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Harnessing the thermotolerant methylotroph Bacillus methanolicus for methanol-based synthetic L-proline production
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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.
Springer Science and Business Media LLC
Title: Harnessing the thermotolerant methylotroph Bacillus methanolicus for methanol-based synthetic L-proline production
Description:
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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