Formate from <scp>THF</scp> ‐ <scp>C1</scp> metabolism induces the <i>AOX1</i> promoter in formate dehydrogenase‐deficient <i>Komagataella phaffii</i>

In Komagataella phaffii (Pichia pastoris), formate is a recognized alternative inducer to methanol for expression systems based on the AOX1 promoter (pAOX1). By disrupting the formate dehydrogenase encoding FDH1 gene, we converted such a system into a self-induced one, as adding any inducer in the culture medium is no longer requested for pAOX1 induction. In cells, formate is generated from serine through the THF-C1 metabolism, and it cannot be converted into carbon dioxide in a FdhKO strain. Under non-repressive culture conditions, such as on sorbitol, the intracellular formate generated from the THF-C1 metabolism is sufficient to induce pAOX1 and initiate protein synthesis. This was evidenced for two model proteins, namely intracellular eGFP and secreted CalB lipase from C. antarctica. Similar protein productivities were obtained for a FdhKO strain on sorbitol and a non-disrupted strain on sorbitol-methanol. Considering a K. Phaffii FdhKO strain as a workhorse for recombinant protein synthesis paves the way for the further development of methanol-free processes in K. phaffii.

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Publication Details

Journal
Microbial Biotechnology
Published
2024-10-01
DOI
https://doi.org/10.1111/1751-7915.70022
Citations
5
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
1.17

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article

Formate from THF ‐ C1 metabolism induces the AOX1 promoter in formate dehydrogenase‐deficient Komagataella phaffii

Patrick Fickers, Julio Berríos, Cristina Bustos
5 citations
Microbial Biotechnology
Microbial Metabolic Engineering and Bioproduction
1.17
article

Formate from THF ‐ C1 metabolism induces the AOX1 promoter in formate dehydrogenase‐deficient Komagataella phaffii

Patrick Fickers, Julio Berríos, Cristina Bustos
article en
5 citations

Abstract

In Komagataella phaffii (Pichia pastoris), formate is a recognized alternative inducer to methanol for expression systems based on the AOX1 promoter (pAOX1). By disrupting the formate dehydrogenase encoding FDH1 gene, we converted such a system into a self-induced one, as adding any inducer in the culture medium is no longer requested for pAOX1 induction. In cells, formate is generated from serine through the THF-C1 metabolism, and it cannot be converted into carbon dioxide in a FdhKO strain. Under non-repressive culture conditions, such as on sorbitol, the intracellular formate generated from the THF-C1 metabolism is sufficient to induce pAOX1 and initiate protein synthesis. This was evidenced for two model proteins, namely intracellular eGFP and secreted CalB lipase from C. antarctica. Similar protein productivities were obtained for a FdhKO strain on sorbitol and a non-disrupted strain on sorbitol-methanol. Considering a K. Phaffii FdhKO strain as a workhorse for recombinant protein synthesis paves the way for the further development of methanol-free processes in K. phaffii.

Microbial BiotechnologyVol. 17(10)
Pontificia Universidad Católica de Valparaíso (CL), University of Liège (BE), Gembloux Agro-Bio Tech (BE)
Universidad Técnica Federico Santa María, Pontificia Universidad Católica de Valparaíso, Wallonie-Bruxelles International, Agencia Nacional de Investigación y Desarrollo, Fondo Nacional de Desarrollo Científico y Tecnológico
Openalex Percentile: Top 22%
Microbial Metabolic Engineering and Bioproduction
1.17
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