Engineering of vitamin prototrophy in Clostridium ljungdahlii and Clostridium autoethanogenum.


Journal

Applied microbiology and biotechnology
ISSN: 1432-0614
Titre abrégé: Appl Microbiol Biotechnol
Pays: Germany
ID NLM: 8406612

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 26 09 2018
accepted: 12 03 2019
revised: 19 02 2019
pubmed: 12 4 2019
medline: 15 8 2019
entrez: 12 4 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30972463
doi: 10.1007/s00253-019-09763-6
pii: 10.1007/s00253-019-09763-6
pmc: PMC6505512
doi:

Substances chimiques

Culture Media 0
Recombinant Proteins 0
Vitamins 0

Types de publication

Journal Article

Langues

eng

Pagination

4633-4648

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/L502030/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/K00283X/1
Pays : United Kingdom

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Auteurs

Florence J Annan (FJ)

BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK.

Bakir Al-Sinawi (B)

University of New-South Wales (UNSW) Sydney, Kensington, Australia.

Christopher M Humphreys (CM)

BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK.

Rupert Norman (R)

BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK.

Klaus Winzer (K)

BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK.

Michael Köpke (M)

LanzaTech Inc., 8045 Lamon Avenue, Suite 400, Skokie, IL, USA.

Sean D Simpson (SD)

LanzaTech Inc., 8045 Lamon Avenue, Suite 400, Skokie, IL, USA.

Nigel P Minton (NP)

BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK.

Anne M Henstra (AM)

BBSRC/EPSRC Synthetic Biology Research Centre, School of Life Sciences, University of Nottingham, Nottingham, NG7 2RD, UK. anne.henstra@nottingham.ac.uk.

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Classifications MeSH