Evading native restriction-modification systems improves electroporation efficiency of the methanotroph Methylococcus capsulatus Bath

Methylococcus capsulatus Bath is a unique methanotrophic bacterium that uses methane (CH₄) as a carbon and energy source and encodes the RubisCO enzyme for inorganic carbon assimilation, positioning it as an excellent candidate for biotechnology to capture atmospheric CH₄ and carbon dioxide (CO₂) for chemical production. However, a limited genetic toolbox and minimal high-throughput methodologies for genetic engineering hinder the development of efficient M. capsulatus biocatalysts. In this work, we developed and optimized an electroporation workflow to transfer circular and linear DNA fragments into M. capsulatus with high efficiency by evading the host restriction-modification (RM) systems that recognize and degrade foreign DNA. To achieve this, we determined the M. capsulatus methylome to identify RM system methyltransferases and express them in Escherichia coli, resulting in DNA methylation in E. coli that mirrors that of M. capsulatus, which improved methanotroph electroporation efficiency. Iterative site-directed mutagenesis of plasmid methylation sites identified a m⁶A motif necessary for the increase in electroporation efficiency. An M. capsulatus knock-out strain with a disrupted Type I RM system linked to the m⁶A motif showed improved transformation efficiency compared to wild type, underscoring the importance of proper m⁶A methylation in successful DNA transfer to M. capsulatus. Notably, plasmid methylation coupled to an optimized electroporation workflow enabled the facile generation of an M. capsulatus genome-wide CRISPR interference library for functional genomic screening. Collectively, our results identify an RM system that has, up to now, limited M. capsulatus transformation and establish a methodology to bypass the RM system and improve transformation efficiency, which will accelerate the development of engineered methanotrophs for CH₄ bioconversion technologies.