Harnessing the thermotolerant methylotroph Bacillus methanolicus for methanol-based synthetic L-proline production

Abstract Background Bacillus methanolicus MGA3 is a thermotolerant methylotroph that utilizes methanol, a renewable C₁ substrate, as its sole carbon and energy source. The strain naturally overproduces and secretes L-glutamate, making it a promising platform for engineering pathways toward L-glutamate-derived amino acids such as L-proline, which has applications in nutrition, stress protection, and industry. Results Heterologous expression of an osmotic stress–responsive L-proline biosynthetic operon from the mesophile Bacillus licheniformis in the thermotolerant B. methanolicus strain MGA3 did not increase L-proline levels but instead led to accumulation of L-citrulline. This was likely due to heat sensitivity of pyrroline-5-carboxylate reductase (ProH), the last enzyme of the osmoregulatory L-proline biosynthetic route, and metabolic crosstalk between L-proline and L-arginine pathways operating in Bacilli. To overcome these limitations, a synthetic operon containing the native anabolic proBA and proI L-proline biosynthetic genes from B. methanolicus MGA3 was engineered to remove transcriptional T-box regulation and biochemical feedback inhibition of ProB enzyme activity. Expression of this engineered operon enhanced L-proline synthesis and triggered its secretion during methanol-based growth of B. methanolicus MGA3 at 50° C. In fed-batch fermentation with methanol as carbon and energy source, extracellular L-proline levels reached 262 ± 20 mg L⁻ 1 after 40 h. During the fermentation process, a stepwise increase in medium osmolarity was observed, likely due to large-scale L-glutamate excretion, which impaired cellular growth. Conclusions This study links osmolarity dynamics to methanol-based fermentation in B. methanolicus MGA3 and demonstrates its potential as a cell factory for L-proline and L-citrulline production. These findings support further strain optimization for producing value-added amino acids and highlight the relevance of methylotrophic thermophiles in sustainable biotechnology.

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Journal
Microbial Cell Factories
Published
2026-05-23
DOI
https://doi.org/10.1186/s12934-026-03032-8
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
0.00

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article

Harnessing the thermotolerant methylotroph Bacillus methanolicus for methanol-based synthetic L-proline production

Christine Frank, Erhard Bremer, Tamara Hoffmann, David Virant et al.
Microbial Cell Factories
Microbial Metabolic Engineering and Bioproduction
article

Harnessing the thermotolerant methylotroph Bacillus methanolicus for methanol-based synthetic L-proline production

Christine Frank, Erhard Bremer, Tamara Hoffmann, David Virant, Gregor Kosec, Max F. Felle, Oskar Zelder
article en

Abstract

Abstract Background Bacillus methanolicus MGA3 is a thermotolerant methylotroph that utilizes methanol, a renewable C₁ substrate, as its sole carbon and energy source. The strain naturally overproduces and secretes L-glutamate, making it a promising platform for engineering pathways toward L-glutamate-derived amino acids such as L-proline, which has applications in nutrition, stress protection, and industry. Results Heterologous expression of an osmotic stress–responsive L-proline biosynthetic operon from the mesophile Bacillus licheniformis in the thermotolerant B. methanolicus strain MGA3 did not increase L-proline levels but instead led to accumulation of L-citrulline. This was likely due to heat sensitivity of pyrroline-5-carboxylate reductase (ProH), the last enzyme of the osmoregulatory L-proline biosynthetic route, and metabolic crosstalk between L-proline and L-arginine pathways operating in Bacilli. To overcome these limitations, a synthetic operon containing the native anabolic proBA and proI L-proline biosynthetic genes from B. methanolicus MGA3 was engineered to remove transcriptional T-box regulation and biochemical feedback inhibition of ProB enzyme activity. Expression of this engineered operon enhanced L-proline synthesis and triggered its secretion during methanol-based growth of B. methanolicus MGA3 at 50° C. In fed-batch fermentation with methanol as carbon and energy source, extracellular L-proline levels reached 262 ± 20 mg L⁻ 1 after 40 h. During the fermentation process, a stepwise increase in medium osmolarity was observed, likely due to large-scale L-glutamate excretion, which impaired cellular growth. Conclusions This study links osmolarity dynamics to methanol-based fermentation in B. methanolicus MGA3 and demonstrates its potential as a cell factory for L-proline and L-citrulline production. These findings support further strain optimization for producing value-added amino acids and highlight the relevance of methylotrophic thermophiles in sustainable biotechnology.

Microbial Cell FactoriesVol. 25(1)
Philipps University of Marburg (DE), BASF (Germany) (DE), Acies Bio (Slovenia) (SI), Loewe Center for Synthetic Microbiology (DE)
Philipps-Universität Marburg
Openalex Percentile: Top 8%
Microbial Metabolic Engineering and Bioproduction
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