Extracellular methylation enzymes modify CpG sites on source DNA to produce controlled methylation levels and patterns.
Engineered polymerase variants control DNA strand movement speed to enable precise single-nucleotide resolution during sequencing.
A cell-free protein synthesis system using isolated plant plastid extracts enables rapid in vitro transcription and translation of genetic designs.
A Kup transporter with a glycine to valine substitution at position 344 increases L-lysine excretion from Corynebacterium glutamicum.
A transposon kit selects plasmid terminal repeats to introduce exogenous genes into host cells.