CRISPR/Cas-mediated pinpoint microbial base editing.
Edited length | Efficiency (%) | Cas system | Donor DNA | Organism | Target gene | Description | Reference |
---|---|---|---|---|---|---|---|
Single base | 99.7 | FnCpf1 | Oligo | Target-mismatched crRNA | [98] | ||
95 | SpCas9 | Oligo | Target-mismatched sgRNAs | [97] | |||
83 | SpCas9 | Oligo | 5’-truncated sgRNAs | [99] | |||
68 | SpdCas9-CBE | - | Curing of the plasmid using |
[101] | |||
65 | SpCas9 | Oligo | Single base substitution for streptomycin resistance acquisition | [42] | |||
30 | SpCas9 | Plasmid | Two-step single nucleotide modification using artificial PAM or two-step indel | [60] | |||
Double bases | 100 | SpCas9 | dsOligo | Short-homology-mediated genome editing | [102] | ||
100 | SpCas9 | Oligo | RecT-aided ssDNA recombineering | [58] | |||
100 | AsCpf1 | Oligo | Comparison of 7 different Cas system | [103] | |||
100 | FnCpf1 | Oligo, PCR products | RecT-aided ssDNA recombineering | [63] | |||
100 | FnCpf1 | Oligo | Plasmid curing system using its native plasmid | [104] | |||
90 | BbCpf1 | Oligo | Comparison of 7 different Cas system | [103] | |||
87.5 | FnCpf1 | Plasmid | λ-red aided two-plasmid system | [56] | |||
76 | FnCpf1 | Oligo | Using X-Gal for blue-white colony screening | [55] | |||
60 | FnCpf1 | Oligo | λ-red aided ssDNA recombineering | [55] | |||
60 | TsCpf1 | Oligo | Comparison of 7 different Cas system | [103] | |||
Triple bases | 100 | SpCas9 | Plasmid | Substitution of PAM sequence | [53] | ||
100 | SpCas9 | Oligo | Amino acid change and creating BtgZⅠ site | [42] | |||
94 ~ 99 | SpCas9 | Oligo, PCR products | λ-red aided ssDNA recombineering | [57] | |||
70 ~ 86.7 | SpCas9 | Oligo | Editing of streptomycin resistance phenotype or integrated fluorescence gene | [51] | |||
71 | SpCas9 | Oligo | Overexpression of Dam to interfere MMR | [105] | |||
Quadruple bases | 47 | FnCpf1 | Oligo | Site-directed mutagenesis using a random mutagenic oligo | [106] | ||
17 | Synthetic Cas9 | PCR products | Introduction of point mutations using two-step PCR with three DNA fragments | [107] |