extended selection options with the pantothenate precursors pantolactone and/or beta-alanine. Similarly, growth was obtained with the biotin precursor pimelate combined with genes bioYDA from C. acetobutylicum. The work raises questions whether alternative steps exist in biotin and thiamine biosynthesis pathways in these acetogens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00253-019-09763-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-65055122019-05-28 Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum Annan, Florence J. Al-Sinawi, Bakir Humphreys, Christopher M. Norman, Rupert Winzer, Klaus Köpke, Michael Simpson, Sean D. Minton, Nigel P. Henstra, Anne M. Appl Microbiol Biotechnol Bioenergy and Biofuels Clostridium autoethanogenum and Clostridium ljungdahlii are physiologically and genetically very similar strict anaerobic acetogens capable of growth on carbon monoxide as sole carbon source. While exact nutritional requirements have not been reported, we observed that for growth, the addition of vitamins to media already containing yeast extract was required, an indication that these are fastidious microorganisms. Elimination of complex components and individual vitamins from the medium revealed that the only organic compounds required for growth were pantothenate, biotin and thiamine. Analysis of the genome sequences revealed that three genes were missing from pantothenate and thiamine biosynthetic pathways, and five genes were absent from the pathway for biotin biosynthesis. Prototrophy in C. autoethanogenum and C. ljungdahlii for pantothenate was obtained by the introduction of plasmids carrying the heterologous gene clusters panBCD from Clostridium acetobutylicum, and for thiamine by the introduction of the thiC-purF operon from Clostridium ragsdalei. Integration of panBCD into the chromosome through allele-coupled exchange also conveyed prototrophy. C. autoethanogenum was converted to biotin prototrophy with gene sets bioBDF and bioHCA from Desulfotomaculum nigrificans strain CO-1-SRB, on plasmid and integrated in the chromosome. The genes could be used as auxotrophic selection markers in recombinant DNA technology. Additionally, transformation with a subset of the genes for pantothenate biosynthesis extended selection options with the pantothenate precursors pantolactone and/or beta-alanine. Similarly, growth was obtained with the biotin precursor pimelate combined with genes bioYDA from C. acetobutylicum. The work raises questions whether alternative steps exist in biotin and thiamine biosynthesis pathways in these acetogens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00253-019-09763-6) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-04-10 2019 /pmc/articles/PMC6505512/ /pubmed/30972463 http://dx.doi.org/10.1007/s00253-019-09763-6 Text en © The Author(s) 2019 Open Access This 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.
spellingShingle Bioenergy and Biofuels
Annan, Florence J.
Al-Sinawi, Bakir
Humphreys, Christopher M.
Norman, Rupert
Winzer, Klaus
Köpke, Michael
Simpson, Sean D.
Minton, Nigel P.
Henstra, Anne M.
Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum
title Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum
title_full Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum
title_fullStr Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum
title_full_unstemmed Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum
title_short Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum
title_sort engineering of vitamin prototrophy in clostridium ljungdahlii and clostridium autoethanogenum
topic Bioenergy and Biofuels
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505512/
https://www.ncbi.nlm.nih.gov/pubmed/30972463
http://dx.doi.org/10.1007/s00253-019-09763-6
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