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Abstract
Base editing technologies enable the direct conversion of nucleotide bases, independent of DNA double-strand breaks.
- Base editors utilize deaminases attached to programmable DNA- or RNA-binding scaffolds for editing.
- Deaminase-free editing strategies are emerging as viable alternatives to traditional methods.
- These technologies facilitate continuous genome evolution and phenotypic diversification in microorganisms.
- Applications include sculpting microbial genomes, redirecting metabolic pathways, and improving stress tolerance.
- Recent advances in in situ bacterial base editing highlight its potential for enhancing industrial strains.
- Current limitations of base editing tools are identified, with proposed strategies for improving their effectiveness.
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