DpnI recognizes methylated GATC sites and can remove the methylated parental plasmid after amplification of an unmethylated mutant product. Thus B. This selective template digestion is why DpnI appears in the mutagenesis workflow rather than an ordinary sequence-cutting enzyme without this methylation requirement.
More Molecular tools: Site-directed mutagenesis, CRISPR-Cas, biosensors, interaction tools, genomics and proteomics approaches questions
GATE 2026 BT Q26– Which component of the CRISPR/Cas9 gene editing system is NOT of natural origin?