Recombinant RimM production in B. licheniformis leverages advanced genetic tools:
Thermosensitive plasmid systems: pUB-MazF enables efficient plasmid curing via MazF endoribonuclease, facilitating stable chromosomal integration of rimM .
Promoter systems:
Case study: A B. licheniformis strain with multi-copy chromosomal integration of amyS (α-amylase gene) achieved 50 U/mL enzyme activity in bioreactors , suggesting similar strategies could amplify rimM expression.
RimM ensures proper 16S rRNA processing and 30S subunit assembly:
In Arabidopsis thaliana chloroplasts, RimM homologs coordinate with RsmD methyltransferase for rRNA methylation (e.g., m²G915) and translation fidelity .
B. licheniformis ribosome content varies with growth rate (12,500–92,000 ribosomes/cell) .
RimM deficiency disrupts ribosome assembly, impairing protein synthesis and stress adaptation .
Recombinant RimM can enhance B. licheniformis as an industrial enzyme producer:
Strain optimization: Overexpression of RimM may accelerate ribosome assembly, boosting yields of:
Probiotic engineering: RimM-assisted ribosome biogenesis could improve stress tolerance in probiotic strains like B. licheniformis NXU98 .
Structural studies: No B. licheniformis RimM structures are available; homology modeling using T. thermophilus data (PDB: 2D9X) is needed.
Metabolic burden: High RimM expression may require balancing with toxin-antitoxin systems (e.g., MazF/MazE) .
Antimycobacterial potential: RimM’s role in ribosome maturation could inform novel tuberculosis therapies via B. licheniformis-derived antimicrobials .
KEGG: bld:BLi01822
STRING: 279010.BLi01822