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Markerless mutagenesis enables isoleucine biosynthesis solely from threonine in Methanothermobacter marburgensis

Veröffentlichungen: Beitrag in FachzeitschriftArtikelPeer Reviewed

Abstract

UNLABELLED: The archaeal model microorganism Methanothermobacter marburgensis has been studied for methane production for decades. However, genetic modifications are required to harness M. marburgensis for the generation of novel archaeal cell factories for industrial-scale production of commodity and high-value chemicals. Only the development of tools for genetic engineering opens up this possibility. Here, we present the establishment of the first markerless mutagenesis system for genetic modification of M. marburgensis. This system allows the recycling of positive selection markers and enables multiple sequential gene deletions or integrations. As a demonstration, we clarified the postulated isoleucine biosynthesis pathway directly from pyruvate via citramalate synthase (CimA). In doing so, we identified a putative CimA in M. marburgensis and deleted the CimA coding gene, resulting in auxotrophy for isoleucine. The complementation of cimA initiated through constitutive expression led to prototrophic growth similar to the wild type, demonstrating that cimA is essential for pyruvate-derived isoleucine biosynthesis in M. marburgensis. As it has been shown vice versa in Escherichia coli before, we were able to complement isoleucine biosynthesis with the integration of a synthetic isoleucine biosynthesis pathway from threonine for the first time in a methanogenic archaeon. This was achieved via genome integration of the characterized thermostable threonine deaminase from Geobacillus stearothermophilus. The successful integration of an alternative pathway for isoleucine production paves the road for future application of multi-gene biosynthetic pathways to overproduce industrially relevant chemicals.

IMPORTANCE: The autotrophic, hydrogenotrophic methanogen Methanothermobacter marburgensis is one of the best-studied model organisms in the field of thermophilic archaea. The fact that M. marburgensis shows robust growth and scalability in bioreactor systems makes it a highly suitable candidate for industrial-scale bioprocesses. Additionally, the reported study provides the tools for genetic engineering that enable sequential genome modification in M. marburgensis. Scalable bioreactor cultivation, the ability to genetically engineer, and the recent discovery of natural amino acid secretion in M. marburgensis set the cornerstone for the generation of the first cell factories in archaeal biotechnology to economically produce carbon dioxide-derived commodity and high-value chemicals at industrial scale.


Open access data

Klein M., Hilts A.S., Fennessy R.T., Trattnig N., Stehrer-Polášek T., Rittmann S.K.-M.R., Fink C. (2025) Supplemental material to: Markerless mutagenesis enables isoleucine biosynthesis solely from threonine in Methanothermobacter marburgensis, https://doi.org/10.25365/phaidra.643

 

Klein M., Hilts A.S., Fennessy R.T., Trattnig N., Stehrer-Polášek T., Rittmann S.K.-M.R., Fink C. (2025) Raw data to: Markerless mutagenesis enables isoleucine biosynthesis solely from threonine in Methanothermobacter marburgensis, https://doi.org/10.25365/phaidra.644

OriginalspracheEnglisch
Aufsatznummere0306824
FachzeitschriftMicrobiology Spectrum
Jahrgang13
Ausgabenummer6
Frühes Online-Datum17 Apr. 2025
DOIs
PublikationsstatusVeröffentlicht - Juni 2025

Fördermittel

Research was partially funded by The COMET center ACIB: Next Generation Bioproduction, which is funded by BMK, BMAW, SFG, Standortagentur Tirol, and the Government of Lower Austria and Vienna Business Agency in the framework of COMET\u2014Competence Centers for Excellent Technologies. The COMET-Funding Program is managed by the Austrian Research Promotion Agency FFG. Research was also partially funded by FFG through Industrienahe Dissertationen to A.S.H. (FFG NASPA [FO999901140]). Thanks to Logan Hodgskiss for proofreading the manuscript. Open access funding provided by the University of Vienna. R.T.F., S.K.-M.R.R., and C.F. designed the experiments. M.K. and C.F. performed laboratory experimentation. A.S.H. generated the phylogenetic tree and the multisequence alignment. M.K., R.T.F., and C.F. analyzed the data. N.T. and T.S.-P. established the method for amino acid quantification and performed the analysis. A.S.H. and S.K.-M.R.R. acquired funding. S.K.-M.R.R. and C.F. supervised research. M.K. and C.F. wrote the manuscript. All authors edited the manuscript and approved the submission. Austrian Centre of Industrial Biotechnology Simon K.-M. R. Rittmann Christian Fink \u00D6sterreichische Forschungsf\u00F6rderungsgesell FO999901140 Angus S. Hilts schaft

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

ÖFOS 2012

  • 209006 Industrielle Biotechnologie

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