Development of a genome-targeting mutator for the adaptive evolution of microbial cells.
Ga-Eul EomHyunbin LeeSeokhee KimPublished in: Nucleic acids research (2022)
Methods that can randomly introduce mutations in the microbial genome have been used for classical genetic screening and, more recently, the evolutionary engineering of microbial cells. However, most methods rely on either cell-damaging agents or disruptive mutations of genes that are involved in accurate DNA replication, of which the latter requires prior knowledge of gene functions, and thus, is not easily transferable to other species. In this study, we developed a new mutator for in vivo mutagenesis that can directly modify the genomic DNA. Mutator protein, MutaEco, in which a DNA-modifying enzyme is fused to the α-subunit of Escherichia coli RNA polymerase, increases the mutation rate without compromising the cell viability and accelerates the adaptive evolution of E. coli for stress tolerance and utilization of unconventional carbon sources. This fusion strategy is expected to accommodate diverse DNA-modifying enzymes and may be easily adapted to various bacterial species.
Keyphrases
- genome wide
- escherichia coli
- induced apoptosis
- microbial community
- copy number
- cell cycle arrest
- circulating tumor
- dna methylation
- single molecule
- endoplasmic reticulum stress
- stem cells
- cancer therapy
- drinking water
- crispr cas
- oxidative stress
- signaling pathway
- cystic fibrosis
- cell therapy
- genome wide identification
- cell proliferation
- biofilm formation
- pseudomonas aeruginosa
- multidrug resistant
- transcription factor
- protein protein